Associate Professor Janice Fullerton

Tabs

Main

University role:

Senior Research Scientist

Phone:

02 9399 1836

Email:

j.fullerton@unsw.edu.au

Dr Jan Fullerton is a Senior Research Scientist at NeuRA and a Conjoint Associate Professor at UNSW.

She completed her PhD in human genetics at The University of Melbourne in 2001. Dr Fullerton completed five years postdoctoral training at The Wellcome Trust Centre for Human Genetics, University of Oxford (UK), where she developed her career interest in psychiatric genetics and complex trait analysis. Here she studied the genetic contributors to personality, depression and anxiety in both humans and mice.

Dr Fullerton returned to Australia in 2006 on a NHMRC Howard Florey Fellowship, which allowed her to join NeuRA to study the genetics of major mental illnesses, with a particular focus on bipolar disorder. In 2013, Dr Fullerton was promoted to Group Leader at NeuRA, where she heads a number of projects in gene discovery using the latest genomics technologies, as well as projects examining the role of specific genes in risk of major psychiatric conditions.

Qualifications:

Doctor of Philosophy (Medicine): The University of Melbourne: Australia

Honours Degree (First Class): The University of Melbourne: Australia

Bachelor of Science: The University of Melbourne: Australia

Grants:

In the last 5 years FTE (2014-2020) I have secured $7.55m in research funding/awards as a CI, of which $3.3m was category 1 and $5.5m was as CIA.

2020-2022 NHMRC Medical Research Futures Fund - Emerging Priorities and Consumer Driven Research Initiative - Mental Health Pharmacogenomics APP1200428 "A multifaceted approach to the pharmacogenomic signatures of bipolar disorder for improving treatment outcomes" CIs: Fullerton, Green, Schofield, Toma; AIs: O'Donnell, Mitchell. Budget: $1,009,678

2019-2020 UNSW Mindgardens Neuroscience Network Alliance “Bipolar 45 and Up Study: clinical course and long-term health outcomes of people with BD using electronic health record data” Budget: $300,000

2019 NSW Health Biospecimen Collection Grant. 45 and Up Bipolar Study (EOI submitted 31 August 2018, invited for full application which was submitted 9 Dec 2018). Budget: $100,000

2017 NSW Health Office of Health and Medical Research - Sydney Collaborative Genomics “Genetic contributors, clinical course and pharmacogenomics of Bipolar Disorder using data linkage in NSW” CIs: Fullerton, Mitchell, Schofield, Havard, Toma, Maryanne O’Donnell. AIs: Green. ($2,460,000)

2017 NAB Foundation “Stronger Minds” grant “Identification of mutant genes that contribute to bipolar disorder” CIs: A Cooper, JM Fullerton ($100,000)

2016 MLC Community Foundation "Whole Genome Sequencing of families with mental illness: 9 nuclear families with bipolar disorder". CI: A Cooper, Collaborator: JM Fullerton ($70,000)

2014-2017 NHMRC project grant APP1063960 “Unravelling the genetic causes of bipolar disorder: lessons from rare but highly penetrant variants in very heritable forms of illness” CIA: JM Fullerton, CIB: PR Schofield ($684,890)

2014-2017 NHMRC project grant APP1066177 “The biology of risk for bipolar disorder: genetic effects in a high-risk longitudinal study” CIA: JM Fullerton, CIB: R Lenroot, CIC: JI Nurnberger Jr ($833,835)

Awards:

2014 Dean’s Rising Star Award, UNSW: “Significant contribution to research”.

2013 UNSW Silver star award CIA: J Fullerton, CIB: PR Schofield

2012 UNSW Gold star award CIA: J Fullerton, CIB: PR Schofield, CIC: JA Donald, CID: PB Mitchell

2010 UNSW Gold star award CIA: J Fullerton, CIB: PR Schofield, CIC: JA Donald, CID: PB Mitchell

2007 - 2008 NARSAD Young Investigator Award awarded by the National Alliance for Research on Schizophrenia and Depression, New York, USA (US$60,000). CI: J Fullerton, Sponsor: PR Schofield

2007 Brain Sciences UNSW 2007 Symposium Post-doctoral “Best Poster Award” awarded to J Fullerton

2005 – 2007 Howard Florey Centenary Research Fellowship awarded by the National Health and Medical Research Council, Australia. Grant #: 325643. CI: J Fullerton, Sponsor: PR Schofield

Keywords:

bipolar disorder

genomics

psychiatry

prodromal phase

epigenomics

genome-wide association

pharmacogenomics

electronic health records

neuroimaging

cognition

next generation sequencing

Research

Research activities:

My group is interested in identifying and characterising genes which increase risk to mental illness, particularly bipolar disorder and schizophrenia. While these are clinically distinct disorders, bipolar disorder and schizophrenia share a common genetic foundation, as well as overlapping constellations of symptoms. Understanding the genetic contributors to mental illness enable us to improve our understanding of the biological basis of these psychiatric conditions, identify similarities and differences across disorders, and ultimately improve treatment of psychiatric disorders through these discoveries. Identifying the specific genes which are impaired in mental illness also helps to demystify the functioning of the human brain, and to comprehend the orchestration of events which leads to development of a healthy or unhealthy brain.

