Psychiatric genomics

About

Our primary research goals are (i) to identify susceptibility genes for schizophrenia and related disorders and (ii) understand both their normal and pathologic functions in the brain. To investigate these two broad areas of research, we use a wide range of methodologies and techniques ranging from high-throughput sequencing technologies, quantitative genetics, systems biology and deep learning, through to animal models and cutting-edge microscopy.  Our research is organised into the following themes:

Statistical genetics, bioinformatics and systems biology

Genome-wide common and rare variant association analyses using high-throughput genotyping technologies

We have conducted a number of Genome Wide Association Studies (GWAS) over many years, to identify key genetic contributors to schizophrenia and other related psychiatric disorders. These have been a mixture of collaborative efforts (contributing several Australian datasets to the worldwide Psychiatric Genomics Consortium series of GWASs), and our own studies based on ethnically homogeneous populations from which we have collected blood samples, clinical histories, and extensive family histories.

As well as GWAS, recent focuses for other sequencing projects have included RNA transcriptome analysis from post-mortem brain sections, whole exome sequencing from a southern Indian cohort, and targeted resequencing of a genetic region from one of our unique sample cohorts which showed a very strong linkage to schizophrenia.

Post GWAS computational approaches for investigating molecular mechanisms underlying genotype-phenotype associations

In addition to in-house data generation, we also use publicly available high-throughput data sources such as regulatory, epigenetic and spatio-temporal brain gene expression data for: 1) Modelling the Impact of schizophrenia GWAS loci during human brain development to facilitate in silico prediction of the impact of loci on transcription factor dynamics during human brain development; 2) Fine-mapping of GWAS loci using data from differential binding of regulatory factors; 3) Developing intelligent solutions for automating and rapid translation of GWAS findings to medical interventions using deep learning(DL) approaches. The goal is to develop novel predictive computational models to facilitate in silico investigations of the molecular mechanisms underlying genotype-phenotype associations. The outcome will be a novel automated solution using transparent DL to accelerate the process of GWAS fine-mapping, gene discovery and mechanistic understanding­­­ of the disease/trait.

Biological and animal models

Understanding the normal and pathologic neuronal function of schizophrenia susceptibility genes using the zebrafish model.

This work aims to characterise the neurodevelopmental and neuronal role of schizophrenia susceptibility genes by using the zebrafish animal model – specifically taking advantage of the fast-developing nervous system to characterise the roles of these genes in neurodevelopmental processes. To do this, we are using a combination of state-of-the-art genetic techniques (transgenesis, CRISPR), microscopy (confocal, super-resolution), and calcium imaging, as well as automatic behavioural profiling. Our ultimate goal is to unveil the role of these risk-genes in the development, progression and severity of schizophrenia and other brain disorders.

This work is supported by an NHMRC project grant (number APP1165850, 2019-2022) to Prof Bryan Mowry and Dr Jean Giacomotto and as well as a Rebecca L. Cooper Medical Research project grant to Dr Jean Giacomotto (2019-2021).

Finding new neuroactive drugs and characterise the neuronal effect of current medication.

In this aim, we are testing and screening diverse catalogues of molecules, from drug-like small molecules to peptides, to search for new neuroactive compounds that could be useful as either therapeutics or chemical genetic tools for our research. We are also using state-of-the-art microscopy tools such as light-sheet and super-resolution microscopy (available at QBI) coupled with calcium imaging to study and characterise the neuronal effect of current anti-psychotic and anti-depressant medication.

Side projects – Understanding and finding treatments against MND

Dr Jean Giacomotto has also been recently supported by international (CureSMA of America ; CIHR Canada) and national (MNDRIA of Australia) grant schemes to develop research models of MNDs, including spinal muscular atrophy (SMA) and amyotrophic lateral sclerosis (ALS). His group is working at manipulating genes known to be associated with those diseases to further establish stable models for both basic research and drug discovery. For more information or to be part of these projects, please contact Dr Giacomotto.

Group Publications

Research Areas

  • Schizophrenia Genetics (GWAS)
  • DNA, RNA Sequencing
  • Gene Expression and editing
  • Neuroimmunology of schizophrenia
  • Zebrafish models and functional genetics
  • Microscopy
  • Drug discovery
  • Chemical genetics
  • Statistical genomics and computational biology
  • Applications of deep learning in biomedicine

Apply for a PhD

Group Leader


Research Members


Students

NHMRC Project Grant APP1165850 (2019-2021, Prof Mowry and Dr Giacomotto) - $481,890. Investigating the neuro-developmental role of schizophrenia-associated genes using the zebrafish. 9546049-01-441-21-022840

Rebecca L. Cooper Medical Research Project Grant (2019-2021, Dr Giacomotto) - $100,000. Unveiling the pathogenic role of the schizophrenia and autism risk-gene NRXN1 in synaptogenesis. https://www.cooperfoundation.org.au/2019-grant-recipients. 9546049-01-475-21-022958

CIHR (Canadian NIH-equivalent) research grant (2018-2022, Dr Patten and Dr Giacomotto), CA$627,300 Deciphering the mechanisms of synaptic dysfunction in a genetic model of spinal muscular atrophy.

CureSMA research grant (2017-2019, Dr Giacomotto), - $101,985 - Zebrafish models of Spinal Muscular Atrophy optimized for chemical genetics and drug discovery. From proof-of-principle to new insights and treatments. http://www.curesma.org/news/grant-awarded-to-jean-giacomotto.html 9546049-01-477-21-020485

MNDRIA research grant (2017-2018, Dr Giacomotto) - $99,611.89 - New and innovative polygenic approach for understanding and modelling MNDs in zebrafish. http://www.mndaust.asn.au/Discover-our-research/Latest-research/Research-reports.aspx

Rebecca L. Cooper Grant grant (2016, Dr Giacomotto) - $23.,900 - Using the Zebrafish to fight psychiatric disorders. From proof-of-principle to new insights and treatments.

Investigating the aetiopathogenic role of autoantibodies against the M1 muscarinic acetylcholine receptor in patients with first episode of schizophrenia
(2016–2020) NHMRC Project Grant

  • GWAS analyses in Indian and Sarawak populations, comparing the results with the latest results for European-ancestry schizophrenia from the Psychiatric Genomics Consortium.
     
  • Phase 2 Indian schizophrenia GWAS using additional samples from India and UK Biobank.
     
  • Targeted resequencing analyses of a previously identified chromosomal region in an Indian sample.
     
  • Identification of de novo and transmitted mutations using whole exome sequence data from Indian family based schizophrenia cohort.
     
  • Functional characterisation of top Indian GWAS locus in zebrafish and cellular models.
     
  • Investigation of top Indian locus in NAD pathway using Indian plasma samples.
     
  • In silico Investigation of the impact of schizophrenia GWAS loci during human brain development using spatio-temporal brain gene expression data.
     
  • Using deep learning to predict disease mechanisms from GWAS in psychiatric disorders.
     
  • Developing deep learning models to predict differential binding of regulators in schizophrenia-associated loci.
     
  • Generating disease specific genetic interaction data investigate relationships between genotype and phenotype using genome-wide GWAS data.
     
  • Investigating the normal and pathogenic in vivo role of genes recently associated with brain disorders and schizophrenia in particular, using the zebrafish as research model (PhD Projects available)
     
  • Identifying new neuroactive drugs using national and international chemical libraries and the zebrafish as a screening tool  (PhD Projects available).
     
  • Understanding the cellular and molecular effect of current anti-psychotic drugs using the zebrafish and state-of-the-art microscopy technologies (PhD Projects available).

 

2019

Huckins LM1,2,3,4, Dobbyn A5,6, Ruderfer DM7, Hoffman G5,8, Wang W5,6, Pardiñas AF9, Rajagopal VM10,11,12, Als TD10,11,12, T Nguyen H5,6, Girdhar K5,6, Boocock J13, Roussos P5,6,14,8, Fromer M5,6, Kramer R15, Domenici E16, Gamazon ER7,17, Purcell S5,6,8; CommonMind Consortium; The Schizophrenia Working Group of the Psychiatric Genomics Consortium; iPSYCH-GEMS Schizophrenia Working Group, Demontis D10,11,12, Børglum AD10,11,12, Walters JTR9, O'Donovan MC9, Sullivan P18,19, Owen MJ9, Devlin B20, Sieberts SK21, Cox NJ7, Im HK22, Sklar P5,6,14,8, Stahl EA5,6,14,8 (2019). Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.

Nat Genet. 2019 Apr;51(4):659-674. Epub 2019 Mar 25.

https://doi:10.1038/s41588-019-0364-4.   

PMID:30911161   

 

Harold D1,2, Connolly S1, Riley BP3, Kendler KS3, McCarthy SE4, McCombie WR4, Richards A5, Owen MJ5, O'Donovan MC5, Walters J5; Wellcome Trust Case Control Consortium 2; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Donohoe G6, Gill M1, Corvin A1, Morris DW6 (2019). Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.

Am J Med Genet B Neuropsychiatr Genet. 2019 Apr;180(3):223-231. Epub 2019 Feb 23.

https://doi:10.1002/ajmg.b.32716.   

PMID:30801977   

 

van Erp TGM1, Walton E2, Hibar DP3, Schmaal L4, Jiang W5, Glahn DC6, Pearlson GD6, Yao N6, Fukunaga M7, Hashimoto R8, Okada N9, Yamamori H10, Clark VP11, Mueller BA12, de Zwarte SMC13, Ophoff RA14, van Haren NEM15, Andreassen OA16, Gurholt TP17, Gruber O18, Kraemer B19, Richter A19, Calhoun VD11, Crespo-Facorro B20, Roiz-Santiañez R20, Tordesillas-Gutiérrez D21, Loughland C22, Catts S23, Fullerton JM24, Green MJ25, Henskens F26, Jablensky A27, Mowry BJ28, Pantelis C29, Quidé Y25, Schall U30, Scott RJ31, Cairns MJ31, Seal M32, Tooney PA33, Rasser PE34, Cooper G34, Shannon Weickert C35, Weickert TW25, Hong E36, Kochunov P36, Gur RE37, Gur RC37, Ford JM38, Macciardi F39, Mathalon DH38, Potkin SG39, Preda A39, Fan F40, Ehrlich S41, King MD42, De Haan L43, Veltman DJ44, Assogna F45, Banaj N46, de Rossi P47, Iorio M46, Piras F45, Spalletta G48, Pomarol-Clotet E49, Kelly S50, Ciufolini S51, Radua J52, Murray R51, Marques TR51, Simmons A51, Borgwardt S53, Schönborn-Harrisberger F53, Riecher-Rössler A53, Smieskova R53, Alpert KI54, Bertolino A55, Bonvino A56, Di Giorgio A56, Neilson E57, Mayer AR42, Yun JY58, Cannon DM59, Lebedeva I60, Tomyshev AS60, Akhadov T61, Kaleda V60, Fatouros-Bergman H62, Flyckt L62; Karolinska Schizophrenia Project, Rosa PGP63, Serpa MH63, Zanetti MV63, Hoschl C64, Skoch A65, Spaniel F64, Tomecek D66, McIntosh AM67, Whalley HC57, Knöchel C68, Oertel-Knöchel V68, Howells FM69, Stein DJ70, Temmingh HS69, Uhlmann A71, Lopez-Jaramillo C72, Dima D73, Faskowitz JI74, Gutman BA75, Jahanshad N74, Thompson PM74, Turner JA76 (2019). Reply to: New Meta- and Mega-analyses of Magnetic Resonance Imaging Findings in Schizophrenia: Do They Really Increase Our Knowledge About the Nature of the Disease Process?

Biol Psychiatry. 2019 Apr 1;85(7):e35-e39. Epub 2018 Nov 22.

https://doi:10.1016/j.biopsych.2018.10.003.  

PMID:30470561   

 

2018

 

Ni G1,2, Gratten J3,4, Wray NR3,4, Lee SH5,6,7; Schizophrenia Working Group of the Psychiatric Genomics Consortium (2018). Age at first birth in women is genetically associated with increased risk of schizophrenia.

Sci Rep. 2018 Jul 5;8(1):10168.

Https://doi:10.1038/s41598-018-28160-z.

PMID:29977057    

van Erp TGM1, Walton E2, Hibar DP3, Schmaal L4, Jiang W5, Glahn DC6, Pearlson GD6, Yao N6, Fukunaga M7, Hashimoto R8, Okada N9, Yamamori H10, Bustillo JR11, Clark VP12, Agartz I13, Mueller BA14, Cahn W15, de Zwarte SMC15, Hulshoff Pol HE15, Kahn RS15, Ophoff RA16, van Haren NEM17, Andreassen OA18, Dale AM19, Doan NT20, Gurholt TP21, Hartberg CB20, Haukvik UK18, Jørgensen KN21, Lagerberg TV22, Melle I18, Westlye LT23, Gruber O24, Kraemer B24, Richter A24, Zilles D25, Calhoun VD12, Crespo-Facorro B26, Roiz-Santiañez R26, Tordesillas-Gutiérrez D27, Loughland C28, Carr VJ29, Catts S30, Cropley VL31, Fullerton JM32, Green MJ33, Henskens FA34, Jablensky A35, Lenroot RK33, Mowry BJ36, Michie PT37, Pantelis C38, Quidé Y33, Schall U39, Scott RJ40, Cairns MJ40, Seal M41, Tooney PA42, Rasser PE43, Cooper G43, Shannon Weickert C33, Weickert TW33, Morris DW44, Hong E45, Kochunov P45, Beard LM46, Gur RE46, Gur RC46, Satterthwaite TD46, Wolf DH46, Belger A47, Brown GG48, Ford JM49, Macciardi F50, Mathalon DH49, O'Leary DS51, Potkin SG50, Preda A50, Voyvodic J52, Lim KO14, McEwen S53, Yang F54, Tan Y54, Tan S54, Wang Z54, Fan F54, Chen J54, Xiang H55, Tang S55, Guo H56, Wan P56, Wei D57, Bockholt HJ58, Ehrlich S59, Wolthusen RPF60, King MD61, Shoemaker JM61, Sponheim SR62, De Haan L63, Koenders L63, Machielsen MW63, van Amelsvoort T64, Veltman DJ65, Assogna F66, Banaj N67, de Rossi P68, Iorio M67, Piras F66, Spalletta G69, McKenna PJ70, Pomarol-Clotet E70, Salvador R70, Corvin A71, Donohoe G44, Kelly S72, Whelan CD73, Dickie EW74, Rotenberg D74, Voineskos AN74, Ciufolini S75, Radua J76, Dazzan P77, Murray R75, Reis Marques T75, Simmons A75, Borgwardt S78, Egloff L78, Harrisberger F78, Riecher-Rössler A78, Smieskova R78, Alpert KI79, Wang L80, Jönsson EG81, Koops S15, Sommer IEC82, Bertolino A83, Bonvino A84, Di Giorgio A84, Neilson E85, Mayer AR61, Stephen JM61, Kwon JS86, Yun JY87, Cannon DM88, McDonald C88, Lebedeva I89, Tomyshev AS89, Akhadov T90, Kaleda V89, Fatouros-Bergman H91, Flyckt L91; Karolinska Schizophrenia Project, Busatto GF92, Rosa PGP92, Serpa MH92, Zanetti MV92, Hoschl C93, Skoch A94, Spaniel F93, Tomecek D95, Hagenaars SP96, McIntosh AM97, Whalley HC85, Lawrie SM85, Knöchel C98, Oertel-Knöchel V98, Stäblein M98, Howells FM99, Stein DJ100, Temmingh HS99, Uhlmann A101, Lopez-Jaramillo C102, Dima D103, McMahon A73, Faskowitz JI73, Gutman BA104, Jahanshad N73, Thompson PM73, Turner JA105. (2018). Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium. Biol Psychiatry. 2018 Nov 1;84(9):644-654.Epub 2018 May14 https://doi:10.1016/j.biopsych.2018.04.023                                                        PMID:29960671   

Duan J1,2, Göring HHH3, Sanders AR4,5, Moy W4,5, Freda J4, Drigalenko EI6, Kos M3, He D4, Gejman PV7,8; MGS.(2018). Transcriptomic signatures of schizophrenia revealed by dopamine perturbation in an ex vivo model. Transl Psychiatry. 2018 Aug 16;8(1):158. https://doi:10.1038/s41398-018-0216-5

PMID:30115913     

Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium. (2018). Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. Cell. 2018 Jun 14;173(7):1705-1715.e16.

https://doi:10.1016/j.cell.2018.05.046

PMID:29906448      

 

Ni G1, Moser G1; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Wray NR2, Lee SH3.(2018). Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood.

Am J Hum Genet. 2018 Jun 7;102(6):1185-1194. Epub 2018 May 10.

https://doi:0.1016/j.ajhg.2018.03.021.  

PMID:29754766     

 

Sudesh, Ravi, Thalamuthu, Anbupalam, John, Sujit, Thara, Rangaswamy, Mowry, Bryan and Munirajan, Arasamabattu Kannan (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 2018 Sep;199:189-194  Epub 2018 Mar 26.

https://doi.org/10.1016/j.schres.2018.03.028   

PMID:29599094        

 

Dzafic, Ilvana, Burianová, Hana, Martin, Andrew K. and Mowry, Bryan (2018). Neural correlates of dynamic emotion perception in schizophrenia and the influence of prior expectations. Schizophrenia Research. 2018 Dec;202:129-137  Epub 2018 Jun 14.

https://doi.org/10.1016/j.schres.2018.06.015   

PMID:29910121       

 

Dzafic, Ilvana, Burianová, Hana, Periyasamy, Sathish and Mowry, Bryan (2018). Association between schizophrenia polygenic risk and neural correlates of emotion perception. Psychiatry research: Neuroimaging. 2018 Jun 30;276:33-40. Epub 2018 Apr 25.

https://doi.org/10.1016/j.pscychresns.2018.04.005 

PMID:29723776      

 

2017

 

Lim YW1, Lo HP1, Ferguson C2, Martel N1, Giacomotto J3, Gomez GA4, Yap AS1, Hall TE5, Parton RG6.(2017). Caveolae Protect Notochord Cells against Catastrophic Mechanical Failure during Development. Curr Biol. 2017 Jul 10;27(13):1968-1981.e7. Epub 2017 Jun 22.

https://doi:10.1016/j.cub.2017.05.067

PMID:28648821   

 

Cassandra Westcott, Geoffrey Waghorn, Duncan McLean, Dixie Statham, Bryan Mowry (2017). Correlates of employment interest among adults with schizophrenia.

International Journal of Therapy and Rehabilitation 2 December 2017 Vol. 24, No. 12 Published Online:15 Dec 2017 ISSN (online): 1759-779X  

https://doi:org/10.12968/ijtr.2017.24.12.510

   

NO PMID       

 

Kelly, S., Jahanshad, N., Zalesky, A., Kochunov, P., Agartz, I., Alloza, C., Andreassen, O. A., Arango, C., Banaj, N., Bouix, S., Bousman, C. A., Brouwer, R. M., Bruggemann, J., Bustillo, J., Cahn, W., Calhoun, V., Cannon, D., Carr, V., Catts, S., Chen, J., Chen, J. -x., Chen, X., Chiapponi, C., Cho, Kl K., Ciullo, V., Corvin, A. S., Crespo-Facorro, B., Cropley, V., De Rossi, P., Diaz-Caneja, C. M., Dickie, E. W., Ehrlich, S., Fan, F. -m., Faskowitz, J., Fatouros-Bergman, H., Flyckt, L., Ford, J. M., Fouche, J. -P., Fukunaga, M., Gill, M., Glahn, D. C., Gollub, R., Goudzwaard, E. D., Guo, H., Gur, R. E., Gur, R. C., Gurholt, T. P., Hashimoto, R., Hatton, S. N., Henskens, F. A., Hibar, D. P., Hickie, I. B., Hong, L. E., Horacek, J., Howells, F. M., Hulshoff Pol, H. E., Hyde, C. L., Isaev, D., Jablensky, A., Jansen, P. R., Janssen, J., Jönsson, E. G., Jung, L. A., Kahn, R. S., Kikinis, Z., Liu, K., Klauser, P., Knöchel, C., Kubicki, M., Lagopoulos, J., Langen, C., Lawrie, S., Lenroot, R. K., Lim, K. O., Lopez-Jaramillo, C., Lyall, A., Magnotta, V., Mandl, R. C. W., Mathalon, D. H., McCarley, R. W., McCarthy-Jones, S., McDonald, C., McEwen, S., McIntosh, A., Melicher, T., Mesholam-Gately, R. I., Michie, P. T., Mowry, B., Mueller, B. A., Newell, D. T., O’Donnell, P., Oertel-Knöchel, V., Oestreich, L., Paciga, S. A., Pantelis, C., Pasternak, O., Pearlson, G., Pellicano, G. R., Pereira, A., Pineda Zapata, J., Piras, F., Potkin, S. G., Preda, A., Rasser, P. E., Roalf, D. R., Roiz, R., Roos, A., Rotenberg, D., Satterthwaite, T. D., Savadjiev, P., Schall, U., Scott, R. J., Seal, M. L., Seidman, L. J., Shannon Weickert, C., Whelan, C. D., Shenton, M. E., Kwon, J. S., Spalletta, G., Spaniel, F., Sprooten, E., Stäblein, M., Stein, D. J., Sundram, S., Tan, Y., Tan, S., Tang, S., Temmingh, H. S., Westlye, L. T., Tønnesen, S., Tordesillas-Gutierrez, D., Doan, N. T., Vaidya, J., van Haren, N. E. M., Vargas, C. D., Vecchio, D., Velakoulis, D., Voineskos, A., Voyvodic, J. Q., Wang, Z., Wan, P., Wei, D., Weickert, T. W., Whalley, H., White, T., Whitford, T. J., Wojcik, J. D., Xiang, H., Xie, Z., Yamamori, H., Yang, F., Yao, N., Zhang, G., Zhao, J., van Erp, T. G. M., Turner, J., Thompson, P. M. and Donohoe, G.  (2017). Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group. Molecular Psychiatry 2018 May;23(5):1261-1269. Epub 2017 Oct 17

https://doi.org/10.1038/mp.2017.170    

PMID:29038599

 

Benyamin, Beben, He, Ji, Zhao, Qiongyi, Gratten, Jacob, Garton, Fleur, Leo, Paul J., Liu, Zhijun, Mangelsdorf, Marie, Al-Chalabi, Ammar, Anderson, Lisa, Butler, Timothy J., Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Devine, Matthew, Edson, Janette, Fifita, Jennifer A., Furlong, Sarah, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K., Jeffree, Rosalind L., Jin, Zi-Bing, Li, Zhongshan, Li, Ting, Li, Mengmeng, Lin, Yong, Liu, Xiaolu, Marshall, Mhairi, McCann, Emily P., Mowry, Bryan J., Ngo, Shyuan T., Pamphlett, Roger, Ran, Shu, Reutens, David C., Rowe, Dominic B., Sachdev, Perminder, Shah, Sonia, Song, Sharon, Tan, Li-Jun, Tang, Lu, van den Berg, Leonard H., van Rheenen, Wouter, Veldink, Jan H., Wallace, Robyn H., Wheeler, Lawrie, Williams, Kelly L., Wu, Jinyu, Wu, Xin, Yang, Jian, Yue, Weihua, Zhang, Zong-Hong, Zhang, Dai, Noakes, Peter G., Blair, Ian P., Henderson, Robert D., McCombe, Pamela A., Visscher, Peter M., Xu, Huji, Bartlett, Perry F., Brown, Matthew A., Wray, Naomi R. and Fan, Dongsheng  (2017). Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. Nature Communications 2017 Sep 20;8(1):611.

https://doi.org/10.1038/s41467-017-00471-1   

PMID:28931804

 

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, 2017 Nov 17;9(1):97

 https://doi.org/10.1186/s13073-017-0487-0  

PMID:29149916

 

CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium*; Psychosis Endophenotypes International Consortium. * Mowry BJ listed as author under Schizophrenia Working Group of the Psychiatric Genomics Consortium (2017). Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.  Nature Genetics 2017 Jan;49(1):27-35.  RGMS ID P02644159 (grants) Epub 2016 Nov 21

 https://dx.doi.org/10.1038/ng.3725

PMID:27869829

 

Ravi Sudesh, Priya Thirunavukkarasu, R Preeti, Sujit John, Thara Rangasamy, Bryan Mowry, Arasamabattu Kannan Munirajan. (2017). Minor allele C of rs12807809 polymorphism in NRGN contributes to the severity of psychosis in patients with Schizophrenia in South Indian population. Neuroscience Letters. 2017 May 10;649:107-111.

Epub 2017 Apr 4.

 https://doi.org/10.1016/j.neulet.2017.04.008  

PMID:28389239

 

McLaughlin, Russell L., Schijven, Dick, Van Rheenen, Wouter, Van Eijk, Kriste R., O'Brien, Margaret, Kahn, Rene S., Ophoff, Roel A., Goris, An, Bradley, Daniel G., Al-Chalabi, Ammar, Van Den Berg, Leonard H., Luykx, Jurjen J., Hardiman, Orla, Veldink, Jan H., Project MinE GWAS Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Catts, Stanley V., Gratten, Jacob, Lee, S. Hong, Wray, Naomi R., Visscher, Peter M. and Mowry, Bryan J.  (2017). Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Nature Communications 2017 Mar 21;8:14774. https://doi.org/10.1038/ncomms14774    

PMID:28322246

 

Klauser P1,2,3, Baker ST2, Cropley VL1, Bousman C1,4, Fornito A1,2, Cocchi L5, Fullerton JM6,7, Rasser P8,9,10, Schall U8,9,10, Henskens F11, Michie PT8,9,10,12, Loughland C6,13, Catts SV14, Mowry B15,16, Weickert TW1,6,10,17, Shannon Weickert C1,6,10,17, Carr V10,17,18, Lenroot R6,10,17, Pantelis C1,4,10,19, Zalesky A1.(2017). White Matter Disruptions in Schizophrenia Are Spatially Widespread and Topologically Converge on Brain Network Hubs. Schizophr Bull. 2017 Mar 1;43(2):425-435.

https://doi:10.1093/schbul/sbw100.    

PMID:27535082

 

Sanders, Alan R., Beecham, Gary W., Guo, Shengru, Dawood, Khytam, Rieger, Gerulf, Badner, Judith A., Gershon, Elliot S., Krishnappa, Ritesha S., Kolundzija, Alana B., Duan, Jubao, Shi, Jianxin, Levinson, Douglas F., Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Svrakic, Dragan M., Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Freedman, Robert, Gejman, Pablo V., Bailey, J. Michael, Martin, Eden R., MGS Collaboration. (2017). Genome-wide association study of male sexual orientation. Scientific Reports 2017 Dec 7;7(1):16950.

https://doi.org/10.1038/s41598-017-15736-4  

PMID:29217827

 

Sanders, A. R., Drigalenko, E. I., Duan, J., Moy, W., Freda, J., Göring, H. H.H., Gejman, P. V., Levinson, D. F., Shi, J., Buccola, N. G., Mowry, B. J., Freedman, R., Olincy, A., Amin, F., Black, D. W., Silverman, J. M., Byerley, W. F., Cloninger, C. R. and Svrakic, D. M. Show less (2017). Transcriptome sequencing study implicates immune-related genes differentially expressed in schizophrenia: new data and a meta-analysis. Translational Psychiatry 2017 Apr 18;7(4):e1093

https://doi.org/10.1038/tp.2017.47   

PMID:28418402

 

Ragan, C.; Patel, K.; Edson, J.; Zhang, Z. H.; Gratten, J.; Mowry, B. (2017). Small non-coding RNA expression from anterior cingulate cortex in schizophrenia shows sex specific regulation.  Schizophrenia Research 2017 May;183:82-87.  RGMS ID P13952322

https://dx.doi.org/10.1016/j.schres.2016.11.024  

PMID:27916288

 

2016

 

Franke B, Stein JL, Ripke S, Anttila V, Hibar DP, van Hulzen KJ, Arias-Vasquez A, Smoller JW, Nichols TE, Neale MC, McIntosh AM, Lee P, McMahon FJ, Meyer-Lindenberg A, Mattheisen M, Andreassen OA, Gruber O, Sachdev PS, Roiz-Santianez R, Saykin AJ, Ehrlich S, Mather KA, Turner JA, Schwarz E, Thalamuthu A, Yao Y, Ho YY, Martin NG, Wright MJ, O'Donovan MC, Thompson PM, Neale BM, Medland SE, Sullivan PF & Schizophrenia Working Group of the Psychiatric Genomics Consortium [includes Gratten J LS, Wray NR, Visscher PM & Mowry BJ], (2016). Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nature Neuroscience 2016 Mar;19(3):420-431. RGMS ID P02384952 (grants) Epub 2016 Feb 1

https://doi.org/10.1038/nn.4228     

PMID:26854805

 

Bigdeli TB, Ripke S, Bacanu SA, Lee SH, Wray NR, Gejman PV, Rietschel M, Cichon S, St Clair D, Corvin A, Kirov G, McQuillin A, Gurling H, Rujescu D, Andreassen OA, Werge T, Blackwood DH, Pato CN, Pato MT, Malhotra AK, O'Donovan MC, Kendler KS, Schizophrenia Working Group of the Psychiatric Genomics Consortium [includes Gratten J LS, Visscher PM, Wray NR & Mowry BJ], & Fanous AH (2016). Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 2016 Mar;171B(2):276-89. Epub 2015 Dec 11

https://doi.org/10.1002/ajmg.b.32402

PMID:26663532

 

Giacomotto J., Carroll A., Rinkwitz S., Mowry B., Cairns MJ., Becker TS. (2016). Developmental suppression of schizophrenia-associated miR-137 alters sensorimotor function in zebrafish. Translational Psychiatry 2016 May 24;6:1-10 e818.  

https://doi.org/10.1038/tp.2016.88.   

PMID:27219344

 

Martin AK and Mowry B. (2016). Increased rare duplication burden genomewide in patients with treatment resistant schizophrenia. Psychological Medicine 2016 Feb;46(3):469-76. Epub 2015 Sep 9.

https://doi.org/10.1017/S0033291715001701    

PMID:26349998

 

Dzafic I, Martin AK, Hocking J, Mowry B, Burianova H (2016). Dynamic emotion perception and prior expectancy. Neuropsychologia 2016 Jun;86:131-40. Epub 2016 Apr 26.

https://doi.org/10.1016/j.neuropsychologia.2016.04.025   

PMID:27126841

 

Martin AK, Gibson EC, Mowry B, Robinson GA (2016). Verbal initiation,

Suppression, and Strategy Use and the Relationship with Clinical Symptoms in

Schizophrenia. J Int Neuropsychol Soc 2016 Aug;22(7):735-43. Epub 2016 Jun 22.

https://doi.org/10.1017/S1355617716000552   

PMID:27329682

 

Martin AK, Dzafic I, Robinson GA, Reutens D, Mowry B (2016). Mentalizing in schizophrenia: A multivariate functional MRI study. Neuropsychologia 2016 Dec;93(Pt A):158-166. Epub 2016 Oct 26

 https://doi.org/10.1016/j.neuropsychologia.2016.10.013   

PMID:27793657

 

Edwards, A. C., Bigdeli, T. B., Docherty, A. R., Bacanu, S., Lee, D., de Candia, T. R., Moscati, A., Thiselton, D. L., Maher, B. S., Wormley, B. K., Molecular Genetics of Schizophrenia Collaboration (MGS)*, Walsh, D., O’Neill, F. A., Kendler, K. S., Riley, B. P., Fanous, A. H. * Mowry BJ listed as author under the Molecular Genetics of Schizophrenia Consortium. (2016). Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes. Schizophrenia Bulletin, 2016 Mar;42(2):279-87. Epub 2015 Aug 27

https://doi.org/10.1093/schbul/sbv119    

PMID:26316594

 

Mehta D, Tropf F, Gratten J, Bakshi A, Zhu Z, Bacanu SA, Hemani G, Magnusson PKE, Barban N, Esko T, Metspalu A, Snieder H, Mowry BJ, Kendler KS, Yang J, Visscher PM, McGrath JJ, Mills MC, Wray NR, Lee SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium; LifeLines Cohort Study; Twins UK. (2016). Evidence for genetic overlap between schizophrenia and age at first birth in women. JAMA Psychiatry 2016 May 1;73(5):497-505   RGMS ID P02280502

https://doi.org/10.1001/jamapsychiatry.2016.0129   

PMID:27007234

 

Johnson EC, Bjelland DW, Howrigan DP, Abdellaoui A, Breen G, Borglum A, Cichon S, Degenhardt, F, Forstner AJ, Frank J, Genovese G, Heilmann-Heimbach S, Herms S, Hoffman P, Maier W, Mattheisen M, Morris D, Mowry B, Muller-Mhysok B, Neale B, Nenadic I, Nothen MM, O'Dushlaine C, Rietschel M, Ruderfer DM, Rujescu D, Schulze TG, Simonson MA, Stahl E,  Strohmaier J, Witt SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Sullivan PF, Keller, MC.  (2016). No Reliable Association Between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.  PLOS Genetics 2016 Oct 28;12(10):e1006343. RGMS ID P02490402 (grants) eCollection 2016 Oct.

https://dx.doi.org/10.1371/journal.pgen.1006343  

PMID:27792727

 

Sekar A, Bialas AR, de Rivera H, Davis A, Hammond TR, Kamitaki N, Tooley K, Presumey J, Baum M, Van Doren V, Genovese G, Rose SA, Handsaker RE; Scizophrenia Working Group of the Psychiatric Genomics Consortium*, Daly MJ, Carroll MC, Stevens B, McCarroll SA. * Mowry BJ listed as author under Schizophrenia Working Group of the Psychiatric Genomics Consortium. (2016). Schizophrenia risk from complex variation of complement component 4. Nature 2016 Feb 11;530(7589):177-83. RGMS ID P02280523 (grants) Epub 2016 Jan 27   

https://dx.doi.org/10.1038/nature16549

PMID:26814963

 

2015

 

Martin AK, Mowry B, Reutens D, Robinson GA (2015). Executive functioning in schizophrenia: Unique and shared variance with measures of fluid intelligence. Brain and Cognition 2015 Oct;99:57-67 Epub 2015 Aug 7

https://doi.org/10.1016/j.bandc.2015.07.009   

PMID:26263380

 

Martin, Andrew K, Robinson, G, Reutens, D and Mowry, B (2015). Common genetic risk variants are associated with positive symptoms and decision-making ability in patients with schizophrenia. Psychiatry Research, 2015 Sep 30;229(1-2):606-8. Epub 2015 May 29.

https://doi.org/10.1016/j.psychres.2015.04.045    

PMID:26070766

 

Martin AK, Robinson G, Reutens D and Mowry B (2015). Clinical and parental age characteristics associated with rare copy number variants in patients with schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 2015 Jul;168B(5):374-82.  Epub 2015 May 5.

 https://doi.org/10.1002/ajmg.b.32321     

PMID:25943776

 

Westcott C, Waghorn G., McLean, D., Strathan, D., Mowry, B. (2015). Role functioning among adults with schizophrenia. British Journal of Occupational Therapy March 16, 2015 78(3) 158-165.

https://doi.org/10.1177/0308022615573372     

NO PMID

 

McLean D, Barrett R, Loa P, Thara R, John S, McGrath J, Gratten J, Mowry B. (2015). Comparing schizophrenia symptoms in the Iban of Sarawak with other populations to elucidate clinical heterogeneity. Asia-Pacific Psychiatry 2015 Mar;7(1):36-44. Epub 2013 Aug 22.

https://doi.org/10.1111/appy.12093  

PMID:24038814

 

Westcott C, Waghorn G, McLean D, Statham D, Mowry B. (2015). Interest in employment among people with schizophrenia.  American Journal of Psychiatric Rehabilitation.  18 (2) 187 – 207.   RGMS ID P01870705 (grants) Published online: 09 Jun 2015

https://doi.org/10.1080/15487768.2014.954162

NO PMID

 

Yu H, Wang L, Lv L, Ma C, Du B, Lu T, Jin C, Yan H, Yang Y, Li W, Ruan Y, Zhang H, Zhang H, Mi W, Mowry B, Ma W, Li K, Zhang D, Yue W. (2015). Genome-Wide Association Study Suggested the PTPRD Polymorphisms Were Associated with Weight Gain Effects of Atypical Antipsychotic Medications.  Schizophrenia Bulletin.  2016 May;42(3):814-23. RGMS ID P02280538  Epub 2015 Dec 9 

https://doi.org/10.1093/schbul/sbv179

PMID:26656879

 

 

Maier R, Moser G, Chen GB, Ripke S, Cross-Disorder Working Group of the Psychiatric Genomics Consortium*, Coryell W, Potash JB, Scheftner WA, Shi J, Weissman MM, Hultman CM, Landén M, Levinson DF, Kendler KS, Smoller JW, Wary NR, Lee SH

* Mowry BJ listed as author under Cross-Disorder Working Group of the Psychiatric Genomics Consortium. (2015). Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder.  American Journal of Human Genetics 2015 Feb 5;96(2):283-94. RGMS ID P02283780 Epub 2015 Jan 29.

https://doi.org/10.1016/j.ajhg.2014.12.006    

PMID:25640677

 

Loh, Po-Ru, Bhatia, Gaurav, Gusev, Alexander, Finucane, Hilary K., Bulik-Sullivan, Brendan K., Pollack, Samuela J., de Candia, Teresa R., Lee, Sang Hong, Wray, Naomi R., Kendler, Kenneth S., O'Donovan, Michael C., Neale, Benjamin M., Patterson, Nick, Price, Alkes L., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Visscher, Peter M. and Mowry, Bryan J. (2015). Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis. Nature Genetics, 2015 Dec;47(12):1385-92. Epub 2015 Nov 2.

https://doi.org/10.1038/ng.3431

PMID:26523775

 

Bulik-Sullivan BK, Loh PR, Finucane HK, Ripke S, Yang J; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Patterson N, Daly MJ, Price AL, Neale BM. * Mowry BJ listed as author under Schizophrenia Working Group of the Psychiatric Genomics Consortium. (2015). LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.  Nature Genetics 2015 Mar;47(3):291-5. RGMS ID P02167678  Epub 2015 Feb 2.   

https://doi.org/10.1038/ng.3211

PMID:25642630

 

Vilhjálmsson BJ, Yang J, Finucane HK, Gusev A, Lindström S, Ripke S, Genovese G, Loh PR, Bhatia G, Do R, Hayeck T, Won HH; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) study, Kathiresan S, Pato M, Pato C, Tamimi R, Stahl E, Zaitlen N, Pasaniuc B, Belbin G, Kenny EE, Schierup MH, De Jager P, Patsopoulos NA, McCarroll S, Daly M, Purcell S, Chasman D, Neale B, Goddard M, Visscher PM, Kraft P, Patterson N, Price AL.*Mowry BJ listed under Schizophrenia Working Group of the Psychiatric Genomics Consortium. (2015). Modelling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.  American Journal of Human Genetics 2015 Oct 1;97(4):576-92

RGMS ID P02385188  

https://dx.doi.org/10.1016/j.ajhg.2015.09.001

PMID:26430803

 

Lee, S. Hong, Byrne, Enda M., Hultman, Christina M., Kahler, Anna, Vinkhuyzen, Anna A. E., Ripke, Stephan, Andreassen, Ole A., Frisell, Thomas, Gusev, Alexander, Hu, Xinli, Karlsson, Robert, Mantzioris, Vasilis X., McGrath, John J., Mehta, Divya, Stahl, Eli A., Zhao, Qiongyi, Kendler, Kenneth S., Sullivan, Patrick F., Price, Alkes L., O'Donovan, Michael, Okada, Yukinori, Mowry, Bryan J., Raychaudhuri, Soumya, Wray, Naomi R., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Rheumatoid Arthritis Consortium International and Visscher, Peter M . (2015). New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.

International Journal of Epidemiology, 2015 Oct;44(5):1706-21.  RGMS ID P02285091  

https://doi.org/10.1093/ije/dyv136    

PMID:26286434

 

The Network and Pathway Analysis Subgroup of the Psychiatric Genomics Consortium*.

* Mowry BJ listed as author under Schizophrenia Working Group of the Psychiatric Genomics Consortium. (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways.  Nature Neuroscience 2015 Feb;18(2):199-209.  RGMS ID P01916824 (grants) Epub 2015 Jan 19

https://doi.org/10.1038/nn.3922

PMID:25599223

 

Garrison, Jane R., Fernyhough, Charles, McCarthy-Jones, Simon, Haggard, Mark, The Australian Schizophrenia Research Bank, Carr, Vaughan, Schall, Ulrich, Scott, Rodney, Jablensky, Assen, Mowry, Bryan, Michie, Patricia, Catts, Stanley, Henskens, Frans, Pantelis, Christos, Loughland, Carmel and Simons, Jon S. (2015) Paracingulate sulcus morphology is associated with hallucinations in the human brain. Nature Communications, 2015 Nov 17;6:8956.  RGMS ID P02283639     https://doi.org/10.1038/ncomms9956

PMID:26573408

 

Duan, J., Sanders, A. R., Moy, W., Drigalenko, E. I., Brown, E. C., Freda, J., Leites, C., Göring H. H. H., Molecular Genetics of Schizophrenia Collaboration*, Gejman, P. V.

* Mowry BJ listed as author under Molecular Genetics of Schizophrenia Collaboration. (2015). Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants.  Human Molecular Genetics 2015 Aug 15;24(16):4674-85.   RGMS ID P02173092 Epub 2015 May 28.  

https://doi.org/10.1093/hmg/ddv199

PMID:26022996

 

Arnedo J1, Svrakic DM, Del Val C, Romero-Zaliz R, Hernández-Cuervo H; Molecular Genetics of Schizophrenia Consortium*, Fanous AH, Pato MT, Pato CN, de Erausquin GA, Cloninger CR, Zwir I.* Mowry B listed as author under the Molecular Genetics of Schizophrenia Collaboration (2015). Uncovering the hidden risk architecture of the schizophrenias: confirmation in three independent genome-wide association studies.  American Journal of Psychiatry 2015 Feb 1;172(2):139-53. RGMS ID P02285034 Epub 2014 Oct 31.

https://doi.org/10.1176/appi.ajp.2014.14040435    

PMID:25219520

 

Andreassen OA, Harbo HF, Wang Y, Thompson WK, Schork AJ, Mattingsdal M, Zuber V, Bettella F, Ripke S, Kelsoe JR, Kendler KS10, O'Donovan MC, Sklar P; The Psychiatric Genomics Consortium* (PGC) Bipolar Disorder and Schizophrenia Work Groups; The International Multiple Sclerosis Genetics Consortium (IMSGC), McEvoy LK, Desikan RS, Lie BA, Djurovic S, Dale AM. *Mowry BJ listed as author under Psychiatric Genome Consortium. (2015). Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci.  Molecular Psychiatry 2015 Feb;20(2):207-14.  RGMS ID P01834525 (grants) Epub 2014 Jan 28

https://doi.org/10.1038/mp.2013.195    

PMID:24468824

 

2014

 

Duan J, Shi J, Fiorentino A, Leites C, Chen X, Moy W, Chen J, Alexandrov BS, Usheva A, He D, Freda J, O'Brien NL; Molecular Genetics of Schizophrenia collaboration; Genomic Psychiatric Cohort consortium, McQuillin A, Sanders AR, Gershon ES, DeLisi LE, Bishop AR, Gurling HM, Pato MT, Levinson DF, Kendler KS, Pato CN, Gejman PV. * Mowry BJ listed as author under Molecular Genetics of Schizophrenia collaboration. (2014). A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder.  American Journal of Human Genetics 2014 Dec 4;95(6):744-53   RGMS ID P01916834 (grants)  Epub 2014 Nov 26.

https://doi.org/10.1016/j.ajhg.2014.11.001      

PMID:25434007

 

Jones, Amanda L., Mowry, Bryan J., McLean, Duncan E., Mantzioris, Basil X., Pender, Michael P. and Greer, Judith M. (2014). Elevated levels of autoantibodies targeting the M1 muscarinic acetylcholine receptor and neurofilament medium in sera from subgroups of patients with schizophrenia. Journal of Neuroimmunology, 2014 Apr 15;269(1-2):68-75.  Epub 2014 Feb 25.    

https://doi.org/10.1016/j.jneuroim.2014.02.008

PMID:24636402

 

Martin AK, Robinson G, Reutens D and Mowry B (2014). Cognitive and structural neuroimaging characteristics of schizophrenia patients with large, rare copy number deletions. Psychiatry Research: Neuroimaging 2014 Dec 30;224(3):311-8. Epub 2014 Oct 18.

https://doi.org/10.1016/j.pscychresns.2014.10.006     

PMID:25453991

 

Martin A, Robinson G, Dzafic I, Reutens D, Mowry B, (2014). Theory of Mind and the Social Brain: Implications for Understanding the Genetic Basis of Schizophrenia. Genes Brain & Behaviour 2014 Jan;13(1):104-17. Epub 2013 Aug 24.

https://doi.org/10.1111/gbb.12066

PMID:23927712

Martin AK, Robinson G, Reutens D and Mowry B (2014). Copy number deletion burden is associated with cognitive, structural, and resting-state network differences in patients with schizophrenia. Behavioural Brain Research 2014 Oct 1;272:324-34. Epub 2014 Jul 15.

https://doi.org/10.1016/j.bbr.2014.07.002    

PMID:25036426

 

Martin AK, Robinson G, Reutens D and Mowry B (2014). Cannabis abuse and age at onset in schizophrenia patients with large, rare copy number variants. Schizophrenia Research 2014 May;155(1-3):21-5.  Epub 2014 Mar 29.   

https://doi.org/10.1016/j.schres.2014.03.004

PMID:24685822

 

McLean D, Thara R, John S, Barrett R, Loa P, McGrath J and Mowry B (2014). DSM-IV “criterion A” schizophrenia symptoms across ethnically different populations: evidence for differing psychotic symptom content or structural organization? Culture, Medicine and Psychiatry 2014 Sep;38(3):408-26.

https://doi.org/10.1007/s11013-014-9385-8

PMID:24981830

 

Schizophrenia Working Group of the Psychiatric Genomics Consortium, Catts, Stanley V., Gratten, Jacob, Lee, S. Hong, Wray, Naomi R., Visscher, Peter M., Mowry, Bryan J., Nertney, Deborah A., Psychosis Endophenotypes International Consortium and Wellcome Trust Case-Control Consortium 2 (2014). Biological insights from 108 schizophrenia-associated genetic loci. Nature, 2014 Jul 24;511(7510):421-7. Epub 2014 Jul 22. 

https://doi.org/10.1038/nature13595    

PMID:25056061

 

Nicodemus KK, Hargreaves A, Morris D, Anney R, Gill M, Corvin A, Donohoe G; Schizophrenia Psychiatric Genome-wide Association Study (GWAS) Consortium*; Wellcome Trust Case Control Consortium 2. * Mowry BJ listed as author under the Schizophrenia Psychiatric Genome-wide Association Study (GWAS) Consortium. (2014).   Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway.  JAMA Psychiatry 2014 Jul 1;71(7):778-785. RGMS ID P02285949

https://doi.org/10.1001/jamapsychiatry.2014.528   

PMID:24828433

 

Gusev A, Lee SH, Trynka G, Finucane H, Vilhjálmsson BJ, Xu H, Zang C, Ripke S, Bulik-Sullivan B, Stahl E; Schizophrenia Working Group of the Psychiatric Genomics Consortium; SWE-SCZ Consortium, Kähler AK, Hultman CM, Purcell SM, McCarroll SA, Daly M, Pasaniuc B, Sullivan PF, Neale BM, Wray NR, Raychaudhuri S, Price AL; Schizophrenia Working Group of the Psychiatric Genomics Consortium*; SWE-SCZ Consortium. *Mowry BJ listed as author under Schizophrenia Working Group of the Psychiatric Genomics Consortium. (2014). Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.  American Journal of Human Genetics 2014 Nov 6;95(5):535-52.  RGMS ID P02285146  Epub 2014 Nov 6.   

 https://doi.org/10.1016/j.ajhg.2014.10.004

PMID:25439723

 

 

Mulle, Jennifer Gladys, Pulver, Ann E., McGrath, John A., Wolyniec, Paula S., Dodd, Anne F., Cutler, David J., Sebat, Jonathan, Malhotra, Dheeraj, Nestadt, Gerald, Conrad, Donald F., Hurles, Matthew, Barnes, Chris P., Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Mitchell, Adele A., Peter, Inga, Sklar, Pamela, O'Dushlaine, Colm T., Grozeva, Detelina, O'Donovan, Michael C., Owen, Michael J., Hultman, Christina M., Kahler, Anna K., Sullivan, Patrick F., The Molecular Genetics of Schizophrenia Consortium, Kirov, George, Warren, Stephen T. and Mowry, Bryan J.  (2014.). Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia. Biological Psychiatry 2014 Mar 1;75(5):371-7. Epub 2013 Jul 17.

https://doi.org/10.1016/j.biopsych.2013.05.040

PMID:23871472

 

2013

 

Filippich, Cheryl, Wolvetang, Ernst J. and Mowry, Bryan J. (2013). Will brain cells derived from induced pluripotent stem cells or directly converted from somatic cells (iNs) be useful for schizophrenia research?. Schizophrenia Bulletin 2013 Sep;39(5):948-54.  Epub 2013 Jul 24.

https://doi.org/10.1093/schbul/sbt103    

PMID:23884351

 

 Ripke, Stephan, O'Dushlaine, Colm, Chambert, Kimberly, Moran, Jennifer L., Kaehler, Anna K., Akterin, Susanne, Bergen, Sarah E., Collins, Ann L., Crowley, James J., Fromer, Menachem, Kim, Yunjung, Lee, Sang Hong, Magnusson, Patrik K. E., Sanchez, Nick, Stahl, Eli A., Williams, Stephanie, Wray, Naomi R., Xia, Kai, Bettella, Francesco, Borglum, Anders D., Bulik-Sullivan, Brendan K., Cormican, Paul, Craddock, Nick, de Leeuw, Christiaan, Durmishi, Naser, Gill, Michael, Golimbet, Vera, Hamshere, Marian L., Holmans, Peter, Hougaard, David M., Kendler, Kenneth S., Lin, Kuang, Morris, Derek W., Mors, Ole, Mortensen, Preben B., Neale, Benjamin M., O'Neill, Francis A., Owen, Michael J., Milovancevic, Milica Pejovic, Posthuma, Danielle, Powell, John, Richards, Alexander L., Riley, Brien P., Ruderfer, Douglas, Rujescu, Dan, Sigurdsson, Engilbert, Silagadze, Teimuraz, Smit, August B., Stefansson, Hreinn, Steinberg, Stacy, Suvisaari, Jaana, Tosato, Sarah, Verhage, Matthijs, Walters, James T., Multicenter Genetic Studies of Schizophrenia Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Control Consortium 2,, Bramon, Elvira, Corvin, Aiden P., O'Donovan, Michael C., Stefansson, Kari, Scolnick, Edward, Purcell, Shaun, McCarroll, Steven A., Sklar, Pamela, Hultman, Christina M., Sullivan, Patrick F., Mowry, Bryan J., Nertney, Deborah A. and Brown, Matthew A (2013). Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics, 2013 Oct;45(10):1150-9.  RGMS ID P11946000 (grants) Epub 2013 Aug 25      

https://doi.org/10.1038/ng.2742

PMID:23974872

 

de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, Bryan J., Goddard, Michael E., O'Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, The International Schizophrenia Consortium, The Molecular Genetics of Schizophrenia Collaboration, Visscher, Peter M., Wray, Naomi R. and Keller, Matthew C. (2013). Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. American Journal of Human Genetics, 2013 Sep 5;93(3):463-70. Epub 2013 Aug 15.   

https://doi.org/10.1016/j.ajhg.2013.07.007

PMID:23954163

 

Cross-Disorder Group of the Psychiatric Genomics Consortium*

*Mowry, Bryan J.  (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, 2013 Sep;45(9):984-94.  RGMS ID P11946002 (grants) Epub 2013 Aug 11

https://doi.org/10.1038/ng.2711

PMID:23933821

 

Gratten, Jacob, Visscher, Peter M., Mowry, Bryan J. and Wray, Naomi R. (2013). Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nature Genetics, 2013 Mar;45(3):234-8.  

https://doi.org/10.1038/ng.2555

PMID:23438595

 

Schork, Andrew J., Thompson, Wesley K., Pham, Phillip, Torkamani, Ali, Roddey, J. Cooper, Sullivan, Patrick F., Kelsoe, John R., O'Donovan, Michael C., Furberg, Helena, The Tobacco and Genetics Consortium, The Bipolar Disorder Psychiatric Genomics Consortium, The Schizophrenia Psychiatric Genomics Consortium, Schork, Nicholas J., Andreassen, Ole A., Dale, Anders M., McGrath, John J., Mowry, Bryan and Visscher, Peter (2013). All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PloS Genetics, 2013 Apr;9(4):e1003449 Epub 2013 Apr 25.   

https://doi.org/10.1371/journal.pgen.1003449

PMID:23637621

 

Andreassen OA, Djurovic S, Thompson WK, Schork AJ, Kendler KS, O'Donovan MC, Rujescu D, Werge T, van de Bunt M, Morris AP, McCarthy MI; International Consortium for Blood Pressure GWAS; Diabetes Genetics Replication and Meta-analysis Consortium; Psychiatric Genomics Consortium Schizophrenia Working Group*, *Mowry BJ listed as author under the Psychiatric Genomics Consortium Schizophrenia Working Group Roddey JC, McEvoy LK, Desikan RS, Dale AM. (2013). Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. American Journal of Human Genetics. 2013 Feb 7;92(2):197-209. Epub 2013 Jan 31.

 https://doi.org/10.1016/j.ajhg.2013.01.001    

PMID:23375658

 

Terwisscha van Scheltinga, Afke F., Bakker, Steven C., van Haren, Neeltje E. M., Derks, Eske M., Buizer-Voskamp, Jacobine E., Boos, Heleen B. M., Cahn, Wiepke, Pol, Hilleke E. Hulshoff, Ripke, Stephan, Ophoff, Roel A., Kahn, Rene S., Psychiatric Genome-wide Association Study Consortium, Mowry, Bryan J., McGrath, John J ., Nertney, Deborah A ., Brown, Matthew A., Danoy, Patrick A. and Catts, Stanley V. (2013). Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biological Psychiatry, 2013 Mar 15;73(6):525-31. Epub 2012 Oct 3.  

https://doi.org/10.1016/j.biopsych.2012.08.017

PMID:23039932

 

Terwisscha van Scheltinga, A. F., Bakker, S. C., Van Haren, N. E. M., Derks, E. M., Buizer-Voskamp, J. E., Cahn, W., Ripke, S., Ophoff, R. A., Kahn, R. S., Psychiatric Genomic-Wide Association Study (GWAS) Consortium, Visscher, P. M., Mowry, B. J., Brown, M. A. and McGrath, J. J. (2013). Schizophrenia genetic variants are not associated with intelligence. Psychological Medicine 2013 Dec;43(12):2563-70. RGMS ID P01834533 (grants) Epub 2013 Feb 15.   

https://doi.org/10.1017/S0033291713000196

PMID:23410598

 

Sanders AR, Göring HHH, Duan J, Drigalenko EI, Moy W, Freda J, He D, Shi J, *Molecular Genetics of Schizophrenia (MGS) Collaboration, Gejman PV.

