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:

2019 4 publication excellence awards: UNSW Promoting High Quality Research Papers Scheme

2018 6 publication excellence awards: UNSW Promoting High Quality Research Papers Scheme

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:

I have supervised 9 PhD students, including 6 who have completed. My current students are:

Sonia Hesam Shariati

Javad Jamshidi

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.

Media

LinkedIn:

https://www.linkedin.com/in/jan-fullerton-57882485/

Twitter Account:

https://twitter.com/FullertonJan

Publications related to this Person

Journal articles

Jamshidi J; Schofield PR; Gatt JM; Fullerton JM, 2022, 'Phenotypic and genetic analysis of a wellbeing factor score in the UK Biobank and the impact of childhood maltreatment and psychiatric illness', Translational Psychiatry, vol. 12, pp. 113, http://dx.doi.org/10.1038/s41398-022-01874-5

Hu B; Cha J; Fullerton JM; Hesam-Shariati S; Nakamura K; Nurnberger JI; Anand A, 2022, 'Genetic and environment effects on structural neuroimaging endophenotype for bipolar disorder: a novel molecular approach', Translational Psychiatry, vol. 12, pp. 137, http://dx.doi.org/10.1038/s41398-022-01892-3

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Hesam-Shariati S; Overs BJ; Roberts G; Toma C; Watkeys OJ; Green MJ; Pierce KD; Edenberg HJ; Wilcox HC; Stapp EK; McInnis MG; Hulvershorn LA; Nurnberger JI; Schofield PR; Mitchell PB; Fullerton JM, 2022, 'Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder', Translational Psychiatry, vol. 12, http://dx.doi.org/10.1038/s41398-022-02079-6

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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

Sinclair D; Fullerton J; Webster M; Shannon Weickert C, 2012, 'Glucocorticoid receptor 1B and 1C mRNA transcript alterations in schizophrenia and bipolar disorder, and their possible regulation by GR gene variants', PLoS One, vol. 7, pp. Article no. e31720, http://dx.doi.org/10.1371/journal.pone.0031720

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

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

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

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

Overs B; Toma C; Havard A; Green M; O'Donnell M; Mitchell P; Schofield P; Fullerton J, 2021, 'Medical morbidity and mortality in Australians with bipolar disorder from linked administrative data', in BIPOLAR DISORDERS, WILEY, pp. 51 - 52, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000663051300119&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Mitchell P; Lenroot R; Overs B; Fullerton J; Leung V; Stuart A; Frankland A; Levy F; Hadzi-Pavlovic D; Breakspear M, 2020, 'Accelerated cortical thinning and volume reduction over time in young people at high genetic risk for bipolar disorder', in BIPOLAR DISORDERS, WILEY, ELECTR NETWORK, pp. 48 - 48, presented at 22nd Annual Conference of the International-Society-for-Bipolar-Disorders (ISBD), ELECTR NETWORK, 18 June 2020 - 21 June 2020, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000540293800095&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Hesam-Shariati S; Overs B; Toma C; Watkeys O; Green M; Roberts G; Leung V; Stuart A; Schofield PR; Mitchell PB; Fullerton J, 2019, 'EPIGENOME-WIDE ASSOCIATION STUDY (EWAS) OF YOUNG PEOPLE WITH FAMILIAL RISK OF BIPOLAR DISORDER', in EUROPEAN NEUROPSYCHOPHARMACOLOGY, ELSEVIER, Los Angeles, CA, pp. S192 - S192, 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.2019.08.149

Mitchell PB; Roberts G; Frankland A; Lenroot R; Green M; Breakspear M; Schofield PR; Fullerton J, 2016, 'Integration of Brain Imaging, Genetic, Neuropsychological and Clinical Information to Predict Onset of Major Mood Disorders in Young People at High Risk of Bipolar Disorder', in BIOLOGICAL PSYCHIATRY, ELSEVIER SCIENCE INC, pp. 163S - 163S, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000432440802063&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