Genetic and epigenetic contributors to bipolar disorder in a high risk cohort

The offspring of individuals with bipolar disorder are at increased risk of mental illness, but our tools to predict which of these genetically at-risk young people will eventually develop disorder are very imprecise. Longitudinal studies that ascertain at-risk participants and monitor them prospectively are an effective approach for identifying early clinical and biological markers of future illness. This study examines genomic risk load of genetic and epigenetic factors, early structural brain changes and clinical information to determine if we can use biological signatures to predict which individuals will ultimately transition to illness, and identify targets for intervention prior to onset of symptoms which lead to a clinical diagnosis.

Genetic contributors, clinical course and pharmacogenomics of Bipolar Disorder in a large population cohort

Bipolar Disorder is a severe and debilitating psychiatric condition, for which the clinical course is highly variable between individuals, and the specific genetic causes remain largely obscure. This landmark study aims to use linked administrative health record data and state-of-the-art genomics technologies to address four key knowledge gaps: 1) identification of genes and molecular pathways which increase risk of illness; 2) pharmacogenomics studies to identify genetic signatures which may predict responsiveness to commonly used medicinal treatments; 3) examination of the impact of rare disruptive genetic variants on disease severity; and 4) consideration of the genetic correlates of both the course and severity of illness, and relationships to general medical conditions which more commonly present in people with bipolar disorder (such as cardiovascular disease, type II diabetes and asthma) and which further reduce quality of life and significantly impact overall health of people living with this condition.

Investigation of rare variants which increase risk to bipolar disorder in families with a high density of illness

Advances in technology have enabled sequencing at the level of the entire genome to become a reality. We have access to number of rare families with highly heritable forms of bipolar disorder, for which we will apply this powerful technology to identify specific genetic factors which increase disease risk. We assess loss-of-function variation within genes, at both the level of single base mutations and variation in gene copy number, which track with illness in these families to identify new genes which contribute to illness.

International collaborative consortia involvement

We are active contributors to a number of large international collaborative studies, including the Psychiatric Genomics Consortium (PGC), the Bipolar Sequencing Consortium (BSC), the Bipolar High Risk Consortium, and have contributed to a number of projects through the Enhancing Neuroimaging Genetics through Meta-Analysis (ENIGMA) consortia. These efforts aim to identify risk genes which contribute to disease, and examine their effect on brain structure, function and disease.

Field of Research (FOR) Tag:

Neurogenetics

Genomics

Pharmacogenomics

Psychiatry

Socio-economic Objective (SEO) tags:

Mental Health

Public Health (excl. Specific Population Health) not elsewhere classified

Teaching & Supervision

I am available to supervise:

Yes

Areas of supervision:

ILP, Honours, Masters, PhD.

Currently supervising:

Sonia Hesam Shariati

Javad Jamshidi

Oliver Watkeys

Hayley North

Jessica Chandra

Supervision keywords:

bipolar disorder

epigenomics

genetics

genomics

electronic health records

next generation sequencing

pharmacogenomics

mental health

resilience

high risk

longitudinal studies

psychiatry

genome-wide association

prodromal phase

neuroimaging

cognitive ability

Teaching:

Seeking ILP students and clinicians for short-term research training project on the "Genetic contributors, clinical course and pharmacogenomics of Bipolar Disorder in a large population cohort" project, supported by the Mindgardens Neuroscience Network initiative.

Publications related to this Person

Journal articles

Stone W; Nunes A; Akiyama K; Akula N; Ardau R; Aubry JM; Backlund L; Bauer M; Bellivier F; Cervantes P; Chen HC; Chillotti C; Cruceanu C; Dayer A; Degenhardt F; Del Zompo M; Forstner AJ; Frye M; Fullerton JM; Grigoroiu-Serbanescu M; Grof P; Hashimoto R; Hou L; Jiménez E; Kato T; Kelsoe J; Kittel-Schneider S; Kuo PH; Kusumi I; Lavebratt C; Manchia M; Martinsson L; Mattheisen M; McMahon FJ; Millischer V; Mitchell PB; Nöthen MM; O’Donovan C; Ozaki N; Pisanu C; Reif A; Rietschel M; Rouleau G; Rybakowski J; Schalling M; Schofield PR; Schulze TG; Severino G; Squassina A; Veeh J; Vieta E; Trappenberg T; Alda M, 2021, 'Prediction of lithium response using genomic data', Scientific Reports, vol. 11, http://dx.doi.org/10.1038/s41598-020-80814-z

Mullins N; Forstner AJ; O'Connell KS; Coombes B; Coleman JR; Qiao Z; Als TD; Bigdeli TB; Borte S; Bryois J; Charney AW; Drange OK; Gandal MJ; Hagenaars SP; Ikeda M; Kamitaki N; Kim M; Krebs K; Panagiotaropoulou G; Schilder BM; Sloofman LG; Steinberg S; Trubetskoy V; Winsvold BS; Won H-H; Abramova L; Adorjan K; Agerbo E; Al Eissa M; Albani D; Alliey-Rodriguez N; Anjorin A; Antilla V; Antoniou A; Awasthi S; Baek JH; Baekvad-Hansen M; Bass N; Bauer M; Beins EC; Bergen SE; Birner A; Pedersen CB; Boen E; Boks MP; Bosch R; Brum M; Brumpton BM; Brunkhorst-Kanaan N; Budde M; Bybjerg-Grauholm J; Byerley W; Cairns M; Casas M; Cervantes P; Clarke T-K; Cruceanu C; Cuellar-Barboza A; Cunningham J; Curtis D; Czerski PM; Dale AM; Dalkner N; David FS; Degenhardt F; Djurovic S; Dobbyn AL; Douzenis A; Elvsashagen T; Escott-Price V; Ferrier IN; Fiorentino A; Foroud TM; Forty L; Frank J; Frei O; Freimer NB; Frisen L; Gade K; Garnham J; Gelernter J; Pedersen MG; Gizer IR; Gordon SD; Gordon-Smith K; Greenwood TA; Grove J; Guzman-Parra J; Ha K; Haraldsson M; Hautzinger M; Heilbronner U; Hellgren D; Herms S; Hoffmann P; Holmans PA; Huckins L; Jamain S; Johnson JS; Kalman JL; Kamatani Y; Kennedy JL; Kittel-Schneider S; Knowles JA; Kogevinas M; Koromina M; Kranz TM; Kranzler HR; Kubo M; Kupka R; Kushner SA; Lavebratt C; Lawrence J; Leber M; Lee H-J; Lee PH; Levy SE; Lewis C; Liao C; Lucae S; Lundberg M; MacIntyre DJ; Maier W; Maihofer A; Malaspina D; Maratou E; Martinsson L; Mattheisen M; McCarroll SA; McGregor NW; McGuffin P; McKay JD; Medeiros H; Medland SE; Millischer V; Montgomery GW; Moran JL; Morris DW; Muhleisen TW; O'Brien N; O'Donovan C; Loohuis LMO; Oruc L; Papiol S; Pardinas AF; Perry A; Pfennig A; Porichi E; Potash JB; Quested D; Raj T; Rapaport MH; DePaulo JR; Regeer EJ; Rice JP; Rivas F; Rivera M; Roth J; Roussos P; Ruderfer DM; Sanchez-Mora C; Schulte EC; Senner F; Sharp S; Shilling PD; Sigurdsson E; Sirignano L; Slaney C; Smeland OB; Sobell JL; Hansen CS; Artigas MS; Spijker AT; Stein DJ; Strauss JS; Swiatkowska B; Terao C; Thorgeirsson TE; Toma C; Tooney P; Tsermpini E-E; Vawter MP; Vedder H; Walters JTR; Witt SH; Xi S; Xu W; Yang JMK; Young AH; Young H; Zandi PP; Zhou H; Zillich L; Adolfsson R; Agartz I; Alda M; Alfredsson L; Babadjanova G; Backlund L; Baune BT; Bellivier F; Bengesser S; Berrettini WH; Blackwood DHR; Boehnke M; Borglum AD; Breen G; Carr VJ; Catts S; Corvin A; Craddock N; Dannlowski U; Dikeos D; Esko T; Etain B; Ferentinos P; Frye M; Fullerton JM; Gawlik M; Gershon ES; Goes F; Green MJ; Grigoroiu-Serbanescu M; Hauser J; Henskens F; Hillert J; Hong KS; Hougaard DM; Hultman CM; Hveem K; Iwata N; Jablensky A; Jones I; Jones LA; Kahn RS; Kelsoe JR; Kirov G; Landen M; Leboyer M; Lewis CM; Li QS; Lissowska J; Lochner C; Loughland C; Martin NG; Mathews CA; Mayoral F; McElroy SL; McIntosh AM; McMahon FJ; Melle I; Michie P; Milani L; Mitchell PB; Morken G; Mors O; Mortensen PB; Mowry B; Muller-Myhsok B; Myers RM; Neale BM; Nievergelt CM; Nordentoft M; Nothen MM; ODonovan MC; Oedegaard KJ; Olsson T; Owen MJ; Paciga SA; Pantelis C; Pato C; Pato MT; Patrinos GP; Perlis RH; Posthuma D; Ramos-Quiroga JA; Reif A; Reininghaus EZ; Ribases M; Rietschel M; Ripke S; Rouleau GA; Saito T; Schall U; Schalling M; Schofield PR; Schulze TG; Scott LJ; Scott RJ; Serretti A; Weickert CS; Smoller JW; Stefansson H; Stefansson K; Stordal E; Streit F; Sullivan PF; Turecki G; Vaaler AE; Vieta E; Vincent JB; Waldman ID; Weickert TW; Werge T; Wray NR; Zwart J; Biernacka JM; Nurnberger J; Cichon S; Edenberg HJ; Stahl EA; McQuillin A; Di Florio A; Ophoff RA; Andreassen OA, 2021, 'Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology', NATURE GENETICS, vol. 53, pp. 817 - +, http://dx.doi.org/10.1038/s41588-021-00857-4

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; Degenhardt F; 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; Frank J; Fraser C; Freimer NB; Frisén L; Gade K; Gage D; Garnham J; Giambartolomei C, 2021, 'Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders', Molecular Psychiatry, vol. 26, pp. 1286 - 1298, http://dx.doi.org/10.1038/s41380-019-0558-2

Overs BJ; Lenroot RK; Roberts G; Green MJ; Toma C; Hadzi-Pavlovic D; Pierce KD; Schofield PR; Mitchell PB; Fullerton JM, 2021, 'Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder', Psychiatry Research - Neuroimaging, vol. 309, pp. 111258 - 111258, http://dx.doi.org/10.1016/j.pscychresns.2021.111258

