Objects
Le Hellard, Stephanie, Wang, Yunpeng, Schork, Andrew J., Thompson, Wesley K., Dale, Anders M., Djurovic, Srdjan, Andreassen, Ole A., Cairns, Murray J., Henskens, Frans, Kelly, Brian J., Loughland, Carmel, Michie, Patricia T., Witoelar, Aree, Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Zuber, Verena, Bettella, Francesco, Hugdahl, Kenneth, Espeseth, Thomas, Steen, Vidar M., Melle, Ingrid, Desikan, Rahul. Oxford University Press; 2017. Identification of gene loci that overlap between schizophrenia and educational attainment.
Srinivasan, Saurabh, Bettella, Francesco, Mattingsdal, Morten, Wang, Yunpeng, Witoelar, Aree, Schork, Andrew J., Thompson, Wesley K., Zuber, Verena, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, International Headache Genetics Consortium, Winsvold, Bendik S., Zwart, John-Anker, Collier, David A., Desikan, Rahul S., Melle, Ingrid, Werge, Thomas, Dale, Anders M., Djurovic, Srdjan, Andreassen, Ole A., Henskens, Frans A., Cairns, Murray J., Kelly, Brian J., Loughland, Carmel M., Schall, Ulrich, Tooney, Paul A., Mitchie, Patricia T., Scott, Rodney J.. Elsevier; 2016. Genetic markers of human evolution are enriched in schizophrenia.
Ripke, Stephan, Neale, Benjamin M., Pers, Tune H., Julià, Antonio, Kahn, René S., Kalaydjieva, Luba, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C., Kennedy, James L., Khrunin, Audrey, Kim, Yunjung, Agartz, Iingrid, Klovins, Janis, Knowles, James A., Konte, Bettina, Kucinskas, Vaidutis, Ausrele Kucinskiene, Zita, Kuzelova-Ptackova, Hana, Kähler, Anna K., Laurent, Claudine, Lee Chee Keong, Jimmy, Hong Lee, S., Agerbo, Esben, Legge, Sophie E., Lerer, Bernard, Li, Miaoxin, Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lubinski, Jan, Lönnqvist, Jouko, Albus, Margot, Macek Jr, Milan, Magnusson, Patrik K. E., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Marsal, Sara, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W., McDonald, Colm, Alexander, Madeline, McIntosh, Andrew M., Meier, Sandra, Meijer, Carin J., Melegh, Bela, Melle, Iingrid, Mesholam-Gately, Raquelle I., Metspalu, Andres, Michie, Patricia T., Milani, Lili, Milanova, Virha, Amin, Farooq, Mokrab, Younes, Morris, Derek W., Mors, Ole, Murphy, Kieran C., Murray, Robin M., Myin-Germeys, Inez, Müller-Myhsok, Bertram, Nelis, Mari, Nenadic, Igor, Nertney, Deborah A., Bacanu, Silviu 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, Begemann, Martin, Olsen, Line, Van Os, Jim, Psychosis Endophenotypes International Consortium, Pantelis, Christos, Papadimitriou, George N., Papiol, Sergi, Parkhomenko, Elena, Pato, Michele T., Paunio, Tiina, Pejovic-Milovancevic, Milica, Belliveau Jr, Richard A., Perkins, Diana O., Pietiläinen, Olli, Pimm, Jonathan, Pocklington, Andrew J., Powell, John, Price, Alkes, Pulver, Ann E., Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Bene, Judit, Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roffman, Joshua L., Roussos, Panos, Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R., Schall, Ulrich, Schubert, Christian R., Corvin, Aiden, Bergen, Sarah E., Schulze, Thomas G., Schwab, Sibylle G., Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Shi, Jianxin, Sigurdsson, Engilbert, Silagadze, Teimuraz, Silverman, Jeremy M., Sim, Kang, Bevilacqua, Elizabeth, 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, Bigdeli, Tim B., Strohmaier, Jana, Scott Stroup, T., Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M., Szatkiewicz, Jin P., Söderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Black, Donald W., Veijola, Juha, Waddington, John, Walsh, Dermot, Wang, Dai, Wang, Qiang, Webb, Bradley T., Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Bruggeman, Richard, Witt, Stephanie H., Wolen, Aaron R., Wong, Emily H. M., Wormley, Brandon K., Simon Xi, Hualin, Zai, Clement C., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Stefansson, Kari, Buccola, Nancy G., Visscher, Peter M., Welcome Trust Case-Control Consortium,, Adolfsson, Rolf, Andreassen, Ole A., Blackwood, Douglas H. 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Bigdeli, Tim B., Ripke, Stephan, Kirov, George, McQuillin, Andrew, Gurling, Hugh, Rujescu, Dan, Andreassen, Ole A., Werge, Thomas, Blackwood, Douglas H. R., Pato, Carlos N., Pato, Michele T., Malhotra, Anil K., Bacanu, Silviu-Alin, O'Donovan, Michael C., Kendler, Kenneth S., Fanous, Ayman H., Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Henskens, Frans A., Lee, Sang Hong, Wray, Naomi R., Gejman, Pablo V., Rietschel, Marcella, Cichon, Sven, St Clair, David, Corvin, Aiden. Wiley-Blackwell Publishing; 2016. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.
Franke, Barbara, Stein, Jason L., Ripke, Stephan, Anttila, Verneri, Hibar, Derrek P., van Hulzen, Kimm J. E.JE, Arias-Vasquez, Alejandro, Smoller, Jordan W., Nichols, Thomas E., Neale, Michael C., McIntosh, Andrew M., Lee, Phil, McMahon, Francis J., Meyer-Lindenberg, Andreas, Mattheisen, Manuel, Andreassen, Ole A., Gruber, Oliver, Sachdev, Perminder S., Roiz-Santiañez, Roberto, Saykin, Andrew J., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Enigma Consortium, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulli, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Hansen, Mitchell, Lee, Steve, Liu, Xiaochun. ; 2016. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept.
van Erp, Theo G. M., Walton, Esther, Hibar, Derek P., Schmaal, Lianne, Jiang, Wenhao, Glahn, David C., Pearlson, Godfrey D., Yao, Nailin, Fukunaga, Masaki, Hashimoto, Ryota, Okada, Naohiro, Yