Psychiatric genomics

About

The primary research goal is to identify and functionally characterise susceptibility genes for schizophrenia and related disorders. A special focus is on the study of large collaborative samples and ethnically homogeneous populations.

Key methodologies used in the lab include genome-wide association studies (GWAS), next-generation sequencing, transcriptome profiling of post-mortem brain samples, neurocognitive and neuroimaging phenotyping and induced pluripotent stem cells.The Mowry laboratory aims to identify and functionally characterise susceptibility genes for schizophrenia and related disorders.

The group aims to achieve this by using genome-wide association studies (GWAS), DNA and RNA sequencing, and gene expression studies.

The group hopes to further characterise the function of discovered genetic variants by studying these in zebrafish and in neuronal cells derived from induced pluripotent stem cells (iPSC) sourced from patients. 

A successful NHMRC grant (2016–2018), Investigating the aetiopathogenic role of autoantibodies against the M1 muscarinic acetylcholine receptor in patients with first episode of schizophrenia, with colleagues, Associate Professor Judith Greer and Associate Professor James Scott will enable the Mowry laboratory to study the relationship between higher levels of antibodies and particular disease symptoms. The group will further investigate how these antibodies may worsen specific symptoms.


Group Publications

 

Research Areas

 

  • Schizophrenia Genetics
  • DNA, RNA Sequencing
  • Gene Expression
  • Pluripotent Stem Cells
  • Zebrafish
  • Pharmacogenomics

Group Leader


Research Members


  • Continuing recruitment of southern Indian schizophrenia families and unrelated cases and controls in collaboration with Dr Thara, Director, Schizophrenia Research Foundation, Chennai
     
  • Neuroimaging and neuropsychological phenotyping of selected schizophrenia patients and a matched sample of healthy individuals
     
  • GWAS analyses in homogeneous Indian and Sarawak populations, comparing the results with the latest results for European-ancestry schizophrenia from the Psychiatric Genomics Consortium
     
  • Targeted resequencing analyses of a previously identified chromosomal region in an Indian sample
     
  • Establishing iPSC from selected schizophrenia patients and controls in order to test disease hypotheses; (6) studying the function of the group’s top Indian GWAS locus in zebrafish and cellular models. 


Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Marshall, Christian R., Howrigan, Daniel P., Merico, Daniele, Thiruvahindrapuram, Bhooma, Wu, Wenting, Greer, Douglas S., Antaki, Danny, Shetty, Aniket, Holmans, Peter A., Pinto, Dalila, Gujral, Madhusudan, Brandler, William M., Malhotra, Dheeraj, Wang, Zhouzhi, Fuentes Fajarado, Karin V., Maile, Michelle S., Ripke, Stephan, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amin, Farooq, Atkins, Joshua, Bacanu, Silviu A., Belliveau, Richard A., Jr., Bergen, Sarah E., Bertalan, Marcelo, Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Bruggeman, Richard, Buccola, Nancy G., Buckner, Randy L., Bulik-Sullivan, Brendan, Byerley, William, Cahn, Wiepke, Cai, Guiqing, Cairns, Murray J., Campion, Dominique, Cantor, Rita M., Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chambert, Kimberley D., Cheng, Wei, Cloninger, C. Robert, Cohen, David, Cormican, Paul, Craddock, Nick, Crespo-Facorro, Benedicto, Crowley, James J., Curtis, David, Davidson, Michael, Davis, Kenneth L., Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E., Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H., Farh, Kai-How, Farrell, Martilias S., Frank, Josef, Franke, Lude, Freedman, Robert, Freimer, Nelson B., Friedman, Joseph I., Forstner, Andreas J., Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Gershon, Elliot S., Giegling, Ina, Giusti-Rodriguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I., Gratten, Jacob, De Haan, Lieuwe, Hamshere, Marian L., Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hofman, Andrea, Huang, Hailiang, Ikeda, Masashi, Joa, Inge, Kahler, Anna K., Kahn, René S., Kalaydjieva, Luba, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C., Kelly, Brian J., Kennedy, James L., Kim, Yunjung, Knowles, James A., Konte, Bettina, Laurent, Claudine, Lee, Phil, Lee, S. Hong, Legge, Sophie E., Lerer, Bernard, Levy, Deborah L., Liang, Kung-Yee, Lieberman, Jeffrey, Lonnqvist, Jouko, Loughland, Carmel M., Magnusson, Patrik K. E., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W., McDonald, Colm, McIntosh, Andrew M., Meier, Sandra, Meijer, Carin J., Melle, Ingrid, Mesholam-Gately, Raquelle I., Metspalu, Andres, Michie, Patricia T., Milani, Lili, Milanova, Vihra, Mokrab, Younes, Morris, Derek W., Muller-Myhsok, Bertram, Murphy, Kieran C., Murray, Robin M., Myin-Germeys, Inez, Nenadic, Igor, Nertney, Deborah A., Nestadt, Gerald, Nicodemus, Kristin K., Nisenbaum, Laura, Nordin, Annelie, O'Callaghan, Eadbhard, O'Dushlaine, Colm, Oh, Sang-Yun, Olincy, Ann, Olsen, Line, O'Neill, F. Anthony, Van Os, Jim, Pantelis, Christos, Papadimitriou, George N., Parkhomenko, Elena, Pato, Michele T., Paunio, Tiina, Perkins, Diana O., Pers, Tune H., Pietilainen, Olli, Pimm, Jonathan, Pocklington, Andrew J., Powell, John, Price, Alkes, Pulver, Ann E., Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roffman, Joshua L., Roussos, Panos, Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R., Savitz, Adam, Schall, Ulrich, Schulze, Thomas G., Schwab, Sibylle G., Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Shi, Jianxin, Silverman, Jeremy M., Smoller, Jordan W., Soderman, Erik, Spencer, Chris C. A., Stahl, Eli A., Strengman, Eric, Strohmaier, Jana, Stroup, T. Scott, Suvisaari, Jaana, Svrakic, Dragan M., Szatkiewicz, Jin P., Thirumalai, Srinivas, Tooney, Paul A., Veijola, Juha, Visscher, Peter M., Waddington, John, Walsh, Dermot, Webb, Bradley T., Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Witt, Stephanie H., Wolen, Aaron R., Wormley, Brandon K., Wray, Naomi R., Wu, Jing Qin, Zai, Clement C., Adolfsson, Rolf, Andreassen, Ole A., Blackwood, Douglas H. R., Bramon, Elvira, Buxbaum, Joseph D., Cichon, Sven, Collier, David A., Corvin, Aiden, Daly, Mark J., Darvasi, Ariel, Domenici, Enrico, Esko, Tõnu, Gejman, Pablo V., Gill, Michael, Gurling, Hugh, Hultman, Christina M., Iwata, Nakao, Jablensky, Assen V., Jonsson, Erik G., Kendler, Kenneth S., Kirov, George, Knight, Jo, Levinson, Douglas F., Li, Qingqin S., McCarroll, Steven A., McQuillin, Andrew, Moran, Jennifer L., Mowry, Bryan J., Nothen, Markus M., Ophoff, Roel A., Owen, Michael J., Palotie, Aarno, Pato, Carlos N., Petryshen, Tracey L., Posthuma, Danielle, Rietschel, Marcella, Riley, Brien P., Rujescu, Dan, Sklar, Pamela, St Clair, David, Walters, James T. R., Werge, Thomas, Sullivan, Patrick F., O'Donovan, Michael C., Scherer, Stephen W., Neale, Benjamin M. and Sebat, Jonathan (2017) Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nature Genetics49 1: 27-35. doi:10.1038/ng.3725

Mentalizing in schizophrenia: A multivariate functional MRI study

Martin, Andrew K., Dzafic, Ilvana, Robinson, Gail A., Reutens, David and Mowry, Bryan (2016) Mentalizing in schizophrenia: A multivariate functional MRI study. Neuropsychologia93 158-166. doi:10.1016/j.neuropsychologia.2016.10.013

No reliable association between runs of homozygosity and schizophrenia in a well-powered replication study

Johnson, Emma C., Bjelland, Douglas W., Howrigan, Daniel P., Abdellaoui, Abdel, Breen, Gerome, Borglum, Anders, Cichon, Sven, Degenhardt, Franziska, Forstner, Andreas J., Frank, Josef, Genovese, Giulio, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hoffman, Per, Maier, Wolfgang, Mattheisen, Manuel, Morris, Derek, Mowry, Bryan, Muller-Mhysok, Betram, Neale, Benjamin, Nenadic, Igor, Nothen, Markus M., O'Dushlaine, Colm, Rietschel, Marcella, Ruderfer, Douglas M., Rujescu, Dan, Schulze, Thomas G., Simonson, Matthew A., Stahl, Eli, Strohmaier, Jana, Witt, Stephanie H., Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau, Richard A., Bene, Judit, Bergen, Sarah E., Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Bruggeman, Richard, Buccola, Nancy G., Buckner, Randy L., Byerley, William, Cahn, Wiepke, Cai, Guiqing, Campion, Dominique, Cantor, Rita M., Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chambert, Kimberly D., Chan, Raymond C. K., Chen, Ronald Y. L., Chen, Eric Y. H., Cheng, Wei, Cheung, Eric F. C., Chong, Siow Ann, Cloninger, C. Robert, Cohen, David, Cohen, Nadine, Cormican, Paul, Craddock, Nick, Crowley, James J., Curtis, David, Davidson, Michael, Davis, Kenneth L., Del Favero, Jurgen, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H., Farrell, Martilias S., Franke, Lude, Freedman, Robert, Freimer, Nelson B., Friedl, Marion, Friedman, Joseph I., Fromer, Menachem, Georgieva, Lyudmila, Giegling, Ina, Giusti-Rodriguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I., Golimbet, Vera, Gopal, Srihari, Gratten, Jacob, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian L., Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Hirschhorn, Joel N., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Joa, Inge, Julia, Antonio, Kahn, René S., Kalaydjieva, Luba, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Kennedy, James L., Khrunin, Andrey, Kim, Yunjung, Klovins, Janis, Knowles, James A., Konte, Bettina, Kucinskas, Vaidutis, Kucinskiene, Zita Ausrele, Kuzelova-Ptackova, Hana, Kahler, Anna K., Laurent, Claudine, Chee Keong, Jimmy Lee, Lee, S. Hong, Legge, Sophie E., Lerer, Bernard, Li, Miaoxin, Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lubinski, Jan, Lonnqvist, Jouko, Macek, Milan, Magnusson, Patrik K. E., Maher, Brion S., Mallet, Jacques, Marsal, Sara, Mattingsdal, Morten, McCarley, Robert W., McDonald, Colm, McIntosh, Andrew M., Meier, Sandra, Meijer, Carin J., Melegh, Bela, Melle, Ingrid, Mesholam-Gately, Raquelle I., Metspalu, Andres, Michie, Patricia T., Milani, Lili, Milanova, Vihra, Mokrab, Younes, Morris, Derek W., Mors, Ole, Murphy, Kieran C., Murray, Robin M., Myin-Germeys, Inez, Muller-Myhsok, Bertram, Nelis, Mari, Nertney, Deborah A., Nestadt, Gerald, Nicodemus, Kristin K., Nikitina-Zake, Liene, Nisenbaum, Laura, Nordin, Annelie, O'Callaghan, Eadbhard, O'Dushlaine, Colm, O'Neill, F. Anthony, Oh, Sang-Yun, Olincy, Ann, Olsen, Line, Van Os, Jim, Pantelis,Christos, Papadimitriou, George N., Papiol, Sergi, Parkhomenko, Elena, Pato, Michele T., Paunio, Tiina, Pejovic-Milovancevic, Milica, Perkins, Diana O., Pietilainen, Olli, Pimm, Jonathan, Pocklington, Andrew J., Powell, John, Price, Alkes, Pulver, Ann E., Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roffman, Joshua L., Roussos, Panos, Salomaa, Veikko, Sanders, Alan R., Schall, Ulrich, Schubert, Christian R., Schwab, Sibylle G., Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Shi, Jianxin, Sigurdsson, Engilbert, Silagadze, Teimuraz, Silverman, Jeremy M., Sim, Kang, Slominsky, Petr, Smoller, Jordan W., So, Hon-Cheong, Spencer, Chris C. A., Stahl, Eli A., Stefansson, Hreinn, Steinberg, Stacy, Stogmann, Elisabeth, Straub, Richard E., Strengman, Eric, Stroup, T. Scott, Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M., Szatkiewicz, Jin P., Soderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Waddington, John, Walsh, Dermot, Wang, Dai, Wang, Qiang, Webb, Bradley T., Weiserb, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Wolen, Aaron R., Wong, Emily H. M., Wormley, Brandon K., Xi, Hualin Simon, Zai, Clement C., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Stefansson, Kari, Visscher, Peter M., Adolfsson, Rolf, Andreassen, Ole A., Blackwood, Douglas H. R., Bramon, Elvira, Buxbaum, Joseph D., Borglum, Anders D., Darvasi, Ariel, Domenici, Enrico, Ehrenreich, Hannelore, Esko, Tõnu, Gejman, Pablo V., Gill, Michael, Gurling, Hugh, Hultman, Christina M., Iwata, Nakao, Jablensky, Assen V., Jonsson, Erik G., Kendler, Kenneth S., Kirov, George, Knight, Jo, Lencz, Todd, Levinson, Douglas F., Li, Qingqin S., Liu, Jianjun, Malhotra, Anil K., McCarroll, Steven A., McQuillin, Andrew, Moran, Jennifer L., Mortensen, Preben B., Mowry, Bryan J., Nothen, Markus M., Ophoff, Roel A., Owen, Michael J., Palotie, Aarno, Pato, Carlos N., Petryshen, Tracey L., Posthuma, Danielle, Riley, Brien P., Sham, Pak C., Sklar, Pamela, St Clair, David, Weinberger, Daniel R., Wendland, Jens R., Werge, Thomas, Daly, Mark J., O'Donovan, Michael C., Sullivan, Patrick F. and Keller, Matthew C. (2016) No reliable association between runs of homozygosity and schizophrenia in a well-powered replication study. PLoS Genetics12 10: . doi:10.1371/journal.pgen.1006343

Increased rare duplication burden genomewide in patients with treatment-resistant schizophrenia

Martin, A. K. and Mowry, B. (2016) Increased rare duplication burden genomewide in patients with treatment-resistant schizophrenia. Psychological Medicine46 3: 469-476. doi:10.1017/S0033291715001701

White matter disruptions in schizophrenia are spatially widespread and topologically converge on brain network hubs

Klauser, Paul, Baker, Simon T., Cropley, Vanessa L. , Bousman, Chad, Fornito, Alex, Cocchi, Luca, Fullerton, Janice M., Rasser, Paul, Schall, Ulrich, Henskens, Frans , Michie, Patricia T., Loughland, Carmel, Catts, Stanley V. , Mowry, Bryan, Weickert, Thomas W., Shannon Weickert, Cynthia, Carr, Vaughan, Lenroot, Rhoshel, Pantelis, Christos and Zalesky, Andrew (2016) White matter disruptions in schizophrenia are spatially widespread and topologically converge on brain network hubs. Schizophrenia Bulletin, . doi:10.1093/schbul/sbw100

Verbal initiation, suppression, and strategy use and the relationship with clinical symptoms in schizophrenia

Martin, Andrew K., Gibson, Emily C., Mowry, Bryan and Robinson,Gail A. (2016) Verbal initiation, suppression, and strategy use and the relationship with clinical symptoms in schizophrenia. Journal of the International Neuropsychological Society22 7: 735-743. doi:10.1017/S1355617716000552

Dynamic emotion perception and prior expectancy

Dzafic, Ilvana, Martin, Andrew K., Hocking, Julia, Mowry, Bryan and Burianová, Hana (2016) Dynamic emotion perception and prior expectancy. Neuropsychologia86 131-140. doi:10.1016/j.neuropsychologia.2016.04.025

Developmental suppression of schizophrenia-associated miR-137 alters sensorimotor function in zebrafish

Giacomotto, J., Carroll, A. P., Rinkwitz, S., Mowry, B., Cairns, M. J. and Becker, T. S. (2016) Developmental suppression of schizophrenia-associated miR-137 alters sensorimotor function in zebrafish. Translational Psychiatry6 1-10. doi:10.1038/tp.2016.88

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

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 Genetics47 12: 1385-1392. doi:10.1038/ng.3431

Paracingulate sulcus morphology is associated with hallucinations in the human brain

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 Communications6 8956.1-8956.6. doi:10.1038/ncomms9956

Executive functioning in schizophrenia: Unique and shared variance with measures of fluid intelligence

Martin A.K, Mowry, B, Reutens, D and Robinson, G.A (2015) Executive functioning in schizophrenia: Unique and shared variance with measures of fluid intelligence. Brain and Cognition99 57-67. doi:10.1016/j.bandc.2015.07.009

Common genetic risk variants are associated with positive symptoms and decision-making ability in patients with schizophrenia

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 Research229 1-2: 606-608. doi:10.1016/j.psychres.2015.04.045

Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia

Martin, Andrew K., Robinson, Gail, Reutens, David and Mowry, Bryan (2015) Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics168 5: 374-382. doi:10.1002/ajmg.b.32321

Interest in employment among people with schizophrenia

Westcot, Cassandra, Waghorn, Geoffrey, McLean, Duncan, Statham, Dixie and Mowry, Bryan (2015) Interest in employment among people with schizophrenia. American Journal of Psychiatric Rehabilitation18 2: 187-207. doi:10.1080/15487768.2014.954162

Role functioning among adults with schizophrenia

Westcott, Cassandra, Waghorn, Geoff, McLean, Duncan, Statham, Dixie and Mowry, Bryan (2015) Role functioning among adults with schizophrenia. British Journal of Occupational Therapy78 3: 158-165. doi:10.1177/0308022615573372

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

Bulik-Sullivan, Brendan K., Loh, Po-Ru, Finucane, Hilary K., Ripke, Stephen, Yang, Jian, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Patterson, Nick, Daly, Mark J., Price, Alkes L., Neale, Benjamin M., Nertney, Deborah A., Mowry, Bryan J. and Catts, Stanley V. (2015) LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics47 3: 291-295. doi:10.1038/ng.3211

Uncovering the hidden risk architecture of the schizophrenias: confirmation in three independent genome-wide association studies

Arnedo, Javier, Svrakic, Dragan M., del Val, Coral, Romero-Zaliz, Rocio, Hernandez-Cuervo, Helena, Fanous, Ayman H., Pato, Michele T., Pato, Carlos N., de Erausquin, Gabriel A., Cloninger, C. Robert, Zwir, Igor, Molecular Genetics of Schizophrenia Consortium and Mowry, B. J. (2015) Uncovering the hidden risk architecture of the schizophrenias: confirmation in three independent genome-wide association studies. American Journal of Psychiatry172 2: 139-153. doi:10.1176/appi.ajp.2014.14040435