Blokland GAM; Grove J; Chen C-Y; Cotsapas C; Tobet S; Handa R; Schizophrenia Working Group of the Psychiatric Genomics Consortium ; St Clair D; Lencz T; Mowry BJ; Periyasamy S; Cairns MJ; Tooney PA; Wu JQ; Kelly B; Kirov G; Sullivan PF; Corvin A; Riley BP; Esko T; Milani L; Jönsson EG; Palotie A; Ehrenreich H; Begemann M; Steixner-Kumar A; Sham PC; Iwata N; Weinberger DR; Gejman PV; Sanders AR; Buxbaum JD; Rujescu D; Giegling I; Konte B; Hartmann AM; Bramon E; Murray RM; Pato MT; Lee J; Melle I; Molden E; Ophoff RA; McQuillin A; Bass NJ; Adolfsson R; Malhotra AK; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium ; Martin NG; Fullerton JM; Mitchell PB; Schofield PR; Forstner AJ; Degenhardt F; Schaupp S; Comes AL; Kogevinas M; Guzman-Parra J; Reif A; Streit F; Sirignano L; Cichon S; Grigoroiu-Serbanescu M; Hauser J; Lissowska J; Mayoral F; Müller-Myhsok B; Świątkowska B; Schulze TG; Nöthen MM; Rietschel M; Kelsoe J; Leboyer M; Jamain S; Etain B; Bellivier F; Vincent JB; Alda M; O'Donovan C; Cervantes P; Biernacka JM; Frye M; McElroy SL; Scott LJ; Stahl EA; Landén M; Hamshere ML; Smeland OB; Djurovic S; Vaaler AE; Andreassen OA; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium ; Baune BT; Air T; Preisig M; Uher R; Levinson DF; Weissman MM; Potash JB; Shi J; Knowles JA; Perlis RH; Lucae S; Boomsma DI; Penninx BWJH; Hottenga J-J; de Geus EJC; Willemsen G; Milaneschi Y; Tiemeier H; Grabe HJ; Teumer A; Van der Auwera S; Völker U; Hamilton SP; Magnusson PKE; Viktorin A; Mehta D; Mullins N; Adams MJ; Breen G; McIntosh AM; Lewis CM; Sex Differences Cross-Disorder Analysis Group of the Psychiatric Genomics Consortium ; iPSYCH ; Hougaard DM; Nordentoft M; Mors O; Mortensen PB; Werge T; Als TD; Børglum AD; Petryshen TL; Smoller JW; Goldstein JM, 2021, 'Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.', Biol Psychiatry, http://dx.doi.org/10.1016/j.biopsych.2021.02.972

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

Toma C; Shaw AD; Heath A; Pierce KD; Mitchell PB; Schofield PR; Fullerton JM, 2021, 'A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21', Journal of Psychiatry and Neuroscience, vol. 46, pp. E247 - E257, http://dx.doi.org/10.1503/jpn.200083

McWhinney SR; Abé C; Alda M; Benedetti F; Bøen E; del Mar Bonnin C; Borgers T; Brosch K; Canales-Rodríguez EJ; Cannon DM; Dannlowski U; Díaz-Zuluaga AM; Elvsåshagen T; Eyler LT; Fullerton JM; Goikolea JM; Goltermann J; Grotegerd D; Haarman BCM; Hahn T; Howells FM; Ingvar M; Kircher TTJ; Krug A; Kuplicki RT; Landén M; Lemke H; Liberg B; Lopez-Jaramillo C; Malt UF; Martyn FM; Mazza E; McDonald C; McPhilemy G; Meier S; Meinert S; Meller T; Melloni EMT; Mitchell PB; Nabulsi L; Nenadic I; Opel N; Ophoff RA; Overs BJ; Pfarr JK; Pineda-Zapata JA; Pomarol-Clotet E; Raduà J; Repple J; Richter M; Ringwald KG; Roberts G; Salvador R; Savitz J; Schmitt S; Schofield PR; Sim K; Stein DJ; Stein F; Temmingh HS; Thiel K; van Haren NEM; Gestel HV; Vargas C; Vieta E; Vreeker A; Waltemate L; Yatham LN; Ching CRK; Andreassen O; Thompson PM; Hajek T, 2021, 'Association between body mass index and subcortical brain volumes in bipolar disorders–ENIGMA study in 2735 individuals', Molecular Psychiatry, http://dx.doi.org/10.1038/s41380-021-01098-x

Weissleder C; North HF; Bitar M; Fullerton JM; Sager R; Barry G; Piper M; Halliday GM; Webster MJ; Shannon Weickert C, 2021, 'Reduced adult neurogenesis is associated with increased macrophages in the subependymal zone in schizophrenia', Molecular Psychiatry, http://dx.doi.org/10.1038/s41380-021-01149-3