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

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, https://www.webofscience.com/api/gateway?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 Convention and Meeting of the Society-of-Biological-Psychiatry on Stress, Emotion, Neurodevelopment and Psychopathology, Toronto, CANADA, 14 May 2015 - 16 May 2015, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, 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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, 2022, '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. 52, pp. 1344 - 1355, 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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?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, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000332833800274&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Preprints

Liu D; Meyer D; Fennessy B; Feng C; Cheng E; Johnson J; Park YJ; Rieder M-K; Ascolillo S; de Pins A; Dobbyn A; Lebovitch D; Moya E; Nguyen T-H; Wilkins L; Hassan A; Burdick K; Buxbaum J; Domenici E; Frangou S; Hartmann A; Malhotra D; Pato C; Pato M; Ressler K; Roussos P; Rujescu D; Arango C; Bertolino A; Blasi G; Bocchio-Chiavetto L; Campion D; Carr V; Fullerton J; Gennarelli M; González-Peñas J; Levinson D; Mowry B; Nimgaokar V; Pergola G; Rampino A; Rivera-Sanchez M; Schwab S; Wildenauer D; Daly M; Neale B; Singh T; O’Donovan M; Owen M; Walters J; Ayub M; Malhotra A; Lencz T; Sullivan P; Sklar P; Stahl E; Huckins L; Charney A; Psychiatric Genomics Consortium Phase 3 Targeted Sequencing of Schizophrenia Study Team ; Schizophrenia Exome Meta-analysis Consortium , 2022, Rare schizophrenia risk variant burden is conserved in diverse human populations, http://dx.doi.org/10.1101/2022.01.03.22268662

van Velzen L; Dauvermann M; Colic L; Villa L; Savage H; Toenders Y; Zhu A; Bright J; Campos A; Salminen L; Ambrogi S; Ayesa-Arriola R; Banaj N; Başgöze Z; Bauer J; Blair K; Blair RJ; Brosch K; Cheng Y; Colle R; Connolly C; Corruble E; Couvy-Duchesne B; Crespo-Facorro B; Cullen K; Dannlowski U; Davey C; Dohm K; Fullerton J; Gonul AS; Gotlib I; Grotegerd D; Hahn T; Harrison B; He M; Hickie I; Ho T; Iorfino F; Jansen A; Jollant F; Kircher T; Klimes-Dougan B; Klug M; Leehr E; Lippard ETC; McLaughlin K; Meinert S; Miller AB; Mitchell P; Mwangi B; Nenadić I; Ojha A; Overs B; Pfarr J-K; Piras F; Ringwald K; Roberts G; Romer G; Sanches M; Sheridan M; Soares J; Spalletta G; Stein F; Teresi G; Tordesillas-Gutiérrez D; Uyar-Demir A; van der Wee NJA; van der Werff S; Vermeiren RRJM; Winter A; Wu M-J; Yang T; Thompson P; Rentería M; Jahanshad N; Blumberg H; van Harmelen A-L; Schmaal L, 2021, Structural brain alterations associated with suicidal thoughts and behaviors in young people: results across 21 international studies from the ENIGMA Suicidal Thoughts and Behaviours consortium, http://dx.doi.org/10.1101/2021.09.27.21264068

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Mullins N; Kang J; Campos AI; Coleman JRI; Edwards AC; Galfalvy H; Levey DF; Lori A; Shabalin A; Starnawska A; Su M-H; Watson HJ; Adams M; Awasthi S; Gandal M; Hafferty JD; Hishimoto A; Kim M; Okazaki S; Otsuka I; Ripke S; Ware EB; Bergen AW; Berrettini WH; Bohus M; Brandt H; Chang X; Chen WJ; Chen H-C; Crawford S; Crow S; DiBlasi E; Duriez P; Fernández-Aranda F; Fichter MM; Gallinger S; Glatt SJ; Gorwood P; Guo Y; Hakonarson H; Halmi KA; Hwu H-G; Jain S; Jamain S; Jiménez-Murcia S; Johnson C; Kaplan AS; Kaye WH; Keel PK; Kennedy JL; Klump KL; Levitan RD; Li D; Liao S-C; Lieb K; Lilenfeld L; Liu C-M; Magistretti PJ; Marshall CR; Mitchell JE; Monson ET; Myers RM; Pinto D; Powers A; Ramoz N; Roepke S; Rotondo A; Rozanov V; Scherer SW; Schmahl C; Sokolowski M; Strober M; Thornton LM; Treasure J; Tsuang MT; Via MCL; Witt SH; Woodside DB; Yilmaz Z; Zillich L; Adolfsson R; Agartz I; Air TM; Alda M; Alfredsson L; Andreassen OA; Anjorin A; Appadurai V; Artigas MS; Van der Auwera S; Azevedo MH; Bass N; Bau CHD; Baune BT; Bellivier F; Berger K; Biernacka JM; Bigdeli TB; Binder EB; Boehnke M; Boks M; Bosch R; Braff DL; Bryant R; Budde M; Byrne EM; Cahn W; Casas M; Castelao E; Cervilla JA; Chaumette B; Cichon S; Corvin A; Craddock N; Craig D; Degenhardt F; Djurovic S; Edenberg HJ; Fanous AH; Foo JC; Forstner AJ; Frye M; Fullerton JM; Gatt JM; Gejman PV; Giegling I; Grabe HJ; Green MJ; Grevet EH; Grigoroiu-Serbanescu M; Gutierrez B; Guzman-Parra J; Hamilton SP; Hamshere ML; Hartmann A; Hauser J; Heilmann-Heimbach S; Hoffmann P; Ising M; Jones I; Jones LA; Jonsson L; Kahn RS; Kelsoe JR; Kendler KS; Kloiber S; Koenen KC; Kogevinas M; Konte B; Krebs M-O; Landén M; Lawrence J; Leboyer M; Lee PH; Levinson DF; Liao C; Lissowska J; Lucae S; Mayoral F; McElroy SL; McGrath P; McGuffin P; McQuillin A; Medland S; Mehta D; Melle I; Milaneschi Y; Mitchell PB; Molina E; Morken G; Mortensen PB; Müller-Myhsok B; Nievergelt C; Nimgaonkar V; Nöthen MM; O’Donovan MC; Ophoff RA; Owen MJ; Pato C; Pato MT; Penninx BWJH; Pimm J; Pistis G; Potash JB; Power RA; Preisig M; Quested D; Ramos-Quiroga JA; Reif A; Ribasés M; Richarte V; Rietschel M; Rivera M; Roberts A; Roberts G; Rouleau GA; Rovaris DL; Rujescu D; Sánchez-Mora C; Sanders AR; Schofield PR; Schulze TG; Scott LJ; Serretti A; Shi J; Shyn SI; Sirignano L; Sklar P; Smeland OB; Smoller JW; Sonuga-Barke EJS; Spalletta G; Strauss JS; Świątkowska B; Trzaskowski M; Turecki G; Vilar-Ribó L; Vincent JB; Völzke H; Walters JTR; Weickert CS; Weickert TW; Weissman MM; Williams LM; Wray NR; Zai C; Agerbo E; Børglum AD; Breen G; Erlangsen A; Esko T; Gelernter J; Hougaard DM; Kessler RC; Kranzler HR; Li QS; Martin NG; McIntosh AM; Medland SE; Mors O; Nordentoft M; Olsen CM; Porteous D; Ursano RJ; Wasserman D; Werge T; Whiteman DC; Bulik CM; Coon H; Demontis D; Docherty AR; Kuo P-H; Lewis CM; Mann JJ; Rentería ME; Smith DJ; Stahl EA; Stein MB; Streit F; Willour V; Ruderfer DM, Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors, http://dx.doi.org/10.1101/2020.12.01.20241281

