Professor Peter Schofield
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Publications related to this Person
Book Chapters
Brooks WS; Loy CT; Kwok JBJ; Schofield PR, 2012, 'Genetics of dementia', in Cognitive Neurology: A Clinical Textbook, http://dx.doi.org/10.1093/acprof:oso/9780198569275.003.0016
Brooks WS; Loy CT; Kwok JB; Schofield PR, 2008, 'Genetics of Dementia', in Gendelman HE (ed.), Cognitive Neurology: a clinical textbook, Oxford University Press, Oxford, pp. 321 - 345, http://dx.doi.org/10.1016/S0140-6736(13)60630-3
Karlstrom H; Brooks WS; Kwok JB; Kril J; Halliday GM; Schofield PR, 2005, 'Variable phenotype of Alzheimer's Disease with spastic paraparesis', in Cummings J; Hardy J; Poncet M ; Christen Y (ed.), Genotype-Proteotype-Phenotype Relationships in Neurodegenerative Diseases, edn. 1, Springer-Verlag, Heidelberg, Germany, pp. 73 - 92
Dennis JA; Windsor PA; Schofield PR; Healy PJ, 2005, 'Bovine hyperekplexia', in LeDoux M (ed.), Animal Models of Movement Disorders, Elsevier, Amsterdam, pp. 479 - 486, http://dx.doi.org/10.1016/B978-012088382-0/50044-X
Kwok JB; Li Q; Hallupp M; Milward L; Whyte S; Schofield PR, 1999, 'Novel familial early-onset Alzheimer`s disease mutation (Leu723Pro) in amyloid precursor protein (APP) gene increases production of 42(43) amino acid isoform of amyloid beta peptide', in Iqbal K; Swaab DF; Winblad B; Wisniewski HM (ed.), Alzheimer`s Disease and Related Disorders, John Wiley & Sons, Sussex England, pp. 69 - 79, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000080188100010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Schofield PR, 1997, 'Cellular expression of cloned and mutated ion channels', in Neuroscience Methods: a guide for advanced students, edn. Original, Harwood Academic Publishers, Sydney, pp. 187 - 191
Rajendra S; Lynch JW; Schofield PR, 1997, 'The glycine receptor', in Pharmacology and Therapeutics, edn. 2, Pergamon-Elsevier Science Ltd, Kidlington, Oxford, England, pp. 121 - 146, http://dx.doi.org/10.1016/S0163-7258(96)00163-5
Journal articles
Franzmeier N; Ren J; Damm A; Monté-Rubio G; Boada M; Ruiz A; Ramirez A; Jessen F; Düzel E; Rodríguez Gómez O; Benzinger T; Goate A; Karch CM; Fagan AM; McDade E; Buerger K; Levin J; Duering M; Dichgans M; Suárez-Calvet M; Haass C; Gordon BA; Lim YY; Masters CL; Janowitz D; Catak C; Wolfsgruber S; Wagner M; Milz E; Moreno-Grau S; Teipel S; Grothe MJ; Kilimann I; Rossor M; Fox N; Laske C; Chhatwal J; Falkai P; Perneczky R; Lee JH; Spottke A; Boecker H; Brosseron F; Fliessbach K; Heneka MT; Nestor P; Peters O; Fuentes M; Menne F; Priller J; Spruth EJ; Franke C; Schneider A; Westerteicher C; Speck O; Wiltfang J; Bartels C; Araque Caballero MÁ; Metzger C; Bittner D; Salloway S; Danek A; Hassenstab J; Yakushev I; Schofield PR; Morris JC; Bateman RJ; Ewers M, 2021, 'The BDNF
Joseph-Mathurin N; Wang G; Kantarci K; Jack CR; McDade E; Hassenstab J; Blazey TM; Gordon BA; Su Y; Chen G; Massoumzadeh P; Hornbeck RC; Allegri RF; Ances BM; Berman SB; Brickman AM; Brooks WS; Cash DM; Chhatwal JP; Chui HC; Correia S; Cruchaga C; Farlow MR; Fox NC; Fulham M; Ghetti B; Graff-Radford NR; Johnson KA; Karch CM; Laske C; Lee AKW; Levin J; Masters CL; Noble JM; O'Connor A; Perrin RJ; Preboske GM; Ringman JM; Rowe CC; Salloway S; Saykin AJ; Schofield PR; Shimada H; Shoji M; Suzuki K; Villemagne VL; Xiong C; Yakushev I; Morris JC; Bateman RJ; Benzinger TLS; Dominantly Inherited Alzheimer Network , 2021, 'Longitudinal Accumulation of Cerebral Microhemorrhages in Dominantly Inherited Alzheimer Disease.', Neurology, http://dx.doi.org/10.1212/WNL.0000000000011542
Patel Y; Parker N; Shin J; Howard D; French L; Thomopoulos SI; Pozzi E; Abe Y; Abé C; Anticevic A; Alda M; Aleman A; Alloza C; Alonso-Lana S; Ameis SH; Anagnostou E; McIntosh AA; Arango C; Arnold PD; Asherson P; Assogna F; Auzias G; Ayesa-Arriola R; Bakker G; Banaj N; Banaschewski T; Bandeira CE; Baranov A; Bargalló N; Bau CHD; Baumeister S; Baune BT; Bellgrove MA; Benedetti F; Bertolino A; Boedhoe PSW; Boks M; Bollettini I; Del Mar Bonnin C; Borgers T; Borgwardt S; Brandeis D; Brennan BP; Bruggemann JM; Bülow R; Busatto GF; Calderoni S; Calhoun VD; Calvo R; Canales-Rodríguez EJ; Cannon DM; Carr VJ; Cascella N; Cercignani M; Chaim-Avancini TM; Christakou A; Coghill D; Conzelmann A; Crespo-Facorro B; Cubillo AI; Cullen KR; Cupertino RB; Daly E; Dannlowski U; Davey CG; Denys D; Deruelle C; Di Giorgio A; Dickie EW; Dima D; Dohm K; Ehrlich S; Ely BA; Erwin-Grabner T; Ethofer T; Fair DA; Fallgatter AJ; Faraone SV; Fatjó-Vilas M; Fedor JM; Fitzgerald KD; Ford JM; Frodl T; Fu CHY; Fullerton JM; Gabel MC; Glahn DC; Roberts G; Gogberashvili T; Goikolea JM; Gotlib IH; Goya-Maldonado R; Grabe HJ; Green MJ; Grevet EH; Groenewold NA; Grotegerd D; Gruber O; Gruner P; Guerrero-Pedraza A, 2021, 'Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders', JAMA Psychiatry, vol. 78, pp. 47 - 63, http://dx.doi.org/10.1001/jamapsychiatry.2020.2694
Luo J; Agboola F; Grant E; Masters CL; Albert MS; Johnson SC; McDade EM; Vöglein J; Fagan AM; Benzinger T; Massoumzadeh P; Hassenstab J; Bateman RJ; Morris JC; Perrin RJ; Chhatwal J; Jucker M; Ghetti B; Cruchaga C; Graff-Radford NR; Schofield PR; Mori H; Xiong C, 2020, 'Sequence of Alzheimer disease biomarker changes in cognitively normal adults: A cross-sectional study', Neurology, vol. 95, pp. e3104 - e3116, http://dx.doi.org/10.1212/WNL.0000000000010747
Hofer E; Roshchupkin GV; Adams HHH; Knol MJ; Lin H; Li S; Zare H; Ahmad S; Armstrong NJ; Satizabal CL; Bernard M; Bis JC; Gillespie NA; Luciano M; Mishra A; Scholz M; Teumer A; Xia R; Jian X; Mosley TH; Saba Y; Pirpamer L; Seiler S; Becker JT; Carmichael O; Rotter JI; Psaty BM; Lopez OL; Amin N; van der Lee SJ; Yang Q; Himali JJ; Maillard P; Beiser AS; Decarli C; Karama S; Lewis L; Harris M; Bastin ME; Deary IJ; Witte AV; Beyer F; Loeffler M; Mather KA; Schofield PR; Thalamuthu A; Kwok JB; Wright MJ; Ames D; Trollor J; Jiang J; Brodaty H; Wen W; Vernooij MW; Hofman A; Uitterlinden AG; Niessen WJ; Wittfeld K; Bülow R; Völker U; Pausova Z; Pike GB; Maingault S; Crivello F; Tzourio C; Amouyel P; Mazoyer B; Neale MC; Franz CE; Lyons MJ; Panizzon MS; Andreassen OA; Dale AM; Logue M; Grasby KL; Jahanshad N; Painter JN; Colodro-Conde L; Bralten J; Hibar DP; Lind PA; Pizzagalli F; Stein JL; Thompson PM; Medland SE; Sachdev PS; Kremen WS; Wardlaw JM; Villringer A; van Duijn CM; Grabe HJ; Longstreth WT; Fornage M; Paus T; Debette S; Ikram MA; Schmidt H; Schmidt R; Seshadri S; Ching CRK, 2020, 'Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults', Nature Communications, vol. 11, http://dx.doi.org/10.1038/s41467-020-18367-y
Karystianis G; Simpson A; Adily A; Schofield P; Greenberg D; Wand H; Nenadic G; Butler T, 2020, 'Prevalence of mental illnesses in domestic violence police records: Text mining study', Journal of Medical Internet Research, vol. 22, pp. e23725, http://dx.doi.org/10.2196/23725
Sargurupremraj M; Suzuki H; Jian X; Sarnowski C; Evans TE; Bis JC; Eiriksdottir G; Sakaue S; Terzikhan N; Habes M; Zhao W; Armstrong NJ; Hofer E; Yanek LR; Hagenaars SP; Kumar RB; van den Akker EB; McWhirter RE; Trompet S; Mishra A; Saba Y; Satizabal CL; Beaudet G; Petit L; Tsuchida A; Zago L; Schilling S; Sigurdsson S; Gottesman RF; Lewis CE; Aggarwal NT; Lopez OL; Smith JA; Valdés Hernández MC; van der Grond J; Wright MJ; Knol MJ; Dörr M; Thomson RJ; Bordes C; Le Grand Q; Duperron MG; Smith AV; Knopman DS; Schreiner PJ; Evans DA; Rotter JI; Beiser AS; Maniega SM; Beekman M; Trollor J; Stott DJ; Vernooij MW; Wittfeld K; Niessen WJ; Soumaré A; Boerwinkle E; Sidney S; Turner ST; Davies G; Thalamuthu A; Völker U; van Buchem MA; Bryan RN; Dupuis J; Bastin ME; Ames D; Teumer A; Amouyel P; Kwok JB; Bülow R; Deary IJ; Schofield PR; Brodaty H; Jiang J; Tabara Y; Setoh K; Miyamoto S; Yoshida K; Nagata M; Kamatani Y; Matsuda F; Psaty BM; Bennett DA; De Jager PL; Mosley TH; Sachdev PS; Schmidt R; Warren HR; Evangelou E; Trégouët DA; Amouyel P; de Andrade M; Basu S; Berr C; Brody JA; Chasman DI; Dartigues JF; Folsom AR; Germain M, 2020, 'Cerebral small vessel disease genomics and its implications across the lifespan', Nature Communications, vol. 11, http://dx.doi.org/10.1038/s41467-020-19111-2
Jamshidi J; Williams LM; Schofield PR; Park HRP; Montalto A; Chilver MR; Bryant RA; Toma C; Fullerton JM; Gatt JM, 2020, 'Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores', Genes, Brain and Behavior, vol. 19, pp. e12694, http://dx.doi.org/10.1111/gbb.12694
Coleman JRI; Gaspar HA; Bryois J; Byrne EM; Forstner AJ; Holmans PA; de Leeuw CA; Mattheisen M; McQuillin A; Whitehead Pavlides JM; Pers TH; Ripke S; Stahl EA; Steinberg S; Trubetskoy V; Trzaskowski M; Wang Y; Abbott L; Abdellaoui A; Adams MJ; Adolfsson AN; Agerbo E; Akil H; Albani D; Alliey-Rodriguez N; Als TD; Andlauer TFM; Anjorin A; Antilla V; Van der Auwera S; Awasthi S; Bacanu SA; Badner JA; Bækvad-Hansen M; Barchas JD; Bass N; Bauer M; Beekman ATF; Belliveau R; Bergen SE; Bigdeli TB; Binder EB; Bøen E; Boks M; Boocock J; Budde M; Bunney W; Burmeister M; Buttenschøn HN; Bybjerg-Grauholm J; Byerley W; Cai N; Casas M; Castelao E; Cerrato F; Cervantes P; Chambert K; Charney AW; Chen D; Christensen JH; Churchhouse C; St Clair D; Clarke TK; Colodro-Conde L; Coryell W; Couvy-Duchesne B; Craig DW; Crawford GE; Cruceanu C; Czerski PM; Dale AM; Davies G; Deary IJ; Degenhardt F; Del-Favero J; DePaulo JR; Derks EM; Direk N; Djurovic S; Dobbyn AL; Dolan CV; Dumont A; Dunn EC; Eley TC; Elvsåshagen T; Escott-Price V; Fan CC; Finucane HK; Fischer SB; Flickinger M; Foo JC; Foroud TM; Forty L; Frank J; Fraser C; Freimer NB; Frisén L; Gade K; Gage D; Garnham J, 2020, 'The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls', Biological Psychiatry, vol. 88, pp. 169 - 184, http://dx.doi.org/10.1016/j.biopsych.2019.10.015
Armstrong NJ; Mather KA; Sargurupremraj M; Knol MJ; Malik R; Satizabal CL; Yanek LR; Wen W; Gudnason VG; Dueker ND; Elliott LT; Hofer E; Bis J; Jahanshad N; Li S; Logue MA; Luciano M; Scholz M; Smith AV; Trompet S; Vojinovic D; Xia R; Alfaro-Almagro F; Ames D; Amin N; Amouyel P; Beiser AS; Brodaty H; Deary IJ; Fennema-Notestine C; Gampawar PG; Gottesman R; Griffanti L; Jack CR; Jenkinson M; Jiang J; Kral BG; Kwok JB; Lampe L; Liewald DCM; Maillard P; Marchini J; Bastin ME; Mazoyer B; Pirpamer L; Romero JR; Roshchupkin GV; Schofield PR; Schroeter ML; Stott DJ; Thalamuthu A; Trollor J; Tzourio C; van der Grond J; Vernooij MW; Witte VA; Wright MJ; Yang Q; Morris Z; Siggurdsson S; Psaty B; Villringer A; Schmidt H; Haberg AK; van Duijn CM; Wouter Jukema J; Dichgans M; Sacco RL; Wright CB; Kremen WS; Becker LC; Thompson PM; Mosley TH; Wardlaw JM; Ikram MA; Adams HHH; Seshadri S; Sachdev PS; Smith SM; Launer L; Longstreth W; DeCarli C; Schmidt R; Fornage M; Debette S; Nyquist PA, 2020, 'Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities', Stroke, vol. 51, pp. 2112 - 2121, http://dx.doi.org/10.1161/STROKEAHA.119.027544
Scott J; Bellivier F; Manchia M; Schulze T; Alda M; Etain B; Cervantes P; Garnham J; Nunes A; O'Donovan C; Slaney C; Bauer M; Pfennig A; Reif A; Kittel-Schneider S; Veeh J; Zompo MD; Ardau R; Chillotti C; Severino G; Kato T; Ozaki N; Kusumi I; Hashimoto R; Akiyama K; Kelso J, 2020, 'Can network analysis shed light on predictors of lithium response in bipolar I disorder?', Acta Psychiatrica Scandinavica, vol. 141, pp. 522 - 533, http://dx.doi.org/10.1111/acps.13163
Wong MWK; Thalamuthu A; Braidy N; Mather K; Liu Y; Ciobanu L; Baune B; Armstrong N; Kwok J; Schofield P; Wright M; Ames D; Pickford R; Lee T; Poljak A; Sachdev P, 2020, 'Genetic and environmental determinants of variation in the plasma lipidome of older Australian twins', , http://dx.doi.org/10.1101/2020.05.05.075606
Van Der Meer D; Sønderby IE; Kaufmann T; Walters GB; Abdellaoui A; Ames D; Amunts K; Andersson M; Armstrong NJ; Bernard M; Blackburn NB; Blangero J; Boomsma DI; Brodaty H; Brouwer RM; Bülow R; Cahn W; Calhoun VD; Caspers S; Cavalleri GL; Ching CRK; Cichon S; Ciufolini S; Corvin A; Crespo-Facorro B; Curran JE; Dalvie S; Dazzan P; De Geus EJC; De Zubicaray GI; De Zwarte SMC; Delanty N; Den Braber A; Desrivieres S; Di Forti M; Doherty JL; Donohoe G; Ehrlich S; Eising E; Espeseth T; Fisher SE; Fladby T; Frei O; Frouin V; Fukunaga M; Gareau T; Glahn DC; Grabe HJ; Groenewold NA; Gústafsson Ó; Haavik J; Haberg AK; Hashimoto R; Hehir-Kwa JY; Hibar DP; Hillegers MHJ; Hoffmann P; Holleran L; Hottenga JJ; Hulshoff Pol HE; Ikeda M; Jacquemont S; Jahanshad N; Jockwitz C; Johansson S; Jönsson EG; Kikuchi M; Knowles EEM; Kwok JB; Le Hellard S; Linden DEJ; Liu J; Lundervold A; Lundervold AJ; Martin NG; Mather KA; Mathias SR; McMahon KL; McRae AF; Medland SE; Moberget T; Moreau C; Morris DW; Mühleisen TW; Murray RM; Nordvik JE; Nyberg L; Olde Loohuis LM; Ophoff RA; Owen MJ; Paus T; Pausova Z; Peralta JM; Pike B; Prieto C; Quinlan EB; Reinbold CS; Reis Marques T; Rucker JJH; Sachdev PS, 2020, 'Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region with Cortical and Subcortical Morphology and Cognition', JAMA Psychiatry, vol. 77, pp. 420 - 430, http://dx.doi.org/10.1001/jamapsychiatry.2019.3779
Grasby KL; Jahanshad N; Painter JN; Colodro-Conde L; Bralten J; Hibar DP; Lind PA; Pizzagalli F; Ching CRK; McMahon MAB; Shatokhina N; Zsembik LCP; Thomopoulos SI; Zhu AH; Strike LT; Agartz I; Alhusaini S; Almeida MAA; Alnæs D; Amlien IK; Andersson M; Ard T; Armstrong NJ; Ashley-Koch A; Atkins JR; Bernard M; Brouwer RM; Buimer EEL; Bülow R; Bürger C; Cannon DM; Chakravarty M; Chen Q; Cheung JW; Couvy-Duchesne B; Dale AM; Dalvie S; de Araujo TK; de Zubicaray GI; de Zwarte SMC; den Braber A; Doan NT; Dohm K; Ehrlich S; Engelbrecht HR; Erk S; Fan CC; Fedko IO; Foley SF; Ford JM; Fukunaga M; Garrett ME; Ge T; Giddaluru S; Goldman AL; Green MJ; Groenewold NA; Grotegerd D; Gurholt TP; Gutman BA; Hansell NK; Harris MA; Harrison MB; Haswell CC; Hauser M; Herms S; Heslenfeld DJ; Ho NF; Hoehn D; Hoffmann P; Holleran L; Hoogman M; Hottenga JJ; Ikeda M; Janowitz D; Jansen IE; Jia T; Jockwitz C; Kanai R; Karama S; Kasperaviciute D; Kaufmann T; Kelly S; Kikuchi M; Klein M; Knapp M; Knodt AR; Krämer B; Lam M; Lancaster TM; Lee PH; Lett TA; Lewis LB; Lopes-Cendes I; Luciano M; Macciardi F; Marquand AF; Mathias SR; Melzer TR; Milaneschi Y, 2020, 'The genetic architecture of the human cerebral cortex', Science, vol. 367, http://dx.doi.org/10.1126/science.aay6690
Sønderby IE; Gústafsson Ó; Doan NT; Hibar DP; Martin-Brevet S; Abdellaoui A; Ames D; Amunts K; Andersson M; Armstrong NJ; Bernard M; Blackburn N; Blangero J; Boomsma DI; Bralten J; Brattbak HR; Brodaty H; Brouwer RM; Bülow R; Calhoun V; Caspers S; Cavalleri G; Chen CH; Cichon S; Ciufolini S; Corvin A; Crespo-Facorro B; Curran JE; Dale AM; Dalvie S; Dazzan P; de Geus EJC; de Zubicaray GI; de Zwarte SMC; Delanty N; den Braber A; Desrivières S; Donohoe G; Draganski B; Ehrlich S; Espeseth T; Fisher SE; Franke B; Frouin V; Fukunaga M; Gareau T; Glahn DC; Grabe H; Groenewold NA; Haavik J; Håberg A; Hashimoto R; Hehir-Kwa JY; Heinz A; Hillegers MHJ; Hoffmann P; Holleran L; Hottenga JJ; Hulshoff HE; Ikeda M; Jahanshad N; Jernigan T; Jockwitz C; Johansson S; Jonsdottir GA; Jönsson EG; Kahn R; Kaufmann T; Kelly S; Kikuchi M; Knowles EEM; Kolskår KK; Kwok JB; Hellard SL; Leu C; Liu J; Lundervold AJ; Lundervold A; Martin NG; Mather K; Mathias SR; McCormack M; McMahon KL; McRae A; Milaneschi Y; Moreau C; Morris D; Mothersill D; Mühleisen TW; Murray R; Nordvik JE; Nyberg L; Olde Loohuis LM; Ophoff R; Paus T; Pausova Z; Penninx B; Peralta JM; Pike B; Prieto C, 2020, 'Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia', Molecular Psychiatry, vol. 25, pp. 584 - 602, http://dx.doi.org/10.1038/s41380-018-0118-1
Barthélemy NR; Li Y; Joseph-Mathurin N; Gordon BA; Hassenstab J; Benzinger TLS; Buckles V; Fagan AM; Perrin RJ; Goate AM; Morris JC; Karch CM; Xiong C; Allegri R; Mendez PC; Berman SB; Ikeuchi T; Mori H; Shimada H; Shoji M; Suzuki K; Noble J; Farlow M; Chhatwal J; Graff-Radford NR; Salloway S; Schofield PR; Masters CL; Martins RN; O’Connor A; Fox NC; Levin J; Jucker M; Gabelle A; Lehmann S; Sato C; Bateman RJ; McDade E; Allegri R; Bateman R; Bechara J; Benzinger T; Berman S; Bodge C; Brandon S; Brooks W; Buck J; Chea S; Chrem Mendez P; Chui H; Cinco J; Clifford J; Cruchaga C; Donahue T; Douglas J; Edigo N; Erekin-Taner N; Fagan A; Farlow M; Fitzpatrick C; Flynn G; Franklin E; Fujii H; Gant C; Gardener S; Ghetti B; Goate A; Goldman J; Gordon B; Graff-Radford N; Gray J; Groves A; Hassenstab J; Hoechst-Swisher L; Holtzman D; Hornbeck R; DiBari SH; Ikonomovic S; Jerome G; Karch C; Kasuga K; Kawarabayashi T; Klunk W; Koeppe R; Kuder-Buletta E; Laske C; Lee JH; Levin J; Martins R; Mason NS; Maue-Dreyfus D; McDade E; Mori H; Morris J; Nagamatsu A, 2020, 'A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer’s disease', Nature Medicine, vol. 26, pp. 398 - 407, http://dx.doi.org/10.1038/s41591-020-0781-z
Amare AT; Schubert KO; Hou L; Clark SR; Papiol S; Cearns M; Heilbronner U; Degenhardt F; Tekola-Ayele F; Hsu YH; Shekhtman T; Adli M; Akula N; Akiyama K; Ardau R; Arias B; Aubry JM; Backlund L; Bhattacharjee AK; Bellivier F; Benabarre A; Bengesser S; Biernacka JM; Birner A; Brichant-Petitjean C; Cervantes P; Chen HC; Chillotti C; Cichon S; Cruceanu C; Czerski PM; Dalkner N; Dayer A; Del Zompo M; DePaulo JR; Étain B; Jamain S; Falkai P; Forstner AJ; Frisen L; Frye MA; Fullerton JM; Gard S; Garnham JS; Goes FS; Grigoroiu-Serbanescu M; Grof P; Hashimoto R; Hauser J; Herms S; Hoffmann P; Hofmann A; Jiménez E; Kahn JP; Kassem L; Kuo PH; Kato T; Kelsoe JR; Kittel-Schneider S; Kliwicki S; König B; Kusumi I; Laje G; Landén M; Lavebratt C; Leboyer M; Leckband SG; Tortorella A; Manchia M; Martinsson L; McCarthy MJ; McElroy SL; Colom F; Mitjans M; Mondimore FM; Monteleone P; Nievergelt CM; Nöthen MM; Novák T; O’Donovan C; Ozaki N; Ösby U; Pfennig A; Potash JB; Reif A; Wray NR; Ripke S; Mattheisen M; Trzaskowski M; Byrne EM; Abdellaoui A; Adams MJ; Agerbo E; Air TM; Andlauer TFM; Bacanu SA; Bækvad-Hansen M; Beekman ATF; Bigdeli TB; Binder EB, 2020, 'Association of polygenic score for major depression with response to lithium in patients with bipolar disorder', Molecular Psychiatry, http://dx.doi.org/10.1038/s41380-020-0689-5
Han LKM; Dinga R; Hahn T; Ching CRK; Eyler LT; Aftanas L; Aghajani M; Aleman A; Baune BT; Berger K; Brak I; Filho GB; Carballedo A; Connolly CG; Couvy-Duchesne B; Cullen KR; Dannlowski U; Davey CG; Dima D; Duran FLS; Enneking V; Filimonova E; Frenzel S; Frodl T; Fu CHY; Godlewska BR; Gotlib IH; Grabe HJ; Groenewold NA; Grotegerd D; Gruber O; Hall GB; Harrison BJ; Hatton SN; Hermesdorf M; Hickie IB; Ho TC; Hosten N; Jansen A; Kähler C; Kircher T; Klimes-Dougan B; Krämer B; Krug A; Lagopoulos J; Leenings R; MacMaster FP; MacQueen G; McIntosh A; McLellan Q; McMahon KL; Medland SE; Mueller BA; Mwangi B; Osipov E; Portella MJ; Pozzi E; Reneman L; Repple J; Rosa PGP; Sacchet MD; Sämann PG; Schnell K; Schrantee A; Simulionyte E; Soares JC; Sommer J; Stein DJ; Steinsträter O; Strike LT; Thomopoulos SI; van Tol MJ; Veer IM; Vermeiren RRJM; Walter H; van der Wee NJA; van der Werff SJA; Whalley H; Winter NR; Wittfeld K; Wright MJ; Wu MJ; Völzke H; Yang TT; Zannias V; de Zubicaray GI; Zunta-Soares GB; Abé C; Alda M; Andreassen OA; Bøen E; Bonnin CM; Canales-Rodriguez EJ; Cannon D; Caseras X; Chaim-Avancini TM; Elvsåshagen T; Favre P; Foley SF; Fullerton JM, 2020, 'Brain aging in major depressive disorder: results from the ENIGMA major depressive disorder working group', Molecular Psychiatry, http://dx.doi.org/10.1038/s41380-020-0754-0
de Zwarte SMC; Brouwer RM; Agartz I; Alda M; Alonso-Lana S; Bearden CE; Bertolino A; Bonvino A; Bramon E; Buimer EEL; Cahn W; Canales-Rodríguez EJ; Cannon DM; Cannon TD; Caseras X; Castro-Fornieles J; Chen Q; Chung Y; De la Serna E; del Mar Bonnin C; Demro C; Di Giorgio A; Doucet GE; Eker MC; Erk S; Fatjó-Vilas M; Fears SC; Foley SF; Frangou S; Fullerton JM; Glahn DC; Goghari VM; Goikolea JM; Goldman AL; Gonul AS; Gruber O; Hajek T; Hawkins EL; Heinz A; Hidiroglu Ongun C; Hillegers MHJ; Houenou J; Hulshoff Pol HE; Hultman CM; Ingvar M; Johansson V; Jönsson EG; Kane F; Kempton MJ; Koenis MMG; Kopecek M; Krämer B; Lawrie SM; Lenroot RK; Marcelis M; Mattay VS; McDonald C; Meyer-Lindenberg A; Michielse S; Mitchell PB; Moreno D; Murray RM; Mwangi B; Nabulsi L; Newport J; Olman CA; van Os J; Overs BJ; Ozerdem A; Pergola G; Picchioni MM; Piguet C; Pomarol-Clotet E; Radua J; Ramsay IS; Richter A; Roberts G; Salvador R; Saricicek Aydogan A; Sarró S; Schofield PR; Simsek EM; Simsek F; Soares JC; Sponheim SR; Sugranyes G; Toulopoulou T; Tronchin G; Vieta E; Walter H; Weinberger DR; Whalley HC; Wu MJ; Yalin N; Andreassen OA; Ching CRK; Thomopoulos SI; van Erp TGM; Jahanshad N; Thompson PM, 2020, 'Intelligence, educational attainment, and brain structure in those at familial high-risk for schizophrenia or bipolar disorder', Human Brain Mapping, http://dx.doi.org/10.1002/hbm.25206
Montal V; Vilaplana E; Pegueroles J; Bejanin A; Alcolea D; Carmona-Iragui M; Clarimón J; Levin J; Cruchaga C; Graff-Radford NR; Noble JM; Lee JH; Allegri R; Karch CM; Laske C; Schofield PR; Salloway S; Ances B; Benzinger T; McDale E; Bateman R; Blesa R; Sánchez-Valle R; Lleó A; Fortea J, 2020, 'Biphasic cortical macro- and microstructural changes in autosomal dominant Alzheimer's disease', Alzheimer's and Dementia, http://dx.doi.org/10.1002/alz.12224
Lee PH; Anttila V; Won H; Feng YCA; Rosenthal J; Zhu Z; Tucker-Drob EM; Nivard MG; Grotzinger AD; Posthuma D; Wang MMJ; Yu D; Stahl EA; Walters RK; Anney RJL; Duncan LE; Ge T; Adolfsson R; Banaschewski T; Belangero S; Cook EH; Coppola G; Derks EM; Hoekstra PJ; Kaprio J; Keski-Rahkonen A; Kirov G; Kranzler HR; Luykx JJ; Rohde LA; Zai CC; Agerbo E; Arranz MJ; Asherson P; Bækvad-Hansen M; Baldursson G; Bellgrove M; Belliveau RA; Buitelaar J; Burton CL; Bybjerg-Grauholm J; Casas M; Cerrato F; Chambert K; Churchhouse C; Cormand B; Crosbie J; Dalsgaard S; Demontis D; Doyle AE; Dumont A; Elia J; Grove J; Gudmundsson OO; Haavik J; Hakonarson H; Hansen CS; Hartman CA; Hawi Z; Hervás A; Hougaard DM; Howrigan DP; Huang H; Kuntsi J; Langley K; Lesch KP; Leung PWL; Loo SK; Martin J; Martin AR; McGough JJ; Medland SE; Moran JL; Mors O; Mortensen PB; Oades RD; Palmer DS; Pedersen CB; Pedersen MG; Peters T; Poterba T; Poulsen JB; Ramos-Quiroga JA; Reif A; Ribasés M; Rothenberger A; Rovira P; Sánchez-Mora C; Satterstrom FK; Schachar R; Artigas MS; Steinberg S; Stefansson H; Turley P; Walters GB; Werge T; Zayats T; Arking DE; Bettella F; Buxbaum JD, 2019, 'Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders', Cell, vol. 179, pp. 1469 - 1482.e11, http://dx.doi.org/10.1016/j.cell.2019.11.020
Davies G; Lam M; Harris SE; Trampush JW; Luciano M; Hill WD; Hagenaars SP; Ritchie SJ; Marioni RE; Fawns-Ritchie C; Liewald DCM; Okely JA; Ahola-Olli AV; Barnes CLK; Bertram L; Bis JC; Burdick KE; Christoforou A; DeRosse P; Djurovic S; Espeseth T; Giakoumaki S; Giddaluru S; Gustavson DE; Hayward C; Hofer E; Ikram MA; Karlsson R; Knowles E; Lahti J; Leber M; Li S; Mather KA; Melle I; Morris D; Oldmeadow C; Palviainen T; Payton A; Pazoki R; Petrovic K; Reynolds CA; Sargurupremraj M; Scholz M; Smith JA; Smith AV; Terzikhan N; Thalamuthu A; Trompet S; van der Lee SJ; Ware EB; Windham BG; Wright MJ; Yang J; Yu J; Ames D; Amin N; Amouyel P; Andreassen OA; Armstrong NJ; Assareh AA; Attia JR; Attix D; Avramopoulos D; Bennett DA; Böhmer AC; Boyle PA; Brodaty H; Campbell H; Cannon TD; Cirulli ET; Congdon E; Conley ED; Corley J; Cox SR; Dale AM; Dehghan A; Dick D; Dickinson D; Eriksson JG; Evangelou E; Faul JD; Ford I; Freimer NA; Gao H; Giegling I; Gillespie NA; Gordon SD; Gottesman RF; Griswold ME; Gudnason V; Harris TB; Hartmann AM; Hatzimanolis A; Heiss G; Holliday EG; Joshi PK; Kähönen M; Kardia SLR; Karlsson I; Kleineidam L, 2019, 'Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (Nature Communications, (2018), 9, 1, (2098), 10.1038/s41467-018-04362-x)', Nature Communications, vol. 10, pp. 2068, http://dx.doi.org/10.1038/s41467-019-10160-w
Favre P; Pauling M; Stout J; Hozer F; Sarrazin S; Abé C; Alda M; Alloza C; Alonso-Lana S; Andreassen OA; Baune BT; Benedetti F; Busatto GF; Canales-Rodríguez EJ; Caseras X; Chaim-Avancini TM; Ching CRK; Dannlowski U; Deppe M; Eyler LT; Fatjo-Vilas M; Foley SF; Grotegerd D; Hajek T; Haukvik UK; Howells FM; Jahanshad N; Kugel H; Lagerberg TV; Lawrie SM; Linke JO; McIntosh A; Melloni EMT; Mitchell PB; Polosan M; Pomarol-Clotet E; Repple J; Roberts G; Roos A; Rosa PGP; Salvador R; Sarró S; Schofield PR; Serpa MH; Sim K; Stein DJ; Sussmann JE; Temmingh HS; Thompson PM; Verdolini N; Vieta E; Wessa M; Whalley HC; Zanetti MV; Leboyer M; Mangin JF; Henry C; Duchesnay E; Houenou J, 2019, 'Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals', Neuropsychopharmacology, vol. 44, pp. 2285 - 2293, http://dx.doi.org/10.1038/s41386-019-0485-6
Favre P; Pauling M; Stout J; Hozer F; Sarrazin S; Abé C; Alda M; Alloza C; Alonso-Lana S; Andreassen OA; Baune BT; Benedetti F; Busatto GF; Canales-Rodríguez EJ; Caseras X; Chaim-Avancini TM; Ching CRK; Dannlowski U; Deppe M; Eyler LT; Fatjo-Vilas M; Foley SF; Grotegerd D; Hajek T; Haukvik UK; Howells FM; Jahanshad N; Kugel H; Lagerberg TV; Lawrie SM; Linke JO; McIntosh A; Melloni EMT; Mitchell PB; Polosan M; Pomarol-Clotet E; Repple J; Roberts G; Roos A; Rosa PGP; Salvador R; Sarró S; Schofield PR; Serpa MH; Sim K; Stein DJ; Sussmann JE; Temmingh HS; Thompson PM; Verdolini N; Vieta E; Wessa M; Whalley HC; Zanetti MV; Leboyer M; Mangin JF; Henry C; Duchesnay E; Houenou J, 2019, 'Correction: Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals (Neuropsychopharmacology, (2019), 44, 13, (2285-2293), 10.1038/s41386-019-0485-6)', Neuropsychopharmacology, vol. 44, pp. 2298, http://dx.doi.org/10.1038/s41386-019-0521-6
Satizabal CL; Adams HHH; Hibar DP; White CC; Knol MJ; Stein JL; Scholz M; Sargurupremraj M; Jahanshad N; Roshchupkin GV; Smith AV; Bis JC; Jian X; Luciano M; Hofer E; Teumer A; van der Lee SJ; Yang J; Yanek LR; Lee TV; Li S; Hu Y; Koh JY; Eicher JD; Desrivières S; Arias-Vasquez A; Chauhan G; Athanasiu L; Rentería ME; Kim S; Hoehn D; Armstrong NJ; Chen Q; Holmes AJ; den Braber A; Kloszewska I; Andersson M; Espeseth T; Grimm O; Abramovic L; Alhusaini S; Milaneschi Y; Papmeyer M; Axelsson T; Ehrlich S; Roiz-Santiañez R; Kraemer B; Håberg AK; Jones HJ; Pike GB; Stein DJ; Stevens A; Bralten J; Vernooij MW; Harris TB; Filippi I; Witte AV; Guadalupe T; Wittfeld K; Mosley TH; Becker JT; Doan NT; Hagenaars SP; Saba Y; Cuellar-Partida G; Amin N; Hilal S; Nho K; Mirza-Schreiber N; Arfanakis K; Becker DM; Ames D; Goldman AL; Lee PH; Boomsma DI; Lovestone S; Giddaluru S; Le Hellard S; Mattheisen M; Bohlken MM; Kasperaviciute D; Schmaal L; Lawrie SM; Agartz I; Walton E; Tordesillas-Gutierrez D; Davies GE; Shin J; Ipser JC; Vinke LN; Hoogman M; Jia T; Burkhardt R; Klein M; Crivello F; Janowitz D; Carmichael O; Haukvik UK; Aribisala BS; Schmidt H, 2019, 'Genetic architecture of subcortical brain structures in 38,851 individuals', Nature Genetics, vol. 51, pp. 1624 - 1636, http://dx.doi.org/10.1038/s41588-019-0511-y
Armstrong N; Mather K; Sargurupremraj M; Knol M; Malik R; Satizabal C; Yanek L; Wei W; Gudnason V; Deuker N; Elliott L; Hofer E; Jahanshad N; Li S; Logue M; Luciano M; Scholz M; Smith A; Trompet S; Vojinovic D; Xia R; Alfaro-Almagro F; Ames D; Amin N; Amouyel P; Beiser A; Brodaty H; Deary I; Fennema-Notestine C; Gampwar P; Gottesman R; Griffanti L; Jack C; Jenkinson M; Jain J; Kral B; Kwok J; Lampe L; Liewald DCM; Maillard P; Marchini J; Bastin M; Mazoyer B; Pirpamer L; Romero JR; Roshchupkin G; Schofield P; Schroeter M; Stott D; Thalamuth A; Trollor J; Tzourio C; van der Grond J; Vernooij M; Witte V; Wright M; Yang Q; Zoe M; Siggurdsson S; Villringer A; Schmidt H; Haberg A; Van Duijn C; Jukema W; Dichigans M; Sacco R; Wright C; Kremen W; Becker L; Thompson P; Launer L; Mosley T; Wardlaw J; Ikram A; Adams HHH; Schmidt R; Smith S; Decarli C; Sachdev P; Fornage M; Debbette S; Seshadri S; Nyquist P, 2019, 'Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities', , http://dx.doi.org/10.1101/683367
Vöglein J; Paumier K; Jucker M; Preische O; McDade E; Hassenstab J; Benzinger TL; Noble JM; Berman SB; Graff-Radford NR; Ghetti B; Farlow MR; Chhatwal J; Salloway S; Xiong C; Karch CM; Cairns N; Mori H; Schofield PR; Masters CL; Goate A; Buckles V; Fox N; Rossor M; Chrem P; Allegri R; Ringman JM; Höglinger G; Steiner H; Dieterich M; Haass C; Laske C; Morris JC; Bateman RJ; Danek A; Levin J, 2019, 'Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's disease', Brain, vol. 142, pp. 1429 - 1440, http://dx.doi.org/10.1093/brain/awz050
Vöglein J; Noachtar S; McDade E; Quaid KA; Salloway S; Ghetti B; Noble J; Berman S; Chhatwal J; Mori H; Fox N; Allegri R; Masters CL; Buckles V; Ringman JM; Rossor M; Schofield PR; Sperling R; Jucker M; Laske C; Paumier K; Morris JC; Bateman RJ; Levin J; Danek A, 2019, 'Seizures as an early symptom of autosomal dominant Alzheimer's disease', Neurobiology of Aging, vol. 76, pp. 18 - 23, http://dx.doi.org/10.1016/j.neurobiolaging.2018.11.022