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

Nunes A; Schnack HG; Ching CRK; Agartz I; Akudjedu TN; Alda M; Alnæs D; Alonso-Lana S; Bauer J; Baune BT; Bøen E; Bonnin CDM; Busatto GF; Canales-Rodríguez EJ; Cannon DM; Caseras X; Chaim-Avancini TM; Dannlowski U; Díaz-Zuluaga AM; Dietsche B; Doan NT; Duchesnay E; Elvsåshagen T; Emden D; Eyler LT; Fatjó-Vilas M; Favre P; Foley SF; Fullerton JM; Glahn DC; Goikolea JM; Grotegerd D; Hahn T; Henry C; Hibar DP; Houenou J; Howells FM; Jahanshad N; Kaufmann T; Kenney J; Kircher TTJ; Krug A; Lagerberg TV; Lenroot RK; López-Jaramillo C; Machado-Vieira R; Malt UF; McDonald C; Mitchell PB; Mwangi B; Nabulsi L; Opel N; Overs BJ; Pineda-Zapata JA; Pomarol-Clotet E; Redlich R; Roberts G; Rosa PG; Salvador R; Satterthwaite TD; Soares JC; Stein DJ; Temmingh HS; Trappenberg T; Uhlmann A; van Haren NEM; Vieta E; Westlye LT; Wolf DH; Yüksel D; Zanetti MV; Andreassen OA; Thompson PM; Hajek T, 2020, 'Using structural MRI to identify bipolar disorders – 13 site machine learning study in 3020 individuals from the ENIGMA Bipolar Disorders Working Group', Molecular Psychiatry, vol. 25, pp. 2130 - 2143, http://dx.doi.org/10.1038/s41380-018-0228-9

Radua J; Vieta E; Shinohara R; Kochunov P; Quidé Y; Green MJ; Weickert CS; Weickert T; Bruggemann J; Kircher T; Nenadić I; Cairns MJ; Seal M; Schall U; Henskens F; Fullerton JM; Mowry B; Pantelis C; Lenroot R; Cropley V; Loughland C; Scott R; Wolf D; Satterthwaite TD; Tan Y; Sim K; Piras F; Spalletta G; Banaj N; Pomarol-Clotet E; Solanes A; Albajes-Eizagirre A; Canales-Rodríguez EJ; Sarro S; Di Giorgio A; Bertolino A; Stäblein M; Oertel V; Knöchel C; Borgwardt S; du Plessis S; Yun JY; Kwon JS; Dannlowski U; Hahn T; Grotegerd D; Alloza C; Arango C; Janssen J; Díaz-Caneja C; Jiang W; Calhoun V; Ehrlich S; Yang K; Cascella NG; Takayanagi Y; Sawa A; Tomyshev A; Lebedeva I; Kaleda V; Kirschner M; Hoschl C; Tomecek D; Skoch A; van Amelsvoort T; Bakker G; James A; Preda A; Weideman A; Stein DJ; Howells F; Uhlmann A; Temmingh H; López-Jaramillo C; Díaz-Zuluaga A; Fortea L; Martinez-Heras E; Solana E; Llufriu S; Jahanshad N; Thompson P; Turner J; van Erp T; Glahn D; Pearlson G; Hong E; Krug A; Carr V; Tooney P; Cooper G; Rasser P; Michie P; Catts S; Gur R; Gur R; Yang F; Fan F; Chen J; Guo H; Tan S, 2020, 'Increased power by harmonizing structural MRI site differences with the ComBat batch adjustment method in ENIGMA', NeuroImage, vol. 218, pp. 116956, http://dx.doi.org/10.1016/j.neuroimage.2020.116956

Watkeys OJ; Cohen-Woods S; Quide Y; Cairns MJ; Overs B; Fullerton JM; Green MJ, 2020, 'Derivation of poly-methylomic pro fi le scores for schizophrenia', PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, vol. 101, http://dx.doi.org/10.1101/607309

Watkeys OJ; Cohen-Woods S; Quidé Y; Cairns MJ; Overs B; Fullerton JM; Green MJ, 2020, 'Derivation of poly-methylomic profile scores for schizophrenia', Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol. 101, http://dx.doi.org/10.1016/j.pnpbp.2020.109925

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Fullerton JM; Willis-Owen SAG; Yalcin B; Shifman S; Copley RR; Miller SR; Bhomra A; Davidson S; Oliver PL; Mott R; Flint J, 2008, 'Human-Mouse Quantitative Trait Locus Concordance and the Dissection of a Human Neuroticism Locus', Biological Psychiatry, vol. 63, pp. 874 - 883, http://dx.doi.org/10.1016/j.biopsych.2007.10.019

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

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

Fullerton J, 2006, 'New approaches to the genetic analysis of neuroticism and anxiety', Behavior Genetics, vol. 36, pp. 147 - 161, http://dx.doi.org/10.1007/s10519-005-9000-4

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

Fullerton J; Heath A; Mitchell P; Schofield P, 2006, 'Investigation of circadian disruption in bipolar disorder.', Acta Neuropsychiatr, vol. 18, pp. 251, http://dx.doi.org/10.1017/S0924270800030283

Willis-Owen SAG; Fullerton J; Surtees PG; Wainwright NWJ; Miller S; Flint J, 2005, 'The Val66Met coding variant of the brain-derived neurotrophic factor (BDNF) gene does not contribute toward variation in the personality trait neuroticism', Biological Psychiatry, vol. 58, pp. 738 - 742, http://dx.doi.org/10.1016/j.biopsych.2005.05.014

Yalcin B; Willis-Owen SAG; Fullerton J; Meesaq A; Deacon RM; Rawlins JNP; Copley RR; Morris AP; Flint J; Mott R, 2004, 'Genetic dissection of a behavioral quantitative trait locus shows that Rgs2 modulates anxiety in mice', Nature Genetics, vol. 36, pp. 1197 - 1202, http://dx.doi.org/10.1038/ng1450