Kalman JL; Olde Loohuis LM; Vreeker A; McQuillin A; Stahl EA; Ruderfer D; Grigoroiu-Serbanescu M; Panagiotaropoulou G; Ripke S; Bigdeli TB; Stein F; Meller T; Meinert S; Pelin H; Streit F; Papiol S; Adams MJ; Adolfsson R; Adorjan K; Agartz I; Aminoff SR; Anderson-Schmidt H; Andreassen OA; Ardau R; Aubry J-M; Balaban C; Bass N; Baune BT; Bellivier F; Benabarre A; Bengesser S; Berrettini WH; Boks MP; Bromet EJ; Brosch K; Budde M; Byerley W; Cervantes P; Chillotti C; Cichon S; Clark SR; Comes AL; Corvin A; Coryell W; Craddock N; Craig DW; Croarkin PE; Cruceanu C; Czerski PM; Dalkner N; Dannlowski U; Degenhardt F; DePaulo JR; Djurovic S; Edenberg HJ; Eissa MA; Elvsåshagen T; Etain B; Fanous AH; Fellendorf F; Fiorentino A; Forstner AJ; Frye MA; Fullerton JM; Gade K; Garnham J; George K; Gershon E; Gill M; Goes FS; Gordon-Smith K; Grof P; Guzman-Parra J; Hahn T; Hake M; Hasler R; Heilbronner U; Jamain S; Jimenez E; Jones I; Jones L; Jonsson L; Kahn RS; Kelsoe JR; Kennedy JL; Kircher T; Kittel-Schneider S; Klöhn-Saghatolislam F; Knowles JA; Kranz TM; Lagerberg TV; Landen M; Lawson WB; Leboyer M; Li QS; Maj M; Malaspina D; Manchia M; Mayoral F; McElroy SL; McInnis MG; McIntosh AM; Medeiros H; Melle I; Milanova V; Mitchell PB; Monteleone P; Monteleone AM; Nöthen MM; Novak T; Nurnberger JJ; O’Brien N; O’Connell KS; O’Donovan C; O’Donovan MC; Opel N; Ortiz A; Owen MJ; Pålsson E; Pato C; Pato MT; Pawlak J; Pfarr J-K; Pisanu C; Potash JB; Rapaport MH; Reich-Erkelenz D; Reif A; Reininghaus E; Repple J; Richard-Lepouriel H; Rietschel M; Ringwald K; Roberts G; Rouleau G; Schaupp S; Scheftner WA; Schmitt S; Schofield PR; Schubert KO; Schulte EC; Schweizer B; Senner F; Severino G; Sharp S; Slaney C; Smeland OB; Sobell JL; Squassina A; Stopkova P; Strauss J; Tortorella A; Turecki G; Twarowska-Hauser J; Veldic M; Vieta E; Vincent JB; Xu W; Zai CC; Zandi PP; Del Zompo M; Florio AD; Smoller JW; Biernacka JM; McMahon FJ; Alda M; Muller-Myhsok B; Koutsouleris N; Falkai P; Freimer NB; Andlauer TFM; Schulze TG; Ophoff RA, Characterization of Age and Polarity at Onset in Bipolar Disorder, http://dx.doi.org/10.1101/2021.04.16.21251163

Blokland GAM; Grove J; Chen C-Y; Cotsapas C; Tobet S; Handa R; 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; 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; 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; Hougaard DM; Nordentoft M; Mors O; Mortensen PB; Werge T; Als TD; Børglum AD; Petryshen TL; Smoller JW; Goldstein JM, Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders, http://dx.doi.org/10.1101/2020.08.13.249813

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 K; 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 M-J; Veer IM; Vermeiren RRJM; Walter H; van der Wee NJA; van der Werff SJA; Whalley H; Winter NR; Wittfeld K; Wright MJ; Wu M-J; Völzke H; Yang TT; Zannias V; Zubicaray GID; 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; Goikolea JM; Haarman BCM; Hajek T; Henry C; Houenou J; Howells FM; Ingvar M; Kuplicki R; Lafer B; Landén M; Machado-Vieira R; Malt UF; McDonald C; Mitchell PB; Nabulsi L; Otaduy MCG; Overs BJ; Polosan M; Pomarol-Clotet E; Radua J; Rive MM; Roberts G; Ruhe HG; Salvador R; Sarró S; Satterthwaite TD; Savitz J; Schene AH; Schofield PR; Serpa MH; Sim K; Soeiro-de-Souza MG; Sutherland AN; Temmingh HS; Timmons GM; Uhlmann A; Vieta E; Wolf DH; Zanetti MV; Jahanshad N; Thompson PM; Veltman DJ; Penninx BWJH; Marquand AF; Cole JH; Schmaal L, Brain Aging in Major Depressive Disorder: Results from the ENIGMA Major Depressive Disorder working group, http://dx.doi.org/10.1101/560623

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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; Whitehead Pavlides JM; 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; Bøcker Pedersen C; 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 T-K; Coryell W; Craig DW; Cruceanu C; Curtis D; 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; Giørtz Pedersen M; Goldstein J; Gordon SD; Gordon-Smith K; Green EK; Green MJ; Greenwood TA; Grove J; Guan W; Parra J; Hamshere ML; Hautzinger M; Heilbronner U; Herms S; Hipolito M; Hoffmann P; Holland D; Huckins L; Jamain S; Johnson JS; Juréus A; Kandaswamy R; Karlsson R; Kennedy JL; Kittel-Schneider S; Knott SV; Knowles JA; Kogevinas M; Koller AC; Kupka R; Lavebratt C; Lawrence J; Lawson WB; Leber M; Lee PH; Levy SE; Li JZ; Liu C; Lucae S; Maaser A; MacIntyre DJ; Mahon PB; Maier W; Martinsson L; McCarroll S; McGuffin P; McInnis MG; McKay JD; Medeiros H; Medland SE; Meng F; Milani L; Montgomery GW; Morris DW; Mühleisen TW; Mullins N; Nguyen H; Nievergelt CM; Adolfsson AN; Nwulia EA; O’Donovan C; Olde Loohuis LM; Ori APS; Oruc L; Ösby U; Perlis RH; Perry A; Pfennig A; Potash JB; Purcell SM; Regeer EJ; Reif A; Reinbold CS; Rice JP; Rivas F; Rivera M; Roussos P; Ruderfer DM; Ryu E; Sánchez-Mora C; Schatzberg AF; Scheftner WA; Schork NJ; Weickert CS; Shehktman T; Shilling PD; Sigurdsson E; Slaney C; Smeland OB; Sobell JL; Søholm Hansen C; Spijker AT; St Clair D; Steffens M; Strauss JS; Streit F; Strohmaier J; Szelinger S; Thompson RC; Thorgeirsson TE; Treutlein J; Vedder H; Wang W; Watson SJ; Weickert TW; Witt SH; Xi S; Xu W; Young AH; Zandi P; Zhang P; Zollner S; Adolfsson R; Agartz I; Alda M; Backlund L; Baune BT; Bellivier F; Berrettini WH; Biernacka JM; Blackwood DHR; Boehnke M; Børglum AD; Corvin A; Craddock N; Daly MJ; Dannlowski U; Esko T; Etain B; Frye M; Fullerton JM; Gershon ES; Gill M; Goes F; Grigoroiu-Serbanescu M; Hauser J; Hougaard DM; Hultman CM; Jones I; Jones LA; Kahn R; Kirov G; Landén M; Leboyer M; Lewis CM; Li QS; Lissowska J; Martin NG; Mayoral F; McElroy SL; McIntosh AM; McMahon FJ; Melle I; Metspalu A; Mitchell PB; Morken G; Mors O; Mortensen PB; Müller-Myhsok B; Myers RM; Neale BM; Nimgaonkar V; Nordentoft M; Nöthen MM; O’Donovan MC; Oedegaard KJ; Owen MJ; Paciga SA; Pato C; Pato MT; Posthuma D; Ramos-Quiroga JA; Ribasés M; Rietschel M; Rouleau GA; Schalling M; Schofield PR; Schulze TG; Serretti A; Smoller JW; Stefansson H; Stefansson K; Stordal E; Sullivan PF; Turecki G; Vaaler AE; Vieta E; Vincent JB; Werge T; Nurnberger JI; Wray NR; Di Florio A; Edenberg HJ; Cichon S; Ophoff RA; Scott LJ; Andreassen OA; Kelsoe J; Sklar P, Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder, http://dx.doi.org/10.1101/173062

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