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

O'Dushlaine, Colm, Rossin, Lizzy, Lee, Phil H., Duncan, Laramie, Parikshak, Neelroop N., Newhouse, Stephen, Ripke, Stephan, Neale, Benjamin M., Purcell, Shaun M., Posthuma, Danielle, Nurnberger, John I., Lee, S. Hong, Faraone, Stephen V., Perlis, Roy H., Mowry, Bryan J, Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H., Backlund, Lena, Badner, Judith A., Bailey, Anthony J., Banaschewski, Tobias, Barchas, Jack D., Barnes, Michael R., Barrett, Thomas B., Bass, Nicholas, Battaglia, Agatino, Bauer, Michael, Bayes, Monica, Bellivier, Frank, Bergen, Sarah E., Berrettini, Wade, Betancur, Catalina, Bettecken, Thomas, Biederman, Joseph, Binder, Elisabeth B., Black, Donald W., Blackwood, Douglas H. R., Bloss, Cinnamon S., Boehnke, Michael, Boomsma, Dorret I., Breuer, Rene, Bruggeman, Richard, Cormican, Paul, Buccola, Nancy G., Buitelaar, Jan K., Bunney, William E., Buxbaum, Joseph D., Byerley, William F., Byrne, Enda M, Caesar, Sian, Cahn, Wiepke, Cantor, Rita M., Casas, Miguel, Chakravarti, Aravinda, Chambert, Kimberly, Choudhury, Khalid, Cichon, Sven, Mattheisen, Manuel, Cloninger, C. Robert, Collier, David A., Cook, Edwin H., Coon, Hilary, Cormand, Bru, Corvin, Aiden, Coryell, William H., Craig, David W., Craig, Ian W., Crosbie, Jennifer, Cuccaro, Michael L., Curtis, David, Czamara, Darina, Datta, Susmita, Dawson, Geraldine, Day, Richard, De Geus, Eco J., Degenhardt, Franziska, Djurovic, Srdjan, Donohoe, Gary J., Doyle, Alysa E., Duan, Jubao, Dudbridge, Frank, Duketis, Eftichia, Ebstein, Richard P., Edenberg, Howard J., Elia, Josephine, Ennis, Sean, Etain, Bruno, Fanous, Ayman, Farmer, Anne E., Ferrier, I. Nicol, Flicldnger, Matthew, Fombonne, Eric, Foroud, Tatiana, Frank, Josef, Franke, Barbara, Fraser, Christine, Freedman, Robert, Freimer, Nelson B., Freitag, Christine M., Friedl, Marion, Frisen, Louise, Gailagher, Louise, Gejman, Pablo V., Georgieva, Lyudmila, Gershon, Elliot S., Giegling, Ina, Gill, Michael, Gordon, Scott D., Gordon-Smith, Katherine, Green, Elaine K., Greenwood, Tiffany A., Grice, Dorothy E., Gross, Magdalena, Grozeva, Detelina, Guan, Weihua, Gurling, Hugh, De Haan, Lieuwe, Haines, Jonathan L., Hakonarson, Hakon, Hallmayer, Joachim, Hamilton, Steven P., Hamshere, Marian L., Hansen, Thomas F., Hartmann, Annette M., Hautzinger, Martin, Heath, Andrew C., Henders, Anjali K., Herms, Stefan, Hickie, Ian B., Hipolito, Maria, Hoefels, Susanne, Holsboer, Florian, Hoogendijk, Witte J., Hottenga, Jouke-Jan, Hultman, Christina M., Hus, Vanessa, Ingason, Andres, Ising, Marcus, Jamain, Stephane, Jones, Edward G., Jones, Ian, Jones, Lisa, Tzeng, Jung-Ying, Kaehler, Anna K., Kahn, Rene S., Kandaswamy, Radhika, Keller, Matthew C., Kennedy, James L., Kenny, Elaine, Kent, Lindsey, Kim, Yunjung, Kirov, George K., Klauck, Sabine M., Klei, Lambertus, Knowles, James A., Kohli, Martin A., Koller, Daniel L., Konte, Bettina, Korszun, Ania, Krabbendam, Lydia, Krasucki, Robert, Kuntsi, Jonna, Kwan, Phoenix, Landen, Mikael, Laengstroem, Niklas, Lathrop, Mark, Lawrence, Jacob, Lawson, William B., Leboyer, Marion, Ledbetter, David H., Lencz, Todd, Lesch, Klaus-Peter, Levinson, Douglas F., Lewis, Cathryn M., Li, Jun, Lichtenstein, Paul, Lieberman, Jeffrey A., Lin, Dan-Yu, Linszen, Don H., Liu, Chunyu, Lohoff, Falk W., Loo, Sandra K., Lord, Catherine, Lowe, Jennifer K., Lucae, Susanne, MacIntyre, Donald J., Madden, Pamela A. F., Maestrini, Elena, Magnusson, Patrik K. 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Genome-wide association study suggested the PTPRD polymorphisms were associated with weight gain effects of atypical antipsychotic medications

Yu, Hao, Wang, Lifang, Lv, Luxian, Ma, Cuicui, Du, Bo, Lu, Tianlan, Jin, Chao, Yan, Hao, Yang, Yongfeng, Li, Wenqiang, Ruan, Yanyan, Zhang, Hongyan, Zhang, Hongxing, Mi, Weifeng, Mowry, Bryan, Ma, Wenbin, Li, Keqing, Zhang, Dai and Yue, Weihua (2015) Genome-wide association study suggested the PTPRD polymorphisms were associated with weight gain effects of atypical antipsychotic medications. Schizophrenia Bulletin42 3: 814-823. doi:10.1093/schbul/sbv179

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

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 Epidemiology44 5: 1-16. doi:10.1093/ije/dyv136

Cognitive and structural neuroimaging characteristics of schizophrenia patients with large, rare copy number deletions

Martin, Andrew Kenneth, Robinson, Gail, Reutens, David and Mowry, Bryan (2014) Cognitive and structural neuroimaging characteristics of schizophrenia patients with large, rare copy number deletions. Psychiatry Research: Neuroimaging224 3: 311-318. doi:10.1016/j.pscychresns.2014.10.006

A rare functional noncoding variant at the GWAS-Implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder

Duan, Jubao, Shi, Jianxin, Fiorentino, Alessia, Leites, Catherine, Chen, Xiangning, Moy, Winton, Chen, Jingchun, Alexandrov, Boian S., Usheva, Anny, He, Deli, Freda, Jessica, O'Brien, Niamh L., MGS, GPC, McQuillin, Andrew, Sanders, Alan R., Gershon, Elliot S., DeLisi, Lynn E., Bishop, Alan R., Gurling, Hugh M. D., Pato, Michele T., Levinson, Douglas F., Kendler, Kenneth S., Pato, Carlos N., Gejman, Pablo V. and Mowry, Bryan J. (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 Genetics95 6: 744-753. doi:10.1016/j.ajhg.2014.11.001

Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

Gusev, Alexander, Lee, S. Hong, Trynka, Gosia, Finucane, Hilary, Vilhjálmsson, Bjarni J., Xu, Han, Zang, Chongzhi, Ripke, Stephan, Bulik-Sullivan, Brendan, Stahl, Eli, Schizophrenia Working Group of the Psychiatric Genomics Consortium, SWE-SCZ Consortium, Kaehler, Anna K., Hultman, Christina M., Purcell, Shaun M., McCarroll, Steven A., Daly, Mark, Pasaniuc, Bogdan, Sullivan, Patrick F., Neale, Benjamin M., Wray, Naomi R., Raychaudhuri, Soumya, Price, Alkes L., Visscher, Peter M., Mowry, Bryan J., Psychosis Endophenotypes International Consortium and Wellcome Trust Case Control Consortium (2014) Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases. American Journal of Human Genetics95 5: 535-552. doi:10.1016/j.ajhg.2014.10.004

Copy number deletion burden is associated with cognitive, structural, and resting-state network differences in patients with schizophrenia

Martin, A. K., 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 Research272 324-334. doi:10.1016/j.bbr.2014.07.002

DSM-IV "Criterion A" schizophrenia symptoms across ethnically different populations: evidence for differing psychotic symptom content or structural organization?

