Monoamine oxidase A and childhood adversity as risk factors for conduct disorder in females von Prom-Wormley, E. C., Eaves, L. J., Foley, D. L., Gardner, C. O., Archer, K. J., Wormley, B. K., Maes, H. H., Riley, B. P., Silberg, J. L.

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Defects in intracellular trafficking of fungal cell wall synthases lead to aberrant host immune recognition von Esher, Shannon K, Ost, Kyla S, Kohlbrenner, Maria A, Pianalto, Kaila M, Telzrow, Calla L, Campuzano, Althea, Nichols, Connie B, Munro, Carol, Wormley, Jr, Floyd L, Alspaugh, J Andrew

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Replication of association between schizophrenia and ZNF804A in the Irish Case–Control Study of Schizophrenia sample von Riley, B, Thiselton, D, Maher, B S, Bigdeli, T, Wormley, B, McMichael, G O, Fanous, A H, Vladimirov, V, O'Neill, F A, Walsh, D, Kendler, K S

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Examining interactions between polygenic scores and interpersonal trauma exposure on alcohol consumption and use disorder in an ancestrally diverse college cohort von Sheerin, Christina M, O'Hara-Payne, Rowan K, Lancaster, Eva E, Suarez-Rivas, Hailie, Chatzinakos, Chris, Prom-Wormley, Elizabeth C, Peterson, Roseann E

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Genome-wide association analysis identifies 13 new risk loci for schizophrenia von Ripke, Stephan, O'Dushlaine, Colm, Chambert, Kimberly, Moran, Jennifer L, Kähler, 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, 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

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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects von Merico, Daniele, Antaki, Danny, Shetty, Aniket, Gujral, Madhusudan, Brandler, William M, Malhotra, Dheeraj, Alexander, Madeline, Belliveau, Richard A, Bergen, Sarah E, Bertalan, Marcelo, Bevilacqua, Elizabeth, Cantor, Rita M, Carrera, Noa, Cormican, Paul, Crespo-Facorro, Benedicto, Curtis, David, Davidson, Michael, Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Essioux, Laurent, Farrell, Martilias S, Freedman, Robert, Freimer, Nelson B, Georgieva, Lyudmila, Gershon, Elliot S, Giegling, Ina, Godard, Stephanie, Goldstein, Jacqueline I, Hamshere, Marian L, Hartmann, Annette M, Hofman, Andrea, Kähler, Anna K, Kalaydjieva, Luba, Kelly, Brian J, Lee, S Hong, Legge, Sophie E, Lerer, Bernard, Levy, Deborah L, Maher, Brion S, Mattingsdal, Morten, McDonald, Colm, Metspalu, Andres, Milanova, Vihra, Morris, Derek W, Murray, Robin M, Nestadt, Gerald, Nicodemus, Kristin K, Nordin, Annelie, Oh, Sang-Yun, Olsen, Line, Van Os, Jim, Pantelis, Christos, Pers, Tune H, Powell, John, Price, Alkes, Pulver, Ann E, Purcell, Shaun M, Rasmussen, Henrik B, Richards, Alexander L, Roussos, Panos, Schall, Ulrich, Schwab, Sibylle G, Smoller, Jordan W, Spencer, Chris C A, Stahl, Eli A, Stroup, T Scott, Suvisaari, Jaana, Svrakic, Dragan M, Szatkiewicz, Jin P, Veijola, Juha, Waddington, John, Webb, Bradley T, Williams, Nigel M, Williams, Stephanie, Wolen, Aaron R, Adolfsson, Rolf, Blackwood, Douglas H R, Bramon, Elvira, Buxbaum, Joseph D, Collier, David A, Daly, Mark J, Darvasi, Ariel, Domenici, Enrico, Gill, Michael, Iwata, Nakao, Jablensky, Assen V, Jönsson, Erik G, Kirov, George, Knight, Jo, Levinson, Douglas F, Ophoff, Roel A, Owen, Michael J, Rietschel, Marcella, Rujescu, Dan, O'Donovan, Michael C, Neale, Benjamin M

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Genome-wide association study identifies five new schizophrenia loci von Ripke, Stephan, Sanders, Alan R, Kendler, 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, Stefansson, Hreinn, Steinberg, Stacy, Mowry, Bryan J, Golimbet, Vera, De Hert, Marc, Jonsson, Erik G, Bitter, Istvan, Pietilaeinen, Olli P H, Collier, David A, Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L, Amin, Farooq, Bass, Nicholas, Bergen, Sarah E, Black, Donald W, Boerglum, Anders D, Brown, Matthew A, Bruggeman, Richard, Buccola, Nancy G

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Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes von Edwards, Alexis C, Bigdeli, Tim B, Docherty, Anna R, Bacanu, Silviu, Lee, Donghyung, de Candia, Teresa R, Moscati, Arden, Thiselton, Dawn L, Maher, Brion S, Wormley, Brandon K, Walsh, Dermot, O'Neill, Francis A, Kendler, Kenneth S, Riley, Brien P, Fanous, Ayman H

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Testosterone modifies the effect of APOE genotype on hippocampal volume in middle-aged men von PANIZZON, M. S, HAUGER, R, JACOBSON, K. C, LYONS, M. J, MENDOZA, S. P, NEALE, M. C, PROM-WORMLEY, E. C, SEIDMAN, L. J, TSUANG, M. T, XIAN, H, KREMEN, W. S, DALE, A. M, EAVES, L. J, EYLER, L. T, FISCHL, B, FENNEMA-NOTESTINE, C, FRANZ, C. E, GRANT, M. D, JAK, A. J

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Association between major depression and type 2 diabetes in midlife: findings from the Screening Across the Lifespan Twin Study von Mezuk, Briana, Heh, Victor, Prom-Wormley, Elizabeth, Kendler, Kenneth S, Pedersen, Nancy L

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Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Ortholog of the Mouse Dysbindin Gene, Is Associated with Schizophrenia von Straub, Richard E., Jiang, Yuxin, MacLean, Charles J., Ma, Yunlong, Webb, Bradley T., Myakishev, Maxim V., Harris-Kerr, Carole, Wormley, Brandon, Sadek, Hannah, Kadambi, Bharat, Cesare, Anthony J., Gibberman, Avi, Wang, Xu, O'Neill, F. Anthony, Walsh, Dermot, Kendler, Kenneth S.

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Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms von Holmans, P A, Riley, B, Pulver, A E, Owen, M J, Wildenauer, D B, Gejman, P V, Mowry, B J, Laurent, C, Kendler, K S, Nestadt, G, Williams, N M, Schwab, S G, Sanders, A R, Nertney, D, Mallet, J, Wormley, B, Lasseter, V K, O'Donovan, M C, Duan, J, Albus, M, Alexander, M, Godard, S, Ribble, R, Liang, K Y, Norton, N, Maier, W, Papadimitriou, G, Walsh, D, Jay, M, O'Neill, A, Lerer, F B, Dikeos, D, Crowe, R R, Silverman, J M, Levinson, D F

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Loosening the definition of culture: An investigation of gender and cultural tightness von Wormley, Alexandra S., Scott, Matthew, Grimm, Kevin, Li, Norman P., Choy, Bryan K.C., Cohen, Adam B.

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Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees von 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-Bauché, 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, Dudbridge, Frank, Holmans, Peter A.

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Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibi... von STRAUB, R. E, MACLEAN, C. J, WALSH, D, KENDLER, K. S, MA, Y, WEBB, B. T, MYAKISHEV, M. V, HARRIS-KERR, C, WORMLEY, B, SADEK, H, KADAMBI, B, O'NEILL, F. A

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Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes: Table 1 von Edwards, Alexis C., Bigdeli, Tim B., Docherty, Anna R., Bacanu, Silviu, Lee, Donghyung, de Candia, Teresa R., Moscati, Arden, Thiselton, Dawn L., Maher, Brion S., Wormley, Brandon K., Walsh, Dermot, O’Neill, Francis A., Kendler, Kenneth S., Riley, Brien P., Fanous, Ayman H.

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An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis von Morris, Derek W, Pearson, Richard D, Cormican, Paul, Kenny, Elaine M, O'Dushlaine, Colm T, Perreault, Louis-Philippe Lemieux, Giannoulatou, Eleni, Tropea, Daniela, Maher, Brion S, Wormley, Brandon, Kelleher, Eric, Fahey, Ciara, Molinos, Ines, Bellini, Stefania, Pirinen, Matti, Strange, Amy, Freeman, Colin, Thiselton, Dawn L, Elves, Rachel L, Regan, Regina, Ennis, Sean, Dinan, Timothy G, McDonald, Colm, Murphy, Kieran C, O'Callaghan, Eadbhard, Waddington, John L, Walsh, Dermot, O'Donovan, Michael, Grozeva, Detelina, Craddock, Nick, Stone, Jennifer, Scolnick, Ed, Purcell, Shaun, Sklar, Pamela, Coe, Bradley, Eichler, Evan E, Ophoff, Roel, Buizer, Jacobine, Szatkiewicz, Jin, Hultman, Christina, Sullivan, Patrick, Gurling, Hugh, Mcquillin, Andrew, St Clair, David, Rees, Elliott, Kirov, George, Walters, James, Blackwood, Douglas, Johnstone, Mandy, Donohoe, Gary, O'Neill, Francis A, Kendler, Kenneth S, Gill, Michael, Riley, Brien P, Spencer, Chris C A, Corvin, Aiden

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Multicenter linkage study of schizophrenia loci on chromosome 22q von 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, Bauché, S, Owen, M J, Wormley, B, Sanders, A R, Nestadt, G, Liang, K Y, Duan, J, Ribble, R, Norton, N, Soubigou, S, Maier, W, Ewen-White, K R, deMarchi, N, Carpenter, B, Walsh, D, Williams, H, Jay, M, Albus, M, Nertney, D A, Papadimitriou, G, O'Neill, A, O'Donovan, M C, Deleuze, J-F, Lerer, F B, Dikeos, D, Kendler, K S, Mallet, J, Silverman, J M, Crowe, R R, Levinson, D F

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Association study of SNAP25 and schizophrenia in Irish family and case-control samples von Fanous, A.H., Zhao, Z., van den Oord, E.J.C.G., Maher, B.S., Thiselton, D.L., Bergen, S.E., Wormley, B., Bigdeli, T., Amdur, R.L., O'Neill, F.A., Walsh, D., Kendler, K.S., Riley, B.P.

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A region of 35 kb containing the trace amine associate receptor 6 ( ) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families von Vladimirov, V, Thiselton, D L, Kuo, P-H, McClay, J, Fanous, A, Wormley, B, Vittum, J, Ribble, R, Moher, B, van den Oord, E, O'Neill, F A, Walsh, D, Kendler, K S, Riley, B P

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