*Mowry BJ listed as author under Molecular Genetics of Schizophrenia (MGS) Collaboration.  (2013). Transcriptome study of differential expression in schizophrenia. Human Molecular Genetics 2013 Dec 15;22(24):5001-14. RGMS ID P02096680 Epub 2013 Jul 30.

 https://doi.org/10.1093/hmg/ddt350            

PMID:23904455

 

Mowry, B. J. 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. Molecular Psychiatry, 2013 Jan;18(1):38-52. Epub 2012 May 1.

https://doi.org/10.1038/mp.2012.34 

PMID:22547114

 

2012

 

Fanous, Ayman H., Zhou, Baiyu, Aggen, Steven H., Bergen, Sarah E., Amdur, Richard L., Duan, Jubao, Sanders, Alan R., Shi, Jianxin, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Freedman, Robert, Dudbridge, Frank, Holmans, Peter A., Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, Ripke, Stephan, Gejman, Pablo V., Kendler, Kenneth S. and Levinson, Douglas F. (2012). Genome-Wide Association Study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms. American Journal of Psychiatry, 2012 Dec;169(12):1309-17.  

https://doi.org/10.1176/appi.ajp.2012.12020218

PMID:23212062

 

 Levinson, Douglas F., Shi, Jianxin, Wang, Kai, Oh, Sang, Riley, Brien, Pulver, Ann E., Wildenauer, Dieter B., Laurent, Claudine, Mowry, Bryan J., Gejman, Pablo V., Owen, Michael J., Kendler, Kenneth S., Nestadt, Gerald, Schwab, Sibylle G., Mallet, Jacques, Nertney, Deborah, Sanders, Alan R., Williams, Nigel M., Wormley, Brandon, Lasseter, Virginia K., Albus, Margot, Godard-Bauche, Stephanie, Alexander, Madeline, Duan, Jubao, O'Donovan, Michael C., Walsh, Dermot, O'Neill, Anthony, Papadimitriou, George N., Dikeos, Dimitris, Maier, Wolfgang, Lerer, Bernard, Campion, Dominique, Cohen, David, Jay, Maurice, Fanous, Ayman, Eichhammer, Peter, Silverman, Jeremy M., Norton, Nadine, Zhang, Nancy, Hakonarson, Hakon, Gao, Cynthia, Citri, Ami, Hansen, Mark, Ripke, Stephan, The Schizophrenia Psychiatric GWAS Consortium, Dudbridge, Frank and Holmans, Peter A. (2012). Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees. American Journal of Psychiatry, 2012 Sep;169(9):963-73.   

https://doi.org/10.1176/appi.ajp.2012.11091423

PMID:22885689

 

Ragan, Chikako, Mowry, Bryan J. and Bauer, Denis C. (2012). Hybridization-based reconstruction of small non-coding RNA transcripts from deep sequencing data. Nucleic Acids Research, 2012 Sep;40(16):7633-43. Epub 2012 Jun 16.

https://doi.org/10.1093/nar/gks505

PMID:22705792

 

Derks EM, Vorstman JA, Ripke S, Kahn RS; Schizophrenia Psychiatric Genomic Consortium*, Ophoff RA. *Mowry BJ listed as author under Schizophrenia Psychiatric Genomic Consortium. (2012). Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis. PLoS One.; 2012;7(6):e37852. Epub 2012 Jun 22.

https://doi.org/10.1371/journal.pone.0037852

PMID:22761660

 

Keller MC, Simonson MA, Ripke S, Neale BM, Gejman PV, Howrigan DP, Lee SH, Lencz T, Levinson DF, Sullivan PF; Schizophrenia Psychiatric Genome-Wide Association Study Consortium*. *Mowry BJ listed as author under Schizophrenia Genome-Wide Association Study Consortium. (2012). Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. PLoS Genetics.; 2012;8(4):e1002656. Epub 2012 Apr 12.

https://doi.org/10.1371/journal.pgen.1002656

PMID:22511889

 

 Weickert, C. S., Tiwari, Y., Schofield, P. R., Mowry, B. J. and Fullerton, J. M. (2012). Schizophrenia-associated HapICE haplotype is associated with increased NRG1 type III expression and high nucleotide diversity. Translational Psychiatry, 2012 Apr 17;2:e104. https://doi.org/10.1038/tp.2012.25  

PMID:22832904

 

McLean, Duncan, John, Sujit, Barrett, Robert, McGrath, John, Loa, Peter, Thara, Rangaswamy and Mowry, Bryan (2012). Refining clinical phenotypes by contrasting ethnically different populations with schizophrenia from Australia, India and Sarawak. Psychiatry Research, 2012 Apr 30;196(2-3):194-200.  Epub 2012 Mar 7.

https://doi.org/10.1016/j.psychres.2011.12.027     

PMID:22401968

 

McLean, Duncan, Gladman, Beverley and Mowry, Bryan (2012). Significant relationship between lifetime alcohol use disorders and suicide attempts in an Australian schizophrenia sample. Australian and New Zealand Journal of Psychiatry, 2012 Feb;46(2):132-40. https://doi.org/10.1177/0004867411433211 

PMID:22311529

 

McAuley, Erica Z., Scimone, Anna, Tiwari, Yash, Agahi, Giti, Mowry, Bryan J., Holliday, Elizabeth G., Donald, Jennifer A., Weickert, Cynthia Shannon, Mitchell, Phillip B., Schofield, Peter R. and Fullerton, Janice M. (2012). Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26. Plos One, 2012;7(5):e38172. Epub 2012 May 31. 

https://doi.org/10.1371/journal.pone.0038172

PMID:22693595

 

Richards, A. L., Jones, L., Moskvina, V., Kirov, G., Gejman, P. V., Levinson, D. F., Sanders, A. R., Molecular Genetics of Schizophrenia Collaboration, International Schizophrenia Consortium (ISC), Purcell, S., Visscher, P. M., Craddock, N., Owen, M. J., O'Donovan, M. C., Holmans, P. and Mowry, B.J. (2012). Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry, 2012 Feb;17(2):193-201 Epub 2011 Feb 22.

https://doi.org/10.1038/mp.2011.11

PMID:21339752

 

Andreassen OA, Anney RJ, Asherson P, Ashley-Koch A, Blackwood D, Boomsma DI, Breen G, Buitelaar J, Bulik CM, Cichon S, Collier D, Corvin A, Craddock N, DeLisi LE, Ebstein R, Edenberg HJ, Estivill X, Faraone SV, Farmer AE, Fernandez-Aranda F, Flint J, Foroud T, Franke B, Gelernter J, Gill M, Grabe HJ, Hamilton SP, Hickie IB, Hoogendijk W, Jablensky A, Kalaydjieva L, Kaprio J, Kas M, Keller M, Kelsoe J, Kendler KS, Kennedy M, Kent L, Klump K, Knowles JA, Levinson DF, Lewis CM, Lichtenstein P, Lucae S, Martin NG, McCarroll S, McGough J, McGrath JJ, McGuffin P, Mitchell P, Mowry B, Muglia P, Müller-Myhsok B, Neale B, Nöthen M, Nurnberger JI, Oades RD, O'Donovan M, Ophoff R, Owen M, Pato CN, Pato MT, Penninx BW, Perlis RH, Porjesz B, Posthuma D, Potash JB, Preisig M, Reichborn-Kjennerud T, Rice JP, Rietschel M, Riley B, Ripke S, Rothenberger A, Rujescu D, Santangelo SL, Schachar R, Schellenberg GD, Scherer SW, Schofield P, Schulze TG, Sklar P, Smoller JW, Stefansson H, Stefansson K, Sullivan P, Todorov A, Tozzi F, Tzeng JY, van den Oord EJ, Vorstman JA, Wang K, Weissman MM, Werge T, Wray NR, Zeggini E.  (2012). Editorial. Don't give up on GWAS. Molecular Psychiatry. 2012 Jan;17(1):2-3.  Epub 2011 Aug 9.

https://doi.org/10.1038/mp.2011.94

PMID:21826059

 

Lee SH, DeCandia TR, Ripke S, Yang J; Schizophrenia Psychiatric Genome-Wide Association Study Consortium (PGC-SCZ); International Schizophrenia Consortium (ISC); Molecular Genetics of Schizophrenia Collaboration (MGS)*, Sullivan PF, Goddard ME, Keller MC, Visscher PM, Wray NR. *Mowry BJ listed as author under the Molecular Genetics of Schizophrenia Collaboration. (2012). Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nature Genetics. 2012 Feb 19;44(3):247-50. 

 https://doi.org/10.1038/ng.1108        

PMID:22344220

 

2011

 

The Schizophrenia Psychiatric Genome- Wide Association Study (GWAS) Consortium*

*Mowry, Bryan J. (2011). Genome-wide association study identifies five new schizophrenia loci. Nature Genetics43 (10) 969-976.  

https://doi.org/10.1038/ng.940

PMID:21926974

 

Simonson, Tatum S., Xing, Jinchuan, Barrett, Robert, Jerah, Edward, Loa, Peter, Zhang, Yuhua, Watkins, W. Scott, Witherspoon, David J., Huff, Chad D., Woodward, Scott, Mowry, Bryan and Jorde, Lynn B. (2011). Ancestry of the Iban is predominantly Southeast Asian: Genetic evidence from autosomal, mitochondrial, and Y chromosomes. PLoS One6 (1)e16338.  

https://doi.org/10.1371/journal.pone.0016338  

PMID:21305013

 

Levinson, Douglas F., Duan, Jubao, Oh, Sang, Wang, Kai, Sanders, Alan R., Shi, Jianxin, Zhang, Nancy, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Kendler, Kenneth S., Freedman, Robert, Dudbridge, Frank, Pe'er, Itsik, Hakonarson, Hakon, Bergen, Sarah E., Fanous, Ayman H., Holmans, Peter A. and Gejman, Pablo V. (2011). Copy number variants in Schizophrenia: Confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. American Journal of Psychiatry, 2011 Mar;168(3):302-16.  Epub 2011 Feb 1.

https://doi.org/10.1176/appi.ajp.2010.10060876   

PMID:21285140

 

Harris, Meredith, Gladman, Beverley, Hennessy, Nicole, Lloyd, Chris, Mowry, Bryan and Waghorn, Geoffrey (2011). Reliability and validity of a measure of role functioning among people with psychiatric disabilities. Australian Occupational Therapy Journal, 2011 Jun;58(3):203-8. Epub 2011 Feb 23.   

https://doi.org/10.1111/j.1440-1630.2010.00921.x

PMID:21599686

 

Harris, Meredith, Gladman, Beverley, Hennessy, Nicole, Lloyd, Chris, Mowry, Bryan and Waghorn, Geoffrey (2011).The reliability of an education-related self-efficacy scale for people with psychiatric disabilities. Community Mental Health Journal, 2011 Apr;47(2):136-42.  Epub 2010 Feb 6.

https://doi.org/10.1007/s10597-010-9294-4   

PMID:20140644

 

Fornito, Alex, Zalesky, Andrew, Bassett, Danielle S., Meunier, David, Ellison-Wright, Ian, Yucel, Murat, Wood, Stephen J., Shaw, Karen, O'Connor, Jennifer, Nertney, Deborah, Mowry, Bryan J., Pantelis, Christos and Bullmore, Edward T. (2011). Genetic influences on cost-efficient organization of human cortical functional networks. Journal of Neuroscience, 2011 Mar 2;31(9):3261-70.   

https://doi.org/10.1523/JNEUROSCI.4858-10.2011

PMID:21368038

 

Goes FS, Rongione M, Chen YC, Karchin R, Elhaik E Bipolar Genome Study*, Potash JB. *Mowry BJ listed as author under Bipolar Genome Study. (2011). Exonic DNA sequencing of ERBB4 in bipolar disorder.  PLoS One  6 (5) e20242. RGMS ID P11078145 

https://doi.org/10.1371/journal.pone.0020242

PMID:21637803

 

Belmonte Mahon P, Pirooznia M, Goes FS, Seifuddin F, Steele J, Lee PH, Huang J, Hamshere ML Bipolar Genome Study (BiGS) Consortium*, The Wellcome Trust Case Control Consortium Bipolar Disorder Group, Depaulo JR Jr, Kelsoe JR, Rietschel M, Nöthen M, Cichon S, Gurling H, Purcell S, Smoller JW, Craddock N, Schulze TG, McMahon FJ, Potash JB, Zandi PP. *Mowry BJ listed as author under Bipolar Genome Study (BiGS) Consortium. (2011). Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.  American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 2011 Apr;156B(3):370-8. RGMS ID P11078146 Epub 2011 Feb 8

https://doi.org/10.1002/ajmg.b.31172      

PMID:21305692

 

Waghorn, Geoffrey, Harris, Meredith G., Gladman, Beverly, Hennesey, Nicole, Lloyd, Chris and Mowry, Bryan (2011). Reliability and validity of a measure of work-related subjective experiences among people with psychiatric disabilities. International Journal of Therapy and Rehabilitation 1 March 2011 18 (3) 146-155.  RGMS ID P01871551 (grants)  

https://doi.org/10.12968/ijtr.2011.18.3.146    

NO PMID 

 

2010

 

Stewart, Gavin, Sara, Grant, Harris, Meredith, Waghorn, Geoffrey, Hall, Anna, Sivarajasingam, Siva, Gladman, Beverley and Mowry, Bryan (2010). A brief measure of vocational activity and community participation: Development and reliability of the Activity and Participation Questionnaire. Australian And New Zealand Journal of Psychiatry44 (3) 258-266.   

https://doi.org/10.3109/00048670903487175

PMID:20050719

 

Sanders, Alan R., Levinson, Douglas F., Duan, Jubao, Dennis, J. Michael, Li, Rick, Kendler, Kenneth S., Rice, John P., Shi, Jianxin, Mowry, Bryan J., Amin, Farooq, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Freedman, Robert, Cloninger, C. Robert and Gejman, Pablo V. (2010). The internet-based MGS2 control sample: Self report of mental illness. American Journal of Psychiatry167 (7) 854-865. https://doi.org/10.1176/appi.ajp.2010.09071050   

PMID:20516154

 

Loughland, Carmel, Draganic, Daren, McCabe, Kathryn, Richards, Jacqueline, Nasir, Aslam, Allen, Joanne, Catts, Stanley, Jablensky, Assen, Henskens, Frans, Michie, Patricia, Mowry, Bryan, Pantelis, Christos, Schall, Ulrich, Scott, Rodney, Tooney, Paul and Carr, Vaughan (2010). Australian Schizophrenia Research Bank: A database of comprehensive clinical, endophenotypic and genetic data for aetiological studies of schizophrenia. Australian and New Zealand Journal of Psychiatry44 (11) 1029-1035.   

http://journals.sagepub.com/doi/abs/10.3109/00048674.2010.501758

PMID:21034186

 

Harris, Meredith, Gladman, Beverley, Hennessy, Nicole, Lloyd, Chris, Mowry, Bryan and Waghorn, Geoffrey (2010). Reliability of a scale of work-related self-efficacy for people with psychiatric disabilities. International Journal of Rehabilitation Research33 (2) 183-186. https://doi.org/10.1097/MRR.0b013e32832e98b8     

PMID:19561512

 

Knight, Jo, Rochberg, Nanette S., Saccone, Scott F., Nurnberger, John I., Jr., Rice, John P., NIMH Genetics Initiative Bipolar Disorder Consortium and Mowry, Bryan J. (2010). An Investigation of Candidate Regions for Association with Bipolar Disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 153B (7) 1292-1297. RGMS ID P11078144.

https://doi.org/10.1002/ajmg.b.31100

PMID:20872768

 

2009

 

Xing, J. C., Watkins, W. S., Witherspoon, D. J., Zhang, Y. H., Guthery, S. L., Thara, R., Mowry, B. J., Bulayeva, K., Weiss, R. B. and Jorde, L. B. (2009). Fine-scaled human genetic structure revealed by SNP microarrays. Genome Research19 (5) 815-825. https://doi.org/10.1101/gr.085589.108   

PMID:19411602

 

Thara, R, Srinivasan, T, John, S, Nancarrow, D, Chant, D, Holliday, E and Mowry, B (2009). Design and clinical characteristics of a homogeneous schizophrenia pedigree sample from Tamil Nadu, India. Australian And New Zealand Journal of Psychiatry43 (6) 561-570. https://doi.org/10.1080/00048670902873631    

PMID:19440889

 

Shi, Jianxin, Levison, Douglas F., Duan, Juboa, Sanders, Alan R., Zheng, Yonglan, Pe'er, Itsik, Dudbridge, Frank, Holmans, Peter A., Whittmore, Alice S, Mowry, Bryan J., Olincy, Anne, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Crowe, Raymond R., Oksenberg, Jorge R., Mirel, Daniel B., Kendler, Kenneth S., Freedman, Robert and Gejman, Pablo V. (2009). Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 460 (7256) 753-757.    

https://doi.org/10.1038/nature08192

PMID:19571809

 

O'Donovan MC, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Giegling I, Hartmann AM, Möller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Adolfsson R, Osby U, Terenius L, Jönsson EG, Cichon S, Nöthen MM, Gill M, Corvin AP, Rujescu D, Gejman PV, Kirov G, Craddock N, Williams NM, Owen MJ, Molecular Genetics of Schizophrenia Collaboration*.*Mowry BJ listed as author under the Molecular Genetics of Schizophrenia Collaboration. (2009). Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Molecular Psychiatry. 14(1) 30-36.

https://doi.org/10.1038/mp.2008.108

PMID:18813210

 

Ng MYM, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, Mowry BJ, Brzustowicz LM, Maziade M, Sklar P, Garver DL, Abecasis GR, Lerer B, Fallin MD, Gurling HMD, Gejman PV, Lindholm E, Moises HW, Byerley W, Wijsman EM, Forabosco P, Tsuang MT, Hwu HG, Okazaki Y, Kendler KS, Wormley B, Fanous A, Walsh D, O'Neill FA, Peltonen L, Nestadt G, Lasseter VK, Liang KY, Papadimitriou GM, Dikeos DG, Schwab SG, Owen MJ, O'Donovan MC, Norton N, Hare E, Raventos H, Nicolini H, Albus M, Maier W, Nimgaonkar VL, Terenius L, Mallet J, Jay M, Godard S, Nertney D, Alexander M, Crowe RR, Silverman JM, Bassett AS, Roy MA, Merette C, Pato CN, Pato MT, Roos JL, Kohn Y, Amann-Zalcenstein D, Kalsi G, McQuillin A, Curtis D, Brynjolfson J, Sigmundsson T, Petursson H, Sanders AR, Duan J, Jazin E, Myles-Worsley M, Karayiorgou M, Lewis CM. (2009).  Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry. 14(8) 774-785. 

https://doi.org/10.1038/mp.2008.135

PMID:19349958

 

Jones, Amanda L., Holliday, Elizabeth G., Mowry, Bryan J., McLean, Duncan E., McGrath, John J., Pender, Michael P. and Greer, Judith M. (2009). CTLA-4 single-nucleotide polymorphisms in a Caucasian population with Schizophrenia. Brain, Behavior and Immunity23 (3) 347-350.   

https://doi.org/10.1016/j.bbi.2008.09.008

PMID:18848621

 

Holmans, PA, Riley, B, Pulver, AE, Owen, MJ, Wildenauer, DB, Gejman, PV, Mowry, Bryan, Laurent, C, Kendler, KS, Nestadt, G, Williams, NM, Schwab, SG, Sanders, AR, Nertney, D, Mallet, J, Wormley, B, Lasseter, VK, O'Donovan, MC, Duan, J, Albus, M, Alexander, M, Godard, S, Ribble, R, Liang, KY, Norton, N, Maier, W, Papadimitriou, G, Walsh, D, Jay, M, O'Neill, A, Lerer, FB, Dikeos, D, Crowe, RR, Silverman, JM and Levinson, DF (2009). Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Molecular Psychiatry14 (8) 786-795.   