McLean, Duncan, Thara, Rangaswamy, John, Sujit, Barrett, Robert, Loa, Peter, McGrath, John and Mowry, Bryan (2014) DSM-IV "Criterion A" schizophrenia symptoms across ethnically different populations: evidence for differing psychotic symptom content or structural organization?. Culture, Medicine, and Psychiatry38 3: 408-426. doi:10.1007/s11013-014-9385-8

Cannabis abuse and age at onset in schizophrenia patients with large, rare copy number variants

Martin, Andrew Kenneth, Robinson, Gail, Reutens, David and Mowry, Bryan (2014) Cannabis abuse and age at onset in schizophrenia patients with large, rare copy number variants. Schizophrenia Research155 1-3: 21-25. doi:10.1016/j.schres.2014.03.004

Elevated levels of autoantibodies targeting the M1 muscarinic acetylcholine receptor and neurofilament medium in sera from subgroups of patients with schizophrenia

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 Neuroimmunology269 1-2: 68-75. doi:10.1016/j.jneuroim.2014.02.008

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

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 Psychiatry75 5: 371-377. doi:10.1016/j.biopsych.2013.05.040

Biological insights from 108 schizophrenia-associated genetic loci

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. Nature511 7510: 421-427. doi:10.1038/nature13595

Theory of mind and the social brain: implications for understanding the genetic basis of schizophrenia

Martin, A. K., Robinson, G., Dzafic, I., Reutens, David and Mowry, Bryan (2014) Theory of mind and the social brain: implications for understanding the genetic basis of schizophrenia. Genes, Brain and Behavior13 1: 104-117. doi:10.1111/gbb.12066

Schizophrenia genetic variants are not associated with intelligence

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 Medicine43 12: 2563-2570. doi:10.1017/S0033291713000196

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

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 Genetics45 10: 1150-U282. doi:10.1038/ng.2742

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent

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 Genetics93 3: 463-470. doi:10.1016/j.ajhg.2013.07.007

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Lee, S. Hong, Ripke, Stephan, Neale, Benjamin M., Faraone, Stephen V., Purcell, Shaun M., Perlis, Roy H., Mowry, Bryan J., Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H., Backlund, Lena, Badner, Judith A., Bailey, Anthony J., Banaschewski, Tobias, Barchas, Jack D., Barnes, Michael R., Barrett, Thomas B., Bass, Nicholas, Battaglia, Agatino, Bauer, Michael, Bayes, Monica, Bellivier, Frank, Bergen, Sarah E., Berrettini, Wade, Betancur, Catalina, Bettecken, Thomas, Biederman, Joseph, Binder, Elisabeth B., Black, Donald W., Blackwood, Douglas H. 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E., Mahon, Pamela B., Maier, Wolfgang, Malhotra, Anil K., Mane, Shrikant M., Martin, Christa L., Martin, Nicholas G., Mattheisen, Manuel, Matthews, Keith, Mattingsdal, Morten, McCarroll, Steven A., McGhee, Kevin A., McGough, James J., McGrath, Patrick J., McGuffin, Peter, McInnis, Melvin G., McIntosh, Andrew, McKinney, Rebecca, McLean, Alan W., McMahon, Francis J., McMahon, William M., McQuillin, Andrew, Medeiros, Helena, Medland, Sarah E., Meier, Sandra, Melle, Ingrid, Meng, Fan, Meyer, Jobst, Middeldorp, Christel M., Middleton, Lefkos, Milanova, Vihra, Miranda, Ana, Monaco, Anthony P., Montgomery, Grant W., Moran, Jennifer L., Moreno-De-Luca, Daniel, Morken, Gunnar, Morris, Derek W., Morrow, Eric M., Moskvina, Valentina, Muglia, Pierandrea, Muehleisen, Thomas W., Muir, Walter J., Mueller-Myhsok, Bertram, Murtha, Michael, Myers, Richard M., Myin-Germeys, Inez, Neale, Michael C., Nelson, Stan F., Nievergelt, Caroline M., Nikolov, Ivan, Nimgaonkar, Vishwajit, Nolen, Willem A., Noethen, Markus M., Nurnberger, John I., Nwulia, Evaristus A., Nyholt, Dale R., O'Dushlaine, Colm, Oades, Robert D., Olincy, Ann, Oliveira, Guiomar, Olsen, Line, Ophoff, Roel A., Osby, Urban, Owen, Michael J., Palotie, Aarno, Parr, Jeremy R., Paterson, Andrew D., Pato, Carlos N., Pato, Michele T., Penninx, Brenda W., Pergadia, Michele L., Pericak-Vance, Margaret A., Pickard, Benjamin S., Pimm, Jonathan, Piven, Joseph, Posthuma, Danielle, Potash, James B., Poustka, Fritz, Propping, Peter, Puri, Vinay, Quested, Digby J., Quinn, Emma M., Antoni Ramos-Quiroga, Josep, Rasmussen, Henrik B., Raychaudhuri, Soumya, Rehnstroem, Karola, Reif, Andreas, Ribases, Marta, Rice, John P., Rietschel, Marcella, Roeder, Kathryn, Roeyers, Herbert, Rossin, Lizzy, Rothenberger, Aribert, Rouleau, Guy, Ruderfer, Douglas, Rujescu, Dan, Sanders, Alan R., Sanders, Stephan J., Santangelo, Susan L., Sergeant, Joseph A., Schachar, Russell, Schalling, Martin, Schatzberg, Alan F., Scheftner, William A., Schellenberg, Gerard D., Scherer, Stephen W., Schork, Nicholas J., Schulze, Thomas G., Schumacher, Johannes, Schwarz, Markus, Scolnick, Edward, Scott, Laura J., Shi, Jianxin, Shilling, Paul D., Shyn, Stanley I., Silverman, Jeremy M., Slager, Susan L., Smalley, Susan L., Smit, Johannes H., Smith, Erin N., Sonuga-Barke, Edmund J. S., St Clair, David, State, Matthew, Steffens, Michael, Steinhausen, Hans-Christoph, Strauss, John S., Strohmaier, Jana, Stroup, T. Scott, Sutcliffe, James S., Szatmari, Peter, Szelinger, Szabocls, Thirumalai, Srinivasa, Thompson, Robert C., Todorov, Alexandre A., Tozzi, Federica, Treutlein, Jens, Uhr, Manfred, van den Oord, Edwin J. C. G., Van Grootheest, Gerard, Van Os, Jim, Vicente, Astrid M., Vieland, Veronica J., Vincent, John B., Visscher, Peter M., Walsh, Christopher A., Wassink, Thomas H., Watson, Stanley J., Weissman, Myrna M., Werge, Thomas, Wienker, Thomas F., Wijsman, Ellen M., Willemsen, Gonneke, Williams, Nigel, Willsey, A. Jeremy, Witt, Stephanie H., Xu, Wei, Young, Allan H., Yu, Timothy W., Zammit, Stanley, Zandi, Peter P., Zhang, Peng, Zitman, Frans G., Zoellner, Sebastian, Devlin, Bernie, Kelsoe, John R., Sklar, Pamela, Daly, Mark J., O'Donovan, Michael C., Craddock, Nicholas, Sullivan, Patrick F., Smoller, Jordan W., Kendler, Kenneth S. and Wray, Naomi R. (2013) Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics45 9: 984-995. doi:10.1038/ng.2711

Comparing schizophrenia symptoms in the Iban of Sarawak with other populations to elucidate clinical heterogeneity

McLean, Duncan, Barrett, Robert, Loa, Peter, Thara, Rangaswamy, John, Sujit, McGrath, John, Gratten, Jake and Mowry, Bryan (2013) Comparing schizophrenia symptoms in the Iban of Sarawak with other populations to elucidate clinical heterogeneity. Asia-Pacific Psychiatry7 1: 36-44. doi:10.1111/appy.12093

All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

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 Genetics9 4: . doi:10.1371/journal.pgen.1003449

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

Smoller, Jordan W., Craddock, Nicholas, Kendler, Kenneth, Lee, Phil Hyoun, Neale, Benjamin M., Nurnberger, John I., Ripke, Stephan, Santangelo, Susan, Sullivan, Patrick F., Cross-Disorder Group of the Psychiatric Genomics Consortium and Mowry, Bryan J. (2013) Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. The Lancet381 9875: 1371-1379. doi:10.1016/S0140-6736(12)62129-1

Genetic schizophrenia risk variants jointly modulate total brain and white matter volume

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 Psychiatry73 6: 525-531. doi:10.1016/j.biopsych.2012.08.017

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

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 Genetics45 3: 234-238. doi:10.1038/ng.2555

Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors

Andreassen, Ole A., Djurovic, Srdjan, Thompson, Wesley K., Schork, Andrew J., Kendler, Kenneth S., O'Donovan, Michael C., Rujescu, Dan, Werge, Thomas, van de Bunt, Martijn, Morris, Andrew P., McCarthy, Mark I., Roddey, J. Cooper, McEvoy, Linda K., Desikan, Rahul S., Dale, Anders M., International Consortium for Blood Pressure GWAS and Mowry, Bryan (2013) Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. American Journal of Human Genetics92 2: 197-209. doi:10.1016/j.ajhg.2013.01.001

Will brain cells derived from induced pluripotent stem cells or directly converted from somatic cells (iNs) be useful for schizophrenia research?

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,39 5: 948-954. doi:10.1093/schbul/sbt103

Genome-Wide Association Study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms

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 Psychiatry169 12: 1309-1317. doi:10.1176/appi.ajp.2012.12020218

Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees

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 Psychiatry169 9: 963-973. doi:10.1176/appi.ajp.2012.11091423

Hybridization-based reconstruction of small non-coding RNA transcripts from deep sequencing data

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 Research40 16: 7633-7643. doi:10.1093/nar/gks505

Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26

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 One7 5: e38172.1-e38172.10. doi:10.1371/journal.pone.0038172

The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants

Mowry, B. J. and Gratten, J. (2012) The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants. Molecular Psychiatry18 1: 38-52. doi:10.1038/mp.2012.34

Refining clinical phenotypes by contrasting ethnically different populations with schizophrenia from Australia, India and Sarawak

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 Research196 2-3: 194-200. doi:10.1016/j.psychres.2011.12.027

Schizophrenia-associated HapICE haplotype is associated with increased NRG1 type III expression and high nucleotide diversity

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 Psychiatry2 e104.1-e104.8. doi:10.1038/tp.2012.25

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

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 Psychiatry17 2: 193-201. doi:10.1038/mp.2011.11

Significant relationship between lifetime alcohol use disorders and suicide attempts in an Australian schizophrenia sample

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 Psychiatry46 2: 132-140. doi:10.1177/0004867411433211

Genome-wide association study identifies five new schizophrenia loci

Ripke, Stephan, Sanders, Alan R., Kedler, Kenneth S., Levinson, Douglas F., Sklar, Pamela, Holmans, Peter A., Lin, Dan-Yu, Duan, Jubao, Ophoff, Roel A., Andreassen, Ole A., Scolnick, Edward, Cichon, Sven, St. Clair, David, Corvin, Aiden, Gurling, Hugh, Werge, Thomas, Rujescu, Dan, Blackwood, Douglas H. R., Pato, Carlos N., Malhotra, Anil K., Purcell, Shaun, Dudbridge, Frank, Neale, Benjamin M., Rossin, Lizzy, Visscher, Peter M., Posthuma, Danielle, Ruderfer, Douglas M., Fanous, Ayman, Hreinn, Stefansson, Steinberg, Stacy, Mowry, Bryan J., Golimbet, Vera, De Hert, Marc, Jonsson, Erik G., Bitter, Istvan, Pietilainen, Olli P., Collier, David A., Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L., Amin, Farooq, Bass, Nicholas, Bergen, Sarah E., Black, Donald W., Borglum, Anders D., Brown, Matthew A., Bruggeman, Richard, Buccola, Nancy G., Byerley, William F., Cahn, Wiepke, Cantor, Rita M., Carr, Vaughan J., Catts, Stanley V., Choudhury, Khalid, Cloninger, C. Robert, Cormican, Paul, Craddock, Nicholas, Danoy, Patrick A., Datta, Susmita, de Haan, Lieuwe, Demontis, Ditte, Dikeos, Dimitris, Djurovic, Srdjan, Donnelly, Peter, Donohoe, Gary, Linh, Duong, Dwyer, Sarah, Fink-Jensen, Anders, Freedman, Robert, Freimer, Nelson B., Friedle, Marion, Georgieva, Lyudmila, Giegling, Ina, Gill, Michael, Clenthoj, Birte, Godard, Stephanie, Hamshere, Marian, Hansen, Mark, Hansen, Thomas, Hartmann, Annette M., Henskens, Frans A., Hougaard, David M., Hultman, Christina M., Ingason, Andres, Jablensky, Assen V., Jakobsen, Klaus D., Jay, Maurice, Jurgens, Gesche, Kahn, Rene S., Keller, Matthew C., Kenis, Gunter, Kenny, Elaine, Kim, Yunjung, Kirov, George K., Konnerth, Heike, Konte, Bettina, Krabbendam, Lydia, Krasucki, Robert, Lasseter, Virginia K., Laurent, Claudine, Lawrence, Jacob, Lencz, Todd, Lerer, F. Bernhard, Liang, Kung-Yee, Lichtenstein, Paul, Liebermann, Jeffrey A., Linszen, Don H., Lonnqvist, Jouko, Loughland, Carmel M., Maclean, Alan W., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Malloy, Pat, Mattheisen, Manuel, Mattingsdal, Morten, McGhee, Kevin A., McGrath, John J., McIntosh, Andrew, McLean, Duncan E., McQuillin, Andrew, Melle, Ingrid, Michie, Patricia T., Milanova, Vihra, Morris, Derek W., Mors, Ole, Mortensen, Preben B., Moskvina, Valentina, Muglia, Pierandrea, Myin-Germeys, Inez, Nertney, Deborah A., Nestadt, Gerald, Nielsen, Jimmi, Nikolov, Ivan, Nordentoft, Merete, Norton, Nadine, Nothen, Markus M., O'Dushlaine, Colm T., Olincy, Ann, Olsen, Line, O'Neill, F. Anthony, Orntoft, Torben F., Owen, Michael J., Pantelis, Christos, Papadimitriou, George, Pato, Michele T., Peltonen, Leena, Petursson, Hannes, Pickard, Ben, Pimm, Jonathan, Pulver, Ann E., Puri, Vinay, Quested, Digby, Quinn, Emma M., Rasmussen, Henrik B., Rethelyi, Janos M., Ribble, Robert, Rietschel, Marcella, Riley, Brien P., Ruggeri, Mirella, Schall, Ulrich, Schulze, Thomas G., Schwab, Sibylle G., Scott, Rodney J., Shi, Jianxin, Sigurdson, Engilbert, Silverman, Jeremy M., Spencer, Chris C. A., Stefansson, Kari, Strange, Amy, Strengman, Eric, Stroup, T. Scott, Suvisaari, Jaana, Terenius, Lars, Thirumalai, Srinivasa, Thygesen, Johan H., Timm, Sally, Toncheva, Draga, van den Oord, Edwin, van Os, Jim, van Winkel, Ruud, Veldink, Jan, Walsh, Dermot, Wang, August G., Wiesrma, Durk, Wildenauer, Dieter B., Williams, Hywel J., Williams, Nigel M., Wormley, Brandon, Zammitt, Stan, Sullivan, Patrick F., O'Donovan, Micahel C., Daly, Mark J. and Gejman, Pablo V. (2011) Genome-wide association study identifies five new schizophrenia loci. Nature Genetics43 10: 969-976. doi:10.1038/ng.940

Reliability and validity of a measure of role functioning among people with psychiatric disabilities

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 Journal58 3: 203-208. doi:10.1111/j.1440-1630.2010.00921.x

The reliability of an education-related self-efficacy scale for people with psychiatric disabilities

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 Journal47 2: 136-142. doi:10.1007/s10597-010-9294-4

Copy number variants in Schizophrenia: Confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

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. Americal Journal of Psychiatry168 3: 302-316. doi:10.1176/appi.ajp.2010.10060876

Genetic influences on cost-efficient organization of human cortical functional networks

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 Neuroscience31 9: 3261-3270. doi:10.1523/JNEUROSCI.4858-10.2011

Reliability and validity of a measure of work-related subjective experiences among people with psychiatric disabilities

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 Rehabilitation18 3: 146-157.

Ancestry of the Iban is predominantly Southeast Asian: Genetic evidence from autosomal, mitochondrial, and Y chromosomes

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: 1-8. doi:10.1371/journal.pone.0016338

Australian Schizophrenia Research Bank: A database of comprehensive clinical, endophenotypic and genetic data for aetiological studies of schizophrenia

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. doi:10.3109/00048674.2010.501758

An Investigation of Candidate Regions for Association With Bipolar Disorder

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 Genetics153B 7: 1292-1297. doi:10.1002/ajmg.b.31100

The internet-based MGS2 control sample: Self report of mental illness

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. doi:10.1176/appi.ajp.2010.09071050

Reliability of a scale of work-related self-efficacy for people with psychiatric disabilities

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. doi:10.1097/MRR.0b013e32832e98b8

A brief measure of vocational activity and community participation: Development and reliability of the Activity and Participation Questionnaire

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. doi:10.3109/00048670903487175

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis

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. doi:10.1001/archgenpsychiatry.2009.136

Common variants on chromosome 6p22.1 are associated with schizophrenia

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. Nature460 7256: 753-757. doi:10.1038/nature08192

Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms

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. doi:10.1038/mp.2009.11

Fine-scaled human genetic structure revealed by SNP microarrays

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. doi:10.1101/gr.085589.108

CTLA-4 single-nucleotide polymorphisms in a Caucasian population with schizophrenia

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. doi:10.1016/j.bbi.2008.09.008

Strong Evidence for a Novel Schizophrenia Risk Locus on Chromosome 1p31.1 in Homogeneous Pedigrees From Tamil Nadu, India

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 PSYCHIATRY166 2: 206-215. doi:10.1176/appi.ajp.2008.08030442

Design and clinical characteristics of a homogeneous schizophrenia pedigree sample from Tamil Nadu, India

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. doi:10.1080/00048670902873631

Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders

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 Psychiatry166 5: 540-556. doi:10.1176/appi.ajp.2008.08091354

Meta-analysis of 32 genome-wide linkage studies of schizoph

Ng, M. Y. M., Levinson, D. F., Faraone S. V., Suarez, B. K., DeLisi, L. E., Arinami, T., Riley, B., Paunio, T., Pulver, A. E., Irmansyah, Holmans,P. A., Escamilla, M., Wildenauer, DB, Williams, N. M., Laurent, C., Mowry, Bryan, Brzustowicz, L. M., Maziade, M., Sklar, P., Garver, D. L., Abecasi, G. R., Lerer, B., Fallin, M. D., Gurling, H. M. D., Gejman, P. V., Lindholm, E., Moises, H. W., Byerley, W., Wijsman, E. M., Forabosco, P., Tsuang, M. T., Hwu, H-G., Okazaki, Y., Kendler, K. S., Wormley, B., Fanous, A., Walsh, D., O'Neill, F. A., Peltonen, L., Nestadt, G., Lasseter, V. K., Liang, K. Y., Papadimitriou, G. M., Dikeos, D. G., Schwab, S. G., Owen, M. J., O'Donovan, M. C., Norton, N., Hare, E., Raventos, H., Nicolini, H., Albus, M., Maier, W., Nimgaonkar, V. L., Terenius, L., Mallet, J., Jay, M., Godard, S., Nertney, D., Alexander, M., Crowe, R. R., Silverman, J. M., Bassett, A. S., Roy, M-A., Mérette, C., Pato, C. N., Pato, M. T., Louw Roos, J., Kohn, Y., Amann-Zalcenstein, D., Kalsi, G., McQuillin, A., Curtis, D., Brynjolfson, J., Sigmundsson, T., Petursson, H., Sanders, A. R., Duan, J., Jazin, E., Myles-Worsley, M., Karayiorgou, M. and Lewis, C. M. (2008) Meta-analysis of 32 genome-wide linkage studies of schizoph. Molecular Psychiatry14 8: 774-785. doi:10.1038/mp.2008.135

Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms

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 . doi:10.1186/1471-2156-9-86

A Reanalysis of 409 European-Ancestry and African American Schizophrenia Pedigrees Reveals Significant Linkage to 8p23.3 With Evidence of Locus Heterogeneity

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. doi:10.1002/ajmg.b.30722

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2

O'Donovan, M. C., Norton, N., Williams, H., Peirce, T., Moskvina, V., Nikolov, I., Hamshere, M., Carroll, L., Georgieva, L., Dwyer, S., Holmans, P., Marchini, J. L., Spencer, C. C. A., Howie, B., Leung, H-T, Giegling, I., Hartmann, A. M., Moeller, H.-J., Morris, D. W., Shi, Y., Feng, G., Hoffmann, P., Propping, P., Vasilescu, C., Maier, W., Rietschel, M., Zammit, S., Schumacher, J., Quinn, E. M., Schulze, T. G., Iwata, N., Ikeda, M., Darvasi, A., Shifman, S., He, L., Duan, J., Sanders, A. R., Levinson, D. F., Adolfsson, R., Osby, U., Terenius, L., Jonsson, E. G., Cichon, S., Noethen, M. M., Gill, M., Corvin, A. P., Rujescu, D., Gejman, P. V., Kirov, G., Craddock, N., Williams, N. M., Owen, M. J., Molecular Genetics of Schizophrenia Collaboration and Mowry, B.J. (2008) Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.Molecular Psychiatry14 1: 30-36. doi:10.1038/mp.2008.108

Identification of loci associated with schizophrenia by genome-wide association and follow-up

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. doi:10.1038/ng.201

Fibroblast and lymphoblast gene expression profiles in schizophrenia: Are non-neural cells informative?

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: e2412-1-e2412-5. doi:10.1371/journal.pone.0002412

No significant Association of 14 Candidate Genes With Schizophrenia in a Large European Ancestry Sample: Implications for Psychiatric Genetics

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. doi:10.1176/appi.ajp.2007.07101573

Expression profiling in monozygotic twins discordant for bipolar disorder reveals dysregulation of the WNT signaling pathway

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 signaling pathway. Molecular Psychiatry12 9: 815-825. doi:10.1038/sj.mp.4001998

Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines

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. doi:10.1093/hmg/ddl456

Evidence of altered prefrontal-thalamic circuitry in schizophrenia: An optimised diffusion MRI study

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. doi:10.1016/j.neuroimage.2006.03.003

Olanzapine treatment is associated with reduced high molecular weight adiponectin in serum: A potential mechanism for Olanzapine-induced insulin resistance in patients with schizophrenia

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. doi:10.1097/01.jcp.0000218404.64619.52

Polymorphisms in the vitamin D receptor and their associations with risk of schizophrenia and selected anthropometric measures

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. doi:10.1002/ajhb.20504

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

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. doi:10.1086/500272

Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples

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. doi:10.1375/183242706778025035

Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia

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. doi:10.1038/sj.mp.4001785

Queensland Centre for Mental Health Research: the first 17 years

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

Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia

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. doi:10.1038/sj.mp.4001606

Immune Dysregulation and Self-Reactivity in Schizophrenia: Do Some Cases of Schizophrenia Have an Autoimmune Basis?

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

Dimensions of psychotic illness in schizophrenia pedigrees

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 Genetics138B 1: 125-125.

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

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 Genetics138B 1: 7-7.

Rates of treated schizophrenia and its clinical and cultural features in the population isolate of the Iban of Sarawak: a tri-diagnostic approach

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. doi:10.1017/S0033291704002880

The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data

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

An analysis of DTNBP1 (dysbindin) in Australian and Indian populations

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.

Multicenter linkage study of schizophrenia loci on chromosome 22q

Mowry, B. J., Holmans, P. A., Pulver, A. E., Gejman, P. V., Riley, B., Williams, N. M, Laurent, C., Schwab, S. G., Wildenauer, D.B., Bauche, S., Owen, M. J., Wormley, B., Sanders, A. R., Nestadt, G. and Liang, K. Y. (2004) Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry9 8: 784-795. doi:10.1038/sj.mp.4001481

Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia

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 Genetics75 4: 624-638. doi:10.1086/424887

Low maternal vitamin D as a risk factor for schizophrenia: a pilot study using banked sera

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

Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia-Pacific region

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. doi:10.1002/ajmg.b.20059

Directional and fluctuating asymmetry in finger and a-b ridge counts in psychosis: A case-control study

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 Article 3: . doi:10.1186/1471-244X-3-3

Directional and fluctuating asymmetry in finger and a-b ridge counts in psychosis: a case-control study

Saha, Sukanta, Loesch, Danuta, Chant, David, Welham, Joy, El-Saadi, Ossama, Fananas, 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 . doi:10.1186/1471-244X-3-3

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

Lewis, C. O., Levinson, D., Wise, L., DeLisi, L., Straub, R. and Mowry, B. (2003) Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. American Journal of Human Genetics73 1: 34-48. doi:10.1086/376549

Polymorphisms in the 5 '-untranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression

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. doi:10.1038/sj.mp.4001403

Psychiatric genetics in Australia

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

Is Schizophrenia Linked to Chromosome 1q? (Response to Technical Comments)

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: 2277-2277. doi:10.1126/science.1076508

No Major Schizophrenia Locus Detected on Chromosome 1q in a Large Multicenter Sample

Holmans, P. A., Levinson, D. F., Laurent, C., Riley, B., Pulver, A. E., Gejman, P. V., Schwab, S. G., Williams, N. M., Owen, M. J., Wildenauer, D. B., Sanders, A. R., Nestadt, G., Mowry, B., Wormley, B., Bauche, S., Soubigou, S., Ribble, R., Nertney, D. A., Liang, K. Y., Martinolich, L., Maler, W., Norton, N., Williams, H., Albus, M., Carpenter, E. B., de Marchi, N., Ewen-White, K. R., Walsh, D., Jay, M., Deleuze, J. F., O'Neill, F. A., Papadimitriou, G., Weilbaecher, A., Lerer, B., O'Donovan, M. C., Dikeos, D., Silverman, J. M., Kendler, K. S., Mallet, J., Crowe, R. R. and Walters, M. (2002) No Major Schizophrenia Locus Detected on Chromosome 1q in a Large Multicenter Sample. Science296 5568: 739-741. doi:10.1126/science.1069914

Assessing the co-segregation of disorders within pedigrees: a comparison of two methods

Chant, David, McGrath, John and Mowry, Bryan (2002) Assessing the co-segregation of disorders within pedigrees: a comparison of two methods. Australasian Epidemiologist9 1: 29-33.

Minor physical anomalies and quantitative measures of the head and face in patients with psychosis

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. doi:10.1001/archpsyc.59.5.458

The Lifetime Dimensions of Psychosis Scale (LDPS): description and interrater reliability

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.

Urban birth and migrant status as risk factors for psychosis: An Australian case-control study

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. doi:10.1007/s001270170003

Genetic diversity of the human serotonin receptor 1B (HTR1B) gene

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. Genomics72 1: 1-14. doi:10.1006/geno.2000.6411

Second state of a genome scan of schizophrenia: Study of five positive regions in an expanded sample

Mowry, B., Kelly, R. W., Nancarrow, D. J., Lennon, D. P., Nertney, D. A., Jones, H. L., O'Brien, M. F., Thornley, C. E., Walters, M. K., Crowe, R. R., Silverman, J. M., Endicott, J., Sharpe, L., Hayward, N. K., Gladis, M. M., Foote, S. J. and Levinson, D. F. (2000) Second state of a genome scan of schizophrenia: Study of five positive regions in an expanded sample. American Journal of Medical Genetics (Neuropsychiatric Genetics)96 6: 864-869. doi:10.1002/1096-8628(20001204)96:6

Seasonal variation in hospital admission for bipolar disorder, depression and schizophrenia in Tasmania

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

No support for linkage to the bipolar regions on chromosomes 4p, 18p, or 18q in 43 schizophrenia pedigrees

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

Identification and analysis of error types in high-throughput genotyping

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. doi:10.1086/303048

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophenia linkage collaborative group 111

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) Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophenia linkage collaborative group 111. American Journal of Human Genetics67 3: 652-663. doi:10.1086/303041

No support for linkage to the bipolar regions on chromosomes 4p, 18p or 18q in 43 schizophrenia pedigrees

Nancarrow, D. J., Levinson, D. F., Taylor, J. J., Hayward, N., Walters, M. K., Lennon, D. P., Nertney, D. A., Jones, H. T., Brown, D. M., Kirby, A., Kruglyak, L., Crowe, R. R., Andreasen, N. C., Black, D. W., Silverman, J. M., Mohs, R. C., Siever, L. J., Endicott, J., Sharpe, L., Mowry, B. and Mahtani, M. M. (2000) No support for linkage to the bipolar regions on chromosomes 4p, 18p or 18q in 43 schizophrenia pedigrees. American Journal of Medicaletics (Neuropsych Geniatric Genetics)96 2: 224-227.

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q

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

Scoresheet: structured clinical interview for DSM-IV Axis 1 disorders (clinical version)

Mowry, B (1998) Scoresheet: structured clinical interview for DSM-IV Axis 1 disorders (clinical version). Australian and New Zealand Journal of Psychiatry32 6: 895-896.

Structured interview for DSM-IV personality: SIDP-IV

Mowry, B (1998) Structured interview for DSM-IV personality: SIDP-IV. Australian and New Zealand Journal of Psychiatry32 6: 896-897.

A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12

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, Curtis, D, 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 and Read, CM (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 Research32 2: 115-121.

Comparison between register and structured interview diagnoses of schizophrenia: a case for longitudinal diagnostic profiles

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. doi:10.3109/00048679809065535

Genome scan of schizophrenia

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 and Mowry, BJ (1998) Genome scan of schizophrenia. American Journal of Psychiatry155 6: 741-750.

Predictability of rehospitalisation over 5 years for schizophrenia, bipolar disorder and depression

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. doi:10.3109/00048679809062740

Psychopathology: the evolving science of mental disorder

Mowry, B (1998) Psychopathology: the evolving science of mental disorder. Australian and New Zealand Journal of Psychiatry32 2: 315-316.

Puerperal psychosis: associated clinical features in a psychiatric hospital mother-baby unit

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. doi:10.3109/00048679809062741

Response to E. Fuller Torrey's comments on 'Season of birth and schizophrenia in Tasmania'

Jones, IH, Hay, DA, Kirkby, KC, Daniels, BA and Mowry, BJ (1998) Response to E. Fuller Torrey's comments on 'Season of birth and schizophrenia in Tasmania'. Australian and New Zealand Journal of Psychiatry32 1: 137-138.

Study guide to treatments of psychiatric disorders, 2nd edition

Mowry, B (1998) Study guide to treatments of psychiatric disorders, 2nd edition. Australian and New Zealand Journal of Psychiatry32 1: 152-153.

The molecular genetics of schizophrenia: an update

Mowry, BJ, Nancarrow, DJ and Levinson, DF (1997) The molecular genetics of schizophrenia: an update. Australian and New Zealand Journal of Psychiatry31 5: 704-713. doi:10.3109/00048679709062684

Linkage study of schizophrenia to markers within Xp11 near the MAOB gene

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) Linkage study of schizophrenia to markers within Xp11 near the MAOB gene. Psychiatry Research,70 3: 131-143. doi:10.1016/S0165-1781(97)03138-7

Season of birth and schizophrenia in Tasmania

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. doi:10.3109/00048679709073799

Affected-only multiplex pedigree analysis of GAW10 problem 2

Nancarrow, DJ and Mowry, BJ (1997) Affected-only multiplex pedigree analysis of GAW10 problem 2. Genetic Epidemiology14 6: 1029-1034. doi:10.1002/(SICI)1098-2272(1997)14:6<1029::AID-GEPI78>3.0.CO;2-K

Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study

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.

A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12

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. doi:10.1002/(SICI)1096-8628(19960216)67:1<40::AID-AJMG6>3.0.CO;2-W

Penetrance of schizophrenia-related disorders in multiplex families after correction for ascertainment

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

Pilot study of hirsutism in women with psychiatric disorders

Johansson, A and Mowry, B (1996) Pilot study of hirsutism in women with psychiatric disorders. Biological Psychiatry,39 2: 149-151. doi:10.1016/0006-3223(95)00374-6

Schizophrenia Susceptibility and Chromosome 6P24-22

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. doi:10.1038/ng1195-233

Diagnosis of Schizophrenia in a Matched Sample of Australian Aborigines

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

Delusions in Schizophrenia Spectrum Disorders - Diagnostic Issues

Gladis, MM, Levinson, DF and Mowry, BJ (1994) Delusions in Schizophrenia Spectrum Disorders - Diagnostic Issues.Schizophrenia Bulletin20 4: 747-754.

Genetic-Linkage and Schizophrenia - Methods, Recent Findings and Future-Directions

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. doi:10.1080/00048679309075769

Defining the Schizophrenia Spectrum - Issues for Genetic-Linkage Studies

Levinson, DF and Mowry, BJ (1991) Defining the Schizophrenia Spectrum - Issues for Genetic-Linkage Studies.Schizophrenia Bulletin17 3: 491-514.

Screening the Elderly in the Community for Psychiatric-Disorder

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. doi:10.3109/00048679009077684

Quantification of physical illness in psychiatric research in the elderly

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. doi:10.1002/gps.930050304

Psychiatric-Examination - Notes On Eliciting and Recording Clinical Information in Psychiatric-Patients - Inst-Psychiat-Dept-Psychiat

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 Psychiatry23 2: 284-285.

A Study of Mild Dementia in the Community Using a Wide-Range of Diagnostic-Criteria

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 328-334. doi:10.1192/bjp.153.3.328

The Decline of the Old Medical Regime in Stuart London - Cook,hj

Mowry, BJ (1988) The Decline of the Old Medical Regime in Stuart London - Cook,hj. Annals of Science45 2: 219-220.

From Galen Theory to Harvey,william Theory - a Case-Study in the Rationality of Scientific Theory Change

Mowry, B (1985) From Galen Theory to Harvey,william Theory - a Case-Study in the Rationality of Scientific Theory Change. Studies in History and Philosophy of Science16 1: 49-82. doi:10.1016/0039-3681(85)90007-X

From Galen's Theory To William Harvey's Theory: A Case Study In The Rationality Of Scientific Theory Change

Mowry, Bryan (1985) From Galen's Theory To William Harvey's Theory: A Case Study In The Rationality Of Scientific Theory Change. Studies in the History and Philosophy of Science16 1: 49-82.

Conference Publication

Voxel-Based Morphometry of Patients with Schizophrenia and Schizoaffective Disorders

Shaffer, J., Choupan, J., Mowry, B., Yang, Z. and Reutens, D. (2015). Voxel-Based Morphometry of Patients with Schizophrenia and Schizoaffective Disorders. In: Journal of Investigative Medicine. Southern Regional Meeting of the American-Federation-for-Medical-Research, New Orleans, LA, United States, (443-443). 26-28 February 2015. doi:10.1097/JIM.0000000000000146

Characterizing rare copy number variants in schizophrenia: a clinical, cognitive, and neuroimaging study

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. In: ICON 2014: XII International Conference on Cognitive Neuroscience, Brisbane, QLD, Australia, (). 27-31 July, 2014. doi:10.3389/conf.fnhum.2015.217.00306

It development and management of a live e-research system: Experiences with the Australian Schizophrenia Research Bank

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. In: HEALTHINF 2012 - Proceedings of the International Conference on Health Informatics. HEALTHINF 2012 - International Conference on Health Informatics, Vilamoura, Algarve, (125-130). 1 - 4 February 2012.

The Australian schizophrenia research bank (ASRB): The first 550 schizophrenia sample profile

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. In: Supplement to Schizophrenia Bulletin: Abstracts of the 13th International Congress on Schizophrenia Research (ICOSR). 13th International Congress on Schizophrenia Research (ICOSR), Colorado Springs CO, United States, (54-55). 2-6 April 2011.

Associations between perinatal complications and clinical, neurological and cognitive outcomes in adults with schizophrenia: A preliminary analysis from ASRB Queensland

Diminic, S, Stiller, A, Mowry, B, Catts, S and Australian Schizophrenia Research (2010). Associations between perinatal complications and clinical, neurological and cognitive outcomes in adults with schizophrenia: A preliminary analysis from ASRB Queensland. In: 11th Australasian Schizophrenia Conference. 11th Biennial Australasian Schizophrenia Conference, Sydney, NSW, Australia, (A-44-A-44). 22-24 September 2010. doi:10.3109/00048674.2010.507066

Elevated levels of autoantibodies against neurotransmitter receptor-related molecules in schizophrenia

Jones, Amanda, Mowry, Bryan, Pender, Michael and Greer, Judith (2010). Elevated levels of autoantibodies against neurotransmitter receptor-related molecules in schizophrenia. In: JOURNAL OF NEUROIMMUNOLOGY. 10th Congress of the International-Society-of-Neuroimmunology (ISNI), Sitges SPAIN, (54-54). OCT 26-30, 2010.

Genome wide analysis of DNA copy number in schizophrenia reveals loss of heterozygosity on chromosome 6P22.1 and 16P11.2-11.1

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. In: 11th Australasian Schizophrenia Conference : Abstracts. 11th Australasian Schizophrenia Conference, Sydney, Australia, (A32-A32). 22-24 September 2010.

The Australian Schizophrenia Research Bank (ASRB): An example of eResearch

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. In: H. A. Nasrallah and L. E. DeLisi, Schizophrenia Research. Proceedings of: 2nd Biennial Schizophrenia International Research Conference. 2nd Schizophrenia International Research Society Conference, Florence, Italy, (427-428). 10-14 April 2010. doi:10.1016/j.schres.2010.02.788

The Australian Schizophrenia Research Bank (ASRB): Demographic, clinical and neropsychological profiles for the first 500 participants with schizophrenia

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 neropsychological profiles for the first 500 participants with schizophrenia. In: Schizophrenia Research. 2nd Biennial Schizophrenia International Research Conference. 2nd Biennial Schizophrenia International Research Conference, Florence, Italy, (312-312). April 10-14, 2010. doi:10.1016/j.schres.2010.02.525

The Australian Schizophrenia Research Bank (ASRB): Demographic, clinical and neuropsychological profile of participants with schizophrenia

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. In: 11th Australasian Schizophrenia Conference, Sydney, Australia, (A59-A59). 22-24 September 2010. doi:10.3109/00048674.2010.507066

The Australian Schizophrenia Research Bank (ASRB): Quality assurance and control for a comprehensive clinical, neurospychologial, genetic and neuroimaging data for researchers

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. In: Schizophrenia Research. 2nd Biennial Schizophrenia International Research Conference. 2nd Biennial Schizophrenia International Research Conference, Florence, Italy, (200-200). April 10-14 2010. doi:10.1016/j.schres.2010.02.269

A Database of Comprehensive Clinical, Endophenotypic and Genetic Data for Aetiological Studies of Schizophrenia

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. In: Schizophrenia Bulletin. 12th International Congress on Schizophrenia Research, San Diego Ca, (108-108). Mar 28-Apr 01, 2009.

