Recent Publications


Sudesh, R., Thalamuthu, A., John, S., Thara, R., Mowry, B., & Munirajan, A. K. (2018). Replication of GWAS identified miR-137 and its target gene polymorphisms in Schizophrenia of South Indian population and meta-analysis with Psychiatric Genomics Consortium. Schizophrenia Research.


Kelly, S., Jahanshad, N., Zalesky, A., Kochunov, P., Agartz, I., Alloza, C., … & Bousman, C. A. (2017). Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group. Molecular Psychiatry.

Benyamin, B., He, J., Zhao, Q., Gratten, J., Garton, F., Leo, P. J., … & Butler, T. J. (2017). Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. Nature Communications, 8(1), 611.

CNV Schizophrenia Working Groups of the Psychiatric Genomics Consortium & Consortium, P.E.I. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nat Genet 49, 27-35 (2017).

Gratten, Jacob, Zhao, Qiongyi, Benyamin, Beben, Garton, Fleur, He, Ji, Leo, Paul J, Mangelsdorf, Marie, Anderson, Lisa, Zhang, Zong-Hong, Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Edson, Janette, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K, Jin, Zi-Bing, Li, Zhongshan, Lin, Yong, Liu, Xiaolu, Marshall, Mhairi, Mowry, Bryan J, Ran, Shu, Reutens, David C, Song, Sharon, Tan, Li-Jun, Tang, Lu, Wallace, Robyn H, Wheeler, Lawrie, Wu, Jinyu, Yang, Jian, Xu, Huji, Visscher, Peter M, Bartlett, Perry F, Brown, Matthew A, Wray, Naomi R and Fan, Dongsheng (2017) Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese. Genome medicine, 9 1: 97. doi:10.1186/s13073-017-0487-0


Sekar, A. et al. Schizophrenia risk from complex variation of complement component 4. Nature 530, 177-183 (2016).

Mehta, D. et al. Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women. JAMA Psychiatry 73, 497-505 (2016).

Martin, A.K. & Mowry, B. Increased rare duplication burden genomewide in patients with treatment-resistant schizophrenia. Psychological Medicine 46, 469-476 (2016).

Martin, A.K., Gibson, E.C., Mowry, B. & Robinson, G.A. Verbal Initiation, Suppression, and Strategy Use and the Relationship with Clinical Symptoms in Schizophrenia. J Int Neuropsychol Soc 22, 735-43 (2016).

Johnson, E.C. et al. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. PLoS Genet 12, e1006343 (2016).

Franke, B. et al. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nat Neurosci 19, 420-431 (2016).

Edwards, A.C. et al. Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes. Schizophr Bull 42, 279-87 (2016).

Dzafic, I., Martin, A.K., Hocking, J., Mowry, B. & Burianová, H. Dynamic emotion perception and prior expectancy. Neuropsychologia 86, 131-40 (2016).

Bigdeli, T.B. et al. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. Am J Med Genet B Neuropsychiatr Genet171B, 276-89 (2016).


Yu, H. et al. Genome-Wide Association Study Suggested the PTPRD Polymorphisms Were Associated With Weight Gain Effects of Atypical Antipsychotic Medications. Schizophrenia Bulletin (2015).

Westcott, C., Waghorn, G., McLean, D., Statham, D. & Mowry, B. Interest in Employment Among People with Schizophrenia. American Journal of Psychiatric Rehabilitation 18, 187-207 (2015).

Westcott, C., Waghorn, G., McLean, D., Statham, D. & Mowry, B. Role functioning among adults with schizophrenia. British Journal of Occupational Therapy 78, 158-165 (2015).

Vilhjálmsson, Bjarni J. et al. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. The American Journal of Human Genetics 97, 576-592 (2015).

O’Dushlaine, C. et al. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature neuroscience 18, 199-209 (2015).

McLean, D. et al. Comparing schizophrenia symptoms in the Iban of Sarawak with other populations to elucidate clinical heterogeneity. Asia Pac Psychiatry 7, 36-44 (2015).

Martin, A.K., Robinson, G., Reutens, D. & Mowry, B. Common genetic risk variants are associated with positive symptoms and decision-making ability in patients with schizophrenia.Psychiatry Research 229, 606-608 (2015).

Martin, A.K., Robinson, G., Reutens, D. & Mowry, B. Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168, 374-382 (2015).

Martin, A.K., Mowry, B., Reutens, D. & Robinson, G.A. Executive functioning in schizophrenia: Unique and shared variance with measures of fluid intelligence. Brain and Cognition 99, 57-67 (2015).