Kalman JL; Papiol S; Forstner AJ; Heilbronner U; Degenhardt F; Strohmaier J; Adli M; Adorjan K; Akula N; Alda M; Anderson-Schmidt H; Andlauer TFM; Anghelescu IG; Ardau R; Arias B; Arolt V; Aubry JM; Backlund L; Bartholdi K; Bauer M; Baune BT; Becker T; Bellivier F; Benabarre A; Bengesser S; Bhattacharjee AK; Biernacka JM; Birner A; Brichant-Petitjean C; Budde M; Cervantes P; Chillotti C; Cichon S; Clark SR; Colom F; Comes AL; Cruceanu C; Czerski PM; Dannlowski U; Dayer A; Del Zompo M; DePaulo JR; Dietrich DE; Étain B; Ethofer T; Falkai P; Fallgatter A; Figge C; Flatau L; Folkerts H; Frisen L; Frye MA; Fullerton JM; Gade K; Gard S; Garnham JS; Goes FS; Grigoroiu-Serbanescu M; Gryaznova A; Hake M; Hauser J; Herms S; Hoffmann P; Hou L; Jäger M; Jamain S; Jiménez E; Juckel G; Kahn JP; Kassem L; Kelsoe J; Kittel-Schneider S; Kliwicki S; Klohn-Sagatholislam F; Koller M; König B; Konrad C; Lackner N; Laje G; Landén M; Lang FU; Lavebratt C; Leboyer M; Leckband SG; Maj M; Manchia M; Martinsson L; McCarthy MJ; McElroy SL; McMahon FJ; Mitchell PB; Mitjans M; Mondimore FM; Monteleone P; Nieratschker V; Nievergelt CM; Novák T; Ösby U; Pfennig A; Potash JB, 2019, 'Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study', Bipolar Disorders, vol. 21, pp. 68 - 75, http://dx.doi.org/10.1111/bdi.12659
Preische O; Schultz SA; Apel A; Kuhle J; Kaeser SA; Barro C; Gräber S; Kuder-Buletta E; LaFougere C; Laske C; Vöglein J; Levin J; Masters CL; Martins R; Schofield PR; Rossor MN; Graff-Radford NR; Salloway S; Ghetti B; Ringman JM; Noble JM; Chhatwal J; Goate AM; Benzinger TLS; Morris JC; Bateman RJ; Wang G; Fagan AM; McDade EM; Gordon BA; Jucker M; Allegri R; Amtashar F; Berman S; Bodge C; Brandon S; Brooks W; Buck J; Buckles V; Chea S; Chrem P; Chui H; Cinco J; Clifford J; Cruchaga C; D’Mello M; Donahue T; Douglas J; Edigo N; Erekin-Taner N; Farlow M; Farrar A; Feldman H; Flynn G; Fox N; Franklin E; Fujii H; Gant C; Gardener S; Goldman J; Gray J; Gurney J; Hassenstab J; Hirohara M; Holtzman D; Hornbeck R; DiBari SH; Ikeuchi T; Ikonomovic S; Jerome G; Karch C; Kasuga K; Kawarabayashi T; Klunk W; Koeppe R; Lee JH; Marcus D; Mason NS; Maue-Dreyfus D; Montoya L; Mori H; Nagamatsu A; Neimeyer K; Norton J; Perrin R; Raichle M; Roh JH; Shimada H; Shiroto T; Shoji M; Sigurdson W; Sohrabi H; Sparks P; Suzuki K; Swisher L; Taddei K; Wang J; Wang P; Weiner M; Wolfsberger M, 2019, 'Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer’s disease', Nature Medicine, vol. 25, pp. 277 - 283, http://dx.doi.org/10.1038/s41591-018-0304-3
Chauhan G; Adams HHH; Satizabal CL; Bis JC; Teumer A; Sargurupremraj M; Hofer E; Trompet S; Hilal S; Smith AV; Jian X; Malik R; Traylor M; Pulit SL; Amouyel P; Mazoyer B; Zhu YC; Kaffashian S; Schilling S; Beecham GW; Montine TJ; Schellenberg GD; Kjartansson O; Guðnason V; Knopman DS; Griswold ME; Windham BG; Gottesman RF; Mosley TH; Schmidt R; Saba Y; Schmidt H; Takeuchi F; Yamaguchi S; Nabika T; Kato N; Rajan KB; Aggarwal NT; De Jager PL; Evans DA; Psaty BM; Rotter JI; Rice K; Lopez OL; Liao J; Chen C; Cheng CY; Wong TY; Ikram MK; van der Lee SJ; Amin N; Chouraki V; Destefano AL; Aparicio HJ; Romero JR; Maillard P; Decarli C; Wardlaw JM; Del C. Valdés Hernández M; Luciano M; Liewald D; Deary IJ; Starr JM; Bastin ME; Maniega SM; Slagboom PE; Beekman M; Deelen J; Uh HW; Lemmens R; Brodaty H; Wright MJ; Ames D; Boncoraglio GB; Hopewell JC; Beecham AH; Blanton SH; Wright CB; Sacco RL; Wen W; Thalamuthu A; Armstrong NJ; Chong E; Schofield PR; Kwok JB; van der Grond J; Stott DJ; Ford I; Jukema JW; Vernooij MW; Hofman A; Uitterlinden AG; van der Lugt A; Wittfeld K; Grabe HJ; Hosten N; von Sarnowski B; Völker U; Levi C; Jimenez-Conde J, 2019, 'Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting', Neurology, vol. 92, pp. E486 - E503, http://dx.doi.org/10.1212/WNL.0000000000006851
Mills L; Meiser B; Ahmad R; Schofield PR; Peate M; Levitan C; Trevena L; Barlow-Stewart K; Dobbins T; Christensen H; Sherman KA; Dunlop K; Mitchell PB, 2019, 'A cluster randomized controlled trial of an online psychoeducational intervention for people with a family history of depression 11 Medical and Health Sciences 1117 Public Health and Health Services 11 Medical and Health Sciences 1103 Clinical Sciences', BMC Psychiatry, vol. 19, pp. 29, http://dx.doi.org/10.1186/s12888-018-1994-2
Swarup V; Hinz FI; Rexach JE; Noguchi KI; Toyoshiba H; Oda A; Hirai K; Sarkar A; Seyfried NT; Cheng C; Haggarty SJ; Ferrari R; Rohrer JD; Ramasamy A; Hardy J; Hernandez DG; Nalls MA; Singleton AB; Kwok JBJ; Dobson-Stone C; Brooks WS; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cairns NJ; Cruchaga C; Binetti G; Ghidoni R; Benussi L; Forloni G; Albani D; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Waldö ML; Nilsson K; Nilsson C; Mackenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; McKeith IG; Thomas AJ; Jaros E; Pietrini P; Huey ED; Wassermann EM; Tierney MC; Baborie A; Pastor P; Ortega-Cubero S; Razquin C; Alonso E; Perneczky R; Diehl-Schmid J; Alexopoulos P; Kurz A; Rainero I; Rubino E; Pinessi L; Rogaeva E; George-Hyslop PS; Rossi G; Tagliavini F; Giaccone G; Rowe JB; Schlachetzki JCM; Uphill J; Collinge J; Mead S; Danek A; Van Deerlin VM; Grossman M; Trojanowski JQ; Pickering-Brown S; Momeni P; van der Zee J; Cruts M; Van Broeckhoven C; Cappa SF; Leber I; Brice A; Hannequin D; Golfier V, 2019, 'Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia', Nature Medicine, vol. 25, pp. 152 - 164, http://dx.doi.org/10.1038/s41591-018-0223-3
Mullins N; Bigdeli TB; Børglum AD; Coleman JRI; Demontis D; Mehta D; Power RA; Ripke S; Stahl EA; Starnawska A; Anjorin A; Corvin A; Sanders AR; Forstner AJ; Reif A; Koller AC; Tkowska BS; Baune BT; Müller-Myhsok B; Penninx BWJH; Pato C; Zai C; Rujescu D; Hougaard DM; Quested D; Levinson DF; Binder EB; Byrne EM; Agerbo E; Streit F; Mayoral F; Bellivier F; Degenhardt F; Breen G; Morken G; Turecki G; Rouleau GA; Grabe HJ; Völzke H; Jones I; Giegling I; Agartz I; Melle I; Lawrence J; Walters JTR; Strohmaier J; Shi J; Hauser J; Biernacka JM; Vincent JB; Kelsoe J; Strauss JS; Lissowska J; Pimm J; Smoller JW; Guzman-Parra J; Berger K; Scott LJ; Jones LA; Azevedo MH; Trzaskowski M; Kogevinas M; Rietschel M; Boks M; Ising M; Grigoroiu-Serbanescu M; Hamshere ML; Leboyer M; Frye M; Nöthen MM; Alda M; Preisig M; Nordentoft M; Boehnke M; O’Donovan MC; Owen MJ; Pato MT; Renteria ME; Budde M; Weissman MM; Wray NR; Bass N; Craddock N; Smeland OB; Andreassen OA; Mors O; Gejman PV; Sklar P; McGrath P; Hoffmann P; McGuffin P; Lee PH; Mortensen PB; Kahn RS; Ophoff RA; Adolfsson R; Van der Auwera S; Djurovic S; Kloiber S; Heilmann-Heimbach S, 2019, 'GWAS of suicide attempt in psychiatric disorders and association with major depression polygenic risk scores', American Journal of Psychiatry, vol. 176, pp. 651 - 660, http://dx.doi.org/10.1176/appi.ajp.2019.18080957
Andlauer TFM; Guzman-Parra J; Streit F; Strohmaier J; González MJ; Gil Flores S; Cabaleiro Fabeiro FJ; del Río Noriega F; Perez FP; Haro González J; Orozco Diaz G; de Diego-Otero Y; Moreno-Küstner B; Auburger G; Degenhardt F; Heilmann-Heimbach S; Herms S; Hoffmann P; Frank J; Foo JC; Treutlein J; Witt SH; Cichon S; Kogevinas M; Stahl EA; Breen G; Forstner AJ; McQuillin A; Ripke S; Trubetskoy V; Mattheisen M; Wang Y; Coleman JRI; Gaspar HA; de Leeuw CA; Steinberg S; Pavlides JMW; Trzaskowski M; Pers TH; Holmans PA; Abbott L; Agerbo E; Akil H; Albani D; Alliey-Rodriguez N; Als TD; Anjorin A; Antilla V; Awasthi S; Badner JA; Bækvad-Hansen M; Barchas JD; Bass N; Bauer M; Belliveau R; Bergen SE; Pedersen CB; Bøen E; Boks M; Boocock J; Budde M; Bunney W; Burmeister M; Bybjerg-Grauholm J; Byerley W; Casas M; Cerrato F; Cervantes P; Chambert K; Charney AW; Chen D; Churchhouse C; Clarke TK; Coryell W; Craig DW; Cruceanu C; Czerski PM; Dale AM; de Jong S; Del-Favero J; DePaulo JR; Djurovic S; Dobbyn AL; Dumont A; Elvsåshagen T; Escott-Price V; Fan CC; Fischer SB; Flickinger M; Foroud TM; Forty L; Fraser C; Freimer NB; Frisén L; Gade K; Gage D; Garnham J; Giambartolomei C; Pedersen MG; Goldstein J, 2019, 'Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders', Molecular Psychiatry, http://dx.doi.org/10.1038/s41380-019-0558-2
Jia T; Chu C; Liu Y; van Dongen J; Papastergios E; Armstrong NJ; Bastin ME; Carrillo-Roa T; den Braber A; Harris M; Jansen R; Liu J; Luciano M; Ori APS; Roiz Santiañez R; Ruggeri B; Sarkisyan D; Shin J; Sungeun K; Tordesillas Gutiérrez D; van’t Ent D; Ames D; Artiges E; Bakalkin G; Banaschewski T; Bokde ALW; Brodaty H; Bromberg U; Brouwer R; Büchel C; Burke Quinlan E; Cahn W; de Zubicaray GI; Ehrlich S; Ekström TJ; Flor H; Fröhner JH; Frouin V; Garavan H; Gowland P; Heinz A; Hoare J; Ittermann B; Jahanshad N; Jiang J; Kwok JB; Martin NG; Martinot JL; Mather KA; McMahon KL; McRae AF; Nees F; Papadopoulos Orfanos D; Paus T; Poustka L; Sämann PG; Schofield PR; Smolka MN; Stein DJ; Strike LT; Teeuw J; Thalamuthu A; Trollor J; Walter H; Wardlaw JM; Wen W; Whelan R; Apostolova LG; Binder EB; Boomsma DI; Calhoun V; Crespo-Facorro B; Deary IJ; Hulshoff Pol H; Ophoff RA; Pausova Z; Sachdev PS; Saykin A; Wright MJ; Thompson PM; Schumann G; Desrivières S, 2019, 'Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group', Molecular Psychiatry, http://dx.doi.org/10.1038/s41380-019-0605-z
Fullerton JM; Klauser P; Lenroot RK; Shaw AD; Overs B; Heath A; Cairns MJ; Atkins J; Scott R; Schofield PR; Weickert CS; Pantelis C; Fornito A; Whitford TJ; Weickert TW; Zalesky A, 2018, 'Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls', Translational Psychiatry, vol. 8, http://dx.doi.org/10.1038/s41398-017-0052-z
Toma C; Shaw AD; Allcock RJN; Heath A; Pierce KD; Mitchell PB; Schofield PR; Fullerton JM, 2018, 'An examination of multiple classes of rare variants in extended families with bipolar disorder', Translational Psychiatry, vol. 8, http://dx.doi.org/10.1038/s41398-018-0113-y
Bonham LW; Karch CM; Fan CC; Tan C; Geier EG; Wang Y; Wen N; Broce IJ; Li Y; Barkovich MJ; Ferrari R; Hardy J; Momeni P; Höglinger G; Müller U; Hess CP; Sugrue LP; Dillon WP; Schellenberg GD; Miller BL; Andreassen OA; Dale AM; Barkovich AJ; Yokoyama JS; Desikan RS; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Albani D; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Waldö ML; Nilsson K; Nilsson C; MacKenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; McKeith IG; Thomas AJ; Pietrini P; Huey ED; Wassermann EM; Baborie A; Jaros E; Tierney MC; Pastor P; Razquin C; Ortega-Cubero S; Alonso E; Perneczky R; Diehl-Schmid J; Alexopoulos P; Kurz A; Rainero I; Rubino E; Pinessi L; Rogaeva E; George-Hyslop PS; Rossi G; Tagliavini F; Giaccone G; Rowe JB; Schlachetzki JCM; Uphill J; Collinge J; Mead S; Danek A; Van Deerlin VM; Grossman M; Trojanowski JQ, 2018, 'CXCR4 involvement in neurodegenerative diseases', Translational Psychiatry, vol. 8, http://dx.doi.org/10.1038/s41398-017-0049-7
Davies G; Lam M; Harris SE; Trampush JW; Luciano M; Hill WD; Hagenaars SP; Ritchie SJ; Marioni RE; Fawns-Ritchie C; Liewald DCM; Okely JA; Ahola-Olli AV; Barnes CLK; Bertram L; Bis JC; Burdick KE; Christoforou A; Derosse P; Djurovic S; Espeseth T; Giakoumaki S; Giddaluru S; Gustavson DE; Hayward C; Hofer E; Ikram MA; Karlsson R; Knowles E; Lahti J; Leber M; Li S; Mather KA; Melle I; Morris D; Oldmeadow C; Palviainen T; Payton A; Pazoki R; Petrovic K; Reynolds CA; Sargurupremraj M; Scholz M; Smith JA; Smith AV; Terzikhan N; Thalamuthu A; Trompet S; Van Der Lee SJ; Ware EB; Windham BG; Wright MJ; Yang J; Yu J; Ames D; Amin N; Amouyel P; Andreassen OA; Armstrong NJ; Assareh AA; Attia JR; Attix D; Avramopoulos D; Bennett DA; Böhmer AC; Boyle PA; Brodaty H; Campbell H; Cannon TD; Cirulli ET; Congdon E; Conley ED; Corley J; Cox SR; Dale AM; Dehghan A; Dick D; Dickinson D; Eriksson JG; Evangelou E; Faul JD; Ford I; Freimer NA; Gao H; Giegling I; Gillespie NA; Gordon SD; Gottesman RF; Griswold ME; Gudnason V; Harris TB; Hartmann AM; Hatzimanolis A; Heiss G; Holliday EG; Joshi PK; Kähönen M; Kardia SLR; Karlsson I; Kleineidam L, 2018, 'Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function', Nature Communications, vol. 9, http://dx.doi.org/10.1038/s41467-018-04362-x
Vojinovic D; Adams HH; Jian X; Yang Q; Smith AV; Bis JC; Teumer A; Scholz M; Armstrong NJ; Hofer E; Saba Y; Luciano M; Bernard M; Trompet S; Yang J; Gillespie NA; van der Lee SJ; Neumann A; Ahmad S; Andreassen OA; Ames D; Amin N; Arfanakis K; Bastin ME; Becker DM; Beiser AS; Beyer F; Brodaty H; Bryan RN; Bülow R; Dale AM; De Jager PL; Deary IJ; DeCarli C; Fleischman DA; Gottesman RF; van der Grond J; Gudnason V; Harris TB; Homuth G; Knopman DS; Kwok JB; Lewis CE; Li S; Loeffler M; Lopez OL; Maillard P; El Marroun H; Mather KA; Mosley TH; Muetzel RL; Nauck M; Nyquist PA; Panizzon MS; Pausova Z; Psaty BM; Rice K; Rotter JI; Royle N; Satizabal CL; Schmidt R; Schofield PR; Schreiner PJ; Sidney S; Stott DJ; Thalamuthu A; Uitterlinden AG; Valdés Hernández MC; Vernooij MW; Wen W; White T; Witte AV; Wittfeld K; Wright MJ; Yanek LR; Tiemeier H; Kremen WS; Bennett DA; Jukema JW; Paus T; Wardlaw JM; Schmidt H; Sachdev PS; Villringer A; Grabe HJ; Longstreth WT; van Duijn CM; Launer LJ; Seshadri S; Ikram MA; Fornage M, 2018, 'Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume', Nature Communications, vol. 9, http://dx.doi.org/10.1038/s41467-018-06234-w
Toma C; Pierce KD; Shaw AD; Heath A; Mitchell PB; Schofield PR; Fullerton JM, 2018, 'Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders', PLoS Genetics, vol. 14, pp. e1007535, http://dx.doi.org/10.1371/journal.pgen.1007535
de Jong S; Diniz MJA; Saloma A; Gadelha A; Santoro ML; Ota VK; Noto C; Wray NR; Ripke S; Mattheisen M; Trzaskowski M; Byrne EM; Abdellaoui A; Adams MJ; Agerbo E; Air TM; Andlauer TFM; Bacanu SA; Bækvad-Hansen M; Beekman ATF; Bigdeli TB; Binder EB; Blackwood DHR; Bryois J; Buttenschøn HN; Bybjerg-Grauholm J; Cai N; Castelao E; Christensen JH; Clarke TK; Coleman JRI; Colodro-Conde L; Couvy-Duchesne B; Craddock N; Crawford GE; Davies G; Deary IJ; Degenhardt F; Derks EM; Direk N; Dolan CV; Dunn EC; Eley TC; Escott-Price V; Kiadeh FFH; Finucane HK; Forstner AJ; Frank J; Gaspar HA; Gill M; Goes FS; Gordon SD; Grove J; Hansen CS; Hansen TF; Herms S; Hickie IB; Hoffmann P; Homuth G; Horn C; Hottenga JJ; Hougaard DM; Ising M; Jansen R; Jones I; Jones LA; Jorgenson E; Knowles JA; Kohane IS; Kraft J; Kretzschmar WW; Krogh J; Kutalik Z; Li Y; Lind PA; MacIntyre DJ; MacKinnon DF; Maier RM; Maier W; Marchini J; Mbarek H; McGrath P; McGuffin P; Medland SE; Mehta D; Middeldorp CM; Mihailov E; Milaneschi Y; Milani L; Mondimore FM; Montgomery GW; Mostafavi S; Mullins N; Nauck M; Ng B; Nivard MG; Nyholt DR; Oskarsson H; Owen MJ; Painter JN, 2018, 'Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder', Communications Biology, vol. 1, http://dx.doi.org/10.1038/s42003-018-0155-y
Jia T; Chu C; Liu Y; van Dongen J; Armstrong N; Bastin M; Carrillo-Roa T; den Braber A; Harris M; Jansen R; Liu J; Luciano M; Ori APS; Roiz Santianez R; Ruggeri B; Sarkisyan D; Shin J; Sungeun K; Tordesillas Gutierrez D; van't Ent D; Ames D; Artiges E; Bakalkin G; Banaschewski T; Bokde ALW; Brodaty H; Bromberg U; Brouwer R; Buchel C; Burke Quinlan E; Cahn W; de Zubicaray G; Ekstrom T; Flor H; Frohner J; Frouin V; Garavan H; Gowland P; Heinz A; Ittermann B; Jahanshad N; Jiang J; Kwok J; Martin N; Martinot J-L; Mather K; McMahon K; McRae A; Nees F; Papadopoulos Orfanos D; Paus T; Poustka L; Samann P; Schofield P; Smolka M; Strike L; Teeuw J; Thalamuthu A; Trollor J; Walter H; Wardlaw J; Wen W; Whelan R; Apostolova L; Binder E; Boomsma D; Calhoun V; Crespo-Facorro B; Deary I; Hulshoff Pol H; Ophoff R; Pausova Z; Sachdev P; Saykin A; Wright M; Thompson P; Schumann G; Desrivieres S, 2018, 'Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group', BIORXIV, http://dx.doi.org/10.1101/460444
Gatt JM; Burton KLO; Routledge KM; Grasby KL; Korgaonkar MS; Grieve SM; Schofield PR; Harris AWF; Clark CR; Williams LM, 2018, 'A negative association between brainstem pontine grey-matter volume, well-being and resilience in healthy twins', Journal of Psychiatry and Neuroscience, vol. 43, pp. 386 - 395, http://dx.doi.org/10.1503/jpn.170125
Müller S; Preische O; Sohrabi HR; Gräber S; Jucker M; Ringman JM; Martins RN; McDade E; Schofield PR; Ghetti B; Rossor M; Fox NN; Graff-Radford NR; Levin J; Danek A; Vöglein J; Salloway S; Xiong C; Benzinger T; Buckles V; Masters CL; Sperling R; Bateman RJ; Morris JC; Laske C, 2018, 'Relationship between physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer's disease', Alzheimer's and Dementia, vol. 14, pp. 1427 - 1437, http://dx.doi.org/10.1016/j.jalz.2018.06.3059
McDade E; Wang G; Gordon BA; Hassenstab J; Benzinger TLS; Buckles V; Fagan AM; Holtzman DM; Cairns NJ; Goate AM; Marcus DS; Morris JC; Paumier K; Xiong C; Allegri R; Berman SB; Klunk W; Noble J; Ringman J; Ghetti B; Farlow M; Sperling RA; Chhatwal J; Salloway S; Graff-Radford NR; Schofield PR; Masters C; Rossor MN; Fox NC; Levin J; Jucker M; Bateman RJ, 2018, 'Longitudinal cognitive and biomarker changes in dominantly inherited Alzheimer disease', Neurology, vol. 91, pp. E1295 - E1306, http://dx.doi.org/10.1212/WNL.0000000000006277
Revelas M; Thalamuthu A; Oldmeadow C; Evans TJ; Armstrong NJ; Kwok JB; Brodaty H; Schofield PR; Scott RJ; Sachdev PS; Attia JR; Mather KA, 2018, 'Review and meta-analysis of genetic polymorphisms associated with exceptional human longevity', Mechanisms of Ageing and Development, vol. 175, pp. 24 - 34, http://dx.doi.org/10.1016/j.mad.2018.06.002
Caballero MÁA; Suárez-Calvet M; Duering M; Franzmeier N; Benzinger T; Fagan AM; Bateman RJ; Jack CR; Levin J; Dichgans M; Jucker M; Karch C; Masters CL; Morris JC; Weiner M; Rossor M; Fox NC; Lee JH; Salloway S; Danek A; Goate A; Yakushev I; Hassenstab J; Schofield PR; Haass C; Ewers M, 2018, 'White matter diffusion alterations precede symptom onset in autosomal dominant Alzheimer's disease', Brain, vol. 141, pp. 3065 - 3080, http://dx.doi.org/10.1093/brain/awy229
Hofer E; Roshchupkin G; Adams H; Knol M; Lin H; Li S; Zare H; Ahmad S; Armstrong N; Satizabal C; Bernard M; Bis J; Gillespie N; Luciano M; Mishra A; Scholz M; Teumer A; Xia R; Jian X; Mosley T; Saba Y; Pirpamer L; Seiler S; Becker J; Carmichael O; Rotter J; Psaty B; Lopez O; Amin N; Lee S; Yang Q; Himali J; Maillard P; Beiser A; DeCarli C; Karama S; Lewis L; Bastin M; Harris M; Deary I; Witte V; Beyer F; Loeffler M; Mather K; Schofield P; Thalamuthu A; Kwok J; Wright M; Ames D; Trollor J; Jiang J; Brodaty H; Wen W; Vernooij M; Hofman A; Uitterlinden A; Niessen W; Wittfeld K; Bulow R; Volker U; Pausova Z; Pike B; Maingault S; Crivello F; Tzourio C; Amouyel P; Mazoyer B; Neale M; Franz C; Lyons M; Panizzon M; Andreassen O; Dale A; Logue M; Grasby K; Jahanshad N; Painter J; Colodro-Conde L; Bralten J; Hibar D; Lind P; Pizzagalli F; Stein J; Thompson P; Medland S; Sachdev P; Kremen W; Wardlaw J; Villringer A; Duijn C; Grabe H; Longstreth W; Fornage M; Paus T; Debette S; Ikram A; Schmidt H; Schmidt R; Seshadri S, 2018, 'Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium', BIORXIV, http://dx.doi.org/10.1101/409649
Lim YY; Hassenstab J; Goate A; Fagan AM; Benzinger TLS; Cruchaga C; McDade E; Chhatwal J; Levin J; Farlow MR; Graff-Radford NR; Laske C; Masters CL; Salloway S; Schofield P; Morris JC; Maruff P; Bateman RJ, 2018, 'Effect of BDNFVal66Met on disease markers in dominantly inherited Alzheimer's disease', Annals of Neurology, vol. 84, pp. 424 - 435, http://dx.doi.org/10.1002/ana.25299
Karystianis G; Adily A; Schofield P; Knight L; Galdon C; Greenberg D; Jorm L; Nenadic G; Butler T, 2018, 'Automatic extraction of mental health disorders from domestic violence police narratives: Text mining study', Journal of Medical Internet Research, vol. 20, http://dx.doi.org/10.2196/11548
LeBlanc M; Zuber V; Thompson WK; Andreassen OA; Frigessi A; Andreassen BK; Ripke S; Neale BM; Corvin A; Walters JTR; Farh KH; Lee P; Bulik-Sullivan B; Collier DA; Huang H; Pers TH; Agartz I; Agerbo E; Albus M; Alexander M; Amin F; Bacanu SA; Begemann M; Belliveau RA; Bene J; Bevilacqua E; Bigdeli TB; Black DW; Bruggeman R; Buccola NG; Buckner RL; Cahn W; Cai G; Cairns MJ; Campion D; Cantor RM; Carr VJ; Carrera N; Catts SV; Chambert KD; Chan RCK; Chen RYL; Chen EYH; Cheng W; Cheung EFC; Chong SA; Cloninger CR; Cohen D; Cohen N; Cormican P; Craddock N; Crespo-Facorro B; Crowley JJ; Curtis D; Davidson M; Davis KL; Degenhardt F; Favero JD; DeLisi LE; Demontis D; Dikeos D; Dinan T; Donohoe G; Drapeau E; Duan J; Dudbridge F; Durmishi N; Eichhammer P; Eriksson J; Escott-Price V; Essioux L; Fanous AH; Farrell MS; Frank J; Franke L; Freedman R; Freimer NB; Friedl M; Friedman JI; Fromer M; Genovese G; Georgieva L; Gershon ES; Giegling I; Giusti-Rodriguez P; Godard S; Goldstein JI; Golimbet V; Gopal S; Gratten J; de Haan L; Hammer C; Hamshere ML; Hansen M; Hansen T; Haroutunian V; Hartmann AM; Henskens FA; Herms S; Hirschhorn JN, 2018, 'A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework', BMC Genomics, vol. 19, http://dx.doi.org/10.1186/s12864-018-4859-7
Anttila V; Bulik-Sullivan B; Finucane HK; Walters RK; Bras J; Duncan L; Escott-Price V; Falcone GJ; Gormley P; Malik R; Patsopoulos NA; Ripke S; Wei Z; Yu D; Lee PH; Turley P; Grenier-Boley B; Chouraki V; Kamatani Y; Berr C; Letenneur L; Hannequin D; Amouyel P; Boland A; Deleuze JF; Duron E; Vardarajan BN; Reitz C; Goate AM; Huentelman MJ; Ilyas Kamboh M; Larson EB; Rogaeva E; George-Hyslop PS; Hakonarson H; Kukull WA; Farrer LA; Barnes LL; Beach TG; Yesim Demirci F; Head E; Hulette CM; Jicha GA; Kauwe JSK; Kaye JA; Leverenz JB; Levey AI; Lieberman AP; Pankratz VS; Poon WW; Quinn JF; Saykin AJ; Schneider LS; Smith AG; Sonnen JA; Stern RA; Van Deerlin VM; Van Eldik LJ; Harold D; Russo G; Rubinsztein DC; Bayer A; Tsolaki M; Proitsi P; Fox NC; Hampel H; Owen MJ; Mead S; Passmore P; Morgan K; Nöthen MM; Rossor M; Lupton MK; Hoffmann P; Kornhuber J; Lawlor B; McQuillin A; Al-Chalabi A; Bis JC; Ruiz A; Boada M; Seshadri S; Beiser A; Rice K; Van Der Lee SJ; De Jager PL; Geschwind DH; Riemenschneider M; Riedel-Heller S; Rotter JI; Ransmayr G; Hyman BT; Cruchaga C; Alegret M; Winsvold B; Palta P; Farh KH; Cuenca-Leon E; Furlotte N; Kurth T, 2018, 'Analysis of shared heritability in common disorders of the brain', Science, vol. 360, http://dx.doi.org/10.1126/science.aap8757
Ruderfer DM; Ripke S; McQuillin A; Boocock J; Stahl EA; Pavlides JMW; Mullins N; Charney AW; Ori APS; Loohuis LMO; Domenici E; Di Florio A; Papiol S; Kalman JL; Trubetskoy V; Adolfsson R; Agartz I; Agerbo E; Akil H; Albani D; Albus M; Alda M; Alexander M; Alliey-Rodriguez N; Als TD; Amin F; Anjorin A; Arranz MJ; Awasthi S; Bacanu SA; Badner JA; Baekvad-Hansen M; Bakker S; Band G; Barchas JD; Barroso I; Bass N; Bauer M; Baune BT; Begemann M; Bellenguez C; Belliveau RA; Bellivier F; Bender S; Bene J; Bergen SE; Berrettini WH; Bevilacqua E; Biernacka JM; Bigdeli TB; Black DW; Blackburn H; Blackwell JM; Blackwood DHR; Pedersen CB; Boehnke M; Boks M; Borglum AD; Bramon E; Breen G; Brown MA; Bruggeman R; Buccola NG; Buckner RL; Budde M; Bulik-Sullivan B; Bumpstead SJ; Bunney W; Burmeister M; Buxbaum JD; Bybjerg-Grauholm J; Byerley W; Cahn W; Cai G; Cairns MJ; Campion D; Cantor RM; Carr VJ; Carrera N; Casas JP; Casas M; Catts SV; Cervantes P; Chambert KD; Chan RCK; Chen EYH; Chen RYL; Cheng W; Cheung EFC; Chong SA; Clarke TK; Cloninger CR; Cohen D; Cohen N; Coleman JRI; Collier DA; Cormican P; Coryell W; Craddock N; Craig DW, 2018, 'Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes', Cell, vol. 173, pp. 1705 - 1715.e16, http://dx.doi.org/10.1016/j.cell.2018.05.046
Routledge KM; Williams LM; Harris AWF; Schofield PR; Clark CR; Gatt JM, 2018, 'Genetic correlations between wellbeing, depression and anxiety symptoms and behavioral responses to the emotional faces task in healthy twins', Psychiatry Research, vol. 264, pp. 385 - 393, http://dx.doi.org/10.1016/j.psychres.2018.03.042
Zeraati M; Langley DB; Schofield P; Moye AL; Rouet R; Hughes WE; Bryan TM; Dinger ME; Christ D, 2018, 'I-motif DNA structures are formed in the nuclei of human cells', Nature Chemistry, vol. 10, pp. 631 - 637, http://dx.doi.org/10.1038/s41557-018-0046-3
Reinbold CS; Forstner AJ; Hecker J; Fullerton JM; Hoffmann P; Hou L; Heilbronner U; Degenhardt F; Adli M; Akiyama K; Akula N; Ardau R; Arias B; Backlund L; Benabarre A; Bengesser S; Bhattacharjee AK; Biernacka JM; Birner A; Marie-Claire C; Cervantes P; Chen GB; Chen HC; Chillotti C; Clark SR; Colom F; Cousins DA; Cruceanu C; Czerski PM; Dayer A; Étain B; Falkai P; Frisén L; Gard S; Garnham JS; Goes FS; Grof P; Gruber O; Hashimoto R; Hauser J; Herms S; Jamain S; Jiménez E; Kahn JP; Kassem L; Kittel-Schneider S; Kliwicki S; König B; Kusumi I; Lackner N; Laje G; Landén M; Lavebratt C; Leboyer M; Leckband SG; Jaramillo CAL; MacQueen G; Manchia M; Martinsson L; Mattheisen M; McCarthy MJ; McElroy SL; Mitjans M; Mondimore FM; Monteleone P; Nievergelt CM; Ösby U; Ozaki N; Perlis RH; Pfennig A; Reich-Erkelenz D; Rouleau GA; Schofield PR; Schubert KO; Schweizer BW; Seemüller F; Severino G; Shekhtman T; Shilling PD; Shimoda K; Simhandl C; Slaney CM; Smoller JW; Squassina A; Stamm TJ; Stopkova P; Tighe SK; Tortorella A; Turecki G; Volkert J; Witt SH; Wright AJ; Trevor Young L; Zandi PP; Potash JB; DePaulo JR; Bauer M; Reininghaus E; Novák T; Aubry JM, 2018, 'Analysis of the influence of microRNAs in lithium response in bipolar disorder', Frontiers in Psychiatry, vol. 9, http://dx.doi.org/10.3389/fpsyt.2018.00207
Lee S; Zimmerman ME; Narkhede A; Nasrabady SE; Tosto G; Meier IB; Benzinger TLS; Marcus DS; Fagan AM; Fox NC; Cairns NJ; Holtzman DM; Buckles V; Ghetti B; McDade E; Martins RN; Saykin AJ; Masters CL; Ringman JM; Fӧrster S; Schofield PR; Sperling RA; Johnson KA; Chhatwal JP; Salloway S; Correia S; Jack CR; Weiner M; Bateman RJ; Morris JC; Mayeux R; Brickman AM, 2018, 'White matter hyperintensities and the mediating role of cerebral amyloid angiopathy in dominantly-inherited Alzheimer’s disease', PLoS ONE, vol. 13, http://dx.doi.org/10.1371/journal.pone.0195838
Chhatwal JP; Schultz AP; Johnson KA; Hedden T; Jaimes S; Benzinger TLS; Jack C; Ances BM; Ringman JM; Marcus DS; Ghetti B; Farlow MR; Danek A; Levin J; Yakushev I; Laske C; Koeppe RA; Galasko DR; Xiong C; Masters CL; Schofield PR; Kinnunen KM; Salloway S; Martins RN; McDade E; Cairns NJ; Buckles VD; Morris JC; Bateman R; Sperling RA, 2018, 'Preferential degradation of cognitive networks differentiates Alzheimer's disease from ageing', Brain, vol. 141, pp. 1486 - 1500, http://dx.doi.org/10.1093/brain/awy053
Burnett DL; Langley DB; Schofield P; Hermes JR; Chan TD; Jackson J; Bourne K; Reed JH; Patterson K; Porebski BT; Brink R; Christ D; Goodnow CC, 2018, 'Germinal center antibody mutation trajectories are determined by rapid self/foreign discrimination', Science, vol. 360, pp. 223 - 226, http://dx.doi.org/10.1126/science.aao3859
Hibar DP; Westlye LT; Doan NT; Jahanshad N; Cheung JW; Ching CRK; Versace A; Bilderbeck AC; Uhlmann A; Mwangi B; Krämer B; Overs B; Hartberg CB; Abe C; Dima D; Grotegerd D; Sprooten E; Ben E; Jimenez E; Howells FM; Delvecchio G; Temmingh H; Starke J; Almeida JRC; Goikolea JM; Houenou J; Beard LM; Rauer L; Abramovic L; Bonnin M; Ponteduro MF; Keil M; Rive MM; Yao N; Yalin N; Najt P; Rosa PG; Redlich R; Trost S; Hagenaars S; Fears SC; Alonso-Lana S; Van Erp TGM; Nickson T; Chaim-Avancini TM; Meier TB; Elvsashagen T; Haukvik UK; Lee WH; Schene AH; Lloyd AJ; Young AH; Nugent A; Dale AM; Pfennig A; McIntosh AM; Lafer B; Baune BT; Ekman CJ; Zarate CA; Bearden CE; Henry C; Simhandl C; McDonald C; Bourne C; Stein DJ; Wolf DH; Cannon DM; Glahn DC; Veltman DJ; Pomarol-Clotet E; Vieta E; Canales-Rodriguez EJ; Nery FG; Duran FLS; Busatto GF; Roberts G; Pearlson GD; Goodwin GM; Kugel H; Whalley HC; Ruhe HG; Soares JC; Fullerton JM; Rybakowski JK; Savitz J; Chaim KT; Fatjó-Vilas M; Soeiro-De-Souza MG; Boks MP; Zanetti MV; Otaduy MCG; Schaufelberger MS; Alda M; Ingvar M; Phillips ML; Kempton MJ; Bauer M; Landén M; Lawrence NS, 2018, 'Cortical abnormalities in bipolar disorder: An MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group', Molecular Psychiatry, vol. 23, pp. 932 - 942, http://dx.doi.org/10.1038/mp.2017.73
Franzmeier N; Düzel E; Jessen F; Buerger K; Levin J; Duering M; Dichgans M; Haass C; Suárez-Calvet M; Fagan AM; Paumier K; Benzinger T; Masters CL; Morris JC; Perneczky R; Janowitz D; Catak C; Wolfsgruber S; Wagner M; Teipel S; Kilimann I; Ramirez A; Rossor M; Jucker M; Chhatwal J; Spottke A; Boecker H; Brosseron F; Falkai P; Fliessbach K; Heneka MT; Laske C; Nestor P; Peters O; Fuentes M; Menne F; Priller J; Spruth EJ; Franke C; Schneider A; Kofler B; Westerteicher C; Speck O; Wiltfang J; Bartels C; Araque Caballero MÁ; Metzger C; Bittner D; Weiner M; Lee JH; Salloway S; Danek A; Goate A; Schofield PR; Bateman RJ; Ewers M, 2018, 'Left frontal hub connectivity delays cognitive impairment in autosomal-dominant and sporadic Alzheimer’s disease', Brain, vol. 141, pp. 1186 - 1200, http://dx.doi.org/10.1093/brain/awy008
Jiang J; Thalamuthu A; Ho JE; Mahajan A; Ek WE; Brown DA; Breit SN; Wang TJ; Gyllensten U; Chen MH; Enroth S; Januzzi JL; Lind L; Armstrong NJ; Kwok JB; Schofield PR; Wen W; Trollor JN; Johansson Å; Morris AP; Vasan RS; Sachdev PS; Mather KA, 2018, 'A meta-analysis of genome-wide association studies of growth differentiation factor-15 concentration in blood', Frontiers in Genetics, vol. 9, http://dx.doi.org/10.3389/fgene.2018.00097
Mühleisen TW; Reinbold CS; Forstner AJ; Abramova LI; Alda M; Babadjanova G; Bauer M; Brennan P; Chuchalin A; Cruceanu C; Czerski PM; Degenhardt F; Fischer SB; Fullerton JM; Gordon SD; Grigoroiu-Serbanescu M; Grof P; Hauser J; Hautzinger M; Herms S; Hoffmann P; Kammerer-Ciernioch J; Khusnutdinova E; Kogevinas M; Krasnov V; Lacour A; Laprise C; Leber M; Lissowska J; Lucae S; Maaser A; Maier W; Martin NG; Mattheisen M; Mayoral F; McKay JD; Medland SE; Mitchell PB; Moebus S; Montgomery GW; Müller-Myhsok B; Oruc L; Pantelejeva G; Pfennig A; Pojskic L; Polonikov A; Reif A; Rivas F; Rouleau GA; Schenk LM; Schofield PR; Schwarz M; Streit F; Strohmaier J; Szeszenia-Dabrowska N; Tiganov AS; Treutlein J; Turecki G; Vedder H; Witt SH; Schulze TG; Rietschel M; Nöthen MM; Cichon S, 2018, 'Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder', Journal of Affective Disorders, vol. 228, pp. 20 - 25, http://dx.doi.org/10.1016/j.jad.2017.11.068