IT support for the Australian Schizophrenia Research Bank

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. In: Healthinf 2009: Proceedings of the International Conference On Health Informatics. 2nd International Conference on Health Informatics (HEALTHINF 2009), Oporto, Portugal, (405-410). 14-17 January 2009.

A progress report on the Australian Schizophrenia Research Bank

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. In: Peter Joyce, Australian & New Zealand Journal of Psychiatry: Proceedings of the10th Australasian Schizophrenia Conference. 10th Australasian Schizophrenia Conference, Melbourne, Australia, (A40-A40). 23-24 October 2008. doi:10.1080/00048670802441851

The Australian Schizophrenia Research Bank (ASRB) computer-based Clinical Assessment Software (CAS): Development and application

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. In: Australian and New Zealand Journal of Psychiatry: Australian Society for Psychiatric Research (ASPR) Annual Conference 2008. Australian Society for Psychiatric Research (ASPR) Annual Conference 2008., Newcastle, Australia, (A104-A105). 3-5 December 2008. doi:10.1080/00048670802549646

An overview of the Australian schizophrenia research bank: Linking brain function and structure with genetics in a large sample of schizophrenia cases and controls

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. In: Peter Joyce, Australian & New Zealand Journal of Psychiatry. ASPR Symposium Presentations. World Psychiatric Association International Congress 2007, Melbourne, Australia, (A464-A464). 28 November-2 December 2007. doi:10.1080/00048670701757076

The national recruitment and assessment of people with schizophrenia: The ASRB experience

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. In: Peter Joyce, Abstracts from the WPA International Congress 2007. World Psychiatric Association International Congress 2007, Melbourne, Australia, (A464-A464). 28 November-2 December 2007. doi:10.1080/00048670701757076

Genomewide SNP linkage scan of schizophrenia in a large multicenter sample

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. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics. 14th World Congress on Psychiatric Genetics, Cagliari Italy, (697-697). Oct 28-Nov 01, 2006.

Comprehensive linkage disequilibrium mapping of schizophrenia candidate genes in a large European-ancestry sample

Gejman, PV, Duan, J, Martinez, M, Sanders, AR, Burrell, G, Hou, C, He, D, Schwartz, D, Buccola, NG, Mowry, BJ, Freedman, R, Amin, F, Black, DW, Silverman, JM, Byerley, WF, Crowe, RR, Cloninger, CR and Levinson, DF (2006). Comprehensive linkage disequilibrium mapping of schizophrenia candidate genes in a large European-ancestry sample. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics. 14th World Congress on Psychiatric Genetics,, Italy, (689-689). 28 OCT-01 NOV 2006.

Genetics of schizophrenia: Progress and caveats

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. In: The international journal of neuropsychopharmacology :. XXIVth CINP Congress, Chicago, IL, U.S.A., (S28-S28). 9-13 July, 2006. doi:10.1017/S1461145706007292

Confirmation of the catechol-O-methyltransferase gene contribution to schizophrenia

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. In: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics. 12th World Congress of Psychiatric Genetics, Dublin Ireland, (134-134). Oct 09-13, 2004.

Familiality of symptoms and symptom dimensions in a sample of Indian families

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

Polymorphisms in trace amine receptor 4 (TRAR4) are associated with susceptibility for schizophrenia on chromosome 6q23.2

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.

Caste, geography and genetic structure in Hindu populations.

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.. In: American Journal of Human Genetics.Annual Meeting of the American-Society-of-Human-Genetics, Los Angeles California, (400-400). Nov 04-08, 2003.

Linkage disequilibrium analysis of single nucleotide polymorphisms of the glutamate receptor 6 gene and schizophrenia

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. In: American Journal of Human Genetics. Annual Meeting of the American-Society-of-Human-Genetics, Los Angeles California, (488-488). Nov 04-08, 2003.

Gene-finding approaches in psychosis

Mowry, B (2002). Gene-finding approaches in psychosis. In: Australian and New Zealand Journal of Psychiatry. , , (A30-A30). .

Linkage disequillbrium analysis of 6ql3-q26 schizophrenia candidate genes.

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

The analysis of four candidate chromosomal regions in two schizophrenia datasets from Fiji

Mowry, BJ, Nancarrow, DJ, O'Haeri, J, Walters, MK, Nertney, DA, Hayward, NK, Ott, J and Gordon, D (2002). The analysis of four candidate chromosomal regions in two schizophrenia datasets from Fiji. In: American Journal of Medical Genetics. 10th World Congress of Psychiatric Genetics, Brussels Belgium, (862-862). Oct 09-13, 2002.

Low maternal vitamin D as a risk factor for schizophrenia: A pilot study using banked sera

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. In: Schizophrenia Research. , , (228-229). .

The presence of quasi-psychotic phenomena is associated with minor physical anomalies and craniofacial measures in well controls

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. In: Schizophrenia Research: Abstracts of the XIth Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, February 24–March 1, 2002. XIth Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (232-233). 24 February – 1 March, 2002. doi:10.1016/S0920-9964(01)00381-4

Molecular genetics of schizophrenia

Mowry, B. J. and Nancarrow, D. J. (2001). Molecular genetics of schizophrenia. In: Clinical and Experimental Pharmacology and Physiology. Proceedings of the Australian Neuroscience Society Symposium on Schizophrenia.Australian-Neuroscience-Society Symposium on Schizophrenia, Melbourne, (66-69). January-February 2000. doi:10.1046/j.1440-1681.2001.03399.x

Estimating genotyping error rate in a fine-mapping project.

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.. In: American Journal of Medical Genetics. , , (570-571). .

Genetic diversity of the human serotonin receptor 1B (HTR1B).

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).. In: American Journal of Medical Genetics. , , (564-564). .

Multi-allelic TDT simulation study of indigenous Fijian families with psychosis.

Mowry, B, Nancarrow, D, Ohaeri, J, Gordon, D and Ott, J (2000). Multi-allelic TDT simulation study of indigenous Fijian families with psychosis.. In: American Journal of Medical Genetics. , , (549-550). .

Dysmorphogenesis in psychosis: Quantitative and qualitative measures involving the head and face

McGrath, J., Grim, V., Cardy, S., Chapple, B. and Mowry, B. (2000). Dysmorphogenesis in psychosis: Quantitative and qualitative measures involving the head and face. In: Schizophrenia Research: Abstracts of the Biennial Winter Workshop on Schizophrenia. Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (84-84). 5 February - 11 February 2000. doi:10.1016/S0920-9964(00)90498-5

Endorsement of CIDI psychosis screening items in the Australian Survey of Mental Health and Well being

McGrath, J., White, P., Mowry, B., Chant, D., Slade, T. and Andrews, G. (2000). Endorsement of CIDI psychosis screening items in the Australian Survey of Mental Health and Well being. In: Schizophrenia Research: Abstracts of the Biennial Winter Workshop on Schizophrenia. Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (44-44). 11 - 15 February, 2000. doi:10.1016/S0920-9964(00)90395-5

Endorsement of CIDI psychosis screening items in the Australian Survey of mental Health and Well Being

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. In: L E DeLisi, Abstracts of Tenth Biennial Winter Workshsop on Schizophrenia - Special Issue. Tenth Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (44). 5-11 February 2000.

Increased risk of psychosis in rural-born individuals: An Australian catchment-area study

McGrath, J., Cardy, S., Chapple, B. and Mowry, B. (2000). Increased risk of psychosis in rural-born individuals: An Australian catchment-area study. In: Schizophrenia Research: Biennial Winter Workshop on Schizophrenia. Biennial Winter Workshop on Schizophrenia, Davos, Switzerland, (20-20). 5 February - 11 February 2000. doi:10.1016/S0920-9964(00)90346-3

Increased risk of psychosis in rural-born individuals: an Australian Catchement-area Study

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

The continuum of quasi-psychotic beliefs and experiences in the Australian general public

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The continuum of quasi-psychotic beliefs and experiences in the Australian general public

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Genome scan of schizophrenia: Results of genotyping of positive regions.

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.. In: Molecular Psychiatry. , , (S37-S37). .

Was the pen mightier than the computer? Tasmanian hospital admission registers in the mid-nineteenth century.

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Mutational analysis of the 5-HT1B and 5-HT1E serotonin receptor genes in three datasets with schizophrenia.

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Prevalence of substance use disorder in an Australian schizophrenia spectrum multiply-affected family study

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The Potential of Isonymy in Psychiatric Genetics

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  •  Dr Rangaswamy Thara -  Schizophrenia Research Foundation (SCARF), Chennai, India
  •  Prof Matthew Brown - Diamantina Institute, The University of Queensland
  •  A/Prof Naomi Wray - Queensland Brain Institute, The University of Queensland
  •  Prof Peter Visscher - Queensland Brain Institute, The University of Queensland
  •  Prof David Reutens - Centre for Advanced Imaging, The University of Queensland
  •  Prof Lynn Jorde - University of Utah School of Medicine, Salt Lake City, Utah
  •  Psychiatric Genetics Consortium, Schizophrenia
  •  Molecular Genetics of Schizophrenia Consortium
  •  Australian Schizophrenia Research Bank