https://doi.org/10.1038/mp.2009.11

PMID:19223858

 

Holliday, EG, Nyholt, DR, Tirupati, S, John, S, Ramachandran, P, Ramamurti, M, Ramadoss, AJ, Jeyagurunathan, A, Kottiswaran, S, Smith, HJ, Filippich, C, Nertney, DA, Nancarrow, DJ, Hayward, NK, Watkins, WS, Jorde, LB, Thara, R and Mowry, BJ (2009). Strong Evidence for a Novel Schizophrenia Risk Locus on Chromosome 1p31.1 in Homogeneous Pedigrees from Tamil Nadu, India. American Journal of Psychiatry 166 (2) 206-215. https://doi.org/10.1176/appi.ajp.2008.08030442   

PMID:18829870

 

Holliday, Elizabeth G., McLean, Duncan E., Nyholt, Dale R. and Mowry, Bryan J. (2009). Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis. Archives of General Psychiatry66 (10) 1058-1067.  

https://doi.org/10.1001/archgenpsychiatry.2009.136

PMID:19805696

 

Psychiatric GWAS Consortium Coordinating Committee, Martin, N., Wray, N., Mowry, B. and Holliday, E. (2009). Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders. American Journal of Psychiatry 166 (5) 540-556. https://doi.org/10.1176/appi.ajp.2008.08091354

PMID:19339359

 

Mahon, Pamela Belmonte, Payne, Jennifer L., MacKinnon, Dean F., Mondimore, Francis M., Goes, Fernando S., Schweizer, Barbara, Jancic, Dubravka, NIMH Genetics Initiative Bipolar Disorder Consortium, BiGS Consortium, Coryell, William H., Holmans, Peter A., Shi, Jianxin, Knowles, James A., Scheftner, William A., Weissman, Myrna M., Levinson, Douglas F., DePaulo, J. Raymond, Jr., Zandi, Peter P., Potash, James B. and Mowry, Bryan (2009). Genome-Wide Linkage and Follow-Up Association Study of Postpartum Mood Symptoms. American Journal of Psychiatry 166 (11) 1229-1237. https://doi.org/10.1176/appi.ajp.2009.09030417

PMID:19755578

 

2008

 

Watkins, W. S., Thara, R., Mowry, B. J., Zhang, Y., Witherspoon, D. J., Tolpinrud, W., Bamshad, M. J., Tirupati, S., Padmavati, R., Smith, H., Nancarrow, D., Filippich, C. and Jorde, L. B. (2008). Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms. BMC Genetics9:86.   

https://doi.org/10.1186/1471-2156-9-86

PMID:19077280

 

Sanders, Alan R, Duan, Jubao, Levinson, Douglas F, Jianxin, Shi, He, Deli, Hou, Cuiping, Burrell, Gregory J, Rice, John P, Nertney, Deborah A, Olincy, Ann, Rozic, Pablo, Vinogradov, Sophia, Buccola, Nancy, G and Mowry, Bryan (2008). No significant Association of 14 Candidate Genes with Schizophrenia in a Large European Ancestry Sample: Implications for Psychiatric Genetics. American Journal of Psychiatry165 (4) 497-506.   

https://doi.org/10.1176/appi.ajp.2007.07101573

PMID:18198266

 

O’Donovan, Michael C., Craddock, Nicholas, Norton, Nadine, Williams, Hywel, Peirce, Timothy, Moskvina, Valentina, Nikolov, Ivan, Hamshere, Marian, Carroll, Liam, Georgieva, Lyudmila, Dwyer, Sarah, Holmans, Peter, Marchini, Johnthan L., Spencer, Chris C. A., Howie, Bryan, Leung, Hin-Tak, Hartmann, Annette M., Moller, Hans-Jurgen, Morris, Derek W., Shi, YongYong, Feng, GuoYin, Hoffmann, Per, Propping, Peter, Vasilescu, Catalina, Maier, Wolfgang, Rietschel, Marcella, Zammit, Stanley, Schumacher, Johannes, Quinn, Emma M., Schulze, Thomas G., Williams, Nigel M., Giegling, Ina, Iwata, Nakao, Ikeda, Masashi, Darvasi, Ariel, Shifman, Sagiv, He, Lin, Duan, Jubao, Sanders, Alan R., Levinson, Douglas F., Gejman, Pablo V., Molecular Genetics of Schizophrenia, Cichon, Sven, No¨then, Markus M., Gill, Michael, Corvin, Aiden, Rujescu, Dan, Kirov, George, Owen, Michael J. and Mowry, Bryan (2008). Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nature Genetics40 (9) 1053-1055.   

https://doi.org/10.1038/ng.201

PMID:18677311

 

Matigian, Nicholas A., McCurdy, Richard D., Feron, Francois, Perry, Christopher, Smith, Heather, Filippich, Cheryl, McLean, Duncan, McGrath, John J., Mackay-Sim, Alan, Mowry, Bryan and Hayward, Nicholas K. (2008). Fibroblast and lymphoblast gene expression profiles in schizophrenia: Are non-neural cells informative? PLoS One3(6): e2412.

https://doi.org/10.1371/journal.pone.0002412

PMID:18545665

 

Holliday, E. G., Mowry, B. J. and Nyholt, D. R. (2008). A Reanalysis of 409 European-Ancestry and African American Schizophrenia Pedigrees Reveals Significant Linkage to 8p23.3 With Evidence of Locus Heterogeneity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics147B (7) 1080-1088.   

https://doi.org/10.1002/ajmg.b.30722

PMID:18361422

 

2007

 

McRae, A. F., Matigian, N. A., Vadlamudi, L., Mulley, J. C., Mowry, B., Martin, N. G., Berkovic, S. F., Hayward, N. K. and Visscher, P. M. (2007). Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines. Human Molecular Genetics16 (4) 364-373.    

https://doi.org/10.1093/hmg/ddl456

PMID:17164263

 

Matigian, N., Windus, L., Smith, H., Fillipich, C., Pantelis, C., McGrath, J. J., Mowry, B. and Hayward, N. (2007). Expression profiling in monozygotic twins discordant for bipolar disorder reveals dysregulation of the WNT signalling pathway. Molecular Psychiatry12 (9) 815-825.   

https://doi.org/10.1038/sj.mp.4001998

PMID:17440432

 

2006

 

Suarez, Brian K., Duan, Jubao, Sanders, Alan R., Hinrichs, Anthony L., Jin, Carol H., Hou, Cuiping, Buccola, Nancy G., Hale, Nancy, Weilbaecher, Ann N., Nertney, Deborah A., Olincy, Ann, Green, Susan, Schaffer, Arthur W., Smith, Christopher J., Hannah, Dominique E., Rice, John P., Cox, Nancy J., Martinez, Maria, Mowry, Bryan J., Amin, Farooq, Silverman, Jeremy M., Black, Donald W., Byerley, William F., Crowe, Raymond R., Freedman, Robert C., Cloninger, Robert, Levinson, Douglas F. and Gejman, Pablo V. (2006). Genomewide Linkage Scan of 409 European-ancestry and African American Families with Schizophrenia: Suggestive Evidence of Linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the Combined Sample. American Journal of Human Genetics78 (2) 315-333.  

https://doi.org/10.1086/500272

PMID:16400611

 

Rose, Stephen E., Chalk, Jonathan B., Janke, Andrew L., Strudwick, Mark W., Windus, Louisa C., Hannah, Dominique E., McGrath, John J., Pantelis, Christos, Wood, Stephen J. and Mowry, Bryan J. (2006). Evidence of altered prefrontal-thalamic circuitry in schizophrenia: An optimised diffusion MRI study. NeuroImage32 (1) 16-22. https://doi.org/10.1016/j.neuroimage.2006.03.003    

PMID:16626974

 

Richards, A. A., Hickman, I. J., Wang, A. Y. H., Jones, A. L., Newell, F., Mowry, B. J., Whitehead, J. P., Prins, J. B. and Macdonald, G. A. (2006). Olanzapine treatment is associated with reduced high molecular weight adiponectin in serum: A potential mechanism for Olanzapine-induced insulin resistance in patients with schizophrenia. Journal of Clinical Psychopharmacology26 (3) 232-237.    

https://doi.org/10.1097/01.jcp.0000218404.64619.52

PMID:16702887

 

Mah, S., Nelson, M. R., DeLisi, L. E., Reneland, R. H., Markward, N., James, M. R., Nyholt, D. R., Hayward, N., Handoko, H., Mowry, B., Kammerer, S. and Braun, A. (2006). Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia. Molecular Psychiatry11 (5) 471-478.   

https://doi.org/10.1038/sj.mp.4001785

PMID:16402134

 

Holliday, Elizabeth G., Handoko, Herlina Y., James, Michael R., McGrath, J. J., Nertney, Deborah A., Tirupati, Sujit, Thara, Rangaswamy, Levinson, Douglas F., Hayward, Nicholas K., Mowry, Bryan J. and Nyholt, Dale R. (2006). Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples. Twin Research and Human Genetics9 (4) 531-539.    

https://doi.org/10.1375/183242706778025035

PMID:16899160

 

Handoko, H., Nancarrow, D.J., Mowry, B.J. and McGrath, J.J. (2006). Polymorphisms in the vitamin D receptor and their associations with risk of schizophrenia and selected anthropometric measures. American Journal of Human Biology18 (3) 415-417.

https://doi.org/10.1002/ajhb.20504

PMID:16634022

 

2005

 

Jones, Amanda L., Mowry, Bryan J., Pender, Michael P. and Greer, Judith M. (2005). Immune Dysregulation and Self-Reactivity in Schizophrenia: Do Some Cases of Schizophrenia Have an Autoimmune Basis? Immunology and Cell Biology83 (1) 9-17. https://doi.org/10.1111/j.1440-1711.2005.01305.x   

PMID:15661036

 

Holliday, Elizabeth, Mowry, Bryan, Chant, David and Nyholt, Dale (2005). The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data. Human Genetics117 (2-3) 160-167.   

https://doi.org/10.1007/s00439-005-1282-3

PMID:15843988

 

Handoko, H. Y., Nyholt, D. R., Hayward, N. K., Nertney, D. A., Hannah, D. E., Windus, L. C., McCormack, C. M., Smith, H. J., Filippich, C., James, M. R. and Mowry, B. J. (2005). Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia. Molecular Psychiatry10 (6) 589-597.   

https://doi.org/10.1038/sj.mp.4001606

PMID:15505638

 

Barrett, Robert, Loa, Peter, Jerah, Edward, Nancarrow, Derek, Chant, David and Mowry, Bryan (2005). Rates of treated schizophrenia and its clinical and cultural features in the population isolate of the Iban of Sarawak: a tri-diagnostic approach. Psychological Medicine35 (2) 281-293.    

https://doi.org/10.1017/S0033291704002880

PMID:15841685

 

McGrath, John, Mowry, Bryan and Whiteford, Harvey (2005). Queensland Centre for Mental Health Research: the first 17 years. Australian And New Zealand Journal of Psychiatry39 (7) 533-541.   

https://doi.org/10.1080/j.1440-1614.2005.01624.x

PMID:15996133

 

Levinson, D. F., Murphy-Eberenz, K., Rice, J. P., Amin, F., Buccola, N., Silverman, J. M., Byerley, W., Olincy, A., Black, D. W., Mowry, B. J., Cloninger, C. R. and Gejman, P. V. (2005). Dimensions of psychotic illness in schizophrenia pedigrees. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 138B (1) 125-125.

https://espace.library.uq.edu.au/view/UQ:75318

https://insights.ovid.com/american-medical-genetics/ajmga/2009/09/050/dimensions-psychotic-illness-schizophrenia/451/01445366

NO PMID OR DOI

 

Gejman, P. V., Mowry, B., Freedman, R., Levinson, D. F., Amin, F., Silverman, J. M., Cloninger, C. R., Black, D. W., Byerley, W. F., Crowe, R. R., Hinrichs, A. L., Sanders, A. R., Jin, C. H., Duan, J. and Buccola, N. G.  (2005). Genome-wide scan for schizophrenia in the molecular genetics of schizophrenia (MGS1) collaboration pedigrees suggests linkage in 8p23.3-p12 and 11p11.2-q22.3. results of fine mapping. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 138B (1) 7-7.

 https://espace.library.uq.edu.au/view/UQ:75473

https://insights.ovid.com/american-medical-genetics/ajmga/2005/09/050/genome-wide-scan-schizophrenia-molecular-genetics/17/01445366

NO PMID OR DOI

 

2004

 

Mowry BJ, Holmans PA, Pulver AE, Gejman PV, Riley B, Williams NM, Laurent C, Schwab SG, Wildenauer DB, Bauche S, Owen MJ, Wormley B, Sanders AR, Nestadt G, Liang KY, Duan J, Ribble R, Norton N, Soubigou S, Maier W, Ewen-White KR, deMarchi N, Carpenter B, Walsh D, Williams H, Jay M, Albus M, Nertney DA, Papadimitriou G, O'Neill A, O'Donovan MC, Deleuze JF, Lerer FB, Dikeos D, Kendler KS, Mallet J, Silverman JM, Crowe RR, Levinson DF. (2004). Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry9 (8) 784-795.     

https://doi.org/10.1038/sj.mp.4001481    

PMID:15007391

 

Handoko, HY, Nyholt, DR, Thara, R, Srinivasan, TN, Nertney, DA, Smith, HJ, Filippich, CF, Hannah, DE, McGrath, JJ, Sujit, KJ, Giri, KP and Mowry, BJ (2004). An analysis of DTNBP1 (dysbindin) in Australian and Indian populations. American Journal of Medical Genetics Part B-neuropsychiatric Genetics130B (1) 133-133.

https://espace.library.uq.edu.au/view/UQ:41717

NO PMID OR DOI

 

Duan, JB, Martinez, M, Sanders, AR, Hou, CP, Saitou, N, Kitano, T, Mowry, BJ, Crowe, RR, Silverman, JM, Levinson, DF and Gejman, PV (2004). Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia. American Journal of Human Genetics, 2004 Oct;75(4):624-38. Epub 2004 Aug 24.    

https://doi.org/10.1086/424887

PMID:15329799

 

2003

 

Saha, Sukanta, Loesch, Danuta, Chant, David, Welham, Joy, El-Saadi, Ossama, Fañanás, Lourdes, Mowry, Bryan and McGrath, John (2003). Directional and fluctuating asymmetry in finger and a-b ridge counts in psychosis: A case-control study. BMC Psychiatry3:3.

https://doi.org/10.1186/1471-244X-3-3

PMID:12659652

 

McGrath, J. J., Eyles, Darryl Walter, Mowry, Bryan, Yolken, R. and Buka, S. (2003). Low maternal vitamin D as a risk factor for schizophrenia: a pilot study using banked sera. Schizophrenia Research63 (1 – 2) 73-78.   

https://doi.org/10.1016/S0920-9964(02)00435-8

PMID:12892860

 

Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HMD, Lindholm E, Coon H, Moises HW, Byerley W, Shaw SH, Mesen A, Sherrington R, O'Neill FA, Walsh D, Kendler KS, Ekelund J, Paunio T, Lonnqvist J, Peltonen L, O'Donovan MC, Owen MJ, Wildenauer DB, Maier W, Nestadt G, Blouin JL, Antonarakis SE, Mowry BJ, Silverman JM, Crowe RR, Cloninger CR, Tsuang MT, Malaspina D, Harkavy-Friedman JM, Svrakic DM, Bassett AS, Holcomb J, Kalsi G, McQuillin A, Brynjolfson J, Sigmundsson T, Petursson H, Jazin E, Zoega T, Helgason T. (2003). Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. American Journal of Human Genetics73 (1) 34-48.   

https://doi.org/10.1086/376549

PMID:12802786

 

Handoko, H. Y., Nancarrow, D. J., Hayward, N. K., Ohaeri, J. U., Aghanwa, H., McGrath, J. J., Levinson, D. F., Johns, C., Walters, M. K., Nertney, D. A., Srinivasan, T. N., Thara, R. and Mowry, B. J. (2003). Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia-Pacific region. American Journal of Medical Genetics Part B - Neuropsychiatric Genetics121B (1) 1-6.   

https://doi.org/10.1002/ajmg.b.20059

PMID:12898567

 

Duan, J., Sanders, A. R., Vander Molen, J., Martinolich, L., Mowry, B. J., Levinson, D. F., Crowe, R. R., Silverman, J. M. and Gejman, P. V. (2003). Polymorphisms in the 5 '-untranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression. Molecular Psychiatry8 (11) 901-910.   

https://doi.org/10.1038/sj.mp.4001403

PMID:14593427

 

 Mowry, B. J. (2003). Psychiatric genetics in Australia. Psychiatric Genetics13 (3) 131-141. https://doi.org/10.1097/00041444-200309000-00001        

PMID:12960744

 

2002

 

McGrath, J. J., El-Saadi, O., Grim, V., Cardy, S., Chapple, B., Chant, D., Lieberman, D. and Mowry, B. (2002). Minor physical anomalies and quantitative measures of the head and face in patients with psychosis. Archives of General Psychiatry59 (5) 458-464.    

https://doi.org/10.1001/archpsyc.59.5.458

PMID:11982450

 

Levinson, Douglas F., Mowry, Bryan J., Escamilla, Michael A. and Faraone, Stephen V. (2002). The Lifetime Dimensions of Psychosis Scale (LDPS): description and interrater reliability. Schizophrenia Bulletin28 (4) 683-695.   

https://doi.org/10.1093/oxfordjournals.schbul.a006972

PMID:12795498

 

Chant D, Mowry B, and McGrath, J. (2002). Assessing the co-segregation of disorders within pedigrees: a comparison of two methods. Australasian Epidemiologist. 9 (1)29-33.  

https://search.informit.com.au/documentSummary;res=IELNZC;dn=432440664764460

 NO PMID OR DOI

 

Levinson, Douglas F., Holmans, Peter A., Laurent, Claudine, Mallet, Jacques, Riley, Brien, Kendler, Kenneth S., Pulver, Ann E., Gejman, Pablo V., Sanders, Alan R., Schwab, Sibylle G., Wildenauer, Dieter B., Owen, Michael J. and Mowry, Bryan J. (2002). Is Schizophrenia Linked to Chromosome 1q? (Response to Technical Comments). Science 298 (5602) 2277 - 2279.    

https://doi.org/10.1126/science.298.5602.2279o

NO PMID

 

Levinson DF, Holmans PA, Laurent C, Riley B, Pulver AE, Gejman PV, Schwab SG, Williams NM, Owen MJ, Wildenauer DB, Sanders AR, Nestadt G, Mowry BJ, Wormley B, Bauche S, Soubigou S, Ribble R, Nertney DA, Liang KY, Martinolich L, Maier W, Norton N, Williams H, Albus M, Carpenter EB, deMarchi N, Ewen-White KR, Walsh D, Jay M, Deleuze JF, O'Neill FA, Papadimitriou G, Weilbaecher A, Lerer B, O'Donovan MC, Dikeos D, Silverman JM, Kendler KS, Mallet J, Crowe RR, Walters M. (2002). No Major Schizophrenia Locus Detected on Chromosome 1q in a Large Multicenter Sample. Science296 (5568) 739-741. https://doi.org/10.1126/science.1069914    

PMID:11976456

 

Mowry BJ.  (2002). Finding disease genes in schizophrenia. Today's Life Science 14 (5) 34-38. RGMS ID P01871554   

NO PMID OR DOI

 

Mowry BJ, Nancarrow DJ, O'Haeri J, Walters MK, Nertney DA, Hayward NK, Ott J, Gordon D. (2002). The analysis of four candidate chromosomal regions in two schizophrenia datasets from Fiji.  American Journal of Medical Genetics 114 (7) 862-862.