Gordon BA; Blazey TM; Su Y; Hari-Raj A; Dincer A; Flores S; Christensen J; McDade E; Wang G; Xiong C; Cairns NJ; Hassenstab J; Marcus DS; Fagan AM; Jack CR; Hornbeck RC; Paumier KL; Ances BM; Berman SB; Brickman AM; Cash DM; Chhatwal JP; Correia S; Förster S; Fox NC; Graff-Radford NR; la Fougère C; Levin J; Masters CL; Rossor MN; Salloway S; Saykin AJ; Schofield PR; Thompson PM; Weiner MM; Holtzman DM; Raichle ME; Morris JC; Bateman RJ; Benzinger TLS, 2018, 'Spatial patterns of neuroimaging biomarker change in individuals from families with autosomal dominant Alzheimer's disease: a longitudinal study', The Lancet Neurology, vol. 17, pp. 241 - 250, http://dx.doi.org/10.1016/S1474-4422(18)30028-0
Chang H; Hoshina N; Zhang C; Ma Y; Cao H; Wang Y; Wu DD; Bergen SE; Landén M; Hultman CM; Preisig M; Kutalik Z; Castelao E; Grigoroiu-Serbanescu M; Forstner AJ; Strohmaier J; Hecker J; Schulze TG; Müller-Myhsok B; Reif A; Mitchell PB; Martin NG; Schofield PR; Cichon S; Nöthen MM; Walter H; Erk S; Heinz A; Amin N; Van Duijn CM; Meyer-Lindenberg A; Tost H; Xiao X; Yamamoto T; Rietschel M; Li M; Backlund L; Frisén L; Lavebratt C; Schalling M; Ösby U; Mühleisen TW; Leber M; Degenhardt F; Treutlein J; Mattheisen M; Maaser A; Meier S; Herms S; Hoffmann P; Lacour A; Witt SH; Streit F; Lucae S; Maier W; Schwarz M; Vedder H; Kammerer-Ciernioch J; Pfennig A; Bauer M; Hautzinger M; Wright A; Fullerton JM; Montgomery GW; Medland SE; Gordon SD; Becker T; Schumacher J; Propping P, 2018, 'The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders', Molecular Psychiatry, vol. 23, pp. 400 - 412, http://dx.doi.org/10.1038/mp.2016.231
Kinnunen KM; Cash DM; Poole T; Frost C; Benzinger TLS; Ahsan RL; Leung KK; Cardoso MJ; Modat M; Malone IB; Morris JC; Bateman RJ; Marcus DS; Goate A; Salloway SP; Correia S; Sperling RA; Chhatwal JP; Mayeux RP; Brickman AM; Martins RN; Farlow MR; Ghetti B; Saykin AJ; Jack CRJ; Schofield PR; McDade E; Weiner MW; Ringman JM; Thompson PM; Masters CL; Rowe CC; Rossor MN; Ourselin S; Fox NC, 2018, 'Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial MRI study', Alzheimer's and Dementia, vol. 14, pp. 43 - 53, http://dx.doi.org/10.1016/j.jalz.2017.06.2268
Kinnunen KM; Cash DM; Poole T; Frost C; Benzinger TLS; Ahsan RL; Leung KK; Cardoso MJ; Modat M; Malone IB; Morris JC; Bateman RJ; Marcus DS; Goate A; Salloway SP; Correia S; Sperling RA; Chhatwal JP; Mayeux RP; Brickman AM; Martins RN; Farlow MR; Ghetti B; Saykin AJ; Jack CR; Schofield PR; McDade E; Weiner MW; Ringman JM; Thompson PM; Masters CL; Rowe CC; Rossor MN; Ourselin S; Fox NC, 2018, 'Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial magnetic resonance imaging study', Alzheimer's and Dementia, vol. 14, pp. 43 - 53, http://dx.doi.org/10.1016/j.jalz.2017.06.2268
Vazquez-Lombardi R; Nevoltris D; Luthra A; Schofield P; Zimmermann C; Christ D, 2018, 'Transient expression of human antibodies in mammalian cells', Nature Protocols, vol. 13, pp. 99 - 117, http://dx.doi.org/10.1038/nprot.2017.126
Amare AT; Schubert KO; Hou L; Clark SR; Papiol S; Heilbronner U; Degenhardt F; Tekola-Ayele F; Hsu YH; Shekhtman T; Adli M; Akula N; Akiyama K; Ardau R; Arias B; Aubry JM; Backlund L; Bhattacharjee AK; Bellivier F; Benabarre A; Bengesser S; Biernacka JM; Birner A; Brichant-Petitjean C; Cervantes P; Chen HC; Chillotti C; Cichon S; Cruceanu C; Czerski PM; Dalkner N; Dayer A; Del Zompo M; DePaulo JR; Étain B; Falkai P; Forstner AJ; Frisen L; Frye MA; Fullerton JM; Gard S; Garnham JS; Goes FS; Grigoroiu-Serbanescu M; Grof P; Hashimoto R; Hauser J; Herms S; Hoffmann P; Hofmann A; Jamain S; Jiménez E; Kahn JP; Kassem L; Kuo PH; Kato T; Kelsoe J; Kittel-Schneider S; Kliwicki S; König B; Kusumi I; Laje G; Landén M; Lavebratt C; Leboyer M; Leckband SG; Tortorella A; Manchia M; Martinsson L; McCarthy MJ; McElroy S; Colom F; Mitjans M; Mondimore FM; Monteleone P; Nievergelt CM; Nöthen MM; Novák T; O'Donovan C; Ozaki N; Ösby U; Pfennig A; Potash JB; Reif A; Reininghaus E; Rouleau GA; Rybakowski JK; Schalling M; Schofield PR; Schweizer BW; Severino G; Shilling PD; Shimoda K; Simhandl C; Slaney CM; Squassina A; Stamm T; Stopkova P; Maj M; Turecki G, 2018, 'Association of polygenic score for schizophrenia and HLA antigen and inflammation genes with response to lithium in bipolar affective disorder: A genome-wide association study', JAMA Psychiatry, vol. 75, pp. 65 - 74, http://dx.doi.org/10.1001/jamapsychiatry.2017.3433
Kim WS; Fu Y; Dobson-Stone C; Hsiao JHT; Shang K; Hallupp M; Schofield PR; Garner B; Karl T; Kwok JBJ, 2018, 'Effect of Fluvoxamine on Amyloid-β Peptide Generation and Memory', Journal of Alzheimer's Disease, vol. 62, pp. 1777 - 1787, http://dx.doi.org/10.3233/JAD-171001
Broce I; Karch CM; Wen N; Fan CC; Wang Y; Hong Tan C; Kouri N; Ross OA; Höglinger GU; Muller U; Hardy J; Momeni P; Hess CP; Dillon WP; Miller ZA; Bonham LW; Rabinovici GD; Rosen HJ; Schellenberg GD; Franke A; Karlsen TH; Veldink JH; Ferrari R; Yokoyama JS; Miller BL; Andreassen OA; Dale AM; Desikan RS; Sugrue LP; Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Brooks WS; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Albani D; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Landqvist Waldö M; Nilsson K; Nilsson C; Mackenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; G McKeith I; Thomas AJ; Pietrini P; Huey ED; Wassermann EM; Baborie A; Jaros E; Tierney MC; Pastor P; Razquin C; Ortega-Cubero S; Alonso E; Perneczky R; Diehl-Schmid J; Alexopoulos P; Kurz A; Rainero I; Rubino E; Pinessi L; Rogaeva E; St George-Hyslop P; Rossi G; Tagliavini F; Giaccone G; Rowe JB; Schlachetzki JCM; Uphill J, 2018, 'Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies', PLoS Medicine, vol. 15, http://dx.doi.org/10.1371/journal.pmed.1002487
Müller S; Preische O; Sohrabi HR; Gräber S; Jucker M; Dietzsch J; Ringman JM; Martins RN; McDade E; Schofield PR; Ghetti B; Rossor M; Graff-Radford NR; Levin J; Galasko D; Quaid KA; Salloway S; Xiong C; Benzinger T; Buckles V; Masters CL; Sperling R; Bateman RJ; Morris JC; Laske C, 2017, 'Decreased body mass index in the preclinical stage of autosomal dominant Alzheimer's disease', Scientific Reports, vol. 7, http://dx.doi.org/10.1038/s41598-017-01327-w
Corry J; Green M; Roberts G; Fullerton JM; Schofield PR; Mitchell PB, 2017, 'Does perfectionism in bipolar disorder pedigrees mediate associations between anxiety/stress and mood symptoms?', International Journal of Bipolar Disorders, vol. 5, pp. 34, http://dx.doi.org/10.1186/s40345-017-0102-8
Xiao X; Wang L; Wang C; Yuan TF; Zhou D; Zheng F; Li L; Grigoroiu-Serbanescu M; Ikeda M; Iwata N; Takahashi A; Kamatani Y; Kubo M; Preisig M; Kutalik Z; Castelao E; Pistis G; Amin N; Van Duijn CM; Forstner AJ; Strohmaier J; Hecker J; Schulze TG; Müller-Myhsok B; Reif A; Mitchell PB; Martin NG; Schofield PR; Cichon S; Nöthen MM; Chang H; Luo XJ; Fang Y; Yao YG; Zhang C; Rietschel M; Li M, 2017, 'Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders', Translational Psychiatry, vol. 7, http://dx.doi.org/10.1038/s41398-017-0019-0
Taskesen E; Mishra A; van der Sluis S; Ferrari R; Veldink JH; van Es MA; Smit AB; Posthuma D; Pijnenburg Y; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Albani D; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Waldö ML; Nilsson K; Nilsson C; Mackenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; McKeith IG; Thomas AJ; Pietrini P; Huey ED; Wassermann EM; Baborie A; Jaros E; Tierney MC; Pastor P; Razquin C; Ortega-Cubero S; Alonso E; Perneczky R; Diehl-Schmid J; Alexopoulos P; Kurz A; Rainero I; Rubino E; Pinessi L; Rogaeva E; St George-Hyslop P; Rossi G; Tagliavini F; Giaccone G; Rowe JB; Schlachetzki JCM; Uphill J; Collinge J; Mead S; Danek A; Van Deerlin VM; Grossman M; Trojanowski JQ; van der Zee J; Van Broeckhoven C; Cappa SF; Leber I; Hannequin D; Golfier V; Vercelletto M; Brice A; Nacmias B; Sorbi S; Bagnoli S; Piaceri I; Nielsen JE; Hjermind LE; Riemenschneider M; Mayhaus M, 2017, 'Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS', Scientific Reports, vol. 7, http://dx.doi.org/10.1038/s41598-017-09320-z
Brown BM; Sohrabi HR; Taddei K; Gardener SL; Rainey-Smith SR; Peiffer JJ; Xiong C; Fagan AM; Benzinger T; Buckles V; Erickson KI; Clarnette R; Shah T; Masters CL; Weiner M; Cairns N; Rossor M; Graff-Radford NR; Salloway S; Vöglein J; Laske C; Noble J; Schofield PR; Bateman RJ; Morris JC; Martins RN, 2017, 'Habitual exercise levels are associated with cerebral amyloid load in presymptomatic autosomal dominant Alzheimer's disease', Alzheimer's and Dementia, vol. 13, pp. 1197 - 1206, http://dx.doi.org/10.1016/j.jalz.2017.03.008
van Hulzen KJE; Scholz CJ; Franke B; Ripke S; Klein M; McQuillin A; Sonuga-Barke EJS; Kelsoe JR; Landén M; Andreassen OA; Lesch KP; Weber H; Faraone SV; Arias-Vasquez A; Reif A; Anney RJL; Vasquez AA; Arranz MJ; Asherson P; Banaschewski TJ; Bayés M; Biederman J; Buitelaar JK; Casas M; Charach A; Cormand B; Crosbie J; Dalsgaard S; Daly MJ; Doyle AE; Ebstein RP; Elia J; Freitag C; Gill M; Hakonarson H; Hervas A; Holmans P; Kent L; Kuntsi J; Lambregts-Rommelse N; Langley K; Loo SK; Martin J; McGough JJ; Medland SE; Meyer J; Mick E; Miranda A; Mulas F; Neale BM; Nelson SF; O’Donovan MC; Oades RD; Owen MJ; Palmason H; Ramos-Quiroga JA; Ribasés M; Roeyers H; Romanos J; Romanos M; Rothenberger A; Sánchez-Mora C; Schachar R; Sergeant J; Smalley SL; Steinhausen HC; Thapar A; Todorov A; Walitza S; Wang Y; Warnke A; Williams N; Zhang-James Y; Absher D; Akil H; Anjorin A; Backlund L; Badner JA; Barchas JD; Barrett TB; Bass N; Bauer M; Bellivier F; Bergen SE; Berrettini W; Blackwood D; Bloss CS; Boehnke M; Breen G; Breuer R; Bunney WE; Burmeister M; Byerley W; Caesar S; Chambert K; Cichon S; Collier DA; Corvin A; Coryell W; Craddock N, 2017, 'Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis', Biological Psychiatry, vol. 82, pp. 634 - 641, http://dx.doi.org/10.1016/j.biopsych.2016.08.040
Routledge KM; Burton KLO; Williams LM; Harris A; Schofield PR; Clark CR; Gatt JM, 2017, 'The shared and unique genetic relationship between mental well-being, depression and anxiety symptoms and cognitive function in healthy twins', Cognition and Emotion, vol. 31, pp. 1465 - 1479, http://dx.doi.org/10.1080/02699931.2016.1232242
Chang H; Li L; Peng T; Grigoroiu-Serbanescu M; Bergen SE; Landén M; Hultman CM; Forstner AJ; Strohmaier J; Hecker J; Schulze TG; Müller-Myhsok B; Reif A; Mitchell PB; Martin NG; Cichon S; Nöthen MM; Jamain S; Leboyer M; Bellivier F; Etain B; Kahn JP; Henry C; Rietschel M; Backlund L; Frisén L; Lavebratt C; Schalling M; Ösby U; Mühleisen TW; Leber M; Degenhardt F; Treutlein J; Mattheisen M; Hofmann A; Breuer R; Meier S; Herms S; Hoffmann P; Lacour A; Witt SH; Streit F; Lucae S; Maier W; Schwarz M; Vedder H; Kammerer-Ciernioch J; Pfennig A; Bauer M; Hautzinger M; Wright A; Fullerton JM; Schofield PR; Montgomery GW; Medland SE; Gordon SD; Becker T; Schumacher J; Propping P; Xiao X; Li M, 2017, 'Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1', Molecular Neurobiology, vol. 54, pp. 5166 - 5176, http://dx.doi.org/10.1007/s12035-016-0041-x
Salminen LE; Schofield PR; Pierce KD; Bruce SE; Griffin MG; Tate DF; Cabeen RP; Laidlaw DH; Conturo TE; Bolzenius JD; Paul RH, 2017, 'Vulnerability of white matter tracts and cognition to the SOD2 polymorphism: A preliminary study of antioxidant defense genes in brain aging', Behavioural Brain Research, vol. 329, pp. 111 - 119, http://dx.doi.org/10.1016/j.bbr.2017.04.041
Witt SH; Streit F; Jungkunz M; Frank J; Awasthi S; Reinbold CS; Treutlein J; Degenhardt F; Forstner AJ; Heilmann-Heimbach S; Dietl L; Schwarze CE; Schendel D; Strohmaier J; Abdellaoui A; Adolfsson R; Air TM; Akil H; Alda M; Alliey-Rodriguez N; Andreassen OA; Babadjanova G; Bass NJ; Bauer M; Baune BT; Bellivier F; Bergen S; Bethell A; Biernacka JM; Blackwood DHR; Boks MP; Boomsma DI; Børglum AD; Borrmann-Hassenbach M; Brennan P; Budde M; Buttenschøn HN; Byrne EM; Cervantes P; Clarke TK; Craddock N; Cruceanu C; Curtis D; Czerski PM; Dannlowski U; Davis T; de Geus EJC; Di Florio A; Djurovic S; Domenici E; Edenberg HJ; Etain B; Fischer SB; Forty L; Fraser C; Frye MA; Fullerton JM; Gade K; Gershon ES; Giegling I; Gordon SD; Gordon-Smith K; Grabe HJ; Green EK; Greenwood TA; Grigoroiu-Serbanescu M; Guzman-Parra J; Hall LS; Hamshere M; Hauser J; Hautzinger M; Heilbronner U; Herms S; Hitturlingappa S; Hoffmann P; Holmans P; Hottenga JJ; Jamain S; Jones I; Jones LA; Juréus A; Kahn RS; Kammerer-Ciernioch J; Kirov G; Kittel-Schneider S; Kloiber S; Knott SV; Kogevinas M; Landén M; Leber M; Leboyer M; Li QS; Lissowska J; Lucae S; Martin NG; Mayoral-Cleries F; McElroy SL; McIntosh AM; McKay JD; McQuillin A, 2017, 'Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia', Translational psychiatry, vol. 7, pp. e1155, http://dx.doi.org/10.1038/tp.2017.115
Armstrong NJ; Mather KA; Thalamuthu A; Wright MJ; Trollor JN; Ames D; Brodaty H; Schofield PR; Sachdev PS; Kwok JB, 2017, 'Aging, exceptional longevity and comparisons of the Hannum and Horvath epigenetic clocks', Epigenomics, vol. 9, pp. 689 - 700, http://dx.doi.org/10.2217/epi-2016-0179
Kräutler NJ; Suan D; Butt D; Bourne K; Hermes JR; Chan TD; Sundling C; Kaplan W; Schofield P; Jackson J; Basten A; Christ D; Brink R, 2017, 'Differentiation of germinal center B cells into plasma cells is initiated by high-affinity antigen and completed by Tfh cells', Journal of Experimental Medicine, vol. 214, pp. 1259 - 1267, http://dx.doi.org/10.1084/jem.20161533
Rouet R; Langley DB; Schofield P; Christie M; Roome B; Porebski BT; Buckle AM; Clifton BE; Jackson CJ; Stock D; Christ D, 2017, 'Structural reconstruction of protein ancestry', Proceedings of the National Academy of Sciences of the United States of America, vol. 114, pp. 3897 - 3902, http://dx.doi.org/10.1073/pnas.1613477114
Meiser B; Peate M; Levitan C; Mitchell PB; Trevena L; Barlow-Stewart K; Dobbins T; Christensen H; Sherman KA; Dunlop K; Schofield PR, 2017, 'A Psycho-Educational Intervention for People with a Family History of Depression: Pilot Results', Journal of Genetic Counseling, vol. 26, pp. 312 - 321, http://dx.doi.org/10.1007/s10897-016-0011-5
Forstner AJ; Hecker J; Hofmann A; Maaser A; Reinbold CS; Mühleisen TW; Leber M; Strohmaier J; Degenhardt F; Treutlein J; Mattheisen M; Schumacher J; Streit F; Meier S; Herms S; Hoffmann P; Lacour A; Witt SH; Reif A; Müller-Myhsok B; Lucae S; Maier W; Schwarz M; Vedder H; Kammerer-Ciernioch J; Pfennig A; Bauer M; Hautzinger M; Moebus S; Schenk LM; Fischer SB; Sivalingam S; Czerski PM; Hauser J; Lissowska J; Szeszenia-Dabrowska N; Brennan P; McKay JD; Wright A; Mitchell PB; Fullerton JM; Schofield PR; Montgomery GW; Medland SE; Gordon SD; Martin NG; Krasnov V; Chuchalin A; Babadjanova G; Pantelejeva G; Abramova LI; Tiganov AS; Polonikov A; Khusnutdinova E; Alda M; Cruceanu C; Rouleau GA; Turecki G; Laprise C; Rivas F; Mayoral F; Kogevinas M; Grigoroiu-Serbanescu M; Becker T; Schulze TG; Rietschel M; Cichon S; Fier H; Nöthen MM, 2017, 'Identification of shared risk loci and pathways for bipolar disorder and schizophrenia', PLoS ONE, vol. 12, http://dx.doi.org/10.1371/journal.pone.0171595
Ferrari R; Wang Y; Vandrovcova J; Guelfi S; Witeolar A; Karch CM; Schork AJ; Fan CC; Brewer JB; Momeni P; Schellenberg GD; Dillon WP; Sugrue LP; Hess CP; Yokoyama JS; Bonham LW; Rabinovici GD; Miller BL; Andreassen OA; Dale AM; Hardy J; Desikan RS; Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Albani D; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Landqvist Waldö M; Nilsson K; Nilsson C; Mackenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; McKeith IG; Thomas AJ; Pietrini P; Huey ED; Wassermann EM; Baborie A; Jaros E; Tierney MC; Pastor P; Razquin C; Ortega-Cubero S; Alonso E; Perneczky R; Diehl-Schmid J; Alexopoulos P; Kurz A; Rainero I; Rubino E; Pinessi L; Rogaeva E; St George-Hyslop P; Rossi G; Tagliavini F; Giaccone G; Rowe JB; Schlachetzki JCM; Uphill J; Collinge J; Mead S; Danek A; Van Deerlin VM; Grossman M; Trojanowski JQ; van der Zee J; Cruts M, 2017, 'Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases', Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, pp. 152 - 164, http://dx.doi.org/10.1136/jnnp-2016-314411
Hibar DP; Adams HHH; Jahanshad N; Chauhan G; Stein JL; Hofer E; Renteria ME; Bis JC; Arias-Vasquez A; Ikram MK; Desrivières S; Vernooij MW; Abramovic L; Alhusaini S; Amin N; Andersson M; Arfanakis K; Aribisala BS; Armstrong NJ; Athanasiu L; Axelsson T; Beecham AH; Beiser A; Bernard M; Blanton SH; Bohlken MM; Boks MP; Bralten J; Brickman AM; Carmichael O; Chakravarty MM; Chen Q; Ching CRK; Chouraki V; Cuellar-Partida G; Crivello F; Den Braber A; Doan NT; Ehrlich S; Giddaluru S; Goldman AL; Gottesman RF; Grimm O; Griswold ME; Guadalupe T; Gutman BA; Hass J; Haukvik UK; Hoehn D; Holmes AJ; Hoogman M; Janowitz D; Jia T; Jørgensen KN; Karbalai N; Kasperaviciute D; Kim S; Klein M; Kraemer B; Lee PH; Liewald DCM; Lopez LM; Luciano M; MacAre C; Marquand AF; Matarin M; Mather KA; Mattheisen M; McKay DR; Milaneschi Y; Muñoz Maniega S; Nho K; Nugent AC; Nyquist P; Loohuis LMO; Oosterlaan J; Papmeyer M; Pirpamer L; Pütz B; Ramasamy A; Richards JS; Risacher SL; Roiz-Santiañez R; Rommelse N; Ropele S; Rose EJ; Royle NA; Rundek T; Sämann PG; Saremi A; Satizabal CL; Schmaal L; Schork AJ; Shen L; Shin J; Shumskaya E; Smith AV; Sprooten E; Strike LT; Teumer A, 2017, 'Novel genetic loci associated with hippocampal volume', Nature Communications, vol. 8, http://dx.doi.org/10.1038/ncomms13624
Lipnicki DM; Crawford J; Kochan NA; Trollor JN; Draper B; Reppermund S; Maston K; Mather KA; Brodaty H; Sachdev PS, 2017, 'Risk Factors for Mild Cognitive Impairment, Dementia and Mortality: The Sydney Memory and Ageing Study', Journal of the American Medical Directors Association, vol. 18, pp. 388 - 395, http://dx.doi.org/10.1016/j.jamda.2016.10.014
Mishra A; Ferrari R; Heutink P; Hardy J; Pijnenburg Y; Posthuma D, 2017, 'Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia', Brain, vol. 140, pp. 1437 - 1446, http://dx.doi.org/10.1093/brain/awx066
Adams HHH; Hibar DP; Chouraki V; Stein JL; Nyquist PA; Rentería ME; Trompet S; Arias-Vasquez A; Seshadri S; Desrivières S; Beecham AH; Jahanshad N; Wittfeld K; Van Der Lee SJ; Abramovic L; Alhusaini S; Amin N; Andersson M; Arfanakis K; Aribisala BS; Armstrong NJ; Athanasiu L; Axelsson T; Beiser A; Bernard M; Bis JC; Blanken LME; Blanton SH; Bohlken MM; Boks MP; Bralten J; Brickman AM; Carmichael O; Chakravarty MM; Chauhan G; Chen Q; Ching CRK; Cuellar-Partida G; Braber AD; Doan NT; Ehrlich S; Filippi I; Ge T; Giddaluru S; Goldman AL; Gottesman RF; Greven CU; Grimm O; Griswold ME; Guadalupe T; Hass J; Haukvik UK; Hilal S; Hofer E; Hoehn D; Holmes AJ; Hoogman M; Janowitz D; Jia T; Kasperaviciute D; Kim S; Klein M; Kraemer B; Lee PH; Liao J; Liewald DCM; Lopez LM; Luciano M; Macare C; Marquand A; Matarin M; Mather KA; Mattheisen M; Mazoyer B; McKay DR; McWhirter R; Milaneschi Y; Mirza-Schreiber N; Muetzel RL; Maniega SM; Nho K; Nugent AC; Loohuis LMO; Oosterlaan J; Papmeyer M; Pappa I; Pirpamer L; Pudas S; Pütz B; Rajan KB; Ramasamy A; Richards JS; Risacher SL; Roiz-Santiañez R; Rommelse N; Rose EJ; Royle NA; Rundek T; Sämann PG; Satizabal CL, 2016, 'Novel genetic loci underlying human intracranial volume identified through genome-wide association', Nature Neuroscience, vol. 19, pp. 1569 - 1582, http://dx.doi.org/10.1038/nn.4398
Tang M; Ryman DC; McDade E; Jasielec MS; Buckles VD; Cairns NJ; Fagan AM; Goate A; Marcus DS; Xiong C; Allegri RF; Chhatwal JP; Danek A; Farlow MR; Fox NC; Ghetti B; Graff-Radford NR; Laske C; Martins RN; Masters CL; Mayeux RP; Ringman JM; Rossor MN; Salloway SP; Schofield PR; Morris JC; Bateman RJ, 2016, 'Neurological manifestations of autosomal dominant familial Alzheimer's disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS)', The Lancet Neurology, vol. 15, pp. 1317 - 1325, http://dx.doi.org/10.1016/S1474-4422(16)30229-0
Kindler J; Weickert CS; Schofield PR; Lenroot R; Weickert TW, 2016, 'Raloxifene increases prefrontal activity during emotional inhibition in schizophrenia based on estrogen receptor genotype', European Neuropsychopharmacology, vol. 26, pp. 1930 - 1940, http://dx.doi.org/10.1016/j.euroneuro.2016.10.009
Routledge KM; Burton KLO; Williams LM; Harris A; Schofield PR; Clark CR; Gatt JM, 2016, 'Shared versus distinct genetic contributions of mental wellbeing with depression and anxiety symptoms in healthy twins', Psychiatry Research, vol. 244, pp. 65 - 70, http://dx.doi.org/10.1016/j.psychres.2016.07.016
Lim YY; Hassenstab J; Cruchaga C; Goate A; Fagan AM; Benzinger TLS; Maruff P; Snyder PJ; Masters CL; Allegri R; Chhatwal J; Farlow MR; Graff-Radford NR; Laske C; Levin J; McDade E; Ringman JM; Rossor M; Salloway S; Schofield PR; Holtzman DM; Morris JC; Bateman RJ, 2016, 'BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's disease', Brain, vol. 139, pp. 2766 - 2777, http://dx.doi.org/10.1093/brain/aww200
Hou L; Bergen SE; Akula N; Song J; Hultman CM; Landén M; Adli M; Alda M; Ardau R; Arias B; Aubry JM; Backlund L; Badner JA; Barrett TB; Bauer M; Baune BT; Bellivier F; Benabarre A; Bengesser S; Berrettini WH; Bhattacharjee AK; Biernacka JM; Birner A; Bloss CS; Brichant-Petitjean C; Bui ET; Byerley W; Cervantes P; Chillotti C; Cichon S; Colom F; Coryell W; Craig DW; Cruceanu C; Czerski PM; Davis T; Dayer A; Degenhardt F; Del Zompo M; DePaulo JR; Edenberg HJ; Étain B; Falkai P; Foroud T; Forstner AJ; Frisén L; Frye MA; Fullerton JM; Gard S; Garnham JS; Gershon ES; Goes FS; Greenwood TA; Grigoroiu-Serbanescu M; Hauser J; Heilbronner U; Heilmann-Heimbach S; Herms S; Hipolito M; Hitturlingappa S; Hoffmann P; Hofmann A; Jamain S; Jiménez E; Kahn JP; Kassem L; Kelsoe JR; Kittel-Schneider S; Kliwicki S; Koller DL; König B; Lackner N; Laje G; Lang M; Lavebratt C; Lawson WB; Leboyer M; Leckband SG; Liu C; Maaser A; Mahon PB; Maier W; Maj M; Manchia M; Martinsson L; McCarthy MJ; McElroy SL; McInnis MG; McKinney R; Mitchell PB; Mitjans M; Mondimore FM; Monteleone P; Mühleisen TW; Nievergelt CM; Nöthen MM; Novák T; Nurnberger JI; Nwulia EA; Ösby U, 2016, 'Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder', Human Molecular Genetics, vol. 25, pp. 3383 - 3394, http://dx.doi.org/10.1093/hmg/ddw181
Sachdev PS; Thalamuthu A; Mather KA; Ames D; Wright MJ; Wen W; Bowden J; Lee T; Brodaty H; Crawford J; Duckworth T; Kang K; Garden N; Martin N; Lemmon C, 2016, 'White Matter Hyperintensities Are under Strong Genetic Influence', Stroke, vol. 47, pp. 1422 - 1428, http://dx.doi.org/10.1161/STROKEAHA.116.012532
Lee S; Viqar F; Zimmerman ME; Narkhede A; Tosto G; Benzinger TLS; Marcus DS; Fagan AM; Goate A; Fox NC; Cairns NJ; Holtzman DM; Buckles V; Ghetti B; McDade E; Martins RN; Saykin AJ; Masters CL; Ringman JM; Ryan NS; Förster S; Laske C; Schofield PR; Sperling RA; Salloway S; Correia S; Jack C; Weiner M; Bateman RJ; Morris JC; Mayeux R; Brickman AM, 2016, 'White matter hyperintensities are a core feature of Alzheimer's disease: Evidence from the dominantly inherited Alzheimer network', Annals of Neurology, vol. 79, pp. 929 - 939, http://dx.doi.org/10.1002/ana.24647
Girshkin L; O'Reilly N; Quidé Y; Teroganova N; Rowland JE; Schofield PR; Green MJ, 2016, 'Diurnal cortisol variation and cortisol response to an MRI stressor in schizophrenia and bipolar disorder', Psychoneuroendocrinology, vol. 67, pp. 61 - 69, http://dx.doi.org/10.1016/j.psyneuen.2016.01.021
Mather KA; Thalamuthu A; Oldmeadow C; Song F; Armstrong NJ; Poljak A; Holliday EG; McEvoy M; Kwok JB; Assareh AA; Reppermund S; Kochan NA; Lee T; Ames D; Wright MJ; Trollor JN; Schofield PW; Brodaty H; Scott RJ; Schofield PR; Attia JR; Sachdev PS, 2016, 'Genome-wide significant results identified for plasma apolipoprotein H levels in middle-aged and older adults', Scientific Reports, vol. 6, pp. 23675, http://dx.doi.org/10.1038/srep23675
Hou L; Heilbronner U; Degenhardt F; Adli M; Akiyama K; Akula N; Ardau R; Arias B; Backlund L; Banzato CEM; Benabarre A; Bengesser S; Bhattacharjee AK; Biernacka JM; Birner A; Brichant-Petitjean C; Bui ET; Cervantes P; Chen GB; Chen HC; Chillotti C; Cichon S; Clark SR; Colom F; Cousins DA; Cruceanu C; Czerski PM; Dantas CR; Dayer A; Étain B; Falkai P; Forstner AJ; Frisén L; Fullerton JM; Gard S; Garnham JS; Goes FS; Grof P; Gruber O; Hashimoto R; Hauser J; Herms S; Hoffmann P; Hofmann A; Jamain S; Jiménez E; Kahn JP; Kassem L; Kittel-Schneider S; Kliwicki S; König B; Kusumi I; Lackner N; Laje G; Landén M; Lavebratt C; Leboyer M; Leckband SG; Jaramillo CAL; Macqueen G; Manchia M; Martinsson L; Mattheisen M; McCarthy MJ; McElroy SL; Mitjans M; Mondimore FM; Monteleone P; Nievergelt CM; Nöthen MM; Ösby U; Ozaki N; Perlis RH; Pfennig A; Reich-Erkelenz D; Rouleau GA; Schofield PR; Schubert KO; Schweizer BW; Seemüller F; Severino G; Shekhtman T; Shilling PD; Shimoda K; Simhandl C; Slaney CM; Smoller JW; Squassina A; Stamm T; Stopkova P; Tighe SK; Tortorella A; Turecki G; Volkert J; Witt S; Wright A; Young LT; Zandi PP; Potash JB; Depaulo JR, 2016, 'Genetic variants associated with response to lithium treatment in bipolar disorder: A genome-wide association study', The Lancet, vol. 387, pp. 1085 - 1093, http://dx.doi.org/10.1016/S0140-6736(16)00143-4
Su Y; Blazey TM; Owen CJ; Christensen JJ; Friedrichsen K; Joseph-Mathurin N; Wang Q; Hornbeck RC; Ances BM; Snyder AZ; Cash LA; Koeppe RA; Klunk WE; Galasko D; Brickman AM; McDade E; Ringman JM; Thompson PM; Saykin AJ; Ghetti B; Sperling RA; Johnson KA; Salloway SP; Schofield PR; Masters CL; Villemagne VL; Fox NC; Förster S; Chen K; Reiman EM; Xiong C; Marcus DS; Weiner MW; Morris JC; Bateman RJ; Benzinger TLS, 2016, 'Quantitative Amyloid imaging in autosomal Dominant Alzheimer's disease: Results from the DIAN study group', PLoS ONE, vol. 11, http://dx.doi.org/10.1371/journal.pone.0152082
Franke B; van Hulzen KJE; Arias-Vasquez A; Bralten J; Hoogman M; Klein M; van Donkelaar MMJ; Hakobjan MMH; Heister AJGAM; Makkinje RRR; Naber MAM; van der Marel SSL; Mostert JC; Brunner HG; van Bokhoven H; Zwiers MP; Buitelaar JK; Fernández G; Fisher SE; Francks C; Stein JL; Hibar DP; Thompson PM; Ripke S; Anttila V; Neale BM; Farh KH; Bulik-Sullivan B; Huang H; Fromer M; Goldstein JI; Daly MJ; Walters RK; Smoller JW; Lee P; Belliveau RA; Bergen SE; Bevilacqua E; Chambert KD; Genovese G; O'Dushlaine C; Scolnick EM; McCarroll SA; Moran JL; Palotie A; Petryshen TL; Erk S; Heinz A; Mohnke S; Romanczuk-Seiferth N; Walter H; DeLisi LE; McCarley RW; Mesholam-Gately RI; Seidman LJ; Nichols TE; Neale MC; McIntosh AM; Papmeyer M; Sprooten E; Lawrie SM; Sussmann JE; McMahon FJ; Yao Y; Meyer-Lindenberg A; Schwarz E; Grimm O; Mattheisen M; Agerbo E; Demontis D; Hansen T; Mors O; Olsen L; Rasmussen HB; Børglum AD; Mortensen PB; Werge T; Andreassen OA; Brown AA; Athanasiu L; Hartberg CB; Haukvik U; Melle I; Gruber O; Kraemer B; Keil M; Sachdev PS; Mather KA; Thalamuthu A; Armstrong NJ; Assareh AA; Brodaty H; Reppermund S; Wen W; Roiz-Santiañez R; Perez-Iglesias R; Saykin AJ; Kim S; Nho K; Risacher SL, 2016, 'Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept', Nature Neuroscience, vol. 19, pp. 420 - 431, http://dx.doi.org/10.1038/nn.4228
Li M; Luo XJ; Landén M; Bergen SE; Hultman CM; Li X; Zhang W; Yao YG; Zhang C; Liu J; Mattheisen M; Cichon S; Mühleisen TW; Degenhardt FA; Nöthen MM; Schulze TG; Grigoroiu-Serbanescu M; Li H; Fuller CK; Chen C; Dong Q; Chen C; Jamain S; Leboyer M; Bellivier F; Etain B; Kahn JP; Henry C; Preisig M; Kutalik Z; Castelao E; Wright A; Mitchell PB; Fullerton JM; Schofield PR; Montgomery GW; Medland SE; Gordon SD; Martin NG; Rietschel M; Liu C; Kleinman JE; Hyde TM; Weinberger DR; Su B, 2016, 'Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance', British Journal of Psychiatry, vol. 208, pp. 128 - 137, http://dx.doi.org/10.1192/bjp.bp.114.156976
Salminen LE; Schofield PR; Pierce KD; Zhao Y; Luo X; Wang Y; Laidlaw DH; Cabeen RP; Conturo TE; Tate DF; Akbudak E; Lane EM; Heaps JM; Bolzenius JD; Baker LM; Cagle LM; Paul RH, 2016, 'Neuromarkers of the common angiotensinogen polymorphism in healthy older adults: A comprehensive assessment of white matter integrity and cognition', Behavioural Brain Research, vol. 296, pp. 85 - 93, http://dx.doi.org/10.1016/j.bbr.2015.08.028
Shiner CT; Pierce KD; Thompson-Butel AG; Trinh T; Schofield PR; McNulty PA, 2016, 'BDNF genotype interacts with motor function to influence rehabilitation responsiveness poststroke', Frontiers in Neurology, vol. 7, http://dx.doi.org/10.3389/fneur.2016.00069
Burton KLO; Williams LM; Richard Clark C; Harris A; Schofield PR; Gatt JM, 2015, 'Sex differences in the shared genetics of dimensions of self-reported depression and anxiety', Journal of Affective Disorders, vol. 188, pp. 35 - 42, http://dx.doi.org/10.1016/j.jad.2015.08.053
Ringman JM; Liang LJ; Zhou Y; Vangala S; Teng E; Kremen S; Wharton D; Goate A; Marcus DS; Farlow M; Ghetti B; McDade E; Masters CL; Mayeux RP; Rossor M; Salloway S; Schofield PR; Cummings JL; Buckles V; Bateman R; Morris JC, 2015, 'Erratum: Early behavioural changes in familial Alzheimers disease in the Dominantly Inherited Alzheimer Network (Brain (2015) 138 (103645) (10.1093/brain/awv004))', Brain, vol. 138, pp. e401, http://dx.doi.org/10.1093/brain/awv210
Brautigam H; Moreno CL; Steele JW; Bogush A; Dickstein DL; Kwok JBJ; Schofield PR; Thinakaran G; Mathews PM; Hof PR; Gandy S; Ehrlich ME, 2015, 'Physiologically generated presenilin 1 lacking exon 8 fails to rescue brain PS1-/- phenotype and forms complexes with wildtype PS1 and nicastrin', Scientific Reports, vol. 5, http://dx.doi.org/10.1038/srep17042
Forstner AJ; Hofmann A; Maaser A; Sumer S; Khudayberdiev S; Mühleisen TW; Leber M; Schulze TG; Strohmaier J; Degenhardt F; Treutlein J; Mattheisen M; Schumacher J; Breuer R; Meier S; Herms S; Hoffmann P; Lacour A; Witt SH; Reif A; Müller-Myhsok B; Lucae S; Maier W; Schwarz M; Vedder H; Kammerer-Ciernioch J; Pfennig A; Bauer M; Hautzinger M; Moebus S; Priebe L; Sivalingam S; Verhaert A; Schulz H; Czerski PM; Hauser J; Lissowska J; Szeszenia-Dabrowska N; Brennan P; McKay JD; Wright A; Mitchell PB; Fullerton JM; Schofield PR; Montgomery GW; Medland SE; Gordon SD; Martin NG; Krasnov V; Chuchalin A; Babadjanova G; Pantelejeva G; Abramova LI; Tiganov AS; Polonikov A; Khusnutdinova E; Alda M; Cruceanu C; Rouleau GA; Turecki G; Laprise C; Rivas F; Mayoral F; Kogevinas M; Grigoroiu-Serbanescu M; Propping P; Becker T; Rietsche M; Cichon S; Schratt G; Nöthen MM, 2015, 'Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder', Translational Psychiatry, vol. 5, pp. e678, http://dx.doi.org/10.1038/tp.2015.159
Sachdev PS; Lipnicki DM; Kochan NA; Crawford JD; Thalamuthu A; Andrews G; Brayne C; Matthews FE; Stephan BCM; Lipton RB; Katz MJ; Ritchie K; Carrière I; Ancelin ML; Lam LCW; Wong CHY; Fung AWT; Guaita A; Vaccaro R; Davin A; Ganguli M; Dodge H; Hughes T; Anstey KJ; Cherbuin N; Butterworth P; Ng TP; Gao Q; Reppermund S; Brodaty H; Schupf N; Manly J; Stern Y; Lobo A; Lopez-Anton R; Santabárbara J; Zimmerman M; Derby C; Leung GTY; Chan WC; Polito L; Abbondanza S; Valle E; Colombo M; Vitali SF; Fossi S; Zaccaria D; Forloni G; Villani S; Christensen H; MacKinnon A; Easteal S; Jacomb T; Maxwell K; Bowman A; Burns K; Broe A; Dekker J; Dooley L; De Permentier M; Fairjones S; Fletcher J; French T; Foster C; Nugent-Cleary-Fox E; Gooi C; Harvey E; Helyer R; Hsieh S; Hughes L; Jacek S; Johnston M; McCade D; Meeth S; Milne E; Moir A; O'Grady R; Pfaeffli K; Pose C; Reuser L; Rose A; Schofield P; Shahnawaz Z; Sharpley A; Thompson C; Queisser W; Wong S; Mayeux R; Brickman A; Luchsinger J; Sanchez D; Tang MX; Andrews H; Marcos G; De-La-Cámara C; Saz P; Ventura T; Quintanilla MA; Lobo E, 2015, 'The prevalence of mild cognitive impairment in diverse geographical and ethnocultural regions: The COSMIC Collaboration', PLoS ONE, vol. 10, http://dx.doi.org/10.1371/journal.pone.0142388
Salminen LE; Schofield PR; Pierce KD; Luo X; Zhao Y; Laidlaw DH; Cabeen RP; Conturo TE; Lane EM; Heaps JM; Bolzenius JD; Baker LM; Cooley SA; Scott S; Cagle LM; Paul RH, 2015, 'Genetic markers of cholesterol transport and gray matter diffusion: a preliminary study of the CETP I405V polymorphism', Journal of Neural Transmission, vol. 122, pp. 1581 - 1592, http://dx.doi.org/10.1007/s00702-015-1434-0
Boraxbekk CJ; Ames D; Kochan NA; Lee T; Thalamuthu A; Wen W; Armstrong NJ; Kwok JBJ; Schofield PR; Reppermund S; Wright MJ; Trollor JN; Brodaty H; Sachdev P; Mather KA, 2015, 'Investigating the influence of KIBRA and CLSTN2 genetic polymorphisms on cross-sectional and longitudinal measures of memory performance and hippocampal volume in older individuals', Neuropsychologia, vol. 78, pp. 10 - 17, http://dx.doi.org/10.1016/j.neuropsychologia.2015.09.031
Fullerton JM; Koller DL; Edenberg HJ; Foroud T; Liu H; Glowinski AL; Mcinnis MG; Wilcox HC; Frankland A; Roberts G; Schofield PR; Mitchell PB; Nurnberger JI; Hulvershorn L; Fisher C; Monahan PO; McInnis M; Kamali M; Brucksch C; Glowinski A; Gershon ES; Berrettini W, 2015, 'Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals', American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 168, pp. 617 - 629, http://dx.doi.org/10.1002/ajmg.b.32344
Dobson-Stone C; Shaw AD; Hallupp M; Bartley L; McCann H; Brooks WS; Loy CT; Schofield PR; Mather KA; Kochan NA; Sachdev PS; Halliday GM; Piguet O; Hodges JR; Kwok JBJ, 2015, 'Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?', Brain, vol. 138, pp. e385, http://dx.doi.org/10.1093/brain/awv115
Wang F; Gordon BA; Ryman DC; Ma S; Xiong C; Hassenstab J; Goate A; Fagan AM; Cairns NJ; Marcus DS; McDade E; Ringman JM; Graff-Radford NR; Ghetti B; Farlow MR; Sperling R; Salloway S; Schofield PR; Masters CL; Martins RN; Rossor MN; Jucker M; Danek A; Förster S; Lane CAS; Morris JC; Benzinger TLS; Bateman RJ, 2015, 'Cerebral amyloidosis associated with cognitive decline in autosomal dominant Alzheimer disease', Neurology, vol. 85, pp. 790 - 798, http://dx.doi.org/10.1212/WNL.0000000000001903
Weickert T; Weinberg D; Lenroot R; Catts SV; Wells R; Vercammen A; O'Donnell M; Galletly C; Liu D; Balzan R; Short B; Pellen D; Curtis J; Carr VJ; Kulkarni J; Schofield PR; Weickert CS, 2015, 'Adjunctive raloxifene treatment improves attention and memory in men and women with schizophrenia', Molecular Psychiatry, vol. 20, pp. 685 - 694, http://dx.doi.org/10.1038/mp.2015.11
Hibar DP; Stein JL; Renteria ME; Arias-Vasquez A; Desrivières S; Jahanshad N; Toro R; Wittfeld K; Abramovic L; Andersson M; Aribisala BS; Armstrong NJ; Bernard M; Bohlken MM; Boks MP; Bralten J; Brown AA; Mallar Chakravarty M; Chen Q; Ching CRK; Cuellar-Partida G; Den Braber A; Giddaluru S; Goldman AL; Grimm O; Guadalupe T; Hass J; Woldehawariat G; Holmes AJ; Hoogman M; Janowitz D; Jia T; Kim S; Klein M; Kraemer B; Lee PH; Olde Loohuis LM; Luciano M; MacAre C; Mather KA; Mattheisen M; Milaneschi Y; Nho K; Papmeyer M; Ramasamy A; Risacher SL; Roiz-Santiañez R; Rose EJ; Salami A; Sämann PG; Schmaal L; Schork AJ; Shin J; Strike LT; Teumer A; Van Donkelaar MMJ; Van Eijk KR; Walters RK; Westlye LT; Whelan CD; Winkler AM; Zwiers MP; Alhusaini S; Athanasiu L; Ehrlich S; Hakobjan MMH; Hartberg CB; Haukvik UK; Heister AJGAM; Hoehn D; Kasperaviciute D; Liewald DCM; Lopez LM; Makkinje RRR; Matarin M; Naber MAM; Reese McKay D; Needham M; Nugent AC; Pütz B; Royle NA; Shen L; Sprooten E; Trabzuni D; Van Der Marel SSL; Van Hulzen KJE; Walton E; Wolf C; Almasy L; Ames D; Arepalli S; Assareh AA; Bastin ME; Brodaty H; Bulayeva KB; Carless MA; Cichon S; Corvin A; Curran JE; Czisch M, 2015, 'Common genetic variants influence human subcortical brain structures', Nature, vol. 520, pp. 224 - 229, http://dx.doi.org/10.1038/nature14101
Ringman JM; Liang LJ; Zhou Y; Vangala S; Teng E; Kremen S; Wharton D; Goate A; Marcus DS; Farlow M; Ghetti B; McDade E; Masters CL; Mayeux RP; Rossor M; Salloway S; Schofield PR; Cummings JL; Buckles V; Bateman R; Morris JC, 2015, 'Early behavioural changes in familial Alzheimer's disease in the Dominantly Inherited Alzheimer Network', Brain, vol. 138, pp. 1036 - 1045, http://dx.doi.org/10.1093/brain/awv004
Su Y; Blazey TM; Snyder AZ; Raichle ME; Marcus DS; Ances BM; Bateman RJ; Cairns NJ; Aldea P; Cash L; Christensen JJ; Friedrichsen K; Hornbeck RC; Farrar AM; Owen CJ; Mayeux R; Brickman AM; Klunk W; Price JC; Thompson PM; Ghetti B; Saykin AJ; Sperling RA; Johnson KA; Schofield PR; Buckles V; Morris JC; Benzinger TLS, 2015, 'Partial volume correction in quantitative amyloid imaging', NeuroImage, vol. 107, pp. 55 - 64, http://dx.doi.org/10.1016/j.neuroimage.2014.11.058
Chan JPL; Thalamuthu A; Oldmeadow C; Armstrong NJ; Holliday EG; McEvoy M; Kwok JB; Assareh AA; Peel R; Hancock SJ; Reppermund S; Menant J; Trollor JN; Brodaty H; Schofield PR; Attia JR; Sachdev PS; Scott RJ; Mather KA, 2015, 'Genetics of hand grip strength in mid to late life', Age (Dordrecht, Netherlands), vol. 37, pp. 9745 - 9745, http://dx.doi.org/10.1007/s11357-015-9745-5
Mather KA; Armstrong NJ; Wen W; Kwok JB; Assareh AA; Thalamuthu A; Reppermund S; Duesing K; Wright MJ; Ames D; Trollor JN; Brodaty H; Schofield PR; Sachdev PS, 2015, 'Investigating the genetics of hippocampal volume in older adults without dementia', PLoS ONE, vol. 10, pp. e0116920, http://dx.doi.org/10.1371/journal.pone.0116920
Debette S; Ibrahim Verbaas CA; Bressler J; Schuur M; Smith A; Bis JC; Davies G; Wolf C; Gudnason V; Chibnik LB; Yang Q; DeStefano AL; De Quervain DJF; Srikanth V; Lahti J; Grabe HJ; Smith JA; Priebe L; Yu L; Karbalai N; Hayward C; Wilson JF; Campbell H; Petrovic K; Fornage M; Chauhan G; Yeo R; Boxall R; Becker J; Stegle O; Mather KA; Chouraki V; Sun Q; Rose LM; Resnick S; Oldmeadow C; Kirin M; Wright AF; Jonsdottir MK; Au R; Becker A; Amin N; Nalls MA; Turner ST; Kardia SLR; Oostra B; Windham G; Coker LH; Zhao W; Knopman DS; Heiss G; Griswold ME; Gottesman RF; Vitart V; Hastie ND; Zgaga L; Rudan I; Polasek O; Holliday EG; Schofield P; Choi SH; Tanaka T; An Y; Perry RT; Kennedy RE; Sale MM; Wang J; Wadley VG; Liewald DC; Ridker PM; Gow AJ; Pattie A; Starr JM; Porteous D; Liu X; Thomson R; Armstrong NJ; Eiriksdottir G; Assareh AA; Kochan NA; Widen E; Palotie A; Hsieh YC; Eriksson JG; Vogler C; Van Swieten JC; Shulman JM; Beiser A; Rotter J; Schmidt CO; Hoffmann W; Nöthen MM; Ferrucci L; Attia J; Uitterlinden AG; Amouyel P; Dartigues JF; Amieva H; Räikkönen K; Garcia M, 2015, 'Genome-wide studies of verbal declarative memory in nondemented older people: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium', Biological Psychiatry, vol. 77, pp. 749 - 763, http://dx.doi.org/10.1016/j.biopsych.2014.08.027
Davies G; Armstrong N; Bis JC; Bressler J; Chouraki V; Giddaluru S; Hofer E; Ibrahim-Verbaas CA; Kirin M; Lahti J; Van Der Lee SJ; Le Hellard S; Liu T; Marioni RE; Oldmeadow C; Postmus I; Smith AV; Smith JA; Thalamuthu A; Thomson R; Vitart V; Wang J; Yu L; Zgaga L; Zhao W; Boxall R; Harris SE; Hill WD; Liewald DC; Luciano M; Adams H; Ames D; Amin N; Amouyel P; Assareh AA; Au R; Becker JT; Beiser A; Berr C; Bertram L; Boerwinkle E; Buckley BM; Campbell H; Corley J; De Jager PL; Dufouil C; Eriksson JG; Espeseth T; Faul JD; Ford I; Scotland G; Gottesman RF; Griswold ME; Gudnason V; Harris TB; Heiss G; Hofman A; Holliday EG; Huffman J; Kardia SLR; Kochan N; Knopman DS; Kwok JB; Lambert JC; Lee T; Li G; Li SC; Loitfelder M; Lopez OL; Lundervold AJ; Lundqvist A; Mather KA; Mirza SS; Nyberg L; Oostra BA; Palotie A; Papenberg G; Pattie A; Petrovic K; Polasek O; Psaty BM; Redmond P; Reppermund S; Rotter JI; Schmidt H; Schuur M; Schofield PW; Scott RJ; Steen VM; Stott DJ; Van Swieten JC; Taylor KD; Trollor J; Trompet S; Uitterlinden AG; Weinstein G; Widen E; Windham BG; Jukema JW; Wright AF, 2015, 'Genetic contributions to variation in general cognitive function: A meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)', Molecular Psychiatry, vol. 20, pp. 183 - 192, http://dx.doi.org/10.1038/mp.2014.188
Butt D; Chan TD; Bourne K; Hermes JR; Nguyen A; Statham A; O'Reilly LA; Strasser A; Price S; Schofield P; Christ D; Basten A; Ma CS; Tangye SG; Phan TG; Rao VK; Brink R, 2015, 'FAS Inactivation Releases Unconventional Germinal Center B Cells that Escape Antigen Control and Drive IgE and Autoantibody Production', Immunity, vol. 42, pp. 890 - 902, http://dx.doi.org/10.1016/j.immuni.2015.04.010
Gatt JM; Burton KLO; Williams LM; Schofield PR, 2015, 'Specific and common genes implicated across major mental disorders: A review of meta-analysis studies', Journal of Psychiatric Research, vol. 60, pp. 1 - 13, http://dx.doi.org/10.1016/j.jpsychires.2014.09.014
Kanchibhotla SC; Mather KA; Thalamuthu A; Zhuang L; Schofield PR; Kwok JBJ; Ames D; Wright MJ; Trollor JN; Wen W; Sachdev PS, 2014, 'Genetics of microstructure of the corpus callosum in older adults', PLoS ONE, vol. 9, pp. e113181, http://dx.doi.org/10.1371/journal.pone.0113181
Gatt JM; Burton KLO; Schofield PR; Bryant RA; Williams LM, 2014, 'The heritability of mental health and wellbeing defined using COMPAS-W, a new composite measure of wellbeing', Psychiatry Research, vol. 219, pp. 204 - 213, http://dx.doi.org/10.1016/j.psychres.2014.04.033
Ryman DC; Acosta-Baena N; Aisen PS; Bird T; Danek A; Fox NC; Goate A; Frommelt P; Ghetti B; Langbaum JBS; Lopera F; Martins R; Masters CL; Mayeux RP; McDade E; Moreno S; Reiman EM; Ringman JM; Salloway S; Schofield PR; Sperling R; Tariot PN; Xiong C; Morris JC; Bateman RJ, 2014, 'Symptom onset in autosomal dominant Alzheimer disease: A systematic review and meta-analysis', Neurology, vol. 83, pp. 253 - 260, http://dx.doi.org/10.1212/WNL.0000000000000596
Oldmeadow C; Holliday EG; McEvoy M; Scott R; Kwok JB; Mather K; Sachdev P; Schofield PR; Attia J, 2014, 'Concordance between direct and imputed APOE genotypes using 1000 Genomes data', Journal of Alzheimer's Diseasse, vol. 42, pp. 391 - 393, http://dx.doi.org/10.3233/JAD-140846
Nurnberger JI; Koller DL; Jung J; Edenberg HJ; Foroud T; Guella I; Vawter MP; Kelsoe JR; Sklar P; Ripke S; Scott LJ; Andreassen OA; Cichon S; Craddock N; Rietschel M; Blackwood D; Corvin A; Flickinger M; Guan W; Mattingsdal M; McQuillin A; Kwan P; Wienker TF; Daly M; Dudbridge F; Holmans PA; Lin D; Burmeister M; Greenwood TA; Hamshere ML; Muglia P; Smith EN; Zandi PP; Nievergelt CM; McKinney R; Shilling PD; Schork NJ; Bloss CS; Gershon ES; Liu C; Badner JA; Scheftner WA; Lawson WB; Nwulia EA; Hipolito M; Coryell W; Rice J; Byerley W; McMahon FJ; Schulze TG; Berrettini W; Lohoff FW; Potash JB; Mahon PB; McInnis MG; Zollner S; Zhang P; Craig DW; Szelinger S; Barrett TB; Breuer R; Meier S; Strohmaier J; Witt SH; Tozzi F; Farmer A; McGuffin P; Strauss J; Xu W; Kennedy JL; Vincent JB; Matthews K; Day R; Ferreira MA; O'Dushlaine C; Perlis R; Raychaudhuri S; Ruderfer D; Lee PH; Smoller JW; Li J; Absher D; Bunney WE; Barchas JD; Schatzberg AF; Jones EG; Meng F; Thompson RC; Watson SJ; Myers RM; Akil H; Boehnke M; Chambert K; Moran J; Scolnick EM; Djurovic S; Melle I; Morken G; Gill M; Morris D, 2014, 'Identification of pathways for bipolar disorder: A meta-analysis', JAMA Psychiatry, vol. 71, pp. 657 - 664, http://dx.doi.org/10.1001/jamapsychiatry.2014.176
Mitchell P; Schofield P, 2014, 'Variant GADL1 and Response to Lithium in Bipolar I Disorder', New England Journal of Medicine, vol. 370, pp. 1855 - 1860, http://dx.doi.org/10.1056/NEJMc1401817
Wilde A; Chan HN; Rahman B; Meiser B; Mitchell PB; Schofield PR; Green MJ, 2014, 'A meta-analysis of the risk of major affective disorder in relatives of individuals affected by major depressive disorder or bipolar disorder', Journal of Affective Disorders, vol. 158, pp. 37 - 47, http://dx.doi.org/10.1016/j.jad.2014.01.014
Tadros MA; Farrell KE; Schofield PR; Brichta AM; Graham BA; Fuglevand AJ; Callister RJ, 2014, 'Intrinsic and synaptic homeostatic plasticity in motoneurons from mice with glycine receptor mutations', Journal of Neurophysiology, vol. 111, pp. 1487 - 1498, http://dx.doi.org/10.1152/jn.00728.2013
Shaw AD; Tiwari Y; Kaplan W; Heath A; Mitchell PB; Schofield PR; Fullerton JM, 2014, 'Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder', PLoS ONE, vol. 9, http://dx.doi.org/10.1371/journal.pone.0092556
Mühleisen TW; Leber M; Schulze TG; Strohmaier J; Degenhardt F; Treutlein J; Mattheisen M; Forstner AJ; Schumacher J; Breuer R; Meier S; Herms S; Hoffmann P; Lacour A; Witt SH; Reif A; Müller-Myhsok B; Lucae S; Maier W; Schwarz M; Vedder H; Kammerer-Ciernioch J; Pfennig A; Bauer M; Hautzinger M; Moebus S; Priebe L; Czerski PM; Hauser J; Lissowska J; Szeszenia-Dabrowska N; Brennan P; McKay JD; Wright A; Mitchell PB; Fullerton JM; Schofield PR; Montgomery GW; Medland SE; Gordon SD; Martin NG; Krasnow V; Chuchalin A; Babadjanova G; Pantelejeva G; Abramova LI; Tiganov AS; Polonikov A; Khusnutdinova E; Alda M; Grof P; Rouleau GA; Turecki G; Laprise C; Rivas F; Mayoral F; Kogevinas M; Grigoroiu-Serbanescu M; Propping P; Becker T; Rietschel M; Nöthen MM; Cichon S, 2014, 'Genome-wide association study reveals two new risk loci for bipolar disorder', Nature Communications, vol. 5, http://dx.doi.org/10.1038/ncomms4339
Fagan AM; Xiong C; Jasielec MS; Bateman RJ; Goate AM; Benzinger TLS; Ghetti B; Martins RN; Masters CL; Mayeux R; Ringman JM; Rossor MN; Salloway S; Schofield PR; Sperling RA; Marcus D; Cairns NJ; Buckles VD; Ladenson JH; Morris JC; Holtzman DM, 2014, 'Longitudinal change in CSF biomarkers in autosomal-dominant Alzheimer's disease', Science Translational Medicine, vol. 6, http://dx.doi.org/10.1126/scitranslmed.3007901
Vercammen A; Weickert CS; Skilleter AJ; Lenroot R; Schofield PR; Weickert TW, 2014, 'Common polymorphisms in dopamine-related genes combine to produce a 'schizophrenia-like' prefrontal hypoactivity', Translational Psychiatry, vol. 4, http://dx.doi.org/10.1038/tp.2013.125
McEvoy M; Schofield P; Smith W; Agho K; Mangoni AA; Soiza RL; Peel R; Attia J, 2014, 'Memory Impairment is Associated with Serum Methylarginines in Older Adults', Current Alzheimer Research, vol. 11, pp. 97 - 106, http://dx.doi.org/10.2174/15672050113106660178
Thompson PM; Stein JL; Medland SE; Hibar DP; Vasquez AA; Renteria ME; Toro R; Jahanshad N; Schumann G; Franke B; Wright MJ; Martin NG; Agartz I; Alda M; Alhusaini S; Almasy L; Almeida J; Alpert K; Andreasen NC; Andreassen OA; Apostolova LG; Appel K; Armstrong NJ; Aribisala B; Bastin ME; Bauer M; Bearden CE; Bergmann Ø; Binder EB; Blangero J; Bockholt HJ; Bøen E; Bois C; Boomsma DI; Booth T; Bowman IJ; Bralten J; Brouwer RM; Brunner HG; Brohawn DG; Buckner RL; Buitelaar J; Bulayeva K; Bustillo JR; Calhoun VD; Cannon DM; Cantor RM; Carless MA; Caseras X; Cavalleri GL; Chakravarty MM; Chang KD; Ching CRK; Christoforou A; Cichon S; Clark VP; Conrod P; Coppola G; Crespo-Facorro B; Curran JE; Czisch M; Deary IJ; de Geus EJC; den Braber A; Delvecchio G; Depondt C; de Haan L; de Zubicaray GI; Dima D; Dimitrova R; Djurovic S; Dong H; Donohoe G; Duggirala R; Dyer TD; Ehrlich S; Ekman CJ; Elvsåshagen T; Emsell L; Erk S; Espeseth T; Fagerness J; Fears S; Fedko I; Fernández G; Fisher SE; Foroud T; Fox PT; Francks C; Frangou S; Frey EM; Frodl T; Frouin V; Garavan H; Giddaluru S; Glahn DC; Godlewska B; Goldstein RZ; Gollub RL; Grabe HJ, 2014, 'The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data', Brain Imaging and Behavior, vol. 8, pp. 153 - 182, http://dx.doi.org/10.1007/s11682-013-9269-5
Quinn V; Meiser B; Wilde A; Cousins Z; Barlow-Stewart K; Mitchell PB; Schofield PR, 2014, 'Preferences regarding targeted education and risk assessment in people with a family history of major depressive disorder', Journal of Genetic Counseling, vol. 23, pp. 785 - 795, http://dx.doi.org/10.1007/s10897-013-9685-0
Loy CT; Schofield PR; Turner AM; Kwok JBJ, 2014, 'Genetics of dementia', The Lancet, vol. 383, pp. 828 - 840, http://dx.doi.org/10.1016/S0140-6736(13)60630-3
Salminen LE; Schofield PR; Pierce KD; Lane EM; Heaps JM; Bolzenius JD; Baker LM; Luo X; Paul RH, 2014, 'Triallelic relationships between the serotonin transporter polymorphism and cognition among healthy older adults', International Journal of Neuroscience, vol. 124, pp. 331 - 338, http://dx.doi.org/10.3109/00207454.2013.845822
Zhou YZ; Wilde A; Meiser B; Mitchell PB; Barlow-Stewart K; Schofield PR, 2014, 'Attitudes of medical genetics practitioners and psychiatrists toward communicating with patients about genetic risk for psychiatric disorders', Psychiatric Genetics, vol. 24, pp. 94 - 101, http://dx.doi.org/10.1097/YPG.0000000000000030
Assareh AA; Mather KA; Crawford JD; Wen W; Anstey KJ; Easteal S; Tan X; Mack HA; Kwok JBJ; Schofield PR; Sachdev PS, 2014, 'Renin-angiotensin system genetic polymorphisms and brain white matter lesions in older australians', American Journal of Hypertension, vol. 27, pp. 1191 - 1198, http://dx.doi.org/10.1093/ajh/hpu035
Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Brooks William S. BS; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Waldö ML; Nilsson K; Nilsson C; Mackenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; McKeith IG; Thomas AJ; Pietrini P; Huey ED; Wassermann EM; Baborie A; Jaros E; Tierney MC; Pastor P; Razquin C; Ortega-Cubero S; Alonso E; Perneczky R; Diehl-Schmid J; Alexopoulos P; Kurz A; Rainero I; Rubino E; Pinessi L; Rogaeva E; St George-Hyslop P; Rossi G; Tagliavini F; Giaccone G; Rowe JB; Schlachetzki JCM; Uphill J; Collinge J; Mead S; Danek A; Van Deerlin VM; Grossman M; Trojanowski JQ; Van der Zee J; Deschamps W; Van Langenhove T; Cruts M; Van Broeckhoven C; Cappa SF; Le Ber I; Hannequin D; Golfier V; Vercelletto M; Brice A; Nacmias B; Sorbi S; Bagnoli S; Piaceri I; Nielsen JE; Hjermind LE; Riemenschneider M; Mayhaus M; Ibach B; Gasparoni G; Pichler S; Gu W; Rossor MN, 2014, 'Frontotemporal dementia and its subtypes: A genome-wide association study', The Lancet Neurology, vol. 13, pp. 686 - 699, http://dx.doi.org/10.1016/S1474-4422(14)70065-1
Salminen LE; Schofield PR; Pierce KD; Conturo TE; Tate DF; Lane EM; Heaps JM; Bolzenius JD; Baker LM; Akbudak E; Paul RH, 2014, 'Impact of the AGTR1 A1166C polymorphism on subcortical hyperintensities and cognition in healthy older adults', Age, vol. 36, http://dx.doi.org/10.1007/s11357-014-9664-x
Thomas JB; Brier MR; Bateman RJ; Snyder AZ; Benzinger TL; Xiong C; Raichle M; Holtzman DM; Sperling RA; Mayeux R; Ghetti B; Ringman JM; Salloway S; McDade E; Rossor MN; Ourselin S; Schofield PR; Masters CL; Martins RN; Weiner MW; Thompson PM; Fox NC; Koeppe RA; Jack CR; Mathis CA; Oliver A; Blazey TM; Moulder K; Buckles V; Hornbeck R; Chhatwal J; Schultz AP; Goate AM; Fagan AM; Cairns NJ; Marcus DS; Morris JC; Ances BM, 2014, 'Functional connectivity in autosomal dominant and late-onset Alzheimer disease', JAMA Neurology, vol. 71, pp. 1111 - 1122, http://dx.doi.org/10.1001/jamaneurol.2014.1654
Coupland KG; Mellick GD; Silburn PA; Mather K; Armstrong NJ; Sachdev PS; Brodaty H; Huang Y; Halliday GM; Hallupp M; Kim WS; Dobson-Stone C; Kwok JBJ, 2014, 'DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E In Vitro', Movement Disorders, vol. 29, pp. 1606 - 1614, http://dx.doi.org/10.1002/mds.25784
Steinberg S; de Jong S; Mattheisen M; Costas J; Demontis D; Jamain S; Pietiläinen OPH; Lin K; Papiol S; Huttenlocher J; Sigurdsson E; Vassos E; Giegling I; Breuer R; Fraser G; Walker N; Melle I; Djurovic S; Agartz I; Tuulio-Henriksson A; Suvisaari J; Lönnqvist J; Paunio T; Olsen L; Hansen T; Ingason A; Pirinen M; Strengman E; Hougaard DM; Ørntoft T; Didriksen M; Hollegaard MV; Nordentoft M; Abramova L; Kaleda V; Arrojo M; Sanjuán J; Arango C; Etain B; Bellivier F; Méary A; Schürhoff F; Szoke A; Ribolsi M; Magni V; Siracusano A; Sperling S; Rossner M; Christiansen C; Kiemeney LA; Franke B; van den Berg LH; Veldink J; Curran S; Bolton P; Poot M; Staal W; Rehnstrom K; Kilpinen H; Freitag CM; Meyer J; Magnusson P; Saemundsen E; Martsenkovsky I; Bikshaieva I; Martsenkovska I; Vashchenko O; Raleva M; Paketchieva K; Stefanovski B; Durmishi N; Pejovic Milovancevic M; Lecic Tosevski D; Silagadze T; Naneishvili N; Mikeladze N; Surguladze S; Vincent JB; Farmer A; Mitchell PB; Wright A; Schofield PR; Fullerton JM; Montgomery GW; Martin NG; Rubino IA; van Winkel R; Kenis G; De Hert M; Réthelyi JM; Bitter I; Terenius L; Jönsson EG; Bakker S; van Os J; Jablensky A; Leboyer M; Bramon E; Powell J; Murray R; Corvin A; Gill M; Morris D; O'Neill FA; Kendler K; Riley B; Craddock N; Owen MJ; O'Donovan MC; Thorsteinsdottir U; Kong A; Ehrenreich H; Carracedo A; Golimbet V; Andreassen OA; Børglum AD; Mors O; Mortensen PB; Werge T; Ophoff RA; Nöthen MM; Rietschel M; Cichon S; Ruggeri M; Tosato S; Palotie A; St Clair D; Rujescu D; Collier DA; Stefansson H; Stefansson K, 2014, 'Common variant at 16p11.2 conferring risk of psychosis', Molecular Psychiatry, vol. 19, pp. 108 - 114, http://dx.doi.org/10.1038/mp.2012.157
Assareh AA; Piguet O; Lye TC; Mather KA; Broe GA; Schofield PR; Sachdev PS; Kwok JB, 2014, 'Association of SORL1 gene variants with hippocampal and cerebral atrophy and Alzheimer's disease', Current Alzheimer Research, vol. 11, pp. 558 - 563, http://dx.doi.org/10.2174/1567205011666140618101408
Myers AJ; Williams L; Gatt JM; McAuley-Clark EZ; Dobson-Stone C; Schofield PR; Nemeroff CB, 2014, 'Variation in the oxytocin receptor gene is associated with increased risk for anxiety, stress and depression in individuals with a history of exposure to early life stress', Journal of Psychiatric Research, vol. 59, pp. 93 - 100, http://dx.doi.org/10.1016/j.jpsychires.2014.08.021
Meiser B; Schofield PR; Trevena L; Wilde A; Barlow-Stewart K; Proudfoot J; Peate M; Dobbins T; Christensen H; Sherman KA; Karatas J; Mitchell PB, 2013, 'Cluster randomized controlled trial of a psycho-educational intervention for people with a family history of depression for use in general practice', BMC Psychiatry, vol. 13, http://dx.doi.org/10.1186/1471-244X-13-325
Mills SM; Mallmann J; Santacruz AM; Fuqua A; Carril M; Aisen PS; Althage MC; Belyew S; Benzinger TL; Brooks WS; Buckles VD; Cairns NJ; Clifford D; Danek A; Fagan AM; Farlow M; Fox N; Ghetti B; Goate AM; Heinrichs D; Hornbeck R; Jack C; Jucker M; Klunk WE; Marcus DS; Martins RN; Masters CM; Mayeux R; McDade E; Morris JC; Oliver A; Ringman JM; Rossor MN; Salloway S; Schofield PR; Snider J; Snyder P; Sperling RA; Stewart C; Thomas RG; Xiong C; Bateman RJ, 2013, 'Erratum: Preclinical trials in autosomal dominant AD: Implementation of the DIAN-TU trial (Rev. Neurol. (2013) 169 (10) (737-743))', Revue Neurologique, vol. 169, pp. 1018, http://dx.doi.org/10.1016/j.neurol.2013.10.005
Benzinger TLS; Blazey T; Jack CR; Koeppe RA; Su Y; Xiong C; Raichle ME; Snyder AZ; Ances BM; Bateman RJ; Cairns NJ; Fagan AM; Goate A; Marcus DS; Aisen PS; Christensen JJ; Ercole L; Hornbeck RC; Farrar AM; Aldea P; Jasielec MS; Owen CJ; Xie X; Mayeux R; Brickman A; McDade E; Klunk W; Mathis CA; Ringman J; Thompson PM; Ghetti B; Saykin AJ; Sperling RA; Johnson KA; Salloway S; Correia S; Schofield PR; Masters CL; Rowe C; Villemagne VL; Martins R; Ourselin S; Rossor MN; Fox NC; Cash DM; Weiner MW; Holtzman DM; Buckles VD; Moulder K; Morris JC, 2013, 'Regional variability of imaging biomarkers in autosomal dominant Alzheimer's disease', Proceedings of the National Academy of Sciences of the United States of America, vol. 110, http://dx.doi.org/10.1073/pnas.1317918110
Weickert CS; Fung SJ; Catts VS; Schofield PR; Allen KM; Moore LT; Newell KA; Pellen D; Huang XF; Catts SV; Weickert TW, 2013, 'Molecular evidence of N-methyl-D-aspartate receptor hypofunction in schizophrenia', Molecular Psychiatry, vol. 18, pp. 1185 - 1192, http://dx.doi.org/10.1038/mp.2012.137
Cash DM; Ridgway GR; Liang Y; Ryan NS; Kinnunen KM; Yeatman T; Malone IB; Benzinger TLS; Jack CR; Thompson PM; Ghetti BF; Saykin AJ; Masters CL; Ringman JM; Salloway SP; Schofield PR; Sperling RA; Cairns NJ; Marcus DS; Xiong C; Bateman RJ; Morris JC; Rossor MN; Ourselin S; Fox NC, 2013, 'The pattern of atrophy in familial alzheimer disease: Volumetric MRI results from the DIAN study', Neurology, vol. 81, pp. 1425 - 1433, http://dx.doi.org/10.1212/WNL.0b013e3182a841c6
Xu M; Zou L; Wilde A; Meiser B; Barlow-Stewart K; Chan B; Mitchell PB; Sousa MS; Schofield PR, 2013, 'Exploring culture-specific differences in beliefs about causes, kinship and the heritability of major depressive disorder: The views of anglo-celtic and chinese-Australians', Journal of Genetic Counseling, vol. 22, pp. 613 - 624, http://dx.doi.org/10.1007/s10897-013-9593-3
Bryant RA; Hung L; Dobson-Stone C; Schofield PR, 2013, 'The association between the oxytocin receptor gene (OXTR) and hypnotizability', Psychoneuroendocrinology, vol. 38, pp. 1979 - 1984, http://dx.doi.org/10.1016/j.psyneuen.2013.03.002
Mills SM; Mallmann J; Santacruz AM; Fuqua A; Carril M; Aisen PS; Althage MC; Belyew S; Benzinger TL; Brooks WS; Buckles VD; Cairns NJ; Clifford D; Danek A; Fagan AM; Farlow M; Fox N; Ghetti B; Goate AM; Heinrichs D; Hornbeck R; Jack C; Jucker M; Klunk WE; Marcus DS; Martins RN; Masters CM; Mayeux R; McDade E; Morris JC; Oliver A; Ringman JM; Rossor MN; Salloway S; Schofield PR; Snider J; Snyder P; Sperling RA; Stewart C; Thomas RG; Xiong C; Bateman RJ, 2013, 'Preclinical trials in autosomal dominant AD: Implementation of the DIAN-TU trial', Revue Neurologique, vol. 169, pp. 737 - 743, http://dx.doi.org/10.1016/j.neurol.2013.07.017
Salminen LE; Schofield PR; Lane EM; Heaps JM; Pierce KD; Cabeen R; Laidlaw DH; Akbudak E; Conturo TE; Correia S; Paul RH, 2013, 'Neuronal fiber bundle lengths in healthy adult carriers of the ApoE4 allele: A quantitative tractography DTI study', Brain Imaging and Behavior, vol. 7, pp. 274 - 281, http://dx.doi.org/10.1007/s11682-013-9225-4
Dang TNT; Dobson-Stone C; Glaros EN; Kim WS; Hallupp M; Bartley L; Piguet O; Hodges JR; Halliday GM; Double KL; Schofield PR; Crouch PJ; Kwok JBJ, 2013, 'Endogenous progesterone levels and frontotemporal dementia: Modulation of TDP-43 and Tau levels in vitro and treatment of the A315T TARDBP mouse model', DMM Disease Models and Mechanisms, vol. 6, pp. 1198 - 1204, http://dx.doi.org/10.1242/dmm.011460
Gatto D; Wood K; Caminschi I; Murphy-Durland D; Schofield P; Christ D; Karupiah G; Brink R, 2013, 'Erratum: The chemotactic receptor EBI2 regulates the homeostasis, localization and immunological function of splenic dendritic cells (Nature Immunology (2013) 14 (446-453))', Nature Immunology, vol. 14, pp. 876, http://dx.doi.org/10.1038/ni0813-876e
Manchia M; Adli M; Akula N; Ardau R; Aubry JM; Backlund L; Banzato CEM; Baune BT; Bellivier F; Bengesser S; Biernacka JM; Brichant-Petitjean C; Bui E; Calkin CV; Cheng ATA; Chillotti C; Cichon S; Clark S; Czerski PM; Dantas C; Del Zompo M; DePaulo JR; Detera-Wadleigh SD; Etain B; Falkai P; Frisén L; Frye MA; Fullerton J; Gard S; Garnham J; Goes FS; Grof P; Gruber O; Hashimoto R; Hauser J; Heilbronner U; Hoban R; Hou L; Jamain S; Kahn JP; Kassem L; Kato T; Kelsoe JR; Kittel-Schneider S; Kliwicki S; Kuo PH; Kusumi I; Laje G; Lavebratt C; Leboyer M; Leckband SG; López Jaramillo CA; Maj M; Malafosse A; Martinsson L; Masui T; Mitchell PB; Mondimore F; Monteleone P; Nallet A; Neuner M; Novák T; O'Donovan C; Ösby U; Ozaki N; Perlis RH; Pfennig A; Potash JB; Reich-Erkelenz D; Reif A; Reininghaus E; Richardson S; Rouleau GA; Rybakowski JK; Schalling M; Schofield PR; Schubert OK; Schweizer B; Seemüller F; Grigoroiu-Serbanescu M; Severino G; Seymour LR; Slaney C; Smoller JW; Squassina A; Stamm T; Steele J; Stopkova P; Tighe SK; Tortorella A; Turecki G; Wray NR; Wright A; Zandi PP; Zilles D; Bauer M; Rietschel M; McMahon FJ; Schulze TG; Alda M, 2013, 'Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report', PLoS ONE, vol. 8, http://dx.doi.org/10.1371/journal.pone.0065636
Wilde A; Mitchell PB; Meiser B; Schofield PR, 2013, 'Implications of the use of genetic tests in psychiatry, with a focus on major depressive disorder: A review', Depression and Anxiety, vol. 30, pp. 267 - 275, http://dx.doi.org/10.1002/da.22000
Hsu SC; Sears RL; Lemos RR; Quintans B; Huang A; Spiteri E; Nevarez L; Nevarez C; Zatz M; Pierce KD; Fullerton JM; Adair JC; Berner JE; Bower M; Brodaty H; Carmona O; Dobricic V; Fogel BL; Garcia-Estevez D; Goldman JM; Goudreau J; Goudreau S; Jankovic M; Jauma S; Jen JC; Kirdlarp S; Klepper J; Kostic V; Lang AE; Linglart A; Maisenbacher MK; Manyam BV; Mazzoni P; Miedzybrodzka Z; Mitarnun W; Mitchell PB; Mueller J; Novakovic I; Paucar M; Paulson H; Simpson SA; Svenningsson P; Tuite P; Vitek J; Wetchaphanphesat S; Williams C; Yang M; Schofield PR; Oliveira JRMD; Sobrido MJ; Geschwind DH; Coppola G, 2013, 'Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification', Neurogenetics, vol. 14, pp. 11 - 22, http://dx.doi.org/10.1007/s10048-012-0349-2
Spronk D; Spronk DB; Arns M; Schofield PR; Dobson-Stone C; Ramaekers JG; Franke B; De bruijn ERA; Verkes RJ, 2013, 'DBH - 1021C>T and COMT Val108/158Met genotype are not associated with the P300 ERP in an auditory oddball task', Clinical Neurophysiology, vol. 124, pp. 909 - 915, http://dx.doi.org/10.1016/j.clinph.2012.11.008
Felmingham KL; Dobson-Stone C; Schofield PR; Quirk G; Bryant RA, 2013, 'The Brain-Derived Neurotrophic Factor Val66Met Polymorphism Predicts Response to Exposure Therapy in Posttraumatic Stress Disorder', Biological Psychiatry, vol. 73, pp. 1059 - 1063, http://dx.doi.org/10.1016/j.biopsych.2012.10.033
Dobson-Stone C; Polly P; Korgaonkar M; Williams LM; Gordon E; Schofield PR; Mather KA; Armstrong N; Wen W; Sachdev PS; Kwok JB, 2013, 'GSK3B and MAPT polymorphisms are associated with grey matter and intracranial volume in healthy individuals', PLoS One, vol. 8, pp. e71750, http://dx.doi.org/10.1371/journal.pone.0071750
Kanchibhotla SC; Mather KA; Wen W; Schofield PR; Kwok J; Sachdev PS, 2013, 'Genetics of ageing-related changes in brain white matter integrity - a review', Ageing Research Reviews, vol. 12, pp. 391 - 401, http://dx.doi.org/10.1016/j.arr.2012.10.003
Dobson-Stone C; Luty A; Thompson EM; Blumbergs P; Brooks WS; Short CL; Field C; Panegyres P; Hecker J; Solski JA; Blair I; Fullerton JM; Halliday GM; Schofield PR; Kwok J, 2013, 'Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: Genetic, clinical and neuropathological analysis', ACTA Neuropathologica, vol. 125, pp. 523 - 533, http://dx.doi.org/10.1007/s00401-013-1078-9
Spronk DB; Spronk DB; Arns M; Schofield PR; Dobson-Stone C; Frankel B; De bruijn ERA; Verkes RJ, 2013, 'DBH -1021C>T and COMT Val108/158Met genotype are not associated with the P300 ERP in an auditory oddball task', Clinical Neurophysiology, vol. 124, pp. 909 - 915, http://dx.doi.org/10.1016/j.clinph.2012.11.008
Dobson-Stone C; Hallupp M; Loy CT; Thompson EJ; Haan E; Sue C; Panegyres P; Razquin C; Seijo-Martínez M; Rene R; Gascon J; Campdelacreu J; Schmoll B; Volk AE; Brooks WS; Schofield PR; Pastor P; Kwok J, 2013, 'C9ORF72 Repeat Expansion in Australian and Spanish Frontotemporal Dementia Patients', PLoS ONE, vol. 8, pp. e56899, http://dx.doi.org/10.1371/journal.pone.0056899
Santarelli D; Liu B; Duncan CE; Beveridge NJ; Tooney P; Schofield PR; Cairns MJ, 2013, 'Gene-microRNA interactions associated with antipsychotic mechanisms and the metabolic side effects of olanzapine', Psychopharmacology, vol. 227, pp. 67 - 78, http://dx.doi.org/10.1007/s00213-012-2939-y
Chhatwal JP; Schultz A; Johnson K; Benzinger TLS; Jr CJ; Ances BM; Sullivan CA; Salloway S; Ringman JM; Koeppe RA; Marcus DS; Thompson P; Saykin AJ; Correia S; Schofield PR; Rowe CC; Fox NC; Brickman AM; Mayeux R; McDade E; Bateman R; Fagan AM; Goate A; Xiong C; Buckles V; Morris JC; Sperling R, 2013, 'Impaired default network functional connectivity in autosomal dominant Alzheimer disease', Neurology, vol. 81, pp. 736 - 744, http://dx.doi.org/10.1212/WNL.0b013e3182a1aafe
Felmingham KL; Dobson-Stone C; Schofield PR; Quirk GJ; Bryant RA, 2013, 'The BDNF Val66Met polymorphism predicts response to exposure therapy in posttraumatic stress disorder', Biological Psychiatry, pp. 1059 - 1063, http://dx.doi.org/10.1016/j.biopsych.2012.10.033
Wu MJ; Giersch T; McKay S; Schofield P; Skylas DJ; Cornish G; Hegedus E; Chin J, 2012, 'A novel hardness-related and starch granule-associated protein marker in wheat: LMW-GS-'S'', Journal of Cereal Science, vol. 55, pp. 153 - 159, http://dx.doi.org/10.1016/j.jcs.2011.10.012
Mcauley EZ; Scimone A; Tiwari Y; Agahi G; Mowry BJ; Holliday E; Donald JA; Shannon Weickert C; Mitchell PB; Schofield PR; Fullerton JM, 2012, 'Identification of Sialytransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26', PLoS ONE, vol. 7, pp. 1 - 9, http://dx.doi.org/10.1371/journal.pone.0038172
Bateman R; Xiong C; Benzinger TLS; Fagan AM; Goate A; Fox NC; Marcus DS; Cairns NJ; Xie X; Blazey TM; Holtzman DM; Santacruz A; Buckles V; Oliver A; Moulder K; Aisen PS; Ghetti B; Klunk WE; McDade E; Martins RN; Masters CL; Mayeux R; Ringman JM; Rossor MN; Schofield PR; Sperling R; Salloway S; Morris JC; Dominantly IAN, 2012, 'Clinical and biomarker changes in dominantly inherited Alzheimer's disease', New England Journal of Medicine, vol. 367, pp. 795 - 804, http://dx.doi.org/10.1056/NEJMoa1202753
Weickert CS; Tiwari Y; Schofield PR; Mowry BJ; Fullerton JM, 2012, 'Schizophrenia-associated HapICE haplotype is associated with increased NRG1 type III expression and high nucleotide diversity', Translational Psychiatry, vol. 2, pp. e104, http://dx.doi.org/10.1038/tp.2012.25
Porter MA; Dobson-Stone C; Kwok JB; Schofield PR; Beckett W; Tassabehji M, 2012, 'A Role for Transcription Factor GTF2IRD2 in Executive Function in Williams-Beuren Syndrome', PLoS ONE, vol. 7, pp. Art. No. e47457, http://dx.doi.org/10.1371/journal.pone.0047457
Dobson-Stone C; Hallupp M; Bartley L; Shepherd CE; Halliday GM; Schofield PR; Hodges JR; Kwok J, 2012, 'C9ORF72 repeat expansion in clinical and neuropathological frontotemporal dementia cohorts', Neurology, vol. 79, pp. 995 - 1001, http://dx.doi.org/10.1212/WNL.0b013e3182684634
Gatt JM; Korgaonkar M; Schofield PR; Harris A; Clark R; Oakley K; Ram K; Michaelson H; Yap S; Stanners M; Wise V; Williams LM, 2012, 'The TWIN-E Project in Emotional Wellbeing: Study Protocol and Preliminary Heritability Results Across Four MRI and DTI Measures', Twin research and human genetics, vol. 15, pp. 419 - 441, http://dx.doi.org/10.1017/thg.2012.12
Cichon S; Mühleisen TW; Degenhardt FA; Mattheisen M; Miró X; Strohmaier J; Steffens M; Meesters C; Herms S; Weingarten M; Priebe L; Haenisch B; Alexander M; Vollmer J; Breuer R; Schmäl C; Tessmann P; Moebus S; Wichmann HE; Schreiber S; Müller-Myhsok B; Lucae S; Jamain S; Leboyer M; Bellivier F; Etain B; Henry C; Kahn JP; Heath S; Hamshere M; O'Donovan MC; Owen MJ; Craddock N; Schwarz M; Vedder H; Kammerer-Ciernioch J; Reif A; Sasse J; Bauer M; Hautzinger M; Wright A; Mitchell PB; Schofield PR; Montgomery GW; Medland SE; Gordon SD; Martin NG; Gustafsson O; Andreassen O; Djurovic S; Sigurdsson E; Steinberg S; Stefansson H; Stefansson K; Kapur-Pojskic L; Oruc L; Rivas F; Mayoral F; Chuchalin A; Babadjanova G; Tiganov AS; Pantelejeva G; Abramova LI; Grigoroiu-Serbanescu M; Diaconu CC; Czerski PM; Hauser J; Zimmer A; Lathrop M; Schulze TG; Wienker TF; Schumacher J; Maier W; Propping P; Rietschel M; Nöthen MM, 2011, 'Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder (The American Journal of Human Genetics (2011) 88, (372-381))', American Journal of Human Genetics, vol. 88, pp. 396, http://dx.doi.org/10.1016/j.ajhg.2011.03.001
Sklar P; Ripke S; Scott LJ; Andreassen OA; Cichon S; Craddock N; Edenberg HJ; Nurnberger JI; Rietschel M; Blackwood D; Corvin A; Flickinger M; Guan W; Mattingsdal M; McQuillan A; Kwan P; Wienker TF; Daly MJ; Dudbridge F; Holmans PA; Lin D; Burmeister M; Greenwood TA; Hamshere ML; Muglia P; Smith EN; Zandi PP; Nievergelt CM; McKinney R; Shilling PD; Schork NJ; Bloss CS; Foroud T; Koller DL; Gershon ES; Liu C; Badner JA; Scheftner WA; Lawson WB; Nwulia EA; Hipolito M; Coryell W; Rice J; Byerley W; McMahon FJ; Schulze TG; Berrettini W; Lohoff FW; Potash JB; Mahon AP; McInnis MG; Zollner S; Zhang P; Craig DW; Szelinger S; Barrett TB; Breuer R; Meier S; Strohmaier J; Witt SH; Tozzi F; Farmer A; McGuffin P; Strauss J; Xu W; Kennedy JL; Vincent JB; Matthews K; Day R; Ferreira MA; O'Dushlaine C; Perlis R; Raychaudhuri S; Ruderfer D; Hyoun PL; Smoller JW; Li J; Absher D; Thompson RC; Meng FG; Schatzberg A; Bunney WE; Barchas JD; Jones EG; Watson SJ; Myers RM; Akil H; Boehnke M; Chambert K; Moran J; Scolnick EM; Djurovic S; Melle I; Morken G; Gill M; Morris D; Quinn E; Muhleisen TW; Degenhardt FA; Mattheisen M; Schumacher J; Maier W; Steffens M; Propping P; Nothen MM; Anjorin A; Bass N; Gurling H; Kandaswamy R; Lawrence J; McGhee K; McIntosh A; McLean AW; Muir WJ; Pickard BS; Breen G; St Clair D; Caesar S; Gordon-Smith K; Jones L; Fraser C; Green EK; Grozeva D; Jones IR; Kirov G; Moskvina V; Nikolov I; O'Donovan MC; Owens MJ; Collier DA; Elkin A; Williamson R; Young AH; Ferrier IN; Stefansson K; Stefansson H; Porgeirsson P; Steinberg S; Gustafsson O; Bergen SE; Nimgaonkar V; Hultman C; Landen M; Lichtenstein P; Sullivan P; Schalling M; Osby U; Backlund L; Frisen L; Langstrom N; Jamain S; Leboyer M; Etain B; Bellivier F; Petursson H; Sigurgosson E; Muller-Mysok B; Lucae S; Schwarz M; Schofield PR; Martin N; Montgomery GW; Lathrop M; Oskarsson H; Bauer M; Wright A; Mitchell PB; Hautzinger M; Reif A; Kelsoe JR; Purcell SM, 2011, 'Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4', Nature Genetics, vol. 43, pp. 977 - 985, http://dx.doi.org/10.1038/ng.943
Sachdev PS; Lee T; Lammel A; Crawford J; Trollor JN; Wright MJ; Brodaty H; Ames D; Martin NG, 2011, 'Cognitive functioning in older twins: The Older Australian Twins Study', Australasian Journal on Ageing, vol. 30, pp. 17 - 23, http://dx.doi.org/10.1111/j.1741-6612.2011.00534.x
Assareh A; Mather KA; Schofield PR; Kwok J; Sachdev PS, 2011, 'The Genetics of White Matter Lesions', CNS Neuroscience and Therapeutics, vol. 17, pp. 525 - 540, http://dx.doi.org/10.1111/j.1755-5949.2010.00181.x
Graham B; Tadros M; Schofield PR; Callister RJ, 2011, 'Probing glycine receptor stoichiometry in superficial dorsal horn neurones using the spasmodic mouse', The Journal of Physiology, vol. 589, pp. 2459 - 2479, http://dx.doi.org/10.1113/jphysiol.2011.206326
Cichon S; Muhleisen TW; Degenhardt FA; Mattheisen M; Miro X; Strohmaier J; Steffens M; Meesters C; Herms S; Weingarten M; Priebe L; Haenisch B; Alexander M; Vollmer J; Breuer R; Schmal C; Tessmann P; Moebus S; Wichmann HE; Schreiber S; Muller-Myhsok B; Lucae S; Jamain S; Leboyer M; Bellivier F; Etain B; Henry C; Kahn JP; Heath SC; Hamshere ML; O'Donovan MC; Owen MJ; Craddock N; Schwarz M; Vedder H; Kammerer-Ciernioch J; Reif A; Sasse J; Bauer M; Hautzinger M; Wright A; Mitchell PB; Schofield PR; Montgomery G; Medland SE; Gordon S; Martin NG; Gustafsson O; Andreassen OA; Djurovic S; Sigurdsson E; Steinberg S; Stefansson H; Stefansson K; Kapur-Pojskic L; Oruc L; Rivas F; Mayoral F; Chuchalin A; Babadjanova G; Tiganov AS; Pantelejeva G; Abramova LI; Grigoroiu-Serbanescu M; Diaconu CC; Czerski PM; Hauser J; Zimmer A; Lathrop MG; Schulze TG; Wienker G; Schumacher J; Maier W; Propping P; Rietschel M; Nothen MM, 2011, 'Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder', American Journal of Human Genetics, vol. 88, pp. 372 - 381, http://dx.doi.org/10.1016/j.ajhg.2011.01.017
Lowe DJ; Dudgeon K; Rouet R; Schofield P; Jermutus L; Christ DU, 2011, 'Aggregation, stability, and formulation of human antibody therapeutics', Advances in Protein Chemistry & Structural Biology, vol. 84, pp. 41 - 61, http://dx.doi.org/10.1016/B978-0-12-386483-3.00004-5
Fullerton J; Donald JA; Mitchell PB; Schofield PR, 2010, 'Two-Dimensional Genome Scan Identifies Mltiple Genetic Interactions in Biolar Affective Disorder', Biological Psychiatry, vol. 67, pp. 478 - 486, http://dx.doi.org/10.1016/j.biopsych.2009.10.022
Mitchell PB; Meiser B; Wilde A; Fullerton J; Donald JA; Wilhelm KA; Schofield PR, 2010, 'Predictive and Diagnostic Genetic Testing in Psychiatry', Psychiatric Clinics of North America, vol. 33, pp. 225 - 243, http://dx.doi.org/10.1016/j.psc.2009.10.001
Fullerton J; Tiwari Y; Agahi G; Heath A; Berk M; Mitchell PB; Schofield PR, 2010, 'Assessing Oxidative Pathway Genes as Risk Factors for Bipolar Disorder', Bipolar Disorders, vol. 12, pp. 550 - 556, http://dx.doi.org/10.1111/j.1399-5618.2010.00834.x
Williams L; Gatt JM; Grieve S; Dobson-Stone C; Paul R; Gordon E; Schofield PR, 2010, 'COMT Val108/158Met polymorphism effects on emotional brain function and negativity bias', Neuroimage, vol. 53, pp. 918 - 925, http://dx.doi.org/10.1016/j.neuroimage.2010.01.084
Gatt JM; Williams L; Schofield PR; Dobson-Stone C; Paul R; Grieve S; Clark CR; Gordon E; Nemeroff C, 2010, 'Impact of the HTR3A gene with early life trauma on emotional brain networks and depressed mood.', Depression and Anxiety, vol. 27, pp. 752 - 759, http://dx.doi.org/10.1002/da.20726
Bryant RA; Felmingham KL; Falconer EM; Pe benito L; Dobson-Stone C; Pierce KD; Schofield PR, 2010, 'Preliminary evidence of the short allele of the serotonin transporter gene predicting poor response to cognitive behavior therapy in posttraumatic stress disorder', Biological Psychiatry, vol. 67, pp. 1217 - 1219, http://dx.doi.org/10.1016/j.biopsych.2010.03.016
Cederholm JME; Absalom NL; Sugiharto S; Griffith R; Schofield PR; Lewis TM, 2010, 'Conformational changes in extracellular loop 2 associated with signal transduction in the glycine receptor', Journal of Neurochemistry, vol. 115, pp. 1245 - 1255, http://dx.doi.org/10.1111/j.1471-4159.2010.07021.x
Gatt JM; Nemeroff C; Schofield PR; Paul R; Clark CR; Gordon E; Williams L, 2010, 'Early life stress combined with serotonin 3A receptor and brain-derived neurotrophic factor valine 66 to methionine genotypes impacts emotional brain and arousal correlates of risk for depression', Biological Psychiatry, vol. 68, pp. 818 - 824, http://dx.doi.org/10.1016/j.biopsych.2010.06.025
Camp A; Lim RP; Anderson WP; Schofield PR; Callister RJ; Brichta A, 2010, 'Attenuated glycine receptor function reduces excitability of mouse medial vestibular nucleus neurons', Neuroscience, vol. 170, pp. 348 - 360, http://dx.doi.org/10.1016/j.neuroscience.2010.06.040
Wilde A; Meiser B; Mitchell PB; Schofield PR, 2010, 'Public interest in predictive genetic testing, including direct-to-consumer testing, for susceptibility to major depression: preliminary findings', European Journal of Human Genetics, vol. 18, pp. 47 - 51, http://dx.doi.org/10.1038/ejhg.2009.138
Loy CT; Schofield PR; Kwok JBJ, 2009, 'Reply to García-Gorostiaga, et al', Annals of Neurology, vol. 65, pp. 761 - 762, http://dx.doi.org/10.1002/ana.21718
Dennett AL; Schofield PR; Roake JE; Howes NK; Chin J, 2009, 'Starch swelling power and amylose content of triticale and Triticum timopheevii germplasm', Journal of Cereal Science, vol. 49, pp. 393 - 397, http://dx.doi.org/10.1016/j.jcs.2009.01.005
Mcauley EZ; Fullerton J; Blair I; Donald JA; Mitchell PB; Schofield PR, 2009, 'Association between the serotonin 2A receptor gene and bipolar affective disorder in an Australian cohort', Psychiatric Genetics, vol. 19, pp. 244 - 252, http://dx.doi.org/10.1097/YPG.0b013e32832ceea9
Mcauley EZ; Blair I; Liu Z; Fullerton J; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR, 2009, 'A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26', Molecular Psychiatry, vol. 14, pp. 492 - 500, http://dx.doi.org/10.1038/sj.mp.4002146
Sachdev PS; Lammel A; Trollor JN; Lee T; Wright MJ; Ames D; Wen W; Martin NG; Brodaty H; Schofield PR; Lammel A, 2009, 'A comprehensive neuropsychiatric study of elderly twins: the older australian twin study', Twin research and human genetics, vol. 12, pp. 573 - 582, http://dx.doi.org/10.1375/twin.12.6.573
Williams L; Gatt JM; Kuan SA; Dobson-Stone C; Palmer DM; Paul R; Song L; Costa P; Schofield PR; Gordon E, 2009, 'A polymorphism of the MAOA gene is associated with emotional brain markers and personality traits on an antisocial index', Neuropsychopharmacology, vol. 34, pp. 1797 - 1809, http://dx.doi.org/10.1038/npp.2009.1
Wilhelm KA; Meiser B; Mitchell PB; Finch AW; Siegel JE; Parker GB; Schofield PR, 2009, 'Issues concerning feedback about genetic testing and risk of depression', British Journal of Psychiatry, vol. 194, pp. 404 - 410, http://dx.doi.org/10.1192/bjp.bp.107.047514
Gatt JM; Nemeroff C; Dobson-Stone C; Paul R; Bryant RA; Schofield PR; Gordon E; Kemp A; Williams L, 2009, 'Interactions between BDNF Val66Met polymorphism and early life stress predict brain and arousal pathways to syndromal depression and anxiety', Molecular Psychiatry, vol. 14, pp. 681 - 695, http://dx.doi.org/10.1038/mp.2008.143
Joffe R; Gatt JM; Kemp A; Grieve S; Dobson-Stone C; Kuan SA; Schofield PR; Gordon E; Williams L, 2009, 'Brain derived neurotrophic factor Val66Met polymorphism, the five factor model of personality and hippocampal volume: Implications for depressive illness', Human Brain Mapping, vol. 30, pp. 1246 - 1256, http://dx.doi.org/10.1002/hbm.20592
Schofield PR; Williams L; Paul R; Gatt JM; Brown K; Luty A; Cooper N; Grieve S; Dobson-Stone C; Morris C; Kuan SA; Gordon E, 2009, 'Disturbances in selective information processing associated with the BDNF Val66Met polymorphism: Evidence from cognition, the P300 and fronto-hippocampal systems', Biological Psychology, vol. 80, pp. 176 - 188, http://dx.doi.org/10.1016/j.biopsycho.2008.09.001
Duncan CE; Schofield PR; Shannon-Weickert C, 2009, 'Kv channel interacting protein 3 expression and regulation by haloperidol in midbrain dopaminergic neurons', Brain Research, vol. 1304, pp. 1 - 13, http://dx.doi.org/10.1016/j.brainres.2009.09.045
Wilde A; Meiser B; Mitchell PB; Schofield PR, 2009, 'Community attitudes towards mental health intervention for healthy people on the basis of genetic susceptibility', Australian and New Zealand Journal of Psychiatry, vol. 43, pp. 1070 - 1076, http://dx.doi.org/10.1080/00048670903179152
Absalom NL; Schofield PR; Lewis TM, 2009, 'Pore structure of the Cys-loop ligand-gated ion channels', Neurochemical Research, vol. 34, pp. 1805 - 1815, http://dx.doi.org/10.1007/s11064-009-9971-2
Cederholm JME; Schofield PR; Lewis TM, 2009, 'Gating mechanisms in Cys-loop receptors', European Biophysics Journal, vol. 39, pp. 37 - 49, http://dx.doi.org/10.1007/s00249-009-0452-y
Loy CT; Schofield PR; Kwok JB, 2009, 'Glycogen Synthase Kinase-3 beta and Tau Genes Interact in Parkinson`s and Alzheimer`s Diseases Reply', Annals of Neurology, vol. 65, pp. 761 - 762, http://dx.doi.org/10.1002/ana.21718
Williams L; Gatt JM; Schofield PR; Olivieri G; Peduto A; Gordon E, 2009, '`Negativity bias` in risk for depression and anxiety: Brain-body fear circuitry correlates, 5-HTT-LPR and early life stress', Neuroimage, vol. 47, pp. 804 - 814, http://dx.doi.org/10.1016/j.neuroimage.2009.05.009
Fullerton J; Liu Z; Badenhop RF; Scimone A; Blair I; Van Herten M; Donald JA; Mitchell PB; Schofield PR, 2008, 'Genome screen of 15 Australian bipolar affective disorder pedigrees supports previously identified loci for bipolar susceptibility genes', Psychiatric Genetics, vol. 18, pp. 156 - 161, http://dx.doi.org/10.1097/YPG.0b013e3282fa1861
Chan DK; Mok VW; Ng P; Yeung J; Kwok JB; Fang ZM; Clarke RA; Wong L; Schofield PR; Hattori N, 2008, 'PARK2 mutations and clinical features in a Chinese population with early-onset Parkinson`s disease', Journal of Neural Transmission, vol. 115, pp. 715 - 719, http://dx.doi.org/10.1007/s00702-007-0011-6
Kwok JB; Loy CT; Hamilton G; Lau E; Hallupp M; Williams J; Owen MJ; Broe T; Tang N; Lam L; Powell JM; Lovestone S; Schofield PR, 2008, 'Glycogen synthase kinase-3beta and tau genes interact in Alzheimer`s disease', Annals of Neurology, vol. 64, pp. 446 - 454, http://dx.doi.org/10.1002/ana.21476
Williams L; Gatt JM; Hatch A; Palmer DM; Nagy M; Rennie C; Cooper N; Morris C; Grieve S; Dobson-Stone C; Schofield PR; Clark CR; Gordon E; Arns M; Paul R, 2008, 'The integrate model of emotion, thinking and self regulation: an application to the `paradox of aging`', Journal of Integrative Neuroscience, vol. 7, pp. 367 - 404, http://dx.doi.org/10.1142/S0219635208001939
Luty A; Kwok JB; Thompson E; Blumbergs PC; Brooks WS; Loy CT; Dobson-Stone C; Panegyres P; Hecker J; Nicholson GA; Halliday GM; Schofield PR, 2008, 'Pedigree with frontotemporal lobar degeneration - motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9', BMC NEUROLOGY, vol. 8, http://dx.doi.org/10.1186/1471-2377-8-32
Gatt JM; Kuan SA; Dobson-Stone C; Paul R; Joffe R; Kemp A; Gordon E; Schofield PR; Williams L, 2008, 'Association between BDNF Val66Met polymorphism and trait depression is mediated via resting EEG alpha band activity', Biological Psychology, vol. 79, pp. 275 - 284, http://dx.doi.org/10.1016/j.biopsycho.2008.07.004
Karlstrom H; Brooks WS; Kwok JB; Broe T; Kril J; Mccann H; Halliday GM; Schofield PR, 2008, 'Variable phenotype of Alzheimer's disease with spastic paraparesis', Journal of Neurochemistry, vol. 104, pp. 573 - 583, http://dx.doi.org/10.1111/j.1471-4159.2007.05038.x
Sugiharto S; Lewis TM; Moorhouse AJ; Schofield PR; Barry PH, 2008, 'Anion-cation permeability correlates with hydrated counterion size in glycine receptor channels', Biophysical Journal, vol. 95, pp. 4698 - 4715, http://dx.doi.org/10.1529/biophysj.107.125690
Duffy L; Cappas E; Schofield PR; Scimone A; Karl T, 2008, 'Behavioral profile of a heterozygous mutant mouse model for EGF-like domain neuregulin 1', Behavioral Neuroscience, vol. 122, pp. 748 - 759, http://dx.doi.org/10.1037/0735-7044.122.4.748
Meiser B; Kasparian NA; Mitchell PB; strong K; Simpson JM; Tabassum L; Mireskandari S; Schofield PR, 2008, 'Attitudes to genetic testing in families with multiple cases of bipolar disorder', Genetic Testing, vol. 12, pp. 233 - 243, http://dx.doi.org/10.1089/gte.2007.0100
Duncan CE; Chetcuti A; Schofield PR, 2008, 'Coregulation of genes in the mouse brain following treatment with clozapine, haloperidol, or olanzapine implicates altered potassium channel subunit expression in the mechanism of antipsychotic drug action', Psychiatric Genetics, vol. 18, pp. 226 - 239, http://dx.doi.org/10.1097/YPG.0b013e3283053019
Chetcuti A; Adams LJ; Mitchell PB; Schofield PR, 2008, 'Microarray gene expression profiling of mouse brain mRNA in a model of lithium treatment', Psychiatric Genetics, vol. 18, pp. 64 - 72, http://dx.doi.org/10.1097/YPG.0b013e3282fb0051
Mitchell PB; Fullerton J; Donald JA; Schofield PR, 2008, 'Two-dimensional genome scan identifies complex epistatic interactions in bipolar disorder', Bipolar Disorders, vol. 10, pp. 15 - 15, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000252711100037&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Skene L; Kerridge IH; Marshall B; McCombe P; Schofield PR, 2008, 'The Lockhart Committee: Developing policy through commitment to moral values, community and democratic processes', Journal of Law and Medicine, vol. 16, pp. 132 - 138
Rademakers R; Baker M; Gass J; Adamson J; Huey ED; Momeni P; Spina S; Coppola G; Karydas AM; Stewart H; Johnson N; Hsiung G-Y; Kelley B; Kuntz K; Steinbart E; Wood EM; Yu C-E; Josephs K; Sorenson E; Womack KB; Weintraub S; Pickering-Brown SM; Schopeld PR; Brooks WS; van Deerlin VM; Snowden J; Clark CM; Kertesz A; Boylan K; Ghetti B; Neary D; Schellenberg GD; Beach TG; Mesulam M; Mann D; Grafman J; Mackenzie IR; Feldman H; Bird T; Petersen R; Knopman D; Boeve B; Geschwind DH; Miller B; Wszolek Z; Lippa C; Bigio EH; Dickson D; Graff-Radford N; Hutton M, 2007, 'Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C -> T (Arg493X) mutation: an international initiative', LANCET NEUROLOGY, vol. 6, pp. 857 - 868, http://dx.doi.org/10.1016/S1474-4422(07)70221-1
Gordon E; Liddell BJ; Brown K; Bryant RA; Clark R; Das P; Dobson-Stone C; Falconer EM; Felmingham KL; Kemp A; Flynn G; Gatt JM; Harris A; Hermens D; Hopkinson P; Kuan SA; Lazzuro I; Moyle J; Paul R; Rennie C; Schofield PR; Whitford T; Williams L, 2007, 'Integrating objective gene-brain-behavior markers of psychiatric disorders', Journal of Integrative Neuroscience, vol. 6, pp. 1 - 34, http://dx.doi.org/10.1142/S0219635207001465
Rademakers R; Baker M; Gass J; adamson J; Huey ED; Momeni P; Spina S; Coppola G; Karydas AM; Stewart H; Johnson NA; Hsiung G; Kelley B; Kuntz K; Steinbart E; Wood EF; Yu C; Josephs K; Sorenson E; Womack KB; Weintraub S; Pickering-Brown S; Schofield PR; Brooks WS; Van Deerlin VM; Snowden J; Clark C; Kertesz A; boylan K; Ghetti B; Neary D; Schellenberg G; Beach T; Mesulam M; Mann D; Grafman J; McKenzie IR; Feldman H; Bird T; Petersen RC; Knopman D; Boeve B; Geschwind DH; Miller B; Wszolek Z; Lippa C; Bigio E; Dickson D; Graff-radford N; Hutton M, 2007, 'Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-T (Arg493X) mutation: an international initiative', Lancet Neurology, vol. 6, pp. 857 - 868, http://dx.doi.org/10.1016/S1474-4422(07)70221-1
Karlstrom H; Kwok JB; Gregory GC; Hallupp M; Brooks WS; Schofield PR, 2007, 'No association of spastic paraparesis genes in PSENI Alzheimer`s disease with spastic paraparesis', Neuroreport, vol. 18, pp. 1267 - 1269, http://dx.doi.org/10.1097/WNR.0b013e3282405209
Wilhelm KA; Siegel JE; Finch AW; Hadzi-Pavlovic D; Mitchell PB; Parker GB; Schofield PR, 2007, 'The long and the short of it: associations between 5_HTT genotypes and coping with stress', Psychosomatic Medicine, vol. 69, pp. 614 - 620, http://dx.doi.org/10.1097/PSY.0b013e31814cec64
Dobson-Stone C; Gatt J; Kuan S; Grieve S; Gordon E; Williams L; Schofield PR, 2007, 'Investigation of MCPH1 G37995C and ASPM A44871G polymorphisms and brain size in a healthy cohort', Neuroimage, vol. 37, pp. 394 - 400, http://dx.doi.org/10.1016/j.neuroimage.2007.05.011
Gatt JM; Clark CR; Kemp A; Liddell BJ; Dobson-Stone C; Kuan SA; Schofield PR; Williams L, 2007, 'A genotype-endophenotype-phenotype path model of depressed mood: Integrating cognitive and emotional markers', Journal of Integrative Neuroscience, vol. 6, pp. 75 - 104, http://dx.doi.org/10.1142/S0219635207001398
Alexander D; Williams L; Gatt J; Dobson-Stone C; Kuan S; Todd E; Schofield PR; Cooper N; Gordon E, 2007, 'The contribution of apolipoprotein E alleles on cognitive performance and dynamic neural activity over six decades', Biological Psychology, vol. 75, pp. 229 - 238, http://dx.doi.org/10.1016/j.biopsycho.2007.03.001
Meiser B; Mitchell PB; Kasparian NA; Strong K; Simpson JM; Mireskandari S; Tabassum L; Schofield PR, 2007, 'Attitudes toward childbearing, causal attributions for bipolar disorder and psychological distress A study of families with multiple cases of bipolar disorder', Psychological Medicine, vol. 37, pp. 1601 - 1611, http://dx.doi.org/10.1017/S0033291707000852
Graham BA; Brichta A; Schofield PR; Callister RJ, 2007, 'Altered potassium channel function in the superficial dorsal horn of the spastic mouse', The Journal of Physiology, vol. 584, pp. 121 - 136, http://dx.doi.org/10.1113/jphysiol.2007.138198
Karl T; Duffy L; Scimone A; Harvey RP; Schofield PR, 2007, 'Altered motor activity, exploration and anxiety in heterozygous neuregulin 1 mutant mice: implications for understanding schizophrenia', Genes Brain and Behavior, vol. 6, pp. 677 - 687, http://dx.doi.org/10.1111/j.1601-183X.2006.00298.x
Boucher A; Arnold JC; Duffy L; Schofield PR; Micheau J; Karl T, 2007, 'Heterozygous neuregulin 1 mice are more sensitive to the behavioural effects of Delta(9)-tetrahydrocannabinol', Psychopharmacology, vol. 192, pp. 325 - 336, http://dx.doi.org/10.1007/s00213-007-0721-3
Hickie IB; Ward PB; Scott E; Mitchell PB; Schofield PR; Scimone A; Wilhelm KA; Parker GB; Naismith S, 2007, 'Serotonin transporter gene status predicts caudate nucleus but not amygdala or hippocampal volumes in older persons with major depression', Journal of Affective Disorders, vol. 98, pp. 137 - 142, http://dx.doi.org/10.1016/j.jad.2006.07.010
Sinclair AH; Schofield PR, 2007, 'Human embryonic stem cell research: An Australian perspective', Cell, vol. 128, pp. 221 - 223, http://dx.doi.org/10.1016/j.cell.2007.01.008
Hoth K; Paul R; Williams L; Dobson-Stone C; Todd E; Schofield PR; Gunstad J; Cohen R; Gordon E, 2006, 'Associations between the COMT Val/Met polymorphism, early life stress', Neuropsychiatric Disease and Treatment, vol. 2, pp. 219 - 225, http://dx.doi.org/10.2147/nedt.2006.2.2.219
Blair I; Chetcuti A; Badenhop RF; Scimone A; Moses MJ; Adams LJ; Craddock N; Green E; Kirov G; Owen MJ; Kwok JB; Donald JA; Mitchell PB; Schofield PR, 2006, 'Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele', Molecular Psychiatry, vol. 11, pp. 372 - 383, http://dx.doi.org/10.1038/sj.mp.4001784
Gregory GC; Macdonald V; Schofield PR; Kril J; Halliday GM, 2006, 'Differences in regional brain atrophy in genetic forms of Alzheimer's disease', Neurobiology of Aging, vol. 27, pp. 387 - 393, http://dx.doi.org/10.1016/j.neurobiolaging.2005.03.011
Pickering-Brown S; Baker M; Gass J; Boeve B; Loy CT; Brooks WS; Mackenzie IR; Martins RN; Kwok JB; Halliday GM; Kril J; Schofield PR; Mann DM; Hutton M, 2006, 'Mutations in progranulin explain atypical phenotypes with variants in MAPT', Brain, vol. 129, pp. 3124 - 3126, http://dx.doi.org/10.1093/brain/awl289
Wilhelm KA; Mitchell PB; Niven H; Finch AW; Wedgwood L; Scimone A; Blair I; Parker GB; Schofield PR, 2006, 'Life events, first depression onset and the serotonin transporter gene', British Journal of Psychiatry, vol. 188, pp. 210 - 215, http://dx.doi.org/10.1192/bjp.bp.105.009522