Khoo JP; Nicoli T; Alp NJ; Fullerton J; Flint J; Channon KM, 2004, 'Congenic mapping and genotyping of the tetrahydrobiopterin-deficient hph-1 mouse', Molecular Genetics and Metabolism, vol. 82, pp. 251 - 254, http://dx.doi.org/10.1016/j.ymgme.2004.04.006

Yalcin B; Fullerton J; Miller S; Keays DA; Brady S; Bhomra A; Jefferson A; Volpi E; Copley RR; Flint J; Mott R, 2004, 'Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory mice', Proceedings of the National Academy of Sciences of the United States of America, vol. 101, pp. 9734 - 9739, http://dx.doi.org/10.1073/pnas.0401189101

Fullerton J; Cubin M; Tiwari H; Wang C; Bomhra A; Davidson S; Miller S; Fairburn C; Goodwin G; Neale MC; Fiddy S; Mott R; Allison DB; Flint J, 2003, 'Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative-trait loci that influence variation in the human personality trait neuroticism', American Journal of Human Genetics, vol. 72, pp. 879 - 890, http://dx.doi.org/10.1086/374178

Talbot CJ; Radcliffe RA; Fullerton J; Hitzemann R; Wehner JM; Flint J, 2003, 'Fine scale mapping of a genetic locus for conditioned fear', Mammalian Genome, vol. 14, pp. 223 - 230, http://dx.doi.org/10.1007/s00335-002-3059-5

Fullerton J; Paprocki P; Foote S; Mackey DA; Williamson R; Forrest S, 2002, 'Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia', Human Genetics, vol. 110, pp. 462 - 470, http://dx.doi.org/10.1007/s00439-002-0705-7

Forrest S; Dunn K; Elliott K; Fitzpatrick E; Fullerton J; McCarthy M; Brown J; Hill D; Williamson R, 1999, 'Identifying genes predisposing to atopic eczema', Journal of Allergy and Clinical Immunology, vol. 104, pp. 1066 - 1070, http://dx.doi.org/10.1016/S0091-6749(99)70090-4

Conference Papers

Nurnberger JI; Wilcox H; Glowinsky A; Mitchell P; Fullerton J; Hulvershorn L; Kamali M; Ghaziuddin N; Koller D; Foroud T; Edenberg H, 2015, 'Combined use of clinical and genetic information in the prediction of risk for bipolar disorder', in BIPOLAR DISORDERS, WILEY-BLACKWELL, pp. 11 - 11, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000355338100012&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Nurnberger J; McInnis M; Wilcox H; Glowinski A; Mitchell P; Fullerton J; Hulvershorn L; Kamali M; Ghiazuddin N; Koller D; Foroud T; Edenberg H, 2015, 'Combined Use of Clinical and Genetic Information in the Prediction of Risk for Bipolar Disorder', in BIOLOGICAL PSYCHIATRY, ELSEVIER SCIENCE INC, Toronto, CANADA, 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:000352207501029&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Mitchell P; Roberts G; Frankland A; Breakspear M; Schofield P; Fullerton J, 2014, 'Using brain imaging and genetics to identify those at high risk for bipolar disorder', in INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, CAMBRIDGE UNIV PRESS, Vancouver, CANADA, pp. 14 - 14, presented at 29th CINP World Congress of Neuropsychopharmacology, Vancouver, CANADA, 22 June 2014 - 26 June 2014, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000339769200054&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Mitchell P; Roberts G; Fullerton JM; Green M; Breakspear M; Frankland A; Levy F; Lenroot R; Wen W; Lau P; Joslyn C; Schofield P, 2013, 'Imaging and genetic studies in youth at high risk for bipolar disorder', in BIPOLAR DISORDERS, WILEY-BLACKWELL, Miami Beach, FL, pp. 41 - 41, presented at 10th International Conference on Bipolar Disorder of the International-Society-for-Bipolar-Disorders, Miami Beach, FL, 13 June 2013 - 16 June 2013, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000319826800087&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

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

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

Willis-Owen S; Yalcin B; Fullerton J; Meesaq A; Deacon R; Rawlins N; Copley R; Morris A; Flint J; Mott R, 2005, 'Finding quantitative trait genes that influence mouse behaviour - and investigating their role in human psychopathology', in AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, WILEY, Boston, MA, pp. 94 - 95, 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:000232357300338&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Fullerton J; Brady S; Cubin M; Tiwari H; Wang CX; Bomhra A; Davidson S; Miller S; Fairburn C; Goodwin G; Neale MC; Fiddy S; Mott R; Allison DB; Flint J, 2004, 'Molecular approaches to identifying candidate genes in depression', in BEHAVIOR GENETICS, SPRINGER, Aix en Provence, FRANCE, pp. 639 - 639, presented at 34th Annual Meeting of the Behavior-Genetics-Association, Aix en Provence, FRANCE, 27 June 2004 - 30 June 2004, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000224808200039&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Fullerton J; cubin M; Bhomra A; Davidson S; miller S; turn M; Dolby C; mott R; wang C; Tiwari H; Ailison D; Neale M; fairburn C; Goodwin G; Flint J, 2002, 'Linkage analysis of extremely discordant and concordant sibling pairs identifies QTL that influence variation in a human personality trait.', in AMERICAN JOURNAL OF HUMAN GENETICS, UNIV CHICAGO PRESS, Baltimore, MD, pp. 216 - 216, presented at American Society of Human Genetics, Baltimore, MD, 15 October 2002 - 19 October 2002, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000178025800265&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a