RGMS ID P_9881079    

https://espace.library.uq.edu.au/view/UQ:314248

NO PMID OR DOI

 

Mowry, B (2002). Gene-finding approaches in psychosis. Aust. And NZ J of Psychiatry. 36, (6) (A30-A30)

NO PMID OR DOI

Sanders, AR, Martinez, M, Martinolich, L, Carpenter, EB, Duan, J, Mowry, BJ, Levinson, DF, Crowe, RR, Silverman, JM and Gejman, PV (2002). Linkage disequilibrium analysis of 6ql3-q26 schizophrenia candidate genes. American Journal of Human Genetics 71 (4) 473-473.

https://espace.library.uq.edu.au/view/UQ:314258

NO PMID OR DOI

 

McGrath, J, Eyles, D, Mowry, B, Yolken, R and Buka, S (2002). Low maternal vitamin D as a risk factor for schizophrenia: A pilot study using banked sera. Schizophrenia Research 53 (3) 228-229.

 https://espace.library.uq.edu.au/view/UQ:290740

NO PMID OR DOI

 

Saha, S., Chapple, B., Cardy, S., Chant, D., Mowry, B. and McGrath, J. (2002). The presence of quasi-psychotic phenomena is associated with minor physical anomalies and craniofacial measures in well controls. Schizophrenia Research. 53 (3) Supp 1: 1-269.

https://doi.org/10.1016/S0920-9964(01)00381-4

NO PMID

 

2001

 

Sanders, A. R., Cao, Q., Taylor, J., Levin, T., Badner, J. A., Cravchik, A., Comeron, J. M., Naruya, S., Del Rosario, A., Salvi, D., Walczyk, K., Mowry, B., Levinson, D. F., Crowe, R. R., Silverman, J. M. and Gejman, P. V. (2001). Genetic diversity of the human serotonin receptor 1B (HTR1B) gene. Genomics, 2001 Feb 15;72 (1) 1-14.    

https://doi.org/10.1006/geno.2000.6411

PMID:11247661

 

McGrath, J. J., El-SaadiO, CardyS, ChappleB, ChantD and MowryB (2001). Urban birth and migrant status as risk factors for psychosis: An Australian case-control study. Social Psychiatry and Psychiatric Epidemiology36 (11) 533-536.   

https://doi.org/10.1007/s001270170003

PMID:11824847

 

Mowry, B. J. and Nancarrow, D. J. (2001). Molecular genetics of schizophrenia. In: Clinical and Experimental Pharmacology and Physiology. 2001 Jan-Feb;28(1-2):66-69

https://doi.org/10.1046/j.1440-1681.2001.03399.x  

PMID:11153540

 

2000

 

Nancarrow, Derek J., Levinson, Douglas F., Taylor, Jennifer M., Hayward, Nicholas K., Walters, Marilyn K., Lennon, David P., Nertney, Deborah A., Jones, Helen L., Mahtani, Melanie M., Kirby, Andrew, Kruglyak, Leonid, Brown, Donna M., Crowe, Raymond R., Andreasen, Nancy C., Black, Donald W., Silverman, Jeremy M., Mohs, Richard C., Siever, Larry J., Endicott, Jean, Sharpe, Lawrence and Mowry, Bryan J. (2000). No support for linkage to the bipolar regions on chromosomes 4p, 18p, or 18q in 43 schizophrenia pedigrees. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics96 (2) 224-227.    

https://doi.org/10.1002/(SICI)1096-8628(20000403)96:2<224::AID-AJMG19>3.0.CO;2-2

PMID:10893501

 

Mowry BJ, Ewen KR, Nancarrow DJ, Lennon DP, Nertney DA, Jones HL, O'Brien MS, Thornley CE, Walters MK, Crowe RR, Silverman JM, Endicott J, Sharpe L, Hayward NK, Gladis MM, Foote SJ, Levinson DF. (2000). Second stage of a genome scan of schizophrenia: Study of five positive regions in an expanded sample. American Journal of Medical Genetics. 96 (6) 864-869.   

https://doi.org/10.1002/1096-8628(20001204)96:6%3C864::AID-AJMG35%3E3.0.CO;2-D

PMID:11121199

 

Levinson, D. F., Holmans, P., Straub, R. E., Owen, M. J., Wildenauer, D.B., Gejman, P. V., Pulver, A. E., Laurent, C., Kendler, K., Walsh, D. S., Norton, N., Williams, N. I., Schwab, S.G., Lerer, B., Mowry, B., Sanders, A. R., Antonarakis, S. E., Blouin, J. L., DeLeuze, J. L. and Mallet, J. (2000). Multicentre linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group 111. American Journal of Human Genetics67 (3) 652-663.      

https://doi.org/10.1086/303041

PMID:10924404

 

Ewen, K. R., Bahlo, M., Treloar, S. A., Levinson, D. F., Mowry, B., Barlow, J. W. and Foote, S. J. (2000). Identification and analysis of error types in high-throughput genotyping. American Journal of Human Genetics67 (3) 727-736.    

https://doi.org/10.1086/303048

PMID:10924406

 

Daniels, B. A., Kirkby, K. C., Mitchell, P., Hay, D. and Mowry, B. (2000). Seasonal variation in hospital admission for bipolar disorder, depression and schizophrenia in Tasmania. Acta Psychiatrica Scandinavica102 (1) 38-43.    

https://doi.org/10.1034/j.1600-0447.2000.102001038.x

PMID:10892608  

 

McGrath, J., Grim, V., Cardy, S., Chapple, B. and Mowry, B. (2000). Dysmorphogenesis in psychosis: Quantitative and qualitative measures involving the head and face.  Schizophrenia Research.  41 (1) 84.

https://doi.org/10.1016/S0920-9964(00)90498-5

NO PMID

 

McGrath, J. J., White, P., Mowry, B., Chant, D. C., Slate, T. and Andrews, G. (2000). Endorsement of CIDI psychosis screening items in the Australian Survey of mental Health and Well Being. Schizophrenia Research. 41 (1) 44.

https://doi.org/10.1016/S0920-9964(00)90395-5

NO PMID

 

Levinson, DF, Ewen, KR, Bahlo, M, Treloar, SA, Mowry, B, Barlow, JW and Foote, SJ (2000). Estimating genotyping error rate in a fine-mapping project. Am J of Med Genetics 96, (4) 570-571.

https://espace.library.uq.edu.au/view/UQ:314276

NO PMID OR DOI

 

Sanders, AR, Cao, Q, Taylor, J, Levin, TE, Badner, JA, Cravchik, A, Cameron, JM, Naruya, S, Del Rosario, A, Salvi, DA, Walczyk, KA, Goldin, LR, Mowry, BJ, Levinson, DF, Crowe, RR, Silverman, JM and Gejman, PV  (2000). Genetic diversity of the human serotonin receptor 1B (HTR1B). Am J of Med Genetics 96, (4) 564.

https://espace.library.uq.edu.au/view/UQ:314273

NO PMID OR DOI

 

McGrath, J. J., Cardy, S., Chapple, B. and Mowry, B. (2000). Increased risk of psychosis in rural-born individuals: an Australian Catchement-area Study. Schizophrenia Research. 41 (1) 20.

 https://doi.org/10.1016/S0920-9964(00)90346-3

NO PMID

 

Mowry, B, Nancarrow, D, Ohaeri, J, Gordon, D and Ott, J (2000). Multi-allelic TDT simulation study of indigenous Fijian families with psychosis. Am J of Med Genetics. 96 (4) 549-550.

https://espace.library.uq.edu.au/view/UQ:314254

NO PMID

 

McGrath, J., De Leacy, E., Scheurer, R., Cardy, S. and Mowry, B. (2000). The continuum of quasi-psychotic beliefs and experiences in the Australian general public. Schizophrenia Research. 41 (1) 82.

https://doi.org/10.1016/S0920-9964(00)90493-6

NO PMID

 

1999

 

Martinez, M, Goldin, LR, Cao, QH, Zhang, J, Sanders, AR, Nancarrow, DJ, Taylor, JM, Levinson, DF, Kirby, A, Crowe, RR, Andreasen, NC, Black, DW, Silverman, JM, Lennon, DP, Nertney, DA, Brown, DM, Mowry, BJ, Gershon, ES and Gejman, PV (1999). Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q. American Journal of Medical Genetics88 (4) 337-343.    

https://doi.org/10.1002/(SICI)1096-8628(19990820)88:4<337::AID-AJMG9>3.0.CO;2-A

PMID:10402499

 

Levinson, DF, Mowry, BJ, Ewen, K, Nancarrow, DJ, Hayward, NK, Crowe, RR, Andreasen, NC, Black, DW, Silverman, JM, Endicott, J, Sharpe, L, Mohs, RC, Siever, LJ, Walters, MK, Lennon, DP, Nertney, DA and Foote, SJ (1999). Genome scan of schizophrenia: Results of genotyping of positive regions. Molecular Psychiatry. 4 (S37-S37).

https://espace.library.uq.edu.au/view/UQ:314261

NO PMID OR DOI

 

Kirkby, KC, Daniels, BA, Hay, DA and Mowry, BJ (1999). Was the pen mightier than the computer? Tasmanian hospital admission registers in the mid-nineteenth century. Aust. and NZ J of Psychiatry. Vol 33, A20

https://espace.library.uq.edu.au/view/UQ:314283

NO PMID OR DOI

 

1998

 

Vallada H, Curtis D, Sham P, Kunugi H, Zhao JH, Murray R, McGuffin P, Nanko S, Owen M, Gill M, Collier DA, Antonarakis S, Housman D, Kazazian H, Nestadt G, Pulver AE, Straub RE, MacLean CJ, Walsh D, Kendler KS, DeLisi L, Polymeropoulos M, Coon H, Byerley W, Lofthouse R, Gershon E, Goldin L, Freedman R, Laurent C, Bodeau-Pean S, d'Amato T, Jay M, Campion D, Mallet J, Wildenauer DB, Lerer B, Albus M, Ackenheil M, Ebstein RP, Hallmayer J, Maier W, Gurling H, Kalsi G, Brynjolfsson J, Sigmundson T, Petursson H, Blackwood D, Muri W, StClair D, He L, Maguire S, Moises HW, Hwu HG, Yang L, Wiese C, Kristbjarnarson H, Levinson DF, Mowry BJ, Donis-Keller H, Hayward NK, Crowe RR, Silverman JM, Nancarrow DJ, Read CM, Schizophrenia Collaborative Linkage Grp C.(1998). A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Research. 32 (2) 115-121.

https://DOI.org/10.1016/S0920-9964(98)00048-6

PMID:9713907

 

Mowry, BJ and Lennon, DP (1998). Puerperal psychosis: associated clinical features in a psychiatric hospital mother-baby unit. Australian and New Zealand Journal of Psychiatry32 (2) 287-290.      

https://doi.org/10.3109/00048679809062741

PMID:9588309

 

Levinson DF, Mahtani MM, Nancarrow DJ, Brown DM, Kruglyak L, Kirby A, Hayward NK, Crowe RR, Andreasen NC, Black DW, Silverman JM, Endicott J, Sharpe L, Mohs RC, Siever LJ, Walters MK, Lennon DP, Jones HL, Nertney DA, Daly MJ, Gladis M, Mowry BJ. (1998). Genome scan of schizophrenia. American Journal of Psychiatry. 155 (6) 741-750. 

https://ajp.psychiatryonline.org/doi/abs/10.1176/ajp.155.6.741   

PMID:9619145

 

Jones IH, Hay DA, Kirkby KC, Daniels BA, Mowry BJ. (1998). Response to E. Fuller Torrey's comments on 'Season of birth and schizophrenia in Tasmania'. Australian and New Zealand Journal of Psychiatry. 32 (1) 137-138.

https://espace.library.uq.edu.au/view/UQ:314278

NO PMID OR DOI

 

Kirkby, KC, Hay, DA, Daniels, BA, Jones, IH and Mowry, BJ (1998). Comparison between register and structured interview diagnoses of schizophrenia: a case for longitudinal diagnostic profiles. Australian and New Zealand Journal of Psychiatry32 (3) 410-414. https://doi.org/10.3109/00048679809065535       

PMID:9672732

 

Daniels, BA, Kirkby, KC, Hay, DA, Mowry, BJ and Jones, IH (1998). Predictability of rehospitalisation over 5 years for schizophrenia, bipolar disorder and depression. Australian and New Zealand Journal of Psychiatry32 (2) 281-286.   

https://doi.org/10.3109/00048679809062740

PMID:9588308

 

Taylor, J, Cao, Q, Cravchik, A, Badner, J, Mowry, BJ, Levinson, DF, Crowe, RR, Silverman, JM, Goldin, LR, Gershon, ES and Gejman, PV (1998). Mutational analysis of the 5-HT1B and 5-HT1E serotonin receptor genes in three datasets with schizophrenia. Am J of Med Genetics 81 (6) 504.

https://espace.library.uq.edu.au/view/UQ:707949

NO PMID OR DOI

 

Clair, AL and Mowry, BJ (1998). Prevalence of substance use disorder in an Australian schizophrenia spectrum multiply-affected family study. Schizophrenia Research 29 (1-2) 21-22.

https://doi.org/10.1016/S0920-9964(97)88343-0

NO PMID OR DOI

 

Mowry, B (1998). Psychopathology: the evolving science of mental disorder. Australian and New Zealand Journal of Psychiatry 32 (2) 315-316.

https://espace.library.uq.edu.au/view/UQ:314285

NO PMID OR DOI

 

Mowry, B (1998). Scoresheet: structured clinical interview for DSM-IV Axis 1 disorders (clinical version). Australian and New Zealand Journal of Psychiatry 32 (6) 895-896.

https://espace.library.uq.edu.au/view/UQ:314246

NO PMID OR DOI

 

Mowry, B (1998). Structured interview for DSM-IV personality: SIDP-IV. Australian and New Zealand Journal of Psychiatry 32 (6) 896-897.

 https://espace.library.uq.edu.au/view/UQ:314249

NO PMID OR DOI

 

Mowry, B (1998). Study guide to treatments of psychiatric disorders, 2nd edition. Australian and New Zealand Journal of Psychiatry 32 (1) 152-153.

https://espace.library.uq.edu.au/view/UQ:314272

NO PMID OR DOI

 

1997

 

Nancarrow, DJ and Mowry, BJ (1997). Affected-only multiplex pedigree analysis of GAW10 problem 2. Genetic Epidemiology14 (6) 1029-1034.    

https://doi.org/10.1002/(SICI)1098-2272(1997)14:6<1029::AID-GEPI78>3.0.CO;2-K

PMID:9433619

 

Jones, IH, Hay, DA, Kirkby, KC, Daniels, BA and Mowry, BJ (1997). Season of birth and schizophrenia in Tasmania. Australian and New Zealand Journal of Psychiatry31 (1) 57-61. https://doi.org/10.3109/00048679709073799    

PMID:9088486

 

Dann, J, DeLisi, LE, Devoto, M, Laval, S, Nancarrow, DJ, Shields, G, Smith, A, Loftus, J, Peterson, P, Vita, A, Comazzi, M, Invernizzi, G, Levinson, DF, Wildenauer, D, Mowry, BJ, Collier, D, Powell, J, Crowe, RR, Andreasen, NC, Silverman, JM, Mohs, RC, Murray, RM, Walters, MK, Lennon, DP, Hayward, NK, Albus, M, Lerer, B, Maier, W and Crow, TJ (1997). A Linkage study of schizophrenia to markers within Xp11 near the MAOB gene. Psychiatry Research,70 (3) 131-143.     

https://doi.org/10.1016/S0165-1781(97)03138-7

PMID:9211575

 

Mowry, BJ, Nancarrow, DJ and Levinson, DF (1997). The molecular genetics of schizophrenia: an update. Australian and New Zealand Journal of Psychiatry 31 (5) 704-713. https://doi.org/10.3109/00048679709062684     

PMID:9400877

 

1996

 

Levinson, DF, Wildenauer, DB, Schwab, SG, Albus, M, Hallmayer, J, Lerer, B, Maier, W, Blackwood, D, Muir, W, StClair, D, Morris, S, Moises, HW, Yang, L, Kristbjarnarson, H, Helgason, T, Wiese, C, Collier, DA, Holmans, P, Daniels, J, Rees, M, Asherson, P, Roberts, Q, Cardno, A, Arranz, MJ, Vallada, H, McGuffin, D, Owen, MJ, Pulver, AE, Antonarakis, SE, Babb, R, Blouin, JL, DeMarchi, N, Dombroski, B, Housman, D, Karayiorgou, M, Ott, J, Kasch, L, Kazazian, H, Lasseter, VK, Loetscher, E, Luebbert, H, Nestadt, G, Ton, C, Wolyniec, PS, Laurent, C, deChaldee, M, Thibaut, F, Jay, M, Samolyk, D, Petit, M, Campion, D, Mallet, J, Straub, RE, MacLean, CJ, Easter, SM, ONeill, FA, Walsh, D, Kendler, KS, Gejman, PV, Cao, QH, Gershon, E, Badner, J, Beshah, E, Zhang, J, Riley, BP, Rajagopalan, S, MogudiCarter, M, Jenkins, T, Williamson, R, DeLisi, LE, Garner, C, Kelly, M, LeDuc, C, Cardon, L, Lichter, J, Harris, T, Loftus, J, Shields, G, Comasi, M, Vita, A, Smith, A, Dann, J, Joslyn, G, Gurling, H, Kalsi, G, Brynjolfsson, J, Curtis, D, Sigmundsson, T, Butler, R, Read, T, Murphy, P, Chen, ACH, Petursson, H, Byerley, B, Hoff, M, Holik, J, Coon, H, Nancarrow, DJ, Crowe, RR, Andreasen, N, Silverman, JM, Mohs, RC, Siever, LJ, Endicott, J, Sharpe, L, Walters, MK, Lennon, DP, Hayward, NK, Sandkuijl, LA, Mowry, BJ, Aschauer, HN, Meszaros, K, Lenzinger, E, Fuchs, K, Heiden, AM, Kruglyak, L, Daly, MJ and Matise, TC (1996). Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study. American Journal of Medical Genetics67 (6) 580-594. 