Graham BA; Schofield PR; Sah P; Margrie T; Callister RJ, 2006, 'Distinct physiological mechanisms underlie altered glycinergic synaptic transmission in the murine mutants spastic, spasmodic, and oscillator', Journal of Neuroscience, vol. 26, pp. 4880 - 4890, http://dx.doi.org/10.1523/JNEUROSCI.3991-05.2006
Teber ET; Crawford EN; Bolton K; Van Dyk D; Schofield PR; Kapoor V; Church WB, 2006, 'Djinn Lite: a tool for customised gene transcript modelling, annotation-data enrichment and exploration', BMC bioinformatics, vol. 7, pp. 33 - 41, http://dx.doi.org/10.1186/1471-2105-7-33
Chetcuti A; Adams LJ; Mitchell PB; Schofield PR, 2006, 'Altered gene expression in mice treated with mood stabilizer sodium valproate', International Journal of Neuropsychopharmacology, vol. 9, pp. 267 - 276, http://dx.doi.org/10.1017/S1461145705005717
Gunstad J; Schofield PR; Paul R; Spitznagel M; Cohen R; Williams LA; Kohn M; Gordon E, 2006, 'BDNF Val66Met polymorphism is associated with body mass index in healthy adults', Neuropsychobiology, vol. 53, pp. 153 - 156, http://dx.doi.org/10.1159/000093341
Schofield PR; Blair IP; Chetcuti A; McAuley EZ; Fullerton JM; Donald JA; Mitchell PB, 2006, '03-04 Genetic and genomic approaches to better understanding bipolar disorder.', Acta Neuropsychiatr, vol. 18, pp. 321, http://dx.doi.org/10.1017/S0924270800032038
Finch A; Baikie K; Mitchell P; Parker G; Reddy J; Schofield PR; Showyin T; Siegel J; Wedgwood L; Wilhelm K, 2006, 'Phenotypic correlates of the serotonin transporter gene.', Acta Neuropsychiatr, vol. 18, pp. 249, http://dx.doi.org/10.1017/S0924270800030234
Showyin T; Baikie K; Finch A; Mitchell P; Parker G; Reddy J; Schofield PR; Wedgwood L; Wilhelm K, 2006, 'The Stress Sampler Study II: psychological functioning and coping within a diabetes sample.', Acta Neuropsychiatr, vol. 18, pp. 308, http://dx.doi.org/10.1017/S0924270800031720
Wilhelm K; Meiser B; Mitchell P; Siegel J; Showyin T; Parker G; Schofield PR, 2006, 'Factors influencing the decision to learn 5-HTT genotype results and subsequent impact on the individual.', Acta Neuropsychiatr, vol. 18, pp. 274, http://dx.doi.org/10.1017/S0924270800030891
Attia J; Schofield P, 2005, 'What now for Alzheimer's disease? An epidemiological evaluation of the AD2000 trial', Australian Prescriber, vol. 28, pp. 134 - 135, http://dx.doi.org/10.18773/austprescr.2005.100
Chetcuti A; Adams LJ; Mitchell PB; Schofield PR, 2005, 'Altered gene expression in mice treated with the mood stabilizer sodium valproate', International Journal of Neuropsychopharmacology, vol. 8, pp. 1 - 10
Blair IP; Badenhop RF; Scimone A; Moses MJ; Donald JA; Mitchell PB; Schofield PR, 2005, 'Identification, characterization, and association analysis of novel genes from the bipolar disorder susceptibility locus on chromosome 4q35', Psychiatric Genetics, vol. 15, pp. 199 - 204, http://dx.doi.org/10.1097/00041444-200509000-00011
Halliday GM; Song YC; Lepar GS; Brooks WS; Kwok JB; Kersaitis C; Gregory GC; Shepherd CE; Rahimi F; Schofield PR; Kril J, 2005, 'Pick bodies in a family with presenilin-1 Alzheimer's disease', Annals of Neurology, vol. 57, pp. 139 - 143, http://dx.doi.org/10.1002/ana.20366
Kwok JB; Hallupp M; Loy CT; Chan DK; Woo J; Mellick GD; Buchanan D; Silburn PA; Halliday GM; Schofield PR, 2005, 'GSK3B polymorphisms alter transcription and splicing in Parkinson`s disease', Annals of Neurology, vol. 58, pp. 829 - 839, http://dx.doi.org/10.1002/ana.20691
Blair I; Mitchell PB; Schofield PR, 2005, 'Techniques for the identification of genes involved in psychiatric disorders', Australian and New Zealand Journal of Psychiatry, vol. 39, pp. 542 - 549, http://dx.doi.org/10.1111/j.1440-1614.2005.01625.x
Duncan CE; Chetcuti A; Schofield PR, 2005, 'Identification of genes associated with schizophrenia using gene expression analysis of an animal model of antipsychotic drug action', American Journal of Medical Genetics Part B - Neuropsychiatric Genetics, vol. 138B, pp. 121 - 121, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000232357300436&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Chetcuti A; Adams LJ; Mitchell PB; Schofield PR, 2005, 'Identification of novel valproate regulated genes in the mouse brain', American Journal of Medical Genetics Part B - Neuropsychiatric Genetics, vol. 138B, pp. 75 - 75, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000232357300267&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Panegyres P; Kwok JB; Schofield PR; Blumbergs P, 2005, 'A western Australian kindred with Dutch cerebral amyloid angiopathy', Journal of the Neurological Sciences, vol. 239, pp. 75 - 80, http://dx.doi.org/10.1016/j.jns.2005.08.002
Loy CT; Kwok JB; Blair I; Hallupp M; Todd E; Schofield PR, 2005, 'Tau haplotypes regulate Tau expression in human brains', Journal of the Neurological Sciences, vol. 238, pp. S323 - S323, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000235088003097&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Blair IP; Mitchell PB; Schofield PR, 2005, 'Techniques for the identification of genes involved in psychiatric disorders', Australian and New Zealand Journal of Psychiatry, vol. 39, pp. 542 - 549, http://dx.doi.org/10.1111/j.1440-1614.2005.01625.x
Badenhop RF; Moses MJ; Scimone A; Mitchell PB; Ewen-White KR; Rosso A; Donald JA; Adams LJ; Schofield PR, 2004, 'Erratum: A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19 (Molecular Psychiatry (2002) 7 (851-859) DOI: 10.1038/sj.mp. 4001114)', Molecular Psychiatry, vol. 9, pp. 539, http://dx.doi.org/10.1038/sj.mp.4001510
Verdile G; Groth DM; Matthews P; St George-Hyslop PH; Fraser PE; Ramabhadran T; Kwok J; Schofield PR; Carter T; Gandy SE; Martins RN, 2004, 'P4-265 Baculoviral expression of the presenilin mutation lacking exon 9 increase levels of an amyloid beta - Like protein in SF91NSECTcells', Neurobiology of Aging, vol. 25, pp. S550 - S551
Carter T; Verdile G; Groth DM; Bogush A; Thomas S; Shen P; Fraser PE; Matthews P; Nixon R; Ehrlich M; Kwok JB; George-Hyslop P; Schofield PR; Li Y; Yang A; Martins RN; Gandy SE, 2004, 'Alzheimer amyloid precursor aspartyl proteinase activity in CHAPSO homogenates of Spodoptera frugiperda cells', Alzheimer Disease and Associated Disorders, vol. 18, pp. 261 - 263
Shepherd CE; Gregory GC; Vickers J; Brooks WS; Kwok J; Schofield PR; Kril J; Halliday GM, 2004, 'Positional effects of presenilin-1 mutations on tau phosphorylation in cortical plaques', Neurobiology of Disease, vol. 15, pp. 115 - 119, http://dx.doi.org/10.1016/j.nbd.2003.10.008
Badenhop RF; Jansen J; Fagan PA; Lord RS; Wang Z; Foster W; Schofield PR, 2004, 'The prevalence of SDHB, SDHC, and SDHD mutations in patients with headand neck paraganglioma and association of mutations with clinicalfeatures', Journal of Medical Genetics, vol. 41, http://dx.doi.org/10.1136/jmg.2003.011551
Morris R, 2004, 'In vivo somatic delivery of plasmid DNA and retrograde transport to obtain cell-specific gene expression in the central nervous system', Journal of Neurochemistry, vol. 90, pp. 1445 - 1452, http://dx.doi.org/10.1111/j.1471-4159.2004.02612.x
Piguet O; Brooks WS; Halliday GM; Schofield PR; Stanford PM; Kwok JB; Spillantini M; Yancopoulou D; Nestor PJ; Broe G; Hodges JR, 2004, 'Similar early clinical presentations in familial and non-familial frontotemporal dementia', Journal of Neurosurgery, vol. 75, pp. 1743 - 1745, http://dx.doi.org/10.1136/jnnp.2003.031948
Keramidas A; Moorhouse AJ; Schofield PR; Barry PH, 2004, 'Ligand-gated ion channels: mechanisms underlying ion selectivity', Progress in Biophysics and Molecular Biology, vol. 86, pp. 161 - 204, http://dx.doi.org/10.1016/j.pbiomolbio.2003.09.002
Verdile G; Groth D; Matthews PM; George-Hyslop P; Fraser PE; Ramabhadran T; Kwok JB; Schofield PR; Carter T; Gandy S; Martins RN, 2004, 'Baculoviruses expressing the human familial Alzheimer`s disease presenilin 1 mutation lacking exon 9 increase levels of an amyloid beta-like protein in Sf9 cells', Molecular Psychiatry, vol. 9, pp. 594 - 602, http://dx.doi.org/10.1038/sj.mp.4001458
Kwok J; Teber E; Loy C; Hallupp M; Nicholson GA; Mellick GD; Buchanan DD; Silburn PA; Schofield PR, 2004, 'Tau haplotypes regulate transcription and are associated withParkinson`s disease', Annals of Neurology, vol. 55, pp. 329 - 334, http://dx.doi.org/10.1002/ana.10826
Absalom NL; Lewis TM; Schofield PR, 2004, 'Mechanisms of channel gating of the ligand-gated ion channelsuperfamily inferred from protein structure', Experimental Physiology, vol. 89, pp. 145 - 153, http://dx.doi.org/10.1113/expphysiol.2003.026815
Blair IP; Badenhop RF; Scimone A; Moses MJ; Kerr N; Donald JA; Mitchell PB; Schofield PR, 2004, 'Identification and analysis of candidate genes from the bipolardisorder susceptibility locus on chromosome 4q35', American Journal of Medical Genetics Part A, vol. 130B, pp. 45 - 45, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000223742600167&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Chetcuti A; Adams LD; Schofield PR, 2004, 'Microarray analysis of altered gene expression in the mouse brain aftertreatment with lithium chloride or sodium valproate', American Journal of Medical Genetics Part A, vol. 130B, pp. 149 - 150, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000223742600574&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Mitchell PB; Schofield PR; Donald JA, 2003, 'Major leads in the search for susceptibility genes for depression', Journal of Pharmacogenomics, vol. 3, pp. 305 - 307, http://dx.doi.org/10.1038/sj.tpj.6500212
Segurado R; Detera-Wadleigh SD; Levinson DF; Lewis CR; Gill M; Nurnberger JI; Craddock N; DePaulo R; Baron M; Gershon ES; Ekholm J; Cichon S; Turecki G; Claes S; Kelsoe JR; Schofield PR; Badenhop RF; Morisette J; Coon H; Blackwood D; Curtis D; McInnes A; Foroud T; Edenberg H; Reich T; Donald JA; Rice J; Goate A; McInnis M; McMahon FJ; Goldin JA; Bennett P; Wallour V; Zandi JL; Gilliam C; Juo S; Berrettini WH; Yoshikawa LP; Lonnqvist J; Nothen MM; Schumacher JJ; Windemuth C; Rietschel M; Propping P; Alda M; Grof P; Rouleau GA; Del Favero J; VanBroeckhoven C; Mendlewicz J; Adolfsson R; Spence MA; Luebbert H; Adams LJ; Mitchell PB; Barden N; Shink E; Byerley W; Muir W; Visscher P; Macgregor S; Gurling H; Kalsi G; McQuillan A; Escamilla MA; Reus VI; Leon P; Freimer NB; Ewald H; Kruse T; Mors O; Radhakrishna U; Blouin J; Antonarakis SE; Akarsu N, 2003, 'Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder', American Journal of Human Genetics, vol. 73, pp. 49 - 62, http://dx.doi.org/10.1086/376547
Lee DJ; Keramidas A; Moorhouse AJ; Schofield PR; Barry PH, 2003, 'The contribution of P250 (P-2`D) to ion selectivity and pore diameter in the human glycine receptor.', Neuroscience Letters, vol. 351, pp. 196 - 200, http://dx.doi.org/10.1016/j.neulet.2003.08.005
Absalom NL; Lewis TM; Kaplan W; Pierce KD; Schofield PR, 2003, 'Role of charged residues in coupling ligand binding and channel activation in the extracellular domain of the clycine receptor', The Journal of Biological Chemistry, vol. 278, pp. 50151 - 50157, http://dx.doi.org/10.1074/jbc.M305357200
Graham BA; Schofield PR; Sah P; Callister RJ, 2003, 'Altered inhibitory synaptic transmission in superficial dorsal horn neurones in Spastic and Oscillator mice', The Journal of Physiology, vol. 551, pp. 905 - 916, http://dx.doi.org/10.1113/jphysiol.2003.049064
Lewis TM; Schofield PR; McClellan AM, 2003, 'Kinetic determinants of agonist potency at the recombinant human glycine receptor', The Journal of Physiology, vol. 549, pp. 361 - 374, http://dx.doi.org/10.1113/jphysiol.2002.037796
Kwok J; Schofield PR, 2003, 'The Molecular basis of Alzheimer`s disease and frontotemporal dementia.', The Aging Brain: The Neurobiology and Neurpsychiatry of Ageing, pp. 173 - 185, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000183726900010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Kwok JBJ; Kapoor R; Gotoda T; Iwamoto Y; Iizuka Y; Yamada N; Isaacs KE; Kushwaha VV; Bret Church W; Schofield PR; Kapoor V, 2002, 'A missense mutation in kynurenine aminotransferase-1 in spontaneously hypertensive rats', Journal of Biological Chemistry, vol. 277, pp. 35779 - 35782, http://dx.doi.org/10.1074/jbc.C200303200
Healy PJ; Pierce KD; Dennis JA; Windsor PA; Schofield PR, 2002, 'Bovine myoclonus: Model of human hyperekplexia (startle disease)', Movement Disorders, vol. 17, pp. 743 - 744, http://dx.doi.org/10.1002/mds.10216
Kwok J; Hallupp M; Badenhop RF; Schofield PR; Halliday GM; Brooks WS; Dolois G; Wang R; Murayama O; Takashima A; Vickers J; Gandy SE, 2002, 'Presenilin-1 mutation (L271V) results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy', NEUROBIOLOGY OF AGING, vol. 23, pp. S277 - S277, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000177465301016&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Brooks WS; Broe GA; Kwok JBJ; Schofield PR; Kril JJ, 2002, 'Familial Alzheimer's disease with spastic paraparesis: Two pedigrees with PS-1 exon 9 deletion due to splice acceptor mutations', NEUROBIOLOGY OF AGING, vol. 23, pp. S313 - S313, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000177465301145&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Badenhop RF; Moses MJ; Scimone A; Mitchell PB; Ewen-White KR; Rosso A; Donald JA; Adams LJ; Schofield PR, 2002, 'A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19', Molecular Psychiatry, vol. 7, pp. 851 - 859, http://dx.doi.org/10.1038/sj.mp.4001114
Healy PJ; Dennis JA; Windsor PA; Pierce KD; Schofield PR, 2002, 'Genotyping cattle for inherited congenital myoclonus and maple syrup urine disease', Australian Veterinary Journal, vol. 80, pp. 695 - 697, http://dx.doi.org/10.1111/j.1751-0813.2002.tb11301.x
Schofield PR, 2002, 'The role of glycine and glycine receptors in myoclonus and startle syndromes.', Advances in neurology, vol. 89, pp. 263 - 274
Keramidas A; Moorhouse AJ; Pierce K; Schofield PR; Barry PH, 2002, 'Cation-selective mutations in the M2 domain of the inhibitory glycine receptor channel reveal determinants of ion charge selectivity', Journal of General Physiology, vol. 119, pp. 393 - 410, http://dx.doi.org/10.1085/jgp.20028552
Moorhouse AJ; Keramidas A; Zaikine A; Zaykin A; Schofield PR; Barry PH, 2002, 'Single channel analysis of conductance and rectification in cation-selective, mutant glycine receptor channels', Journal of General Physiology, vol. 119, pp. 411 - 425, http://dx.doi.org/10.1085/jgp.20028553
Munch G; Shepherd CE; Mccann H; Brooks WS; Kwok JB; Arendt T; Hallupp M; Schofield PR; Martins RN; Halliday GM, 2002, 'Intraneuronal advanced glycation endproducts in presenilin-l Alzheimer's disease', Neuroreport, vol. 13, pp. 601 - 604
Brodaty H; Mitchell PB; Luscombe GM; Kwok JB; McKenzie R; Schofield PR; Badenhop RF, 2002, 'Familial idiopathic basal ganglia calcification (Fahr`s disease) without neurological, cognitive and psychiatric symptoms is not linked mto the IBGC1 locus on chromosome 14q', Human Genetics, vol. 110, pp. 8 - 14, http://dx.doi.org/10.1007/s00439-001-0650-x
Rees MI; Lewis TM; Kwok JB; Mortier GR; Govaert P; Snell RG; Schofield PR; Owen MJ, 2002, 'Hyperekplexia associated with compound heterozygote mutations in the β-subunit of the human inhibitory glycine receptor (GLRB).', Human Molecular Genetics, vol. 11, pp. 853 - 860, http://dx.doi.org/10.1093/hmg/11.7.853
Badenhop RF; Moses MJ; Scimone A; Adams LJ; Donald JA; Mitchell PB; Schofield PR, 2001, 'Haplotype analysis defines a 4.7Mb probable disease region for a bipolar affective disorder susceptibility locus on chromosome 4q35', American Journal of Medical Genetics - Neuropsychiatric Genetics, vol. 105, pp. 591
Adams LJ; Schofield PR, 2001, 'Microarray studies of changes in gene expression in mouse brain induced by anti-manic drugs', American Journal of Medical Genetics - Neuropsychiatric Genetics, vol. 105, pp. 582 - 583
Blair IP; Adams LJ; Badenhop RF; Moses MJ; Scimone A; Morris J; Ma L; Austin C; Donald JA; Mitchell PB; Schofield PR, 2001, 'Towards identification of a susceptibility gene for bipolar affective disorder: genomic characterisation of chromosome 4q35.', AMERICAN JOURNAL OF HUMAN GENETICS, vol. 69, pp. 544 - 544, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000171648902130&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Adams LJ; Schofield PR, 2001, 'Identification of genes involved in susceptibility to bipolar affective disorder using GeneChips.', AMERICAN JOURNAL OF HUMAN GENETICS, vol. 69, pp. 465 - 465, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000171648901657&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Collie A; Maruff P; Shafiq-Antonacci R; Smith M; Hallup M; Schofield PR; Masters CL; Currie J, 2001, 'Memory decline in healthy older people: Implications for identifying mild cognitive impairment', Neurology, vol. 56, pp. 1533 - 1538, http://dx.doi.org/10.1212/WNL.56.11.1533
Kwok JB; Raskin S; Morgan G; Antoniuk SA; Bruk I; Schofield PR, 2001, 'Mutations in the glycine receptor alpha1 subunit (GLRA1) gene in hereditary hyperekplexia pedigrees: evidence for non-penetrance of mutation Y279C.', Journal of medical genetics, vol. 38, http://dx.doi.org/10.1136/jmg.38.6.e17
Collie A; Maruff P; Shafiq-Antonacci R; Smith M; Hallup M; Schofield PR; Masters CL; Currie J, 2001, 'Memory decline in healthy older people', Neurology, pp. 1533 - 1538
Badenhop RF; Moses MJ; Scimone A; Mitchell PB; Ewen KR; Rosso A; Donald JA; Adams LJ; Schofield PR, 2001, 'A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q', Molecular Psychiatry, vol. 6, pp. 396 - 403, http://dx.doi.org/10.1038/sj.mp.4000887
Pierce KD; Handford CA; Morris R; Vafa B; Morris JA; Healy PJ; Schofield PR, 2001, 'A nonsense mutation in the alpha1 subunit of the inhibitory glycine receptor associated with bovine myoclonus', Molecular and Cellular Neuroscience, vol. 17, pp. 354 - 363, http://dx.doi.org/10.1006/mcne.2000.0934
Cherian SM; Lord RS; Baysal BE; Taschner PE; Schofield PR; Badenhop RF, 2001, 'Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss', Genes Chromosomes and Cancer, vol. 31, pp. 255 - 263, http://dx.doi.org/10.1002/gcc.1142
Kwok JB; Mclean C; Kril J; Broe T; Nicholson GA; Cappai R; Hallupp M; Cotton R; Schofield PR; Brooks WS; Smith MJ, 2001, 'Variable phenotypes of Alzheimer`s disease with spastic paraparesis', Annals of Neurology, vol. 49, pp. 125 - 129, http://dx.doi.org/10.1002/1531-8249(200101)49:1<125::AID-ANA21>3.0.CO;2-1
Schofield PR, 2001, 'Genetics, an alternative way to discover, characterize and understand ion channels', Clinical and Experimental Pharmacology and Physiology, vol. 28, pp. 84 - 88, http://dx.doi.org/10.1046/j.1440-1681.2001.03409.x
Lynch JW; Han NR; Haddrill J; Pierce KD; Schofield PR, 2001, 'The surface accessibility of the glycine receptor M2-M3 loop is increased in the channel open state', Journal of Neuroscience. 23(33):10559-67, 2003 Nov 19, vol. 21, pp. 2589 - 2599
Stanford PM; Halliday GM; Brooks WS; Kwok JB; Schofield PR, 2001, 'Progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17 and familial tauopathies.', Brain, vol. 124, pp. 1668 - 1670, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000170453400019&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Rees MI; Lewis TM; Vafa B; Ferrie C; Corry P; Muntoni F; Jungbluth H; Stephenson JB; Kerr M; Snell RG; Schofield PR; Owen MJ, 2001, 'Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexia', Human Genetics, vol. 109, pp. 267 - 270, http://dx.doi.org/10.1007/s004390100569
Herrera C; Casado V; Ciruela F; Schofield PR; Mallol J; Lluis C; Franco R, 2001, 'adenosine A2B receptors behave as an alternative anchoring protein for cell surface adenosine deaminase in lymphocytes and cultured cells', Molecular Pharmacology, vol. 59, pp. 127 - 134, http://dx.doi.org/10.1124/mol.59.1.127
Rees MI; Lewis TM; Mortier G; Snell RG; Schofield PR; Owen MJ, 2000, 'A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human beta-subunit of the inhibitory glycine receptor (GLRB).', AMERICAN JOURNAL OF HUMAN GENETICS, vol. 67, pp. 391 - 391, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000089400702194&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Badenhop RF; Moses MJ; Mitchell PB; Donald JA; Adams LJ; Schofield PR, 2000, 'A genome-wide screen for bipolar affective disorder susceptibility loci from 13 Australian pedigrees', American Journal of Medical Genetics - Neuropsychiatric Genetics, vol. 96, pp. 548 - 549
Adams LJ; Badenhop RF; Morris JA; Moses MJ; Scimone A; Ma L; Jones AM; Mathavan K; Donald JA; Hewitt JE; Detera-Wadleigh SD; Mitchell PB; Austin CP; Schofield PR, 2000, 'Analysis of a bipolar affective disorder susceptibility locus on chromosome 4q35', American Journal of Medical Genetics - Neuropsychiatric Genetics, vol. 96, pp. 469
Kwok JBJ; Li QX; Hallupp M; Whyte S; Ames D; Beyreuther K; Masters CL; Schofield PR, 2000, 'Novel Leu723Pro amyloid precursor protein mutation increases amyloid β42(43) peptide levels and induces apoptosis', Annals of Neurology, vol. 47, pp. 249 - 253, http://dx.doi.org/10.1002/1531-8249(200002)47:2<249::AID-ANA18>3.0.CO;2-8
Schofield PR, 2000, 'Comment: The Epidemiology of the Genetic Liability for Schizophrenia', Australian and New Zealand Journal of Psychiatry, vol. 34, pp. S56 - S57, http://dx.doi.org/10.1080/000486700223
Keramidas A; Moorhouse AJ; French CD; Schofield PR; Barry PH, 2000, 'M2 pore mutations convert the glycine receptor channel from being anion- to cation-selective', Biophysical Journal, pp. 247 - 259
Keramidas A; Moorhouse AJ; French C; Schofield PR; Barry PH, 2000, 'M2 pore mutations convert the glycine receptor channel from being anion to cation selective', Biophysical Journal, vol. 78, pp. 247 - 259, http://dx.doi.org/10.1016/S0006-3495(00)76287-4
Stanford PM; Halliday GM; Brooks WS; Kwok JB; Storey CE; Creasey H; Morris J; Fulham MJ; Schofield PR, 2000, 'Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene. Expansion of the disease phenotype caused by tau gene mutations', Brain, vol. 123, pp. 880 - 893, http://dx.doi.org/10.1093/brain/123.5.880
Akinci MK; Schofield PR, 1999, 'Widespread expression of GABA(A) receptor subunits in peripheral tissues', Neuroscience Research, vol. 35, pp. 145 - 153, http://dx.doi.org/10.1016/S0168-0102(99)00078-4
Dowdney L; Wilson R; Maughan B; Allerton M; Schofield P; Skuse D, 1999, 'Psychological disturbance and service provision in parentally bereaved children: Prospective case-control study', British Medical Journal, vol. 319, pp. 354 - 357, http://dx.doi.org/10.1136/bmj.319.7206.354
Heun R; Devi G; Marder K; Schofield P; Tang M; Stern Y; Mayeux R, 1999, 'Validity of family history diagnosis for dementia (multiple letters)', Genetic Epidemiology, vol. 17, pp. 151 - 154, http://dx.doi.org/10.1002/(SICI)1098-2272(1999)17:2<151::AID-GEPI5>3.0.CO;2-K
Devi G; Marder K; Schofield P; Tang M; Stern Y; Mayeux R, 1999, 'Validity of family history diagnosis for dementia - Reply', GENETIC EPIDEMIOLOGY, vol. 17, pp. 152 - 154, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000081186400006&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Barry PH; Schofield PR; Moorhouse AJ, 1999, 'Glycine receptors: What gets in and why?', Clinical and Experimental Pharmacology and Physiology, pp. 935 - 936
Kwok JB; Adams LM; Salmon J; Donald JA; Mitchell PB; Schofield PR, 1999, 'Nonparametric simulation-based statistical analyses for bipolar affective disorder locus on chromosome 21q22.3', American Journal of Medical Genetics Part A, vol. 88, pp. 99 - 102, http://dx.doi.org/10.1002/(SICI)1096-8628(19990205)88:1<99::AID-AJMG18>3.0.CO;2-9
Barry PH; Schofield PR; Moorhouse AJ, 1999, 'Glycine receptors: What gets in and why', Clinical and Experimental Pharmacology and Physiology, vol. 26, pp. 935 - 936, http://dx.doi.org/10.1046/j.1440-1681.1999.03149.x
Moorhouse AJ; Jacques P; Barry PH; Schofield PR, 1999, 'The startle disease mutation Q266H, in the second transmembrane domain of the human glycine receptor, impairs channel gating', Molecular Pharmacology, vol. 55, pp. 386 - 395, http://dx.doi.org/10.1124/mol.55.2.386
Lewis TM; Schofield PR, 1999, 'Structure-function relationships of the human glycine receptor: Insights from hyperekplexia mutations', Annals of the New York Academy of Sciences, vol. 868, pp. 681 - 684, http://dx.doi.org/10.1111/j.1749-6632.1999.tb11345.x
Vafa B; Lewis TM; Cunningham AM; Jacques P; Lynch JP; Schofield PR, 1999, 'Identification of a new ligand binding domain in the alpha1 subunit of the inhibitory glycine receptor', Journal of Neurochemistry, vol. 73, pp. 2158 - 2166
Laws SM; Taddei K; Fisher C; Small D; Clarnette R; Hallmayer J; Brooks WS; Kwok JB; Schofield PR; Gandy SE; Martins RN, 1999, 'Evidence that the butyrylcholinesterase K variant can protect against late-onset Alzheimer`s disease', Alzheimers Reports, vol. 2, pp. 219 - 223
Verdile G; Fraser PE; St George-Hyslop PH; Kwok JB; Schofield PR; Fisher C; Helmerhorst E; Martins RN, 1999, 'Decreased secretion of amyloid precursor protein in Chinese hamster ovary cells overexpressing presenilin 1', Alzheimers Reports, vol. 2, pp. 231 - 239
Lynch JP; Han NR; Schofield PR, 1999, 'Building new function into glycine receptors: A structural model for the activation of the glycine-gated chloride channel', Clinical and Experimental Pharmacology and Physiology, vol. 26, pp. 932 - 934, http://dx.doi.org/10.1046/j.1440-1681.1999.03150.x
Callister RJ; Schofield PR; Sah P, 1999, 'The use of murine mutants to study glycine receptor function', Clinical and Experimental Pharmacology and Physiology, vol. 26, pp. 929 - 931, http://dx.doi.org/10.1046/j.1440-1681.1999.03148.x
Dalpiaz A; Townsend-Nicholson A; Beukers MW; Schofield PR; Ijzerman AP, 1998, 'Thermodynamics of full agonist, partial agonist, and antagonist binding to wild-type and mutant adenosine A
Schofield PR; Adams LJ; Badenhop R; Moses M; Fielder SL; Rosso A; Donald JA; Mitchell PB, 1998, 'Genetic linkage to chromosome 4q35 in bipolar affective disorder', American Journal of Medical Genetics - Neuropsychiatric Genetics, vol. 81, pp. 474 - 475
Donald J; Adams LJ; Mitchell PB; Fielder SL; Rosso A; Schofield PR, 1998, 'Identification of a novel genetic linkage with bipolar affective disorder', EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 6, pp. 137 - 138, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000074522800598&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Dougherty C; Barucha J; Schofield PR; Jacobson KA; Liang BT, 1998, 'Cardiac myocytes rendered ischemia resistant by expressing the human adenosine A
Jacobs DM; Tang MX; Stern Y; Sano M; Marder K; Bell KL; Schofield P; Dooneief G; Gurland B; Mayeux R, 1998, 'Cognitive function in nondemented older women who took estrogen after menopause', Neurology, vol. 50, pp. 368 - 373, http://dx.doi.org/10.1212/WNL.50.2.368
Stern Y; Tang MX; Jacobs DM; Sano M; Marder K; Bell K; Dooneief G; Schofield P; Côté L, 1998, 'Prospective comparative study of the evolution of probable Alzheimer's disease and Parkinson's disease dementia', Journal of the International Neuropsychological Society, vol. 4, pp. 279 - 284, http://dx.doi.org/10.1017/s1355617798002793
Adams LM; Mitchell PB; Fielder SL; Rosso D; Donald J; Schofield PR, 1998, 'A susceptibility locus for bipolar affective disorder on chromosome 4q35.', American Journal of Human Genetics, vol. 62, pp. 1084 - 1091, http://dx.doi.org/10.1086/301826
Vafa B; Schofield PR, 1998, 'Heritable mutations in the glycine GABAa and nicotinic acetyl-choline receptors provide new insights into the ligand-gated ion channel receptor superfamily.', International Review of Neurobiology, vol. 42, pp. 285 - 332
Lynch JP; Jacques P; Pierce K; Schofield PR, 1998, 'Zinc potentiation of the glycine receptor chloride channel is mediated by allosteric pathways.', Journal of Neurochemistry, vol. 71, pp. 2159 - 2168
Taddei K; Kwok JB; Kril J; Halliday GM; Creasey H; Hallupp M; Fisher C; Brooks WS; Chung C; Andrews C; Masters C; Schofield PR; Martins RN, 1998, 'Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's disease.', Neuroreport, vol. 9, pp. 3335 - 3339, http://dx.doi.org/10.1097/00001756-199810050-00034
Camp D; Green J; Kaiser SM; Moni RW; Townsend-Nicholson A; Quinn RJ; Schofield PR, 1998, 'Diimidazo[1,2-c:4`,5`0e] pyrimidines: Adenosine agonist activity demonstrated by micro-physiometry.', Bioorganic and Medicinal Chemistry Letters, vol. 8, pp. 691 - 694, http://dx.doi.org/10.1016/S0960-894X(98)00102-4
Lynch JW; Rajendra S; Pierce K; Handford CA; Barry PH; Schofield PR, 1997, 'Identification of intracellular and extracellular domains mediating signal transduction in the inhiBitory glycine receptor chloride channel', European Molecular Biology Organization, vol. 16, pp. 110 - 120, http://dx.doi.org/10.1093/emboj/16.1.110
Adams LJ; Salmon J; Kwok JB; Vivero C; Donald JA; Mitchell PB; Schofield PR, 1997, 'Exclusion of linkage Between Bipolar affective disorder and chromosome 16 in 12 Australian pedigrees', American Journal of Medical Genetics Part A, vol. 74, pp. 304 - 310, http://dx.doi.org/10.1002/(SICI)1096-8628(19970531)74:3<304::AID-AJMG12>3.0.CO;2-S
Donald JA; Salmon J; Adams LJ; Littlejohn TG; Maher A; Mitchell PB; Schofield PR, 1997, 'Parental sex effects in Bipolar affective disorder pedigrees', Genetic Epidemiology, vol. 14, pp. 611 - 616, http://dx.doi.org/10.1002/(SICI)1098-2272(1997)14:6<611::AID-GEPI10>3.0.CO;2-T
Valenzuela SM; Martin DJ; Warton K; Por SB; Robbins JM; Bootcov MR; Schofield PR; Campbell TJ; Breit SN, 1997, 'Molecular cloning and expression of a chloride ion channel of cell nuclei.', The Journal of Biological Chemistry, vol. 272, pp. 12575 - 12582, http://dx.doi.org/10.1074/jbc.272.19.12575
Atkinson M; Townsend-Nicholson A; Nicholl J; Sutherland GR; Schofield PR, 1997, 'Cloning, characterisation and chromosomal assignment of the human adenosine A3 receptor (ADORA3) gene', Neuroscience Research, vol. 29, pp. 73 - 79, http://dx.doi.org/10.1016/S0168-0102(97)00073-4