Fullerton JM; Paprocki P; Foote S; Mackie D; Williamson R; Forrest S, 1999, 'An association approach using eight affected individuals from Tasmania, Australia maps a locus for keratoconus.', in AMERICAN JOURNAL OF HUMAN GENETICS, UNIV CHICAGO PRESS, pp. A31 - A31, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000082879800159&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Conference Presentations

Lenroot RK; Roberts G; Fullerton J; Overs B; Schofield P; Mitchell P, 2015, 'BIPOLAR DISORDER KIDS & SIBS STUDY: NEUROIMAGING FINDINGS IN YOUNG PEOPLE AT HIGH RISK FOR BIPOLAR DISORDER', in AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, SAGE PUBLICATIONS LTD, Vol. 49, pp. 82 - 82, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000354437500206&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Conference Abstracts

Roberts G; Lenroot R; Overs B; Fullerton J; Leung V; Ridgway K; Stuart A; Frankland A; Levy F; Hadzi-Pavlovic D; Breakspear M; Mitchell PB, 2020, 'Accelerated cortical thinning and volume reduction over time in young people at high genetic risk for bipolar disorder', in Psychological Medicine, WILEY, Sydney, AUSTRALIA, Vol. 21, pp. 66 - 66, presented at 21st Annual ISBD Conference on Global Advances in Bipolar Disorder and Depression, Sydney, AUSTRALIA, 20 March 2019 - 23 March 2019, http://dx.doi.org/10.1017/S0033291720003153

Watkeys O; Fullerton J; Cohen-Woods S; Quide Y; Cairns M; Green M, 2019, 'ASSOCIATIONS BETWEEN DNA METHYLATION PATTERNS AND CLINICAL STATUS ARE MODERATED BY POLYGENIC RISK FOR SCHIZOPHRENIA', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER, Los Angeles, CA, Vol. 29, pp. S214 - S215, presented at 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, 26 October 2019 - 31 October 2019, http://dx.doi.org/10.1016/j.euroneuro.2019.08.190

Mitchell P; Roberts G; Lenroot RK; Overs B; Fullerton J; Leung V; Stuart A; Frankland A; Levy F; Hadzi-Pavlovic D; Breakspear M, 2019, 'ACCELERATED CORTICAL THINNING AND VOLUME REDUCTION OVER TIME IN YOUNG PEOPLE AT HIGH GENETIC RISK FOR BIPOLAR DISORDER', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER, Los Angeles, CA, Vol. 29, pp. S129 - S129, presented at 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, 26 October 2019 - 31 October 2019, http://dx.doi.org/10.1016/j.euroneuro.2019.08.030

Boss P; Loo C; Fullerton J; Mitchell P, 2019, 'The Genes, Clinical Assessment and Depression (GLAD) study', in BIPOLAR DISORDERS, WILEY, Sydney, AUSTRALIA, Vol. 21, pp. 137 - 138, presented at 21st Annual ISBD Conference on Global Advances in Bipolar Disorder and Depression, Sydney, AUSTRALIA, 20 March 2019 - 23 March 2019, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000461513600304&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Hesam-Shariati S; Overs BJ; Green MJ; Roberts G; Leung V; Stuart A; Schofield PR; Mitchell PB; Fullerton JM, 2019, 'Role of epigenetic age and stress in developing bipolar disorder at high familial risk', in BIPOLAR DISORDERS, WILEY, Sydney, AUSTRALIA, Vol. 21, pp. 106 - 106, presented at 21st Annual ISBD Conference on Global Advances in Bipolar Disorder and Depression, Sydney, AUSTRALIA, 20 March 2019 - 23 March 2019, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000461513600238&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Overs B; Toma C; Havard A; Green MJ; Mitchell PB; Schofield PR; Fullerton JM, 2019, 'Identification and characterisation of bipolar disorder in Australia using administrative health data', in BIPOLAR DISORDERS, WILEY, Sydney, AUSTRALIA, Vol. 21, pp. 69 - 70, presented at 21st Annual ISBD Conference on Global Advances in Bipolar Disorder and Depression, Sydney, AUSTRALIA, 20 March 2019 - 23 March 2019, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000461513600148&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Toma C; Shaw AD; Allcock RJN; Heath A; Pierce KD; Cooper A; Mitchell PB; Schofield PR; Fullerton JM, 2019, 'The role of rare variants in bipolar disorder', in BIPOLAR DISORDERS, WILEY, Sydney, AUSTRALIA, Vol. 21, pp. 40 - 41, presented at 21st Annual ISBD Conference on Global Advances in Bipolar Disorder and Depression, Sydney, AUSTRALIA, 20 March 2019 - 23 March 2019, http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000461513600085&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Jamshidi J; Montalto A; Chilver M; Toma C; Schofield PR; Williams L; Fullerton J; Gatt J, 2019, 'Genetic factors influencing quantitative measures of subjective and psychological wellbeing using the COMPAS-W scale in a healthy Australian twin cohort', in Behavior Genetics, Stockholm, Vol. 49, pp. 511 - 511, presented at Behavior Genetics Association, Stockholm

Cohen-Woods S; Watkeys O; Teroganova N; Quide Y; Fullerton J; Cairns M; Green M, 2018, 'IMAGING GENETICS IN PSYCHOSIS STUDY: EPIGENETIC AGE ACCELERATION, TRAUMA, AND PSYCHOSIS OUTCOMES', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER, Glasgow, SCOTLAND, Vol. 29, pp. 1302 - 1302, presented at 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, SCOTLAND, 11 October 2018 - 15 October 2018, http://dx.doi.org/10.1016/j.euroneuro.2018.08.429

Cohen-Woods S; Teroganova N; Quide Y; Fullerton J; Girshkin L; Atkins J; Cairns M; Green M, 2018, 'FKBP5 DNA METHYLATION, CHILDHOOD TRAUMA, AND PSYCHOSIS OUTCOMES', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER, Glasgow, SCOTLAND, Vol. 29, pp. 1147 - 1148, presented at 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, SCOTLAND, 11 October 2018 - 15 October 2018, http://dx.doi.org/10.1016/j.euroneuro.2018.08.150

Fullerton J; Roberts G; Overs B; Lenroot RK; Breakspear M; Frankland A; McInnis M; Glowinski A; Wilcox H; Stapp E; Hulvershorn L; Benke K; Schofield P; Nurnberger J; Mitchell PB, 2018, 'BRAIN CORTICAL TRAJECTORIES, POLYGENIC RISK AND ENVIRONMENTAL INTERACTIONS IN A PROSPECTIVE LONGITUDINAL STUDY OF YOUNG PEOPLE AT-RISK OF BIPOLAR DISORDER', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER, Glasgow, SCOTLAND, Vol. 29, pp. 1307 - 1308, presented at 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, SCOTLAND, 11 October 2018 - 15 October 2018, http://dx.doi.org/10.1016/j.euroneuro.2018.08.441

Lenroot RK; Overs B; Roberts G; Frankland A; Levy F; Toma C; Wieckert CS; Schofield P; Mitchell P; Fullerton J, 2017, 'INTERACTIVE EFFECTS OF FAMILY HISTORY, POLYGENIC RISK AND AGE ON CORTICAL THICKNESS IN YOUNG PEOPLE AT HIGH GENETIC RISK OF BIPOLAR DISORDER', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER SCIENCE BV, Orlando, FL, Vol. 29, pp. S924 - S924, presented at 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, 13 October 2017 - 17 October 2017, http://dx.doi.org/10.1016/j.euroneuro.2017.08.256

Overs BJ; Lenroot RK; Roberts G; Green MJ; Hadzi-Pavlovic D; Frankland A; Levy F; Toma C; Schofield PR; Mitchell PB; Fullerton J, 2017, 'THE RELATIONSHIP BETWEEN FUNCTIONAL DOPAMINE D2 RECEPTOR HAPLOTYPES AND COGNITIVE OUTCOMES, AS MEDIATED BY REGIONAL BRAIN STRUCTURE: A COMPARISON OF CONTROL, AT-RISK, AND BIPOLAR DISORDER SUBJECTS', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER SCIENCE BV, Orlando, FL, Vol. 29, pp. S991 - S992, presented at 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, 13 October 2017 - 17 October 2017, http://dx.doi.org/10.1016/j.euroneuro.2017.08.375

Mitchell P; Frankland A; Roberts G; Holmes-Preston E; Perich T; Levy F; Lenroot R; Hadzi-Pavlovic D; Breakspear M; Fullerton J; Schofield P, 2016, 'PREDICTING CONVERSION TO BIPOLAR DISORDER IN A PROSPECTIVE LONGITUDINAL GENETICALLY HIGH-RISK SAMPLE', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER SCIENCE BV, Jerusalem, ISRAEL, Vol. 27, pp. S516 - S516, presented at 24th World Congress of Psychiatric Genetics (WCPG), Jerusalem, ISRAEL, 30 October 2016 - 04 November 2016, http://dx.doi.org/10.1016/j.euroneuro.2016.09.631

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

Jahanshad N; Kochunov P; Armstrong N; Bastin M; Bearden C; Brouwer R; Cannon D; Caseras X; Costa Rica - Colombia Bipolar Consortium ; Crespo-Facorro B; Dreary I; den Braber A; de Zubicaray G; Donohoe G; Fears S; Franke B; Fullerton J; Hariri A; Hashimoto R; Hibar D; Pol H; Kelly S; Knickmeyer R; Knodt A; Le Hellard S; Lemaitre H; Mandl R; Mitchell P; McDonald C; McMahon K; McIntosh A; Nichols T; Nyberg L; Roberts G; Sachdev PS; Schumann G; Sprooten E; Stein E; Szeszko P; Tordesillas-Gutierrez D; van Hulzen K; vant Ent D; Yang Y; Wardlaw J; Wen W; Zwiers M; The ADNI ; Håberg AK; Wright M; Thompson P; Glahn D, 2015, 'Meta-analyzing genome-wide associations with white matter microstructure - the ENIGMA-DTI group [Poster abstract 3407]', in Proceedings of the 21st Annual Meeting of the Organization for Human Brain Mapping (OHBM), 21st Annual Meeting of the Organization for Human Brain Mapping (OHBM), Honolulu, Hawaii, USA, presented at 21st Annual Meeting of the Organization for Human Brain Mapping (OHBM), Honolulu, Hawaii, USA, 14 June 2015 - 18 June 2015

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

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