Maier, R. et al. Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder. The American Journal of Human Genetics 96, 283-294 (2015).

Loh, P.R. et al. Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis. Nat Genet 47, 1385-92 (2015).

Lee, S.H. et al. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology 44, 1706-1721 (2015).

Garrison, J.R. et al. Paracingulate sulcus morphology is associated with hallucinations in the human brain. Nat Commun 6(2015).

Duan, J. et al. Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants. Human Molecular Genetics 24, 4674-4685 (2015).

Bulik-Sullivan, B.K. et al. LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nat Genet 47, 291-295 (2015).

Arnedo, J. et al. Uncovering the Hidden Risk Architecture of the Schizophrenias: Confirmation in Three Independent Genome-Wide Association Studies. American Journal of Psychiatry172, 139-153 (2015).

Andreassen, O.A. et al. Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci. Mol Psychiatry 20, 207-214 (2015).


Schizophrenia Working Group of the Psychiatric Genomics, C. et al. Biological Insights From 108 Schizophrenia-Associated Genetic Loci. Nature 511, 421-427 (2014).

Nicodemus, K.K., Hargreaves, A., Morris, D. & et al. Variability in working memory performance explained by epistasis vs polygenic scores in the znf804a pathway. JAMA Psychiatry 71, 778-785 (2014).

McLean, D. et al. DSM-IV “criterion A” schizophrenia symptoms across ethnically different populations: evidence for differing psychotic symptom content or structural organization?Culture, medicine and psychiatry 38, 408-426 (2014).

Martin, A.K., Robinson, G., Reutens, D. & Mowry, B. Copy number deletion burden is associated with cognitive, structural, and resting-state network differences in patients with schizophrenia. Behavioural Brain Research 272, 324-334 (2014).

Martin, A.K., Robinson, G., Reutens, D. & Mowry, B. Cannabis abuse and age at onset in schizophrenia patients with large, rare copy number variants. Schizophrenia Research 155, 21-25 (2014).

Kenneth Martin, A., Robinson, G., Reutens, D. & Mowry, B. Cognitive and structural neuroimaging characteristics of schizophrenia patients with large, rare copy number deletions. Psychiatry Research: Neuroimaging 224, 311-318 (2014).

Jones, A.L. et al. Elevated levels of autoantibodies targeting the M1 muscarinic acetylcholine receptor and neurofilament medium in sera from subgroups of patients with schizophrenia. Journal of Neuroimmunology 269, 68-75 (2014).

Gusev, A. et al. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases. The American Journal of Human Genetics 95, 535-552 (2014).

Duan, J. et al. A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder. The American Journal of Human Genetics 95, 744-753 (2014).


Gratten J, Visscher PM, Mowry BJ and Wray NR (2013) Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nat Genet 45:234-238.

Mowry BJ and Gratten J (2013) The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants. Mol Psychiatry 18:38-52.


Fanous AH, …, Mowry BJ, … Levinson DF (2012) Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms. Am J Psychiatry 169:1309-17.

Levinson, D.F. et al. Genome-wide Association Study of Multiplex Schizophrenia Pedigrees. American Journal of Psychiatry. 2012; 169(9): 963-973.

Weickert, C., Tiwari, Y., Schofield, P., Mowry B. & Fullerton, J. Schizophrenia-associated HapICE haplotype is associated with increased NRG1 Type III expression and high nucleotide diversity. Translational Psychiatry (2012).

McAuley, E. et al. Identification of Sialyltransferase 8B as a Generalized Susceptibility Gene for Psychotic and Mood Disorders on Chromosome 15q25-26. PLoS ONE, Accepted 02-05-12 (2012).

McLean D, John S, Barrett R, McGrath J, Loa P, Thara R and Mowry B (2012) Refining clinical phenotypes by contrasting ethnically different populations with schizophrenia from Australia, India and Sarawak. Psychiatry Res 196:194-200.

Lee, S.H. et al. Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nature Genetics 44, 247-250 (2012).

Sullivan, P. Don’t give up on GWAS. Mol Psychiatry 17, 2-3 (2012).

McLean, D., Gladman, B. & Mowry, B. Significant relationship between lifetime alcohol use disorders and suicide attempts in an Australian schizophrenia sample. Australian and New Zealand Journal of Psychiatry 46, 132-140 (2012).

Ragan C, Mowry BJ and Bauer DC (2012) Hybridization-based reconstruction of small non-coding RNA transcripts from deep sequencing data. Nucleic Acids Res 40:7633-43.

Mowry BJ and Gratten J. (In press) The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants. Molecular psychiatry (2012) doi:10.1038/mp.2012.34