Kwok JB; Taddei K; Hallupp M; Fisher C; Brooks WS; Broe T; Hardy J; Fulham MJ; Nicholson GA; Stell R; St George-Hyslop PH; Fraser PE; Kakulas B; Clarnette R; Relkin N; Gandy SE; Schofield PR; Martins RN, 1997, 'Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer`s disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype', Neuroreport, vol. 8, pp. 1537 - 1542, http://dx.doi.org/10.1097/00001756-199704140-00043
Gready JE; Ranganathan S; Schofield PR; Matsuo Y; Nishikawa K, 1997, 'Predicted structure of the extracellular region of ligand-gated ion channel receptors shows SH2-like and SH3-like domains forming the ligand Binding site', Protein Science, vol. 6, pp. 983 - 998, http://dx.doi.org/10.1002/pro.5560060504
Deckert J; Nothen MM; Bryant SE; Schuffenhauer S; Schofield PR; Spurr NK; Propping P, 1997, 'Mapping of the human adenosine A2a receptor gene: relation to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region', Human Genetics, vol. 99, pp. 326 - 328, http://dx.doi.org/10.1007/s004390050366
Baker MA; Kwok JB; Kucera S; Crook R; Farrer M; Houlden H; Isaacs A; Lincoln S; Onstead L; Hardy J; Wittenberg L; Dodd P; Webb SJ; Hayward N; Tannenberg T; Andreadis A; Hallupp M; Schofield PR; Dark F; Hutton M, 1997, 'Localisation of fronto-temporal dementia with Parkinsonism in an Australian kindred to chromosome 17q21-22', Annals of Neurology, vol. 42, pp. 794 - 798, http://dx.doi.org/10.1002/ana.410420516
Marder K; Albert S; Dooneief G; Stern Y; Ramachandran G; Todak G; FriedmanClouse R; Polanco C; Winston T; Schofield P; Mayeux R; Pan GD; Selnes O; Sacktor N; Hasenauer D; Esposito D; NanceSproson L; McArthur J; Kieburtz K; Schifitto G; McDermott M; Palumbo D; Orme C; Zimmerman C; Gelbard H; Hickey C; Casaceli C; Guthrie B; Rumfola L; Epstein L, 1996, 'Clinical confirmation of the American Academy of Neurology algorithm for HIV-associated cognitive/motor disorder', NEUROLOGY, vol. 47, pp. 1247 - 1253, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1996VR42500023&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Tang MX; Jacobs D; Stern Y; Marder K; Schofield P; Gurland B; Andrews H; Mayeux R, 1996, 'Effect of oestrogen during menopause on risk and age at onset of Alzheimer's disease', LANCET, vol. 348, pp. 429 - 432, http://dx.doi.org/10.1016/S0140-6736(96)03356-9
Deckert J; Nöthen MM; Rietschel M; Wildenauer D; Bondy B; Ertl MA; Knapp M; Schofield PR; Albus M; Maier W; Propping P, 1996, 'Human adenosine A
Tang MX; Maestre G; Tsai WY; Liu XH; Lin Chung FY; Chun M; Schofield P; Stern Y; Tycko B; Mayeux R, 1996, 'Relative risk of Alzheimer disease and age-at-onset distributions, based on APOE genotypes among elderly African Americans, Caucasians, and Hispanics in New York City', American Journal of Human Genetics, vol. 58, pp. 574 - 584
Adams LM; Salmon J; Donald J; Mitchell PB; Schofield PR, 1996, 'Non-linkage of D6S260, a putative schizophrenia locus, to bipolar disorder', American Journal of Medical Genetics Part A, pp. 485 - 487
Adams LM; Salmon J; Donald J; Mitchell PB; Schofield PR, 1996, 'Non-linkage of D6S260 a putative schizophrenia locus, to bipolar affective disorder', American Journal of Medical Genetics Part A, vol. 67, pp. 485 - 487
Schofield PR; Lynch JW; Rajendra S; Pierce K; Handford CA; Barry PH, 1996, 'Molecular and genetic insights into ligand binding and signal transduction at the inhibitory glycine receptor.', Cold Spring Harbor Symposia on Quantitative Biology, vol. 61, pp. 333 - 342
Chin CK; Schofield PR; Robertson DM; Gray PP; Chotigeat W; Mahler SM, 1996, 'Biological activity and metabolic clearance of recombinant human follicle stimulating hormone produced in Sp2/0 myeloma cells', Cytotechnology, vol. 21, pp. 171 - 182, http://dx.doi.org/10.1007/BF02215667
Mascia MP; Mihic SJ; Valenzuela CF; Schofield PR; Harris RI, 1996, 'A single amino acid determines differences in ethanol actions on strychnine-sensitive glycine receptors', Molecular Pharmacology, vol. 50, pp. 402 - 406
Le F; Townsend-Nicholson A; Baker E; Sutherland GR; Schofield PR, 1996, 'Characterisation and chromosomal localization of the human adenosine A2a receptor gene:ADORA2A', Biochemical and Biophysical Research Communications, vol. 223, pp. 461 - 467, http://dx.doi.org/10.1006/bbrc.1996.0916
Handford CA; Lynch JP; Baker E; Web GC; Ford J; Sutherland GR; Schofield PR, 1996, 'The human glycine receptor beta subunit: Primary structure, functional characterisation and chromosomal localisation of the human and murine genes', Molecular Brain Research, vol. 35, pp. 211 - 219, http://dx.doi.org/10.1016/0169-328X(95)00218-H
Lago F; Señarís RM; Emson PC; Domínguez F; Diéguez C, 1996, 'Evidence for the involvement of non-androgenic testicular factors in the regulation of hypothalamic somatostatin and GHRH mRNA levels.', Brain Res Mol Brain Res, vol. 35, pp. 220 - 226, https://www.ncbi.nlm.nih.gov/pubmed/8717358
Grossmann M; Szkudlinski MW; Tropea JE; Bishop LA; Thotakura NR; Schofield PR; Weintraub BD, 1995, 'Expression of human thyrotropin in cell lines with different glycosylation patterns combined with mutagenesis of specific glycosylation sites: Characterization of a novel role for the oligosaccharides in the in vitro and in vivo bioactivity', Journal of Biological Chemistry, vol. 270, pp. 29378 - 29385, http://dx.doi.org/10.1074/jbc.270.49.29378
Brooks WS; Martins RN; De Voecht J; Nicholson GA; Schofield PR; Kwok JBJ; Fisher C; Yeung LU; Van Broeckhoven C, 1995, 'A mutation in codon 717 of the amyloid precursor protein gene in an Australian family with Alzheimer's disease', Neuroscience Letters, vol. 199, pp. 183 - 186, http://dx.doi.org/10.1016/0304-3940(95)12046-7
Rajendra S; Schofield PR, 1995, 'Molecular mechanisms of inherited startle syndromes', Trends in Neurosciences, vol. 18, pp. 80 - 82, http://dx.doi.org/10.1016/0166-2236(95)80028-Z
Bishop LA; Nguyen TV; Schofield PR, 1995, 'Both of the β-subunit carbohydrate residues of follicle-stimulating hormone determine the metabolic clearance rate and in vivo potency', Endocrinology, vol. 136, pp. 2635 - 2640, http://dx.doi.org/10.1210/endo.136.6.7750487
Townsend-Nicholson A; Baker E; Sutherland GR; Schofield PR, 1995, 'Localization of the adenosine A2b receptor subtype gene (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybrids', Genomics, vol. 25, pp. 605 - 607, http://dx.doi.org/10.1016/0888-7543(95)80074-V
Townsend-Nicholson A; Baker E; Schofield PR; Sutherland GR, 1995, 'Localization of the adenosine A1 receptor subtype gene (ADORA1) to chromosome 1q32.1', Genomics, vol. 26, pp. 423 - 425, http://dx.doi.org/10.1016/0888-7543(95)80236-F
Townsend Nicholson A; Baker E; Sutherland GR; Schofield PR, 1995, 'Localization of the adenosine A2b receptor subtype gene (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybrids', Genomics, vol. 25, pp. 605 - 607, http://dx.doi.org/10.1016/0888-7543(95)80074-V
Marder K; Liu X; Stern Y; Dooneief G; Bell K; Schofield P; Sacktor N; Todak G; Friedman R; Ehrhardt A; Stein Z; Gorman J; Mayeux R, 1995, 'Neurologic signs and symptoms in a cohort of homosexual men followed for 4.5 years', Neurology, vol. 45, pp. 261 - 267, http://dx.doi.org/10.1212/WNL.45.2.261
Rajendra S; Vandenberg RJ; Pierce K; Cunningham AL; French PW; Barry PH; Schofield PR, 1995, 'Ligand binding and receptor assembly roles of a second extracellular disulphide loop of the glycine receptor', European Molecular Biology Organization, vol. 14, pp. 2987 - 2998
Park JJ; Schofield PR; Edwards MR, 1995, 'The acute response of Giardia intestinalis to hypo-osmotic shock', Microbiology, vol. 141, pp. 2455 - 2462
Knodler LA; Schofield PR; Edwards MR, 1995, 'L-arginine transport and metabolism in giardia intestinalis', Microbiology, vol. 141, pp. 2063 - 2070
Rajendra S; Vandenberg RJ; Pierce K; Cunningham AL; French PW; Barry PH; Schofield PR, 1995, 'The unique extracellular disulfide loop of the glycine receptor is a principal ligand binding element', European Molecular Biology Organization, vol. 14, pp. 2987 - 2998
Rajendra S; Lynch JP; Pierce K; French CD; Barry PH; Schofield PR, 1995, 'Mutation of an arginine residue in the human glycine receptor transforms b-alanine and taurine from agonists into competitive antagonists', Neuron, vol. 14, pp. 169 - 175, http://dx.doi.org/10.1016/0896-6273(95)90251-1
Lynch JP; Rajendra S; Barry PH; Schofield PR, 1995, 'Mutations affecting the glycine receptor agonist transduction mechanism convert the competitive antagonist, picrotoxin into an allosteric potentiator', The Journal of Biological Chemistry, vol. 270, pp. 13799 - 13806, http://dx.doi.org/10.1074/jbc.270.23.13799
Rajendra S; Schofield PR, 1995, 'Molecular mechanisms of inherited startle syndromes', Trends in Neurosciences, vol. 18, pp. 80 - 82, http://dx.doi.org/10.1016/0166-2236(95)80028-z
Rajendra S; Lynch JW; Pierce KD; French CR; Barry PH; Schofield PR, 1994, 'Startle disease mutations reduce the agonist sensitivity of the human inhibitory glycine receptor', Journal of Biological Chemistry, vol. 269, pp. 18739 - 18742
Bishop LA; Robertson DM; Cahir N; Schofield PR, 1994, 'Specific roles for the asparagine-linked carbohydrate residues of recombinant human follicle stimulating hormone in receptor binding and signal transduction', Molecular Endocrinology, vol. 8, pp. 722 - 731, http://dx.doi.org/10.1210/me.8.6.722
Ryan SG; Buckwalter MS; Lynch JW; Handford CA; Segura L; Shiang R; Wasmuth JJ; Camper SA; Schofield P; O'Connell P, 1994, 'A missense mutation in the gene encoding the α
Townsend-Nicholson A; Schofield PB, 1994, 'A threonine residue in the seventh transmembrane domain of the human A
Le F; Mitchell P; Vivero C; Waters B; Donald J; Selbie LA; Shine J; Schofield P, 1994, 'Exclusion of close linkage of bipolar disorder to the G
Baker E; Sutherland GR; Schofield PR, 1994, 'Localization of the glycine receptor α
Bishop LA; Robertson DM; Cahir N; Schofield PR, 1994, 'Specific roles for the asparagine-linked carbohydrate residues of recombinant human follicle stimulating hormone in receptor binding and signal transduction', Molecular Endocrinology, vol. 8, pp. 722 - 731, http://dx.doi.org/10.1210/mend.8.6.7935488
Vandenberg RJ; Rajendra S; French CR; Barry PH; Schofield PR, 1993, 'The extracellular disulfide loop motif of the inhibitory glycine receptor does not form the agonist binding site', Molecular Pharmacology, vol. 44, pp. 198 - 203
Vandenberg RJ; Schofield PR, 1993, 'The importance of being inhibited: Brain GABA(A) and glycine receptors', Today's Life Science, vol. 5, pp. 20 - 26
Cerpa-Poljak A; Bishop LA; Hort YJ; Chin CKH; Dekroon RO; Mahler SM; Smith GM; Stuart MC; Schofield PR, 1993, 'Isoelectric charge of recombinant human follicle-stimulating hormone isoforms determines receptor affinity and in vitro bioactivity', Endocrinology, vol. 132, pp. 351 - 356, http://dx.doi.org/10.1210/endo.132.1.8419133
Cerpa-Poljak A; Bishop LA; Hort YJ; Chin CK; DeKroon R; Mahler SM; Smith GM; Stuart MC; Schofield PR, 1993, 'Isoelectric charge of recombinant human follicle-stimulating hormone isoforms determines receptor affinity and in vitro bioactivity.', Endocrinology, vol. 132, pp. 351 - 356, http://dx.doi.org/10.1210/endo.132.1.8419133
Vandenberg RJ; French CR; Barry PH; Shine J; Schofield PR, 1992, 'Antagonism of ligand-gated ion channel receptors: Two domains of the glycine receptor α subunit form the strychnine-binding site', Proceedings of the National Academy of Sciences of the United States of America, vol. 89, pp. 1765 - 1769, http://dx.doi.org/10.1073/pnas.89.5.1765
Vandenberg RJ; Handford CA; Schofield PR, 1992, 'Distinct agonist- and antagonist-binding sites on the glycine receptor', Neuron, vol. 9, pp. 491 - 496, http://dx.doi.org/10.1016/0896-6273(92)90186-H
Braun T; Schofield PR; Sprengel R, 1991, 'Amino-terminal leucine-rich repeats in gonadotropin receptors determine hormone selectivity', EMBO Journal, vol. 10, pp. 1885 - 1890, http://dx.doi.org/10.1002/j.1460-2075.1991.tb07714.x
Ymer S; Draguhn A; Wisden W; Werner P; Keinanen K; Schofield PR; Sprengel R; Pritchett DB; Seeburg PH, 1990, 'Structural and functional characterization of the γ
Grenningloh G; Schmieden V; Schofield PR; Seeburg PH; Siddique T; Mohandas TK; Becker CM; Betz H, 1990, 'Alpha subunit variants of the human glycine receptor: Primary structures, functional expression and chromosomal localization of the corresponding genes', EMBO Journal, vol. 9, pp. 771 - 776, http://dx.doi.org/10.1002/j.1460-2075.1990.tb08172.x
Schofield PR; Shivers BD; Seeburg PH, 1990, 'The role of receptor subtype diversity in the CNS', Trends in Neurosciences, vol. 13, pp. 8 - 11, http://dx.doi.org/10.1016/0166-2236(90)90052-C
YMER S; DRAGUHN A; KOHLER M; SCHOFIELD PR; SEEBURG PH, 1989, 'SEQUENCE AND EXPRESSION OF A NOVEL GABAA RECEPTOR ALPHA-SUBUNIT', FEBS LETTERS, vol. 258, pp. 119 - 122, http://dx.doi.org/10.1016/0014-5793(89)81630-8
Ymer S; Schofield PR; Shivers BD; Pritchett DB; Lüddens H; Köhler M; Werner P; Sontheimer H; Kettenmann H; Seeburg PH, 1989, 'Molecular studies of the GABA
Schofield PR; Pritchett DB; Sontheimer H; Kettenmann H; Seeburg PH, 1989, 'Sequence and expression of human GABA
Schofield PR, 1989, 'The GABA
Schofield PR; Abbott A, 1989, 'Molecular pharmacology and drug action: structural information casts light on ligand binding', Trends in Pharmacological Sciences, vol. 10, pp. 207 - 212, http://dx.doi.org/10.1016/0165-6147(89)90260-5
Schofield PR; McFarland KC; Hayflick JS; Wilcox JN; Cho TM; Roy S; Lee NM; Loh HH; Seeburg PH, 1989, 'Molecular characterization of a new immunoglobulin superfamily protein with potential roles in opioid binding and cell contact', EMBO Journal, vol. 8, pp. 489 - 495, http://dx.doi.org/10.1002/j.1460-2075.1989.tb03402.x
Ymer S; Schofield PR; Draguhn A; Werner P; Kohler M; Seeburg PH, 1989, 'GABA(A) receptor β subunit heterogeneity: Functional expression of cloned cDNAs', EMBO Journal, vol. 8, pp. 1665 - 1670, http://dx.doi.org/10.1002/j.1460-2075.1989.tb03557.x
Pritchett DB; Sontheimer H; Shivers BD; Ymer S; Kettenmann H; Schofield PR; Seeburg PH, 1989, 'Importance of a novel GABA
Gorman CM; Gies D; Schofield PR; Kado‐Fong H; Malfroy B, 1989, 'Expression of enzymatically active enkephalinase (neutral endopeptidase) in mammalian cells', Journal of Cellular Biochemistry, vol. 39, pp. 277 - 284, http://dx.doi.org/10.1002/jcb.240390307
Shivers BD; Killisch I; Sprengel R; Sontheimer H; Köhler M; Schofield PR; Seeburg PH, 1989, 'Two novel GABA
Schmieden V; Grenningloh G; Schofield PR; Betz H, 1989, 'Functional expression in Xenopus oocytes of the strychnine binding 48 kd subunit of the glycine receptor', EMBO Journal, vol. 8, pp. 695 - 700, http://dx.doi.org/10.1002/j.1460-2075.1989.tb03428.x
Sontheimer H; Becker CM; Pritchett DB; Schofield PR; Grenningloh G; Kettenmann H; Betz H; Seeburg PH, 1989, 'Functional chloride channels by mammalian cell expression of rat glycine receptor subunit', Neuron, vol. 2, pp. 1491 - 1497, http://dx.doi.org/10.1016/0896-6273(89)90195-5
Buckle VJ; Fujita N; Ryder-Cook AS; Derry JMJ; Barnard PJ; Lebo RV; R. Schofield P; Seeburg PH; Bateson AN; Darlison MG; Barnard EA, 1989, 'Chromosomal localization of GABA
Malfroy B; Kuang WJ; Seeburg PH; Mason AJ; Schofield PR, 1988, 'Molecular cloning and amino acid sequence of human enkephalinase (neutral endopeptidase)', FEBS Letters, vol. 229, pp. 206 - 210, http://dx.doi.org/10.1016/0014-5793(88)80828-7
Pritchett DB; Sontheimer H; Gorman CM; Kettenmann H; Seeburg PH; Schofield PR, 1988, 'Transient expression shows ligand gating and allosteric potentiation of GABA
Schofield PR; Darlison MG; Fujita N; Burt DR; Stephenson FA; Rodriguez H; Rhee LM; Ramachandran J; Reale V; Glencorse TA; Seeburg PH; Barnard EA, 1988, 'Sequence and functional expression of the GABA
Levitan ES; Schofield PR; Burt DR; Rhee LM; Wisden W; Köhler M; Fujita N; Rodriguez HF; Stephenson A; Darlison MG; Barnard EA; Seeburg PH, 1988, 'Structural and functional basis for GABA
Schofield PR, 1988, 'Carrier-bound odorant delivery to olfactory receptors', Trends in Neurosciences, vol. 11, pp. 471 - 472, http://dx.doi.org/10.1016/0166-2236(88)90001-X
Barnard EA; Darlison MG; Fujita N; Glencorse TA; Levitan ES; Reale V; Schofield PR; Seeburg PH; Squire MD; Stephenson FA, 1988, 'Molecular biology of the GABAA receptor.', Advances in experimental medicine and biology, vol. 236, pp. 31 - 45, http://dx.doi.org/10.1007/978-1-4757-5971-6_3
SCHOFIELD PR; GIBSON AH; DUDMAN WF; WATSON JM, 1987, 'EVIDENCE FOR GENETIC EXCHANGE AND RECOMBINATION OF RHIZOBIUM SYMBIOTIC PLASMIDS IN A SOIL POPULATION', APPLIED AND ENVIRONMENTAL MICROBIOLOGY, vol. 53, pp. 2942 - 2947, http://dx.doi.org/10.1128/AEM.53.12.2942-2947.1987
Braun T; Schofield PR; Shivers BD; Pritchett DB; Seeburg PH, 1987, 'A novel subtype of muscarinic receptor identified by homology screening', Biochemical and Biophysical Research Communications, vol. 149, pp. 125 - 132, http://dx.doi.org/10.1016/0006-291X(87)91613-5
Schofield PR; Rhee LM; Peralta EG, 1987, 'Primary structure of the human beta-adrenergic receptor gene', Nucleic Acids Research, vol. 15, pp. 3636, http://dx.doi.org/10.1093/nar/15.8.3636
Malfroy B; Schofield PR; Kuang WJ; Seeburg PH; Mason AJ; Henzel WJ, 1987, 'Molecular cloning and amino acid sequence of rat enkephalinase', Biochemical and Biophysical Research Communications, vol. 144, pp. 59 - 66, http://dx.doi.org/10.1016/S0006-291X(87)80475-8
Grenningloh G; Gundelfinger E; Schmitt B; Betz H; Darlison MG; Barnard EA; Schofield PR; Seeburg PH, 1987, 'Glycine vs GABA receptors [4]', Nature, vol. 330, pp. 25 - 26, http://dx.doi.org/10.1038/330025b0
Eipper BA; Park LP; Dickerson IM; Keutmann HT; Thiele EA; Rodriguez H; Schofield PR; Mains RE, 1987, 'Structure of the precursor to an enzyme mediating COOH-terminal amidation in peptide biosynthesis', Molecular Endocrinology, vol. 1, pp. 777 - 790, http://dx.doi.org/10.1210/mend-1-11-777
Djordjevic MA; Innes RW; Wijffelman CA; Schofield PR; Rolfe BG, 1986, 'Nodulation of specific legumes is controlled by several distinct loci in Rhizobium trifolii', Plant Molecular Biology, vol. 6, pp. 389 - 401, http://dx.doi.org/10.1007/BF00027132
Schofield PR; Watson JM, 1986, 'DNA sequence of Rhizobium trifolii nodulation genes reveals a reiterated and potentially regulatory sequence preceding nodABC and nodFE', Nucleic Acids Research, vol. 14, pp. 2891 - 2903, http://dx.doi.org/10.1093/nar/14.7.2891
Djordjevic MA; Schofield PR; Rolfe BG, 1985, 'Tn 5 mutagenesis of Rhizobium trifolii host-specific nodulation genes result in mutants with altered host-range ability', MGG Molecular & General Genetics, vol. 200, pp. 463 - 471, http://dx.doi.org/10.1007/BF00425732
Schofield PR; Watson JM, 1985, 'Conservation of nif- and species-specific domains within repeated promoter sequences from fast-growing Rhizobium species', Nucleic Acids Research, vol. 13, pp. 3407 - 3418, http://dx.doi.org/10.1093/nar/13.10.3407
Watson JM; Schofield PR, 1985, 'Species-specific, symbiotic plasmid-located repeated DNA sequences in Rhizobium trifolii', MGG Molecular & General Genetics, vol. 199, pp. 279 - 289, http://dx.doi.org/10.1007/BF00330270
Djordjevic MA; Schofield PR; Ridge RW; Morrison NA; Bassam BJ; Plazinski J; Watson JM; Rolfe BG, 1985, 'Rhizobium nodulation genes involved in root hair curling (Hac) are functionally conserved', Plant Molecular Biology, vol. 4, pp. 147 - 160, http://dx.doi.org/10.1007/BF02418762
Scott DB; Court CB; Ronson CW; Scott KF; Watson JM; Schofield PR; Shine J, 1984, 'Organisation of nodulation and nitrogen fixation genes on a Rhizobium trifolii symbiotic plasmid', Archives of Microbiology, vol. 139, pp. 151 - 157, http://dx.doi.org/10.1007/BF00401991
Schofield PR; Ridge RW; Rolfe BG; Shine J; Watson JM, 1984, 'Host-specific nodulation is encoded on a 14kb DNA fragment in Rhizobium trifolii', Plant Molecular Biology, vol. 3, pp. 3 - 11, http://dx.doi.org/10.1007/BF00023410
Schofield PR; Djordjevic MA; Rolfe BG; Shine J; Watson JM, 1983, 'A molecular linkage map of nitrogenase and nodulation genes in Rhizobium trifolii', MGG Molecular & General Genetics, vol. 192, pp. 459 - 465, http://dx.doi.org/10.1007/BF00392191
Karystianis G; Adily A; Schofield P; Knight L; Galdon C; Greenberg D; Jorm L; Nenadic G; Butler T, 'Automatic Extraction of Mental Health Disorders From Domestic Violence Police Narratives: Text Mining Study (Preprint)', , http://dx.doi.org/10.2196/preprints.11548
Karystianis G; Adily A; Schofield P; Knight L; Galdon C; Greenberg D; Jorm L; Nenadic G; Butler T, 'Correction: Automatic Extraction of Mental Health Disorders From Domestic Violence Police Narratives: Text Mining Study (Preprint)', , http://dx.doi.org/10.2196/preprints.13007
Karystianis G; Simpson A; Adily A; Schofield P; Greenberg D; Wand H; Nenadic G; Butler T, 'Prevalence of Mental Illnesses in Domestic Violence Police Records: Text Mining Study (Preprint)', , http://dx.doi.org/10.2196/preprints.23725
Conference Papers
Fullerton J; lenroot R; roberts G; overs B; frankland A; schofield P; mitchell P, 2015, 'Neurodevelopmental Trajectories in Young People at High Familial Risk for Bipolar Disorder', in European Neuropsychopharmacology, XXIIIrd World Congress of Psychiatric Genetics, Toronto, presented at XXIIIrd World Congress of Psychiatric Genetics, Toronto, 28 October 2015 - 31 October 2015, http://dx.doi.org/10.1016/j.euroneuro.2015.09.009
Fullerton J; klauser P; lenroot R; shaw A; heath A; cairns M; scott R; schofield P; shannon weickert C; pantellis C; fornito A; whitford T; zalesky A, 2015, 'Differential Effects of Disease Associated ST8SIA2 Haplotype on Cortical White Matter in Schizophrenia', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER SCIENCE BV, Toronto, Canada, pp. S237 - S238, presented at ” XXIII World Congress of Psychiatric Genetics, Toronto, Canada, 28 October 2015 - 30 October 2015, http://dx.doi.org/10.1016/j.euroneuro.2015.09.009
Fullerton J; toma C; shaw A; allcock R; mitchell P; schofield P, 2015, 'Addressing Rare Variant Contributions to the Genetic Architecture of Bipolar Disorder, Utilizing Extended Families with Highly Penetrant Forms of Illness', in European Neuropsychopharmacology, ELSEVIER SCIENCE BV, Toronto, Canada, pp. S293 - S293, presented at XXIII World Congress of Psychiatric Genetics, Toronto, Canada, 28 October 2015 - 30 October 2015, http://dx.doi.org/10.1016/j.euroneuro.2015.09.009
Weickert TW; Weinberg D; Lenroot R; Catts SV; Wells R; Vercammen A; O'Donnell M; Galletly C; Liu D; Balzan R; Short B; Pellen D; Curtis J; Carr VJ; Kulkarni J; Schofield PR; Weickert CS, 2015, 'Adjunctive raloxifene treatment improves attention and memory in men and women with schizophrenia', in Molecular Psychiatry, pp. 685 - 694, http://dx.doi.org/10.1038/mp.2015.11
Dobson-Stone C; Halliday GM; Schofield PR; Crouch PJ; Kwok JB, 2014, 'SIGMAR1 gene in dementia and motor neuron disease', in JOURNAL OF NEUROCHEMISTRY, WILEY-BLACKWELL, Kaohsiung, TAIWAN, pp. 12 - 12, presented at 12th Biennial Meeting of the Asian-Pacific-Society-for-Neurochemistry, Kaohsiung, TAIWAN, 23 August 2014 - 26 August 2014, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000339492800021&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Fullerton J; pierce K; roberts G; levy F; green M; frankland A; wright A; mccormack C; lau P; schofield P; mitchell P, 2012, 'The role of genetic and epigenetic factors in future risk of bipolar disorder: a longitudinal study in a high-risk cohort', in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Wiley: 12 months, Hamburg, Germany, pp. 96 - 121, presented at XXth World Congress on Psychiatric Genetics, Hamburg, Germany, 24 October 2012 - 28 October 2012, http://dx.doi.org/10.1002/ajmg.b.32132
Dobson-Stone C; Luty AA; Thompson EM; Blumbergs P; Brooks WS; Halliday GM; Schofield PR; Kwok JBJ, 2012, 'Identification Of A Locus For Frontotemporal Dementia - Motor Neuron Disease On Chromosome 16p12.1-q12.2', in DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, KARGER, Manchester, ENGLAND, pp. 82 - 82, presented at 8th International Conference on Frontotemporal Dementias, Manchester, ENGLAND, 05 September 2012 - 07 September 2012, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000308612400120&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Weickert CS; Tiwari Y; Schofield PR; Fullerton JM, 2011, 'Linking the NRG1-realted Genetic Risk of Schizophrenia to Increased Type III NRG1 mRNA', in BIOLOGICAL PSYCHIATRY, ELSEVIER SCIENCE INC, San Francisco, CA, pp. 13S - 13S, presented at 66th Annual Meeting of the Society-of-Biological-Psychiatry, San Francisco, CA, 12 May 2011 - 14 May 2011, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000290641800043&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Fullerton JM; Tiwari Y; Schofield PR; Weickert CS, 2010, 'INCREASED FREQUENCY OF NOVEL NRG1 GENE VARIANTS IN SCHIZOPHRENIA AND THE EFFECT OF NUCLEOTIDE VARIATION ON MRNA ISOFORM TRANSCRIPTIONAL REGULATION', in SCHIZOPHRENIA RESEARCH, ELSEVIER SCIENCE BV, Florence, ITALY, pp. 334 - 335, presented at 2nd Conference of the Schizophrenia-International-Research-Society (SIRS), Florence, ITALY, 10 April 2010 - 14 April 2010, http://dx.doi.org/10.1016/j.schres.2010.02.576
Halliday GM; Warden LA; Gregory GC; Kwok JB; Schofield PR; Guillemin GJ; Shepherd CE, 2009, 'Mass buildup of soluble oligomeric Abeta40 occurs in sporadic Alzheimer's disease', in Khachaturian Z (ed.), Alzheimer's and Dementia, Elsevier, Orlando, Florida, pp. P302 - P302, presented at *, Vienna, Austria, 11 July 2009 - 16 July 2009
Schofield PR; Luty A; Kwok JB; Thompson E; Blumbergs P; Brooks WS; Loy CT; Dobson-Stone C; Panegyres P; Hecker J; Nicholson GA; Halliday GM, 2008, 'Linkage to chromosome 9 and examination of candidate genes in a pedigree with FTLD-MND and TDP-43 positive neuropathology', in Dementia and Geriatric Cognitive Disorders, Karger, Basel, Switzerland, pp. 9 - 9, presented at 6th International Conference on Frontotemporal Dementias, Rotterdam, Netherlands, 03 September 2008 - 05 September 2008
Karl T; Boucher A; Dean B; Huang X; Arnold JR; Schofield PR, 2008, 'Environmental modulation of phenotype in neuregulin 1 mutants', in Frazer A (ed.), International Journal of Neuropsychopharmacology, Cambridge University Press, New York, pp. 68 - 69, presented at CINP, Munich, GERMANY, 13 July 2008 - 17 July 2008, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000258855500295&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Wilde A; Meiser B; Mitchell PB; Schofield PR, 2008, 'Public attitudes towards genetic testing for susceptibilityto major depression', in European Journal of Human Genetics, Nature Publishing Group, London, England, pp. EPL2.2 - EPL2.2, presented at European Meeting on Psychosocial Aspects of Genetics (EMPAG), Barcelona, Spain, 31 May 2008 - 03 June 2008
Green MJ; James C; Tabassum L; Schofield PR; Mitchell PB, 2008, 'Cognitive Emotions Regulation in Bipolar disorder', in Australian and New Zealand Journal of Psychiatry, Sage Publications, United Kingdom, pp. A45 - A46, presented at Australian and New Zealand Journal of Psychiatry
Wilhelm KA; Gillis I; Reddy JP; Mitchell PB; Schofield PR, 2008, 'Serotonin transporter gene and gender-specific psychological distress in diabetes patients', in Australian and New Zealand Journal of Psychiatry, Sage Publications, United Kingdom, pp. A107 - A107, presented at Australian and New Zealand Journal of Psychiatry
Barry PH; Sugiharto S; Carland JE; Lewis TM; Schofield PR; Moorhouse AJ, 2008, 'External divalent ions increase anion-cation permeability in glycine receptor channels – consideration of ion activities, surface charge and conductance measurements', in Proceedings of the Australian Physiological and Pharmacological Society, Australian Physiological and Pharmacological Society Conference 2008, presented at Australian Physiological and Pharmacological Society Conference 2008
Sugiharto S; Moorhouse AJ; Lewis TM; Schofield PR; Barry PH, 2007, 'Relative counter-ion permeation in anion-selective glycine receptor channels did not vary between two different anions, supporting an ion pair mechanism', in Proceedings of the Australian Physiological and Pharmacological Society, Australian Physiological and Pharmacological Society Conference 2007, Newcastle, presented at Australian Physiological and Pharmacological Society Conference 2007, Newcastle, 05 December 2007
Sugiharto S; Lewis TM; Moorhouse AJ; Schofield PR; Barry PH, 2007, 'External divalent ions decrease counter-ion permeation in anion-selective glycine receptor channels without changing the minimum pore diameter of the channel', in Proceedings of the Australian Physiological and Pharmacological Society, Australian Physiological and Pharmacological Society Conference 2007, Newcastle, presented at Australian Physiological and Pharmacological Society Conference 2007, Newcastle, 05 December 2007
Williams L; Gatt J; Kuan S; Dobson-Stone C; Paul R; Schofield PR; Gordon E, 2007, 'Genotypes and neural binding in negative affect: The contribution of genetic polymorphisms to 40 hz gamma phase synchrony', in Biological Psychiatry, Elsevier Science Inc, New York, NY, USA, pp. 265S - 265S, presented at 62nd Annual Scientific Convention and meeting of the society of biological psychiatry, San Diego, California, USA, 17 May 2007 - 19 May 2007
Fullerton J; McAuley E; Blair IP; Schofield PR, 2006, 'identification of a bipolar disorder susceptibility locus on chromosome 15q', in Acta Neuropsychiatr, Cagliari, Italy, pp. 261, presented at XIV World Congress on Psychiatric Genetics, Cagliari, Italy, 28 October 2006 - 01 November 2006, http://dx.doi.org/10.1017/S0924270800030544
McAuley EZ; Blair IP; Fullerton JM; Donald JA; Mitchell PB; Schofield PR, 2006, 'Identification of a bipolar disorder susceptibility locus on chromosome 15Q', in AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, WILEY-LISS, Cagliari, ITALY, pp. 695 - 696, presented at 14th World Congress on Psychiatric Genetics, Cagliari, ITALY, 28 October 2006 - 01 November 2006, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000240877700051&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Schofield PR, 2006, 'Current understanding of the molecular pharmacology and physiology of the GABAA and glycine receptors', in Alcoholism : Clinical and Experimental Research, Lippincott Williams & Wilkins, Philadelphia, PA, pp. 61A - 61A, presented at ISBRA World Congress on Alchohol Research, Sydney, 10 September 2006 - 13 September 2006, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000239919900067&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Karl T; Duffy L; Boucher A; Arnold JR; Schofield PR, 2006, 'Genetic animal models for neuregulin 1 - valuable tools for schizophrenia research?', in Australian and New Zealand Journal of Psychiatry, Sage Publications, United Kingdom, pp. A115 - A115, presented at Australasian Schizophrenia Conference, Fremantle, WA, 21 August 2006 - 23 August 2006, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000239520100029&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Sugiharto S; Moorhouse AJ; Lewis TM; Schofield PR; Barry PH, 2006, 'The role of the counter ion in determining the anion-cation permeability ratio in glycine receptor channels of different size', in Proceedings of the Australian Physiological and Pharmacological Society, Australian Physiological and Pharmacological Society Conference 2006, presented at Australian Physiological and Pharmacological Society Conference 2006
Schofield PR, 2005, 'Ion channels: Molecular studies of structure, function and disease', in JOURNAL OF THE NEUROLOGICAL SCIENCES, ELSEVIER SCIENCE BV, Sydney, AUSTRALIA, pp. S38 - S38, presented at 18th World Congress of Neurology, Sydney, AUSTRALIA, 05 November 2005 - 11 November 2005, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000235088000159&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Schofield PR; Williams LA; Luty A; Cooper N; Brown K; Grieve S; Gordon E, 2005, 'Selective errors in declarative memory and hippocampal function associated with brain derived neurotrophic factor polymorphism', in American Journal of Medical Genetics Part B - Neuropsychiatric Genetics, Wiley-Liss, Hoboken, N.J., pp. 91 - 91, presented at XIIIth World Congress on Psychiatric Genetics 2005, Boston, Massachusetts, 14 October 2005 - 18 October 2005, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000232357300326&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
D'Este C; Attia J; Brown A; Schofield P; Tavener M; Gibson R; Horsley K, 2005, 'SHOAMP: The study of health outcomes in aircraft maintenance personnel.', in NEUROTOXICOLOGY, ELSEVIER SCIENCE BV, Res Triangle Park, NC, pp. 886 - 887, presented at 22nd International Neurotoxicology Conference, Res Triangle Park, NC, 11 September 2005 - 14 September 2005, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000240408800057&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Morris R; Gray A; Hort Y; Pierce KD; Schofield PR, 2005, 'A non-invasive adenoviral system for the delivery and expression of genes to spinal cord motor neurones', in Proceedings of Aust Neuroscience Society, 25th Annual Meeting of the Australian Neuroscience Society, Perth, WA, pp. 26 - 26, presented at 25th Annual Meeting of the Australian Neuroscience Society, Perth, WA, 30 January 2005 - 02 February 2005
Gregory GC; Kwok JB; Schofield PR; Halliday GM, 2005, 'Tau accumulation in sporadic and familial Alzheimer's disease', in Proceedings of Aust Neuroscience Society, 25th Annual Meeting of the Australian Neuroscience Society, Perth, WA, pp. 132 - 132, presented at 25th Annual Meeting of the Australian Neuroscience Society, Perth, WA, 30 January 2005 - 02 February 2005
Blair I; Chetcuti A; Badenhop RF; Scimone A; Adams LJ; Craddock N; Green E; Kirov G; Owen MJ; Kennedy MA; Miller A; Donald JA; Joyce PR; Olds R; Mitchell PB; Schofield PR, 2005, 'Positional cloning, association analysis, and expression studies provide convergent evidence that the cadherin gene fat contains a bipolar disorder susceptibility allele', in American Journal of Medical Genetics Part B - Neuropsychiatric Genetics, Wiley-Liss, Boston, MA, pp. 26 - 27, presented at 13th World Congress on Psychiatric Genetics, Boston, MA, 04 September 2005 - 08 September 2005, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000232357300089&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Wilhelm KA; Mitchell PB; Niven H; Finch AW; Wedgwood L; Scimone A; Blair I; Parker GB; Schofield PR, 2005, 'Life events, first depression onset, and the serotonin transporter gene', in American Journal of Medical Genetics Part B - Neuropsychiatric Genetics, Wiley-Liss, Boston, MA, pp. 106 - 106, presented at 13th World Congress on Psychiatric Genetics, Boston, MA, 04 September 2005 - 08 September 2005, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000232357300382&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Lewis TM; Absalom NL; Kaplan W; Schofield PR, 2004, 'Conformational changes in extracellular loop 2 during activation of the α1 glycine receptor', in Proceedings of the Australian Physiological and Pharmacological Society, Australian Physiological Society Conference, presented at Australian Physiological Society Conference, 24 November 2004 - 26 November 2004
Gregory GC; Kwok JB; Shepherd CE; Schofield PR; Halliday GM, 2004, 'Tau deposition in familial Alzheimer`s disease', in Australian Health and Medical Research Congress, Australian Health and Medical Research Congress 2004, Sydney, Convention & Exhibition Centre, pp. 227 - 227, presented at Australian Health and Medical Research Congress 2004, Sydney, Convention & Exhibition Centre, 21 November 2004 - 26 November 2004
Gregory GC; Kwok JB; Xuereb J; Schofield PR; Halliday GM, 2004, 'Beta amyloid toxicity in Alzheimer's disease', in Neurobiology of Aging, Elsevier Science Inc, New York, NY, USA, pp. S157 - S158, presented at 9th International Conference on Alzheimer`s Disease and Related Disorders, Philadelphia, Pennsylvania, 17 July 2004 - 22 July 2004, http://dx.doi.org/10.1016/S0197-4580(04)80530-X
Gregory GC; Kwok JB; Shepherd CE; Brooks WS; Xuereb J; Schofield PR; Halliday GM, 2004, 'Beta-amyloid toxicity in Alzheimer's disease', in Proceedings of Aust Neuroscience Society, 24th Annual Meeting of the Australian Neuroscience Society, Melbourne Convention Centre, pp. 42 - 42, presented at 24th Annual Meeting of the Australian Neuroscience Society, Melbourne Convention Centre, 27 January 2004 - 30 January 2004
Schofield PR, 2003, 'Glycine receptors and startle disease', in JOURNAL OF GENERAL PHYSIOLOGY, ROCKEFELLER UNIV PRESS, MARINE BIOL LAB, WOODS HOLE, MASSACHUSETTS, pp. 8A - 9A, presented at 57th Annual Meeting of the Society-of-General-Physiologists, MARINE BIOL LAB, WOODS HOLE, MASSACHUSETTS, 03 September 2003 - 07 September 2003, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000184087600030&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Bateman GA; Levi CR; Schofield P; Wang Y, 2002, 'Pulse wave encephalopathy: A near spectrum hypothesis in the differentiation between Alzheimer's disease and vascular dementia', in RADIOLOGY, RADIOLOGICAL SOC NORTH AMERICA, CHICAGO, ILLINOIS, pp. 610 - 610, presented at 88th Scientific Assembly and Annual Meeting of the Radiological-Society-of-North-America, CHICAGO, ILLINOIS, 01 December 2002 - 06 December 2002, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000178825101951&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Schofield PR; Blair IP; Badenhop RF; Adams LJ; Scimone A; Ewen-White K; Donald JA; Mitchell PB, 2002, 'Candidate gene analysis of a bipolar affective disorder susceptibility locus on chromosome 4q35', in AMERICAN JOURNAL OF MEDICAL GENETICS, WILEY-LISS, BRUSSELS, BELGIUM, pp. 720 - 721, presented at 10th World Congress of Psychiatric Genetics, BRUSSELS, BELGIUM, 09 October 2002 - 13 October 2002, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000178414400066&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Morgan BS; Morris R; Callister RJ; Schofield PR, 2001, 'Molecular changes to glycine receptors by gene therapy and transgenic approaches for the study of synaptic neurotransmission', in JOURNAL OF NEUROCHEMISTRY, BLACKWELL SCIENCE LTD, pp. 174 - 174, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000170789800623&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Keramidas A; Moorhouse AJ; Barry PH; Schofield PR, 2000, 'Pore mutations that convert a glycine receptor channel from being anion to cation selective', in Proceedings of Aust Neuroscience Society, 20th annual meeting Australian Neuroscience Society, Melbourne Convention Centre, pp. 86, presented at 20th annual meeting Australian Neuroscience Society, Melbourne Convention Centre, 30 January 2000 - 02 February 2000
Kapoor V; Kapoor R; Kwok J; Schofield PR, 1999, 'The prediction and discovery of a point mutation in kynurenine aminotransferase mRNA from spontaneously hypertensive rats - the link to exaggerated `stroke` damage?', in 2nd Biannual Kynurenine Meeting, 2nd Biannual Kynurenine Meeting, University of Sydney, presented at 2nd Biannual Kynurenine Meeting, University of Sydney, 04 December 1999
Keramidas A; Moorhouse AJ; French C; Schofield PR; Barry PH, 1999, 'Mutations in ligand-gated ion channels, such as the glycine receptor channel, that switch anion-to-cation selectivity', in 23rd Annual Meeting of the Australian Society for Biophysics, 23rd Annual Meeting of the Australian Society for Biophysics, Gold Coast, Qld, pp. 33, presented at 23rd Annual Meeting of the Australian Society for Biophysics, Gold Coast, Qld, 30 September 1999
Keramidas A; Moorhouse AJ; Schofield PR; Barry PH, 1999, 'The `Reverse Galzi` triple mutation converts the glycine receptor channel selectivity from anionic to cationic', in Proceedings of the Australian Physiological and Pharmacological Society, 67th Meeting of Physiology and Pharmacology Society, University of Newcastle, NSW, pp. 55P, presented at 67th Meeting of Physiology and Pharmacology Society, University of Newcastle, NSW, 27 September 1999 - 29 September 1999
Keramidas A; Moorhouse AJ; Pierce K; Schofield PR; Barry PH, 1999, 'The effects of various mutations which convert recombinant glycine receptor channels to being cation selective', in Proceedings of the Australian Physiological and Pharmacological Society, 67th Meeting of Physiology and Pharmacology Society, University of Newcastle, NSW, pp. 30, presented at 67th Meeting of Physiology and Pharmacology Society, University of Newcastle, NSW, 27 September 1999 - 29 September 1999
Lee SS; Levy F; Mitchell PB; Schofield PR, 1999, 'DNA and the developing brain in 2000 and beyond molecular genetics in the research of child psychiatric disorders', in Australian and New Zealand Journal of Psychiatry, Sage Publications, United Kingdom, pp. A18, presented at Australian and New Zealand Journal of Psychiatry 1999
Schofield PR; Badenhop RF; Adams LJ; Morrj1 ; Moses MJ; Ma L; Scimone A; Jones AW; Caskey CT; Donald J; Hewitt JE; Mitchell PB; Austin CA, 1999, 'Haplotype analysis of bipolar affective disorder susceptibility locus on chromosome 4q35', in Molecular Psychiatry, Nature Publishing Group, London, England, pp. S20, presented at Molecular Psychiatry, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083600800071&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Badenhop RF; Moses MJ; Mitchell PB; Donald J; Adams LM; Schofield PR, 1999, 'A genome-wide screen for bipolar affective disorder susceptibility loci from 13 Australian pedigrees', in Molecular Psychiatry, Nature Publishing Group, London, England, pp. S69, presented at Molecular Psychiatry, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000083600800235&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Fatima-Shad K; Schofield PR; Barry PH, 1998, 'Ion selectivity in homomeric glycine receptor channels', in Proceedings of the Australian Physiological and Pharmacological Society, 66th Meeting of Physiology and Pharmacology Society, Brisbane, Qld, pp. 58, presented at 66th Meeting of Physiology and Pharmacology Society, Brisbane, Qld, 27 September 1998 - 01 October 1998
Moorhouse AJ; Keramidas A; Barry PH; Schofield PR, 1998, 'Molecular determinants of ligand-gated ion channel conductance: studies using cystein mutagenesis', in Proceedings of the Australian Physiological and Pharmacological Society, 66th Meeting of Physiology and Pharmacology Society, Brisbane, Qld, pp. 56, presented at 66th Meeting of Physiology and Pharmacology Society, Brisbane, Qld, 27 September 1998 - 01 October 1998
Fatima-Shad K; Barry PH; Schofield PR, 1998, 'Anion Permeation through glycine receptor channels in tranfected cells and cultured hippocampal neurons', in Proceedings of Aust Neuroscience Society, 18th Annual meeting Australian Neuroscience Society, Canberra, pp. 89, presented at 18th Annual meeting Australian Neuroscience Society, Canberra, 27 January 1998 - 30 January 1998
Hutton M; Lendon CL; Rizzu P; Kwok JB; Schofield PR, 1998, 'Association of missense and 5`-splice-site mutations in tau with inherited dementia FTDP-17.', in Nature, England, pp. 702 - 705, presented at Nature, http://dx.doi.org/10.1038/31508
Schofield PR; Adams LJ; Kwok JB; Salmon JA; Fielder SL; Rosso D; Reid AR; Donald J; Mitchell PB, 1997, 'Identification of a novel genetic linkage with bipolar affective disorder', in American Journal of Medical Genetics Part A, Wiley-Liss, Hoboken, NJ, USA, pp. 587, presented at 5th World Congress of Psychiatric Genetics, Santa Fe, 19 October 1997 - 23 October 1997, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997YB41400114&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Moorhouse AJ; Barry PH; Schofield PR, 1997, 'The Startle disease mutation Q266H impairs the gating of recombinant human glycine receptors', in Proceedings of the Australian Physiological and Pharmacological Society, 65th Meeting of Physiology and Pharmacology Society, Adelaide, Sth Aust, pp. 44P - 44P, presented at 65th Meeting of Physiology and Pharmacology Society, Adelaide, Sth Aust, 28 September 1997 - 01 October 1997
Stern Y; Tang MX; Jacobs DM; Sano M; Marder K; Bell K; Dooneief G; Schofield P; Cote L, 1997, 'Prospective comparative study of the evolution of probable Alzheimer's disease and Parkinson's disease dementia', in NEUROLOGY, LIPPINCOTT-RAVEN PUBL, pp. 2028 - 2028, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1997XG87100246&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Moorhouse AJ; Keramidas A; Barry PH; Schofield PR, 1997, 'Molecular determinants of ligand-gated ion channel conductance: studies using cystein mutagenesis', in Australian Society of Medical research, Australian Society of Medical research, Garvan Institute, Sydney, pp. 212, presented at Australian Society of Medical research, Garvan Institute, Sydney
Moorhouse AJ; Pierce K; Lynch JW; Barry PH; Schofield PR, 1996, 'The effects of the Startle disease mutation Q266H on recombinant human glycine receptors', in Proceedings of Aust Neuroscience Society, 16th Annual Meeting of the Australian Neuroscience Society, University of Adelaide, pp. 38 - 38, presented at 16th Annual Meeting of the Australian Neuroscience Society, University of Adelaide, 01 February 1996 - 04 February 1996
Tang MX; Maestre G; Tsai WY; Liu XH; Feng L; Chung WY; Chun M; Schofield P; Stern Y; Tycko B; Mayeux R, 1996, 'Relative risk of Alzheimer's disease and age-at-onset distributions based on apolipoprotein E genotypes among elderly African Americans, Caucasians, and Hispanics in New York City', in NEUROLOGY, LITTLE BROWN CO, pp. 5028 - 5028, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1996UA47600782&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Valenzuela S; Martin DK; Por SB; Robbins JM; Bootcov MR; Schofield PR; Campbell TJ; Breit SN, 1996, 'NCC27 - A novel nuclear chloride ion channel associated with macrophage activation.', in JOURNAL OF LEUKOCYTE BIOLOGY, FEDERATION AMER SOC EXP BIOL, pp. 106 - 106, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1996VE90600106&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Chun MR; Schofield P; Stern Y; Tatemichi TK; Mayeux R, 1994, 'The epidemiology of dementia among the elderly: Experience in a community-based registry', in Folstein MF (ed.), NEUROBIOLOGY OF PRIMARY DEMENTIA, AMER PSYCHIATRIC PRESS, INC, TUFTS UNIV, BOSTON, MA, pp. 1 - 26, presented at Conference on Primary Dementia, TUFTS UNIV, BOSTON, MA, 02 December 1994 - 03 December 1994, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000076281600001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
SCHOFIELD P; CHUN M; SACKTOR N; DENARO J; MARDER K; BELL K; DOONEIEF G; GONZALEZ M; SANO M; LANTIGUA R; WILDER D; GURLAND B; STERN Y; MAYEUX R, 1994, 'FREQUENCIES AND CAUSES OF COGNITIVE IMPAIRMENT AND DEMENTIA IN A COMMUNITY-BASED REGISTRY', in NEUROLOGY, LITTLE BROWN CO, pp. A297 - A297, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1994NH01200668&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Conference Proceedings (Editor of)
Wilhelm KA; Siegel JB; Finch AW; Mitchell PB; Schofield PR, (eds.), 2005, 'Australian and New Zealand Journal of Psychiatry', Sage Publications, United Kingdom, presented at Joint CINP/ASPR Scienctific Meeting, Brisbane, Qld, 07 December 2005 - 09 December 2005
Conference Presentations
Cederholm JME; Sugiharto S; Schofield PR; Lewis TM, 2010, 'Loop 9 residues adjacent to loop2 are involved in glycine receptor activation', in Loop 9 residues adjacent to loop2 are involved in glycine receptor activation, Australian Neurosciences Society Annual Scientific Meeting 2010, Sydney, presented at Australian Neurosciences Society Annual Scientific Meeting 2010, Sydney, 31 January 2010 - 03 February 2010
Wilde A; Meiser B; Mitchell PB; Hadzi-Pavlovic D; Schofield PR, 2009, 'Community attitudes to genetic susceptibility-based mental health interventions for healthy people in a large national sample', in Journal of Affective Disorders, Canberra, Vol. 134, pp. 280 - 287, presented at Australian Society for Psychiatric Research Annual Conference, Canberra, 02 December 2009 - 04 December 2009, http://dx.doi.org/10.1016/j.jad.2011.06.023
Wilde A; Meiser B; Mitchell PB; Hadzi-Pavlovic D; Schofield PR, 2009, 'Community interest in predictive genetic testing for suscepitibility to major depression in a large national sample', in Psychological Medicine, San Diego Ca USA, Vol. 41, pp. 1605 - 1613, presented at XVIIth World Congres on Psychiatric Genetics, San Diego Ca USA, http://dx.doi.org/10.1017/S0033291710002394
Sugiharto S; Moorhouse AJ; Lewis TM; Schofield PR; Barry PH, 2007, 'The anion-cation permeability ratio in glycine receptor channels of different pore size is influenced by both counter-ions and divalent ions', in The anion-cation permeability ratio in glycine receptor channels of different pore size is influenced by both counter-ions and divalent ions, 7th International Brain Research Organization World Congress of Neuroscience, Melbourne, Australia, presented at 7th International Brain Research Organization World Congress of Neuroscience, Melbourne, Australia
Conference Abstracts
Sachdev PS; Bowden JL; Lee T; Wen W; Ames D; Baune BT; Brodaty H; Crawford J; Kang K; Mather K; Lammel A; Samaras K; Schofield PR; Thalamuthu A; Trollor JN; Wright MJ, 2016, 'The Older Australian Twins Study - findings from the first 10 years [Oral Abstract]', in Twin Research and Human Genetics, Cambridge University Press (CUP), Vol. 19, pp. 519 - 519, presented at ISTS Satellite Meeting, 20 June 2016, http://dx.doi.org/10.1017/thg.2016.66
Weickert CS; Fullerton JM; Hu S; Kyaw M; Schofield PR; Carr VJ; Laughlin C; Schall U; Scott RJ; Jablensky AV; Mowry B; Michie PT; Catts SV; Henskens FA; Pantellis C; Weickert TW, 2016, 'SCHIZOPHRENIA AND COGNITIVE DYSFUNCTION ASSOCIATED WITH THE ESTROGEN RECEPTOR 1 GENOTYPE', in AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, SAGE PUBLICATIONS LTD, Vol. 50, pp. 77 - 77, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000375591600173&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Gatt JM; Routledge K; Korgaonkar MS; Grieve SM; Clark CR; Schofield PR; Williams LM, 2015, 'Wellbeing and Resilience in the Healthy Twin Brain (chair)', in BIOLOGICAL PSYCHIATRY, ELSEVIER SCIENCE INC, Toronto, CANADA, Vol. 77, presented at 70th Annual Scientific Meeting of the Society-of-Biological-Psychiatry on Stress, Emotion, Neurodevelopment and Psychopathology, Toronto, CANADA, 14 May 2015 - 16 May 2015, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000352207501085&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Weickert T; Weinberg D; Lenroot R; Catts SV; Wells R; Vercammen A; O'Donnell M; Galletly C; Liu D; Balzan R; Short B; Pellen D; Curtis J; Carr VJ; Kulkarni J; Schofield PR; Weickert CS, 2015, 'ADJUNCTIVE RALOXIFENE TREATMENT IMPROVES ATTENTION AND MEMORY IN MEN AND WOMEN WITH SCHIZOPHRENIA', in SCHIZOPHRENIA BULLETIN, OXFORD UNIV PRESS, Colorado Springs, CO, Vol. 41, pp. S339 - S340, presented at 15th International Congress on Schizophrenia Research (ICOSR), Colorado Springs, CO, 28 March 2015 - 01 April 2015, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000353548200898&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Schofield PR; Fullerton JM; Gatt JM; Williams LM; Mitchell PB, 2012, 'Genetic approaches to understanding the etiology of mood disorders', in JOURNAL OF MOLECULAR NEUROSCIENCE, HUMANA PRESS INC, Eilat, ISRAEL, Vol. 51, pp. S107 - S107, presented at 21st Annual Meeting of the Israel-Society-for-Neuroscience / 1st Binational Australian-Israeli Meeting on Neuroscience, Eilat, ISRAEL, 15 December 2012 - 15 December 2012, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000332833800274&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Gatt JM; Korgaonkar M; Schofield PR; Harris A; Clark R; Williams LM, 2012, 'Identifying Risk and Resilience Gene-Brain Markers of Emotional Wellbeing: The TWIN-E Project', in BIOLOGICAL PSYCHIATRY, ELSEVIER SCIENCE INC, Philadelphia, PA, Vol. 71, pp. 14S - 14S, presented at 67th Annual Scientific Convention and Meeting of the Society-of-Biological-Psychiatry, Philadelphia, PA, 03 May 2012 - 05 May 2012, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000302466000045&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Assareh A; Mather KA; Kwok J; Crawford J; Wen W; Brodaty H; Schofield PR; Sachdev PS, 2011, 'Interaction between APOE E4, hypertension and brain white matter lesions [Abstract POS-TUE-121]', in Proceedings of the 31st ANS Annual Meeting, Australian Neuroscience Society, online, pp. 117 - 117, presented at Australian Neuroscience Society 31st Annual Meeting, Auckland, 31 January 2011 - 03 February 2011
Gatt J; Nemeroff CB; Dobson-Stone C; Kuan SA; Paul RH; Bryant RA; Schofield P; Gordon E; Williams L, 2008, 'The impact of gene-environment interactions on neural pathways in risk for syndromal depression and anxiety', in NeuroImage, Elsevier, Vol. 41, pp. S1 - S1, presented at Human Brain Mapping
Williams L; Gatt J; Dobson-Stone C; Paul R; Schofield PR; Gordon E, 2008, 'Neuroimaging endophenotypes for emotion perception? Variation with COMT Val108/158Met genotypes and level of awareness', in NeuroImage, Elsevier, Vol. 41, pp. S1 - S1, presented at Human Brain Mapping
Leuchter BD; Schofield PR; Williams LM; Paul RH; Gatt JM; Brown K; Grieve S; Dobson-Stone C; Kuan S; Gordon E, 2007, 'Disturbances in task-relevant information processing associated with the brain-derived neurotrophic factor Val66Met polymorphism: Evidence from cognition, the P300 endophenotype and neuroimaging', in NEUROLOGY, LIPPINCOTT WILLIAMS & WILKINS, Boston, MA, Vol. 68, pp. A402 - A402, presented at 59th Annual Meeting of the American-Academy-of-Neurology, Boston, MA, 28 April 2007 - 05 May 2007, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000245175002548&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Williams L; Gatt J; Kuan S; Dobson-Stone C; Paul R; Schofield PR; Gordon E, 2007, 'Genotypes and neural binding in negative affect: The contribution of genetic polymorphisms to 40 hz gamma phase synchrony', in Biological Psychiatry, Elsevier Science Inc, San Diego, CA, Vol. 61, pp. 265S - 265S, presented at 62nd Annual Scientific Meeting of the Society-of-Biological-Psychiatry, San Diego, CA, 01 January 2007, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000245698100850&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Williams L; Gatt J; Kuan S; Dobson-Stone C; Paul RH; Schofield PR; Gordon E, 2007, 'Genotypes and neural binding in negative affect: The contribution of genetic polymorphisms to 40 hz gamma phase synchrony', in Biological Psychiatry, Elsevier, Vol. 61, pp. 265S - 265S, presented at Society of Biological Psychiatry
Girgis A; Cockburn J; Butow PN; Schofield PR; Tattersall MH; Bowman D; Doran C; D'Este C; Stojanovski E, 2006, 'Training in communication skills from a distance: an oxymoron or reality', in Psycho-oncology, John Wiley & Sons, New York, Vol. 15, pp. S39 - S40, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000242413900095&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a
Gatt JM; Kuan S; Dobson-Stone C; Paul RH; Schofield PR; Gordon E; Williams LM, 2006, '10-05 Genotypes and neural binding in negative affect: the contribution of genetic polymorphisms to 40 Hz gamma phase synchrony.', in Acta Neuropsychiatr, England, Vol. 18, pp. 337 - 338, England, http://dx.doi.org/10.1017/S0924270800032440
Kuan SA; Gatt JM; Dobson-Stone C; Paul RH; Schofield PR; Gordon E; Williams LM, 2006, '10-04 Identifying markers of negative mood: the gender-specific influence of COMT and MAO-A polymorphisms on emotion processing.', in Acta Neuropsychiatr, England, Vol. 18, pp. 337, England, http://dx.doi.org/10.1017/S0924270800032439
Alexander DM; Gatt JM; Kuan S; Dobson-Stone C; Todd EG; Schofield PR; Gordon E; Williams LM, 2006, '10-02 The neurodevelopmental effects of apolipoprotein E alleles on brain function.', in Acta Neuropsychiatr, England, Vol. 18, pp. 336, England, http://dx.doi.org/10.1017/S0924270800032415
Gatt JM; Kuan S; Dobson-Stone C; Paul RH; Schofield PR; Gordon E; Williams LM, 2006, '10-03 Identifying pathways to depressed mood and cognitive dysfunction: the BDNF Val66Met polymorphism and early life stress.', in Acta Neuropsychiatr, England, Vol. 18, pp. 336 - 337, England, http://dx.doi.org/10.1017/S0924270800032427
Dobson-Stone C; Gatt JM; Kuan S; Paul RH; Gordon E; Williams LM; Schofield PR, 2006, '10-01 Understanding genotype-phenotype relationships using the Brain Resource International Database: Implications for psychiatric conditions.', in Acta Neuropsychiatr, England, Vol. 18, pp. 335 - 336, England, http://dx.doi.org/10.1017/S0924270800032403
Alexander DM; Gatt J; Kuan S; Dobson-Stone C; Todd EG; Schofield PR; Gordon E; Williams LM, 2006, 'The neurodevelopmental effects of apolipoprotein E alleles on brain function.', in Acta Neuropsychiatrica, Cambridge University Press (CUP), Vol. 18, pp. 336 - 336, presented at ASPR Annual Meeting
Gatt J; Kuan S; Dobson-Stone C; Paul RH; Schofield PR; Gordon E; Williams LM, 2006, 'Identifying pathways to depressed mood and cognitive dysfunction: The BDNF Val66Met polymorphism and early life stress.', in Acta Neuropsychiatrica, Cambridge University Press (CUP), Vol. 18, pp. 336 - 336, presented at ASPR
Gatt J; Kuan S; Dobson-Stone C; Paul RH; Schofield PR; Gordon E; Williams LM, 2006, 'Genotypes and neural binding in negative affect: The contribution of genetic polymorphisms to 40 Hz gamma phase synchrony', in Acta Neuropsychiatrica, Cambridge University Press (CUP), Vol. 18, pp. 337 - 337, presented at ASPR
Gatt J; Kuan S; Dobson-Stone C; Brown KJ; Paul RH; Schofield PR; Gordon E; Williams LM, 2006, 'Mapping the BDNF genotype onto cognitive and emotional phenotypes: Integrating EEG, ERPs and MRI', in NeuroImage, Elsevier, Vol. 31, pp. 165 - 165, presented at Human Brain Mapping
Kuan S; Gatt J; Dobson-Stone C; Paul RH; Schofield PR; Gordon E; Williams LM, 2006, 'Identifying markers of negative mood: the gender-specific influence of COMT and MAO-A polymorphisms on emotion processing', in Acta Neuropsychiatrica, Cambridge University Press (CUP), Vol. 18, pp. 337 - 337, presented at ASPR
Kuan S; Gatt J; Dobson-Stone C; Brown KJ; Liddell B; Paul RH; Schofield PR; Gordon E; Williams LM, 2006, 'Neuroimaging endophenotypes associated with the COMT Val108/158Met polymorphism: implications for psychiatric disorders of emotion', in NeuroImage, Elsevier, Vol. 31, pp. 165 - 165, presented at Human Brain Mapping
Gatt J; Kuan S; Dobson-Stone C; Schofield PR; Gordon E; Paul RH; Brown KJ; Williams LM, 2005, 'An integrative approach towards mapping the BDNF genotype onto phenotypes: The identification of mood and memory profiles', in Austrailan and New Zealand Journal of Psychiatry, Vol. 39, pp. A18 - A18, presented at CINP/ASPR Meeting
Kuan S; Gatt J; Dobson-Stone C; Brown KJ; Paul R; Schofield PR; Gordon E; Williams LM, 2005, 'Mapping the COMT genotype onto phenotypes: Implications for psychiatric disorders of cognition and emotion.', in Australian and New Zealand Journal of Psychiatry, SAGE Publications, Vol. 39, pp. A17 - A17, presented at CINP/ASPR Meeting
Reports
Richards LR; Michie PT; Badcock DR; Bartlett PF; Bekkers JM; Bourne JA; Castles A; Egan GF; Fornito A; Hannan AJ; Hickie IB; Mattingley JB; Schofield PR; Shum DHK; Stuart GJ; Vickers JC; Vissel B, 2016, Australian Brain Alliance, http://dx.doi.org/10.1016/j.neuron.2016.10.038