https://doi.org/10.1002/(SICI)1096-8628(19961122)67:6%3C580::AID-AJMG11%3E3.0.CO;2-P

PMID:8950417

 

Levinson, DF, Mowry, BJ, Sharpe, L and Endicott, J (1996). Penetrance of schizophrenia-related disorders in multiplex families after correction for ascertainment. Genetic Epidemiology13 (1) 11-21

https://doi.org/10.1002/(SICI)1098-2272(1996)13:1<11::AID-GEPI2>3.0.CO;2-9

PMID:8647375

 

Johansson, A and Mowry, B (1996). Pilot study of hirsutism in women with psychiatric disorders. Biological Psychiatry,39 (2) 149-151.    

https://doi.org/10.1016/0006-3223(95)00374-6

PMID:8717616

 

Gill, M, Vallada, H, Collier, D, Sham, P, Holmans, P, Murray, R, McGuffin, P, Nanko, S, Owen, M, Antonarakis, S, Housman, D, Kazazian, H, Nestadt, G, Pulver, AE, Straub, RE, MacLean, CJ, Walsh, D, Kendler, KS, DeLisi, L, Polymeropoulos, M, Coon, H, Byerley, W, Lofthouse, R, Gershon, E, Golden, L, Crow, T, Freedman, R, Laurent, C, BodeauPean, S, dAmato, T, Jay, M, Campion, D, Mallet, J, Wildenauer, DB, Lerer, B, Albus, M, Ackenheil, M, Ebstein, RP, Hallmayer, J, Maier, W, Gurling, H, Curtis, D, Kalsi, G, Brynjolfsson, J, Sigmundson, T, Petursson, H, Blackwood, D, Muir, W, StClair, D, He, L, Maguire, S, Moises, HW, Hwu, HG, Yang, L, Wiese, C, Tao, L, Liu, XH, Kristbjarnason, H, Levinson, DF, Mowry, BJ, DonisKeller, H, Hayward, NK, Crowe, RR, Silverman, JM, Nancarrow, DJ and Read, CM (1996). A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12. American Journal of Medical Genetics67 (1) 40-45.  

https://doi.org/10.1002/(SICI)1096-8628(19960216)67:1%3C40::AID-AJMG6%3E3.0.CO;2-W

PMID:8678112

 

1995

 

 Mowry, BJ, Nancarrow, DJ, Lennon, DP, Sandkuijl, LA, Crowe, RR, Silverman, JM, Mohs, RC, Siever, LJ, Endicott, J, Sharpe, L, Walters, MK, Hayward, NK and Levinson, DF (1995). Schizophrenia Susceptibility and Chromosome 6P24-22. Nature Genetics11 (3) 233-234. https://doi.org/10.1038/ng1195-233        

PMID:7581441

 

Hay DA, Hornsby H, Jones I, Mowry B, Mitchell RJ. (1995). The potential of isonymy in psychiatric genetics. Behavior Genetics.; 25 (3) 269-270.

https://espace.library.uq.edu.au/view/UQ:314288

NO PMID OR DOI

 

1994

 

Mowry, BJ, Lennon, DP and Defelice, CN (1994). Diagnosis of Schizophrenia in a Matched Sample of Australian Aborigines. Acta Psychiatrica Scandinavica90 (5) 337-341. https://doi.org/10.1111/j.1600-0447.1994.tb01603.x     

PMID:7872037

 

Gladis MM, Levinson DF, Mowry BJ. (1994). Delusions in schizophrenia spectrum disorders - diagnostic issues. Schizophrenia Bulletin. 20 (4) 747-754.

https://doi.org/10.1093/schbul/20.4.747

PMID:7701280

 

1993

 

Mowry, BJ and Levinson, DF (1993). Genetic-Linkage and Schizophrenia - Methods, Recent Findings and Future-Directions. Australian and New Zealand Journal of Psychiatry27 (2) 200-218

https://doi.org/10.1080/00048679309075769

PMID:8363530

 

1992

 

Black JL, Mowry BJ, Barton DA, De Roach JN. (1992). Auditory P300 studies in schizophrenic subjects and their first-degree relatives. Australasian Physical & Engineering Sciences in Medicine. 15 (2) 65-73.

https://europepmc.org/abstract/med/1642573

PMID:1642573

 

1991

 

Levinson DF, Mowry BJ. (1991). Defining the schizophrenia spectrum - issues for genetic-linkage studies. Schizophrenia Bulletin. 17 (3) 491-514. 

https://doi.org/10.1093/schbul/17.3.491

PMID:1947874

 

1990

 

Mowry, BJ and Burvill, PW (1990). Screening the Elderly in the Community for Psychiatric-Disorder. Australian and New Zealand Journal of Psychiatry24 (2) 203-206.  

https://doi.org/10.3109/00048679009077684

PMID:2396964

 

Burvill, P. W., Mowry, B. and Hall, W. D. (1990). Quantification of physical illness in psychiatric research in the elderly. International Journal of Geriatric Psychiatry5 (3) 161-170.    

https://doi.org/10.1002/gps.930050304

NO PMID

 

1989

 

Mowry, B (1989). Psychiatric-Examination - Notes on Eliciting and Recording Clinical Information in Psychiatric-Patients - Inst-Psychiat-Dept-Psychiat. Australian and New Zealand Journal of Psychiatry 23 (2) 284-285.

https://espace.library.uq.edu.au/view/UQ:314250

NO PMID OR DOI

 

1988

 

Mowry, BJ and Burvill, PW (1988). A Study of Mild Dementia in the Community Using a Wide-Range of Diagnostic-Criteria. British Journal of Psychiatry153 (3) 328-334.  

https://doi.org/10.1192/bjp.153.3.328

PMID:3250669

 

Mowry, BJ (1988). The Decline of the Old Medical Regime in Stuart London - Cook,hj. Annals of Science 45 (2) 219-220.

https://espace.library.uq.edu.au/view/UQ:314259

NO PMID OR DOI

 

1985

 

Mowry B. (1985). From Galen’s theory to William Harvey’s theory - a case-study in the rationality of scientific theory change. Studies in History and Philosophy of Science. 16 (1) 49-82.     

https://doi.org/10.1016/0039-3681(85)90007-X

PMID:11620609

 

Conference Presentations

 

Vinkhuyzen, Anna, John, Sujit, Periyasamy, Sathish, Wray, Naomi, Thara, Rangaswamy and Mowry, Bryan (2017). Genome-wide association study in an Indian population reveals genetic overlap for schizophrenia with Europeans. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto Canada, 16-20 October 2015. Amsterdam, Netherlands: Elsevier. European Neuropsychopharmacology 27, S341-S341 (2017)

https://espace.library.uq.edu.au/view/UQ:697399   

NO PMID OR DOI

 

Shaffer, J., Choupan, J., Mowry, B., Yang, Z. and Reutens, D. (2016). Voxel-Based Morphometry of Patients with Schizophrenia and Schizoaffective Disorders. Southern Regional Meeting of the American-Federation-for-Medical-Research, New Orleans, LA, United States, (443-443) 26-28 February 2015. Philadelphia, United States: Lippincott Williams & Wilkins.  Neurology April 05, 2016; 86 (16 Supplement)  P6-201.

http://n.neurology.org/content/86/16_Supplement/P6.201.short  

NO PMID OR DOI

 

Martin, Andrew K., Robinson, Gail A., Reutens, David C. and Mowry, Bryan (2014). Characterizing rare copy number variants in schizophrenia: a clinical, cognitive, and neuroimaging study. ICON 2014: XII International Conference on Cognitive Neuroscience, Brisbane, QLD, Australia, 27-31 July, 2014. Lausanne, Switzerland: Frontiers Research Foundation.

https://doi.org/10.3389/conf.fnhum.2015.217.00306

NO PMID

 

Paul, D., Henskens, F. A., Loughland, C. M., Bridge, J., McCabe, K., Carr, V. J., Catts, S. V., Jablensky, A., Michie, P. T., Mowry, B. J., Pantelis, C., Schall, U. and Scott, R. J. (2012). It development and management of a live e-research system: Experiences with the Australian Schizophrenia Research Bank. HEALTHINF 2012 - International Conference on Health Informatics, Vilamoura, Algarve, (125-130) 1 - 4 February 2012. Setubal, Portugal: INSTICC Press.

https://espace.library.uq.edu.au/view/UQ:317079

NO PMID OR DOI

 

Loughland, Carmel Lee, McCabe, Kathryn, Catts, S., Jablensky, A., Henskens, F., Michie, P., Mowry, B., Pantelis, C., Schall, U., Tooney, P., Scott, R., Draganic, D., Bridge, J. and Carr, V.  (2011). The Australian schizophrenia research bank (ASRB): The first 550 schizophrenia sample profile. 13th International Congress on Schizophrenia Research (ICOSR), Colorado Springs CO, United States, (54-55) 2-6 April 2011. Oxford, United Kingdom: Oxford University Press.

https://espace.library.uq.edu.au/view/UQ:245623

NO PMID OR DOI

 

Diminic, S, Stiller, A, Mowry, B, Catts, S and Australian Schizophrenia Research Bank. (2010). Associations between perinatal complications and clinical, neurological and cognitive outcomes in adults with schizophrenia: A preliminary analysis from ASRB Queensland. 11th Biennial Australasian Schizophrenia Conference, Sydney, NSW, Australia, (A-44-A-44)

22-24 September 2010. PP07

https://doi.org/10.3109/00048674.2010.507066

NO PMID

 

Jones, Amanda, Mowry, Bryan, Pender, Michael and Greer, Judith (2010). Elevated levels of autoantibodies against neurotransmitter receptor-related molecules in schizophrenia. 10th Congress of the International-Society-of-Neuroimmunology (ISNI), Sitges SPAIN, (54-54)

OCT 26-30, 2010.

https://espace.library.uq.edu.au/view/UQ:226987

NO PMID OR DOI

 

Wu, Jin Qin, Cairns, Murray J., Scott, Rodney J., Carr, Vaughn, Mowry, Bryan, Jablensky, Assen, Pantelis, Christos, Schall, Ulrich, Loughland, Carmel and Tooney, Paul (2010). Genome wide analysis of DNA copy number in schizophrenia reveals loss of heterozygosity on chromosome 6P22.1 and 16P11.2-11.1. 11th Australasian Schizophrenia Conference, Sydney, Australia, (A32-A32) 22-24 September 2010. United Kingdom: Informa Healthcare.

https://espace.library.uq.edu.au/view/UQ:226564

NO PMID OR DOI

 

Henskens, Frans, Carr, Vaughan, Catts, Stan, Jablensky, Assen, Michie, Patricia, Loughland, Carmel, McCabe, Kathryn, Mowry, Bryan, Nasir, Aslam, Pantelis, Christos, Rasser, Paul, Paul, David, Richards, Jacki, Schall, Ulrich and Scott, Rodney (2010). The Australian Schizophrenia Research Bank (ASRB): An example of eResearch. 2nd Schizophrenia International Research Society Conference, Florence, Italy, 10-14 April 2010. (427-428). 10-14 April 2010.  Schizophrenia Research 117 (2-3) 427-428

https://doi.org/10.1016/j.schres.2010.02.788

NO PMID

 

Carr, Vaughan, Loughland, Carmel, McCabe, Kathryn, Nasir, Aslam, Catts, Stan, Jablensky, Assen, Henskens, Frans, Michie, Patricia, Mowry, Bryan, Pantelis, Christos, Schall, Ulrich and Scott, Rodney (2010). The Australian Schizophrenia Research Bank (ASRB): Demographic, clinical and neuropsychological profiles for the first 500 participants with schizophrenia. 2nd Biennial Schizophrenia International Research Conference, Florence, Italy, (312-312). April 10-14, 2010.  Schizophrenia Research 117 (2-3) 312

https://doi.org/10.1016/j.schres.2010.02.525

NO PMID

 

Carr, Vaughan, Loughland, Carmel, McCabe, Kathryn, Nasir, Aslan, Catts, Stanley, Jablensky, Assen, Henskens, Frans, Michie, Patricia, Mowry, Bryan, Pantelis, Christos, Schall, Ulrich, Tooney, Paul and Scott, Rodney (2010). The Australian Schizophrenia Research Bank (ASRB): Demographic, clinical and neuropsychological profile of participants with schizophrenia. 11th Australasian Schizophrenia Conference, Sydney, Australia, (A59-A59). 22-24 September 2010.  PP56

https://doi.org/10.3109/00048674.2010.507066

NO PMID

 

McCabe, Kathryn L., Loughland, Carmel M., Nasir, Aslam, Catts, Stan, Jablensky, Assen, Henskens, Frans, Michie, Patricia, Mowry, Bryan, Pantelis, Christos, Schall, Ulrich, Scott, Rodney and Carr, Vaughan (2010). The Australian Schizophrenia Research Bank (ASRB): Quality assurance and control for a comprehensive clinical, neurospychologial, genetic and neuroimaging data for researchers. 2nd Biennial Schizophrenia International Research Conference, Florence, Italy. April 10-14 2010. Schizophrenia Research 117 (2-3) 200

https://doi.org/10.1016/j.schres.2010.02.269

NO PMID

 

Carr, Vaughan, Loughland, C., Catts, S., Henskens, F., Jablensky, A., Michie, P., Mowry, B., Pantelis, C., Schall, U. and Scott, R. (2009). A Database of Comprehensive Clinical, Endophenotypic and Genetic Data for Aetiological Studies of Schizophrenia. 12th International Congress on Schizophrenia Research, San Diego Ca, (108-108) Mar 28-Apr 01, 2009. OXFORD: OXFORD UNIV PRESS.

https://espace.library.uq.edu.au/view/UQ:304591

NO PMID OR DOI

 

Henskens, F. A., Loughland, C. A., Aphale, M. S., Paul, D., Richards, J. A., Rasser, P., Carr, V. J., Catts, S. V., Jablensky, A., Michie, P. T., Mowry, B. J., Pantelis, C., Schall, U. and Scott, R. J.  (2009). IT support for the Australian Schizophrenia Research Bank. 2nd International Conference on Health Informatics (HEALTHINF 2009), Oporto, Portugal, (405-410) 14-17 January 2009. Setubal, Portugal: INSTICC.

https://espace.library.uq.edu.au/view/UQ:304580

NO PMID OR DOI

 

Carr, V., Loughlan, C., Catts, S., Henskens, F., Jablensky, A., Michie, P., Mowry, B., Pantelis, C., Schall, U. and Scott, R. (2008). A progress report on the Australian Schizophrenia Research Bank. 10th Australasian Schizophrenia Conference, Melbourne, Australia, (A40-A40) 23-24 October 2008. Aust. and NZ J of Psychiatry (Poster)

https://doi.org/10.1080/00048670802441851

NO PMID

 

Richards, Jaci, Loughland, Carmel M., Aphale, Mukta, Henskens, Frans, Carr, Vaughan J., Catts, Stanley V., Jablensky, Assen, Mitchie, Patricia T., Mowry, Bryan J., Pantelis, Christos, Schall, Ulrich, Scott, Rodney J. and Lewin, Terry J. (2008). The Australian Schizophrenia Research Bank (ASRB) computer-based Clinical Assessment Software (CAS): Development and application. Australian Society for Psychiatric Research (ASPR) Annual Conference 2008., Newcastle, Australia, (A104-A105). 3-5 December 2008.  PP50 https://doi.org/10.1080/00048670802549646

NO PMID

 

Carr, V., Schall, U., Michie, P., Scott, R., Jablenski, A., Mowry, B., Catts, S., Henskens, F. and Pantelis, C. (2007). An overview of the Australian schizophrenia research bank: Linking brain function and structure with genetics in a large sample of schizophrenia cases and controls. World Psychiatric Association International Congress 2007, Melbourne, Australia, (A464-A464). 28 November-2 December 2007. Aust. and NZ J of Psychiatry (Poster)

https://doi.org/10.1080/00048670701757076

NO PMID

 

Loughland, C., Carr, V., Michie, P., Stain, H., Badcock, J., Jablenski, A., Draganic, C. D., Lewin, T. J., Schall, U., Scott, R., Mowry, B., Catts, S., Henskens, F. and Pantelis, C.  (2007). The national recruitment and assessment of people with schizophrenia: The ASRB experience. World Psychiatric Association International Congress 2007, Melbourne, Australia, (A464-A464). 28 November-2 December 2007. Aust. and NZ J of Psychiatry (Poster)

https://doi.org/10.1080/00048670701757076

NO PMID

 

Gejman, PV, Duan, J, Martinez, M, Sanders, AR, Burrell, G, Hou, C, He, D, Schwartz, D, Buccola, NG, Mowry, BJ, et al. (2006). Comprehensive linkage disequilibrium mapping of schizophrenia candidate genes in a large European-ancestry sample. 14th World Congress on Psychiatric Genetics, Italy, (689-689). 28 OCT-01 NOV 2006.

https://espace.library.uq.edu.au/view/UQ:79761

NO PMID OR DOI

 

Gejman, P. V., Duan, J., Sanders, A. R., Hou, C., Burrel, G., Buccola, N. G., Mowry, B. J., Amin, F., Silverman, J. M., Black, D. W., Byerley, W. F., Freedman, R., Cloninger, C. R., Levinson, D. F. and Martinez, M.  (2006). Genetics of schizophrenia: Progress and caveats. XXIVth CINP Congress, Chicago, IL, U.S.A., (S28-S28). 9-13 July, 2006. International Journal of Neuropsychopharmacology, 9, Supp 1.

https://doi.org/10.1017/S1461145706007292

NO PMID

 

Levinson, Douglas, Gejman, Pablo V., Laurent, Claudine, Owen, Michael J., Pulver, Ann E., Riley, Brien, Wildenauer, Dieter B., Kendler, Kenneth S., Mallet, Jacques, Mowry, Bryan J., Nestadt, Gerald, O'Donovan, Michael, Sanders, Alan R., Schwab, Sibylle G., Williams, Nigel, Albus, Margot, Bauche, Stephanie, deMarchi, Nicola, Dikeos, Dimitris, Duan, Jubao, Jay, Maurice, Lasseter, Virginia K., Lerer, F. Bernard, Maier, Wolfgang, Nertney, Deborah A., Nikolov, Ivan, Norton, Nadine, O'Neill, Anthony, Papadimitriou, George, Segurado, Ricardo, Silverman, Jeremy M., Walsh, Dermot, Williams, Hywel and Holmans, Peter A.  (2006). Genomewide SNP linkage scan of schizophrenia in a large multicenter sample. 14th World Congress on Psychiatric Genetics, Cagliari Italy, Oct 28-Nov 01, 2006.

https://espace.library.uq.edu.au/view/UQ:314267

NO PMID OR DOI

 

Duan, J, Martinez, M, Sanders, AR, Hou, C, Saitou, N, Kitano, T, Mowry, BJ, Crowe, RR, Silverman, JM, Levinson, DF and Gejman, PV (2004). Polymorphisms in trace amine receptor 4 (TRAR4) are associated with susceptibility for schizophrenia on chromosome 6q23.2. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics.12th World Congress of Psychiatric Genetics, Dublin Ireland, (19-20). Oct 09-13, 2004.

https://espace.library.uq.edu.au/view/UQ:314252

NO PMID OR DOI

 

Handoko, HY, Nyholt, DR, Hayward, NK, James, MR, Hannah, DE, Nertney, DA, Smith, HJ, Filippich, CF and Mowry, BJ (2004). Confirmation of the catechol-O-methyltransferase gene contribution to schizophrenia. 12th World Congress of Psychiatric Genetics, Dublin Ireland, (134-134) Oct 09-13, 2004.

https://espace.library.uq.edu.au/view/UQ:314253

NO PMID OR DOI

 

Srinivasan, TN, Thara, R, Padmavati, R, Sujit, KJ, Giri, KP, Chant, DC and Mowry, BJ (2004). Familiarity of symptoms and symptom dimensions in a sample of Indian families. 12th World Congress of Psychiatric Genetics, Dublin Ireland, (55-55) Oct 09-13, 2004.

https://espace.library.uq.edu.au/view/UQ:314269

NO PMID OR DOI

 

Witherspoon, DJ, Srinivasan, TN, Thara, R, Nancarrow, DJ, Watkins, W, Bamshad, M, Mowry, BJ and Jorde, LB (2003). Caste, geography and genetic structure in Hindu populations. Annual Meeting of the American-Society-of-Human-Genetics, Los Angeles California, (400-400) Nov 04-08, 2003.

https://espace.library.uq.edu.au/view/UQ:314260

NO PMID OR DOI

 

Martinez, M, Sanders, AR, Martinolich, L, Carpenter, EB, Duan, J, Mowry, BJ, Levinson, DF, Crowe, RR, Silverman, JM and Gejman, PV (2003). Linkage disequilibrium analysis of single nucleotide polymorphisms of the glutamate receptor 6 gene and schizophrenia. Annual Meeting of the American-Society-of-Human-Genetics, Los Angeles California, (488-488)

Nov 04-08, 2003.

https://espace.library.uq.edu.au/view/UQ:314274

NO PMID OR DOI

 

Mowry BJ, Nancarrow DJ, O'Haeri J, Walters MK, Nertney DA, Hayward NK, Ott J, Gordon D. (2002). The analysis of four candidate chromosomal regions in two schizophrenia datasets from Fiji.  American Journal of Medical Genetics 114 (7) 862-862. 

10th World Congress of Psychiatric Genetics, Brussels Belgium, Oct 09-13, 2002.

RGMS ID P_9881079   

https://espace.library.uq.edu.au/view/UQ:314248

NO PMID OR DOI

 

Sanders, AR, Martinez, M, Martinolich, L, Carpenter, EB, Duan, J, Mowry, BJ, Levinson, DF, Crowe, RR, Silverman, JM and Gejman, PV (2002). Linkage disequilibrium analysis of 6ql3-q26 schizophrenia candidate genes. 52nd Annual Meeting of the American-Society-of-Human-Genetics, Baltimore Maryland, Oct 15-19, 2002. American Journal of Human Genetics 71 (4) 473-473.

https://espace.library.uq.edu.au/view/UQ:314258

NO PMID OR DOI

 

McGrath, J, Eyles, D, Mowry, B, Yolken, R and Buka, S (2002). Low maternal vitamin D as a risk factor for schizophrenia: A pilot study using banked sera. AMSTERDAM: ELSEVIER SCIENCE BV. In: Schizophrenia Research 53 (3) 228-229.

 https://espace.library.uq.edu.au/view/UQ:290740

NO PMID OR DOI

 

Saha, S., Chapple, B., Cardy, S., Chant, D., Mowry, B. and McGrath, J. (2002). The presence of quasi-psychotic phenomena is associated with minor physical anomalies and craniofacial measures in well controls. XIth Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (232-233). 24 February – 1 March, 2002.  Schizophrenia Research. 53 (3) Supp 1: 1-269.

https://doi.org/10.1016/S0920-9964(01)00381-4

NO PMID

 

Mowry, B. J. and Nancarrow, D. J. (2001). Molecular genetics of schizophrenia. In: Clinical and Experimental Pharmacology and Physiology. 2001 Jan-Feb;28(1-2):66-69

Proceedings of the Australian Neuroscience Society Symposium on Schizophrenia. Australian-Neuroscience-Society Symposium on Schizophrenia, Melbourne, (66-69). January-February 2000.

https://doi.org/10.1046/j.1440-1681.2001.03399.x  

PMID:11153540.

 

McGrath, J., Grim, V., Cardy, S., Chapple, B. and Mowry, B. (2000). Dysmorphogenesis in psychosis: Quantitative and qualitative measures involving the head and face. Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (84-84). 5 February - 11 February 2000.  Schizophrenia Research.  41 (1) 84.

https://doi.org/10.1016/S0920-9964(00)90498-5

NO PMID

 

McGrath, J. J., White, P., Mowry, B., Chant, D. C., Slate, T. and Andrews, G. (2000). Endorsement of CIDI psychosis screening items in the Australian Survey of mental Health and Well Being. Tenth Biennial Winter Workshop on Schizophrenia, Davos, Switzerland. (44-44). 11 - 15 February, 2000. Schizophrenia Research. 41 (1) 44.

https://doi.org/10.1016/S0920-9964(00)90395-5

NO PMID

 

McGrath, J. J., Cardy, S., Chapple, B. and Mowry, B. (2000). Increased risk of psychosis in rural-born individuals: an Australian Catchement-area Study. Tenth Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (20-20). 5 February - 11 February 2000. Schizophrenia Research. 41 (1) 20.

 https://doi.org/10.1016/S0920-9964(00)90346-3

NO PMID

 

McGrath, J., De Leacy, E., Scheurer, R., Cardy, S. and Mowry, B. (2000). The continuum of quasi-psychotic beliefs and experiences in the Australian general public. Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (82-82). 11 - 15 February, 2000. Schizophrenia Research. 41 (1) 82.

https://doi.org/10.1016/S0920-9964(00)90493-6

NO PMID

 

Journal Articles (Reviews)

 

Martin A, Robinson G, Dzafic I, Reutens D, Mowry B, (2014). Theory of Mind and the Social Brain: Implications for Understanding the Genetic Basis of Schizophrenia. Genes Brain & Behaviour 13(1) 104-117.  

https://doi.org/10.1111/gbb.12066

 

Filippich C, Wolvetang EJ, Mowry BJ. (2013). Will Brain Cells Derived from Induced Pluripotent Stem Cells or Directly Converted From Somatic Cells (iNs) Be Useful for Schizophrenia Research? Schizophrenia Bulletin. 39 (5) 948-954.

https://doi.org/10.1093/schbul/sbt103

 

Mowry BJ, 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. Molecular Psychiatry 18 (1) 38-52. 

http://dx.doi.org/10.1038/mp.2012.34

 

Jones AL, Mowry BJ, Pender MP, Greer JM. (2005). Immune dysregulation and self-reactivity in schizophrenia: Do some cases of schizophrenia have an autoimmune basis? Immunology and Cell Biology. 83 (1) 9-17. 

https://doi.org/10.1111/j.1440-1711.2005.01305.x

 

McGrath J, Mowry B, Whiteford H. (2005). Queensland Centre for Mental Health Research: the first 17 years. Australian and New Zealand Journal of Psychiatry. 39 (7) 533-541.

https://doi.org/10.1080/j.1440-1614.2005.01624.x

 

Mowry BJ. (2003). Psychiatric genetics in Australia. Psychiatric Genetics. 13 (3) 131-141.

https://journals.lww.com/psychgenetics/Abstract/2003/09000/Psychiatric_genetics_in_Australia.1.aspx   

 

Mowry BJ, Nancarrow DJ. (2001). Molecular genetics of schizophrenia. Clinical and Experimental Pharmacology and Physiology. 28 (1-2) 66-69.

https://doi.org/10.1046/j.1440-1681.2001.03399.x

 

Mowry BJ, Nancarrow DJ, Levinson DF. (1997). The molecular genetics of schizophrenia: an update. Australian and New Zealand Journal of Psychiatry. 31 (5) 704-713.

https://doi.org/10.3109/00048679709062684

 

Mowry BJ, Levinson DF. (1993). Genetic-linkage and schizophrenia - methods, recent findings and future-directions. Australian and New Zealand Journal of Psychiatry. 27 (2) 200-218.  

https://doi.org/10.1080/00048679309075769

 

Book Chapters

 

Wray, Naomi R., Byrne, Enda M., Stringer, Sven and Mowry, Bryan J. (2014). Future directions in genetics of psychiatric disorders. Behavior Genetics of Psychopathology Advances in Behavior Genetics, vol 2. Chapter 11 311-337. 13 January 2014

Edited by Soo Hyun Rhee and Angelica Ronald. New York, NY, United States: Springer New York. RGMS ID P11414025

https://doi.org/10.1007/978-1-4614-9509-3_11

https://link.springer.com/content/pdf/10.1007/978-1-4614-9509-3.pdf

NO PMID

 

Mowry, Bryan (2010). The status of genetic investigations of schizophrenia. In Secondary schizophrenia. Edited by Perminder S. Sachdev and Matcheri S. Keshavan. Cambridge: Cambridge University Press. Chapter 23 288-308. RGMS ID P_9881119

https://doi.org/10.1017/CBO9780511789977.024

https://books.google.com.au/books?hl=en&lr=&id=44_zy35zFnIC&oi=fnd&pg=PR5&dq=Secondary+Schizophrenia&ots=8j5jWD5wVA&sig=E64h4KaG2I8Ryeq9esLihhTtyMQ

NO PMID

 

Levinson, D.F., and Mowry BJ. (2000). Genetics of Schizophrenia. Genetic influences on neural and behavioural functions. Pfaff, Donald W., Berrettini, Wade H., Maxson, Stephen C., and Joh, Tong H., eds., CRC Press, New York, Chapter 4 pp. 47-82. 1st Edition 1999  RGMS ID P_9881118

https://books.google.com.au/books?hl=en&lr=&id=sjUhzW9crrYC&oi=fnd&pg=PA1&ots=OJDf7IddNZ&sig=iItNSrUYj5ti4_GgjHrHR12tQ8w

NO PMID OR DOI

 

Major Conference Papers (Invited)

Plenary/Keynote: *

 

*Second National Symposium on Translational Psychiatry, Adelaide; 7-8 August, 2013: “Revealing the genetics of schizophrenia: implications for translational medicine”.

 

*International Conference on Schizophrenia (ICONS V), Chennai, India; 21-23 September, 2012: “Genetics of schizophrenia in Tamil Nadu – A genomewide association study.”

 

*First National Symposium on Translational Psychiatry, Canberra; 4-5 April, 2011: “The Genomics Promise: molecular diagnostics and therapeutics for schizophrenia?”

National Health and Medical Research Council (NHMRC) Workshop, Global Health – addressing the health needs of the Asia/Pacific region. Canberra; 25 May, 2010: “Studying the genetics of schizophrenia in India and Sarawak.”

 

*Schering-Plough Senior Medical Research Award. The Royal Australian and New Zealand College of Psychiatrists Annual Congress, Auckland, New Zealand, May 2010. “The challenging reality of schizophrenia genetics.”

 

*International Conference on Schizophrenia (ICONS III), Chennai, India; 17-19 October, 2008: “A genomewide scan of schizophrenia in the Brahmin of Tamil Nadu.”

 

World Psychiatric Association and the Australian Society for Psychiatric Research, Melbourne; November 29, 2007. “Towards identifying genetic risk factors for schizophrenia.”

 

*International Conference on Schizophrenia (ICONS II), Chennai, India; 13-15 October, 2006: “Familiality of symptom dimensions in a sample of Indian families.”

 

3rd National Symposium: Genes, Neurons & Mental Illness. Brain & Mind Institute, Sydney 2005. Molecular Genetics of Schizophrenia

 

*International Conference on Schizophrenia (ICONS I), Chennai, India; 29 Jan – 2 February, 2004: “Recent advances in the genetics of schizophrenia.”

 

Symposium on genetics of schizophrenia and bipolar disorders. XII World Congress of Psychiatry, Yokohama; August, 2002: “Multi-centre linkage and meta-analyses of schizophrenia.”

 

Park City Molecular Psychiatry Meeting, Park City, Utah; USA; 2001. “Multi-allelic TDT simulation study of Fijian families with psychosis.”

 

The Australian Society for Psychiatric Research (ASPR), Annual Scientific Meeting and Meeting, Adelaide; 2000: “A genetic study of schizophrenia among the Iban of Sarawak: Investigating an isolated gene pool.”

 

The Australian Association of Philosophy and Ethics Conference (AAPAE), University of Queensland, Brisbane; 2000. “Ethics and the Research Patient.”

 

Australian Neuroscience Society, Melbourne; 2000: “Molecular Genetics of Schizophrenia. Invited Talk.”

 

Park City Molecular Psychiatry Meeting, Park City, Utah; USA; 1998: “Schizophrenia Genome Scan Update.”

 

21st Annual Scientific meeting of the Human Genetics Society of Australasia, Fremantle; 1997: “The current state of molecular genetics in psychiatry using schizophrenia as an example”.

 

Etiology of Schizophrenia Conference, Mental Health Research Institute, Melbourne; 1997. “The genetics of schizophrenia; Is there light at the end of the tunnel?”

The Royal Australian and New Zealand College of Psychiatrists 32nd Congress, Sydney; 1997. “Latest findings in the molecular genetics of schizophrenia.”

 

Park City Molecular Psychiatry Meeting, Park City, Utah; USA; 1997: “Genome scan of schizophrenia - results.”

 

Australian Society for Medical Research Annual Conference, Gold Coast; 1996: “Latest findings in molecular genetics.”

 

The Royal Australian and New Zealand College of Psychiatrists, Tasmanian Branch, Cradle Mountain, Tasmania; 1996: “Predispositions: latest findings from genetic studies in schizophrenia.”

 

The Fourth Australasian Schizophrenia Conference, Perth; 1996: “Searching for schizophrenia genes: An update.”

 

Mental Health Research Institute, Melbourne; 1995: “The molecular genetics of schizophrenia - an update.”

 

Department of Psychiatry Academic Program, University of New South Wales, Sydney; 1995: “The molecular genetics of schizophrenia - an update.”

 

*The Third Australasian Schizophrenia Research Conference, Brisbane; 1994: “The molecular genetics of schizophrenia.”

 

Third World Congress of Psychiatric Genetics, New Orleans; 1993: “Ethics and psychiatric genetics”. 

 

The Australian Neuroscience Society Annual Meeting, Symposium on the Biology of Brain Disorders, Sydney; 1993: “Molecular genetic linkage and schizophrenia.”

 

The Australian Society for Psychiatric Research, Sydney; 1993: “The molecular genetics of schizophrenia.”

 

Brisbane Philosophy Society, University of Queensland, Brisbane; 1993: “The objectivity of psychiatry: the example of schizophrenia.”

 

The Second Australian Schizophrenia Research Conference, Sydney; 1992: “Genetic linkage in schizophrenia.”

 

Annual Congress of the Australian Philosophical Association, Perth; 1988: “The Objectivity of Psychiatry. Invited paper.”

 

International Collaborations

  • Dr Rangaswamy Thara -  Schizophrenia Research Foundation (SCARF), Chennai, India.
  • Schizophrenia Working Group of the Psychiatric Genetics Consortium.
  • Dr Edor Kabashi – Zebrafish expert from the Brain and Spine Institute, Paris, France.
  • Dr Kessen Patten - INRS, Armand Frappier Institute, Laval, Québec. Joint-CIHR research grant (2018-2022) – Canada.
  • Prof Robert Yolken – Stanley Neurovirology Laboratory, John Hopkins School of Medicine, USA

 

National Collaborators

  • Prof Matthew Brown – Queensland University of Technology at TRI, PA Hospital.
  • Prof Naomi Wray - Institute for Molecular Biology, The University of Queensland.
  • Prof Peter Visscher - Institute for Molecular Biology, The University of Queensland.
  • The Australian Schizophrenia Research Bank.
  • Prof Fred Meunier - Queensland Brain Institute, The University of Queensland.
  • Dr Thomas Hall – Institute for Molecular Biology, The University of Queensland.
  • Dr Jake Gratten – Cognitive Health Genomics Group, Mater Research Institute, TRI
  • Prof Judith Greer – UQ Centre for Clinical Research, Faculty of Medicine, UQ.

PhD project in Neurogenetics

We have a fantastic opportunity funded by the University of Queensland for a PhD student scholarship. The position will be with the Queensland Brain Institute (QBI). This institute focuses on understanding the normal and pathological functions of the nervous system and on looking for treatments against diseases of the brain. The host group, which combine supervision from a senior clinician and a senior research fellow initially trained in the industry (genetics and drug discovery), is currently working at identifying risk-genes involved in neurodevelopmental and mental disorders (mainly schizophrenia) using patients’ samples and at understanding the role of these genes in the nervous system. The main focus of this PhD will be to translate some of their genetics discoveries into functional knowledge. The PhD student will handle several high-priority genes and investigate their function using the zebrafish animal model. The primary goal will be to successfully generate knockout mutant animals and investigate the impact of the corresponding loss-of-function to the brain development and function, with a particular emphasis on synaptogenesis and synaptic function.

The applicant will benefit from an international network and top-notch supervision from experts in the field of mental disorders, genetics, animal models and drug discovery. This is a unique opportunity that, beyond self-development, will enable the applicant to learn state-of-the-art techniques such as animal transgenesis, CRISPR-technology and high-end microscopy (including optogenetics, calcium imaging and super-resolution microscopy). The applicant will also have the opportunity to play a role in side projects focusing on drug discovery using the zebrafish.

 

PhD project in neuro-pharmacology

We also have another great opportunity that would suit an enthusiastic international or national student who is interested in understanding how current anti-psychotic medications and other neuroactive drugs work at the cellular and molecular level in the brain. The applicant will take advantage of the zebrafish animal model and calcium imaging genetic tools as well super-resolution approach (unique within the zebrafish field) to investigate the effect of clozapine and other drugs at the synaptic level. Considering the novelty of this approach, this research will guarantee that the applicant will build a strong and novel set of skills that will set them apart from their peers. The applicant will benefit from co-supervision from a clinician expert in mental health, a senior research fellow expert in genetics and drug discovery as well as a Professor expert in super-resolution microscopy.

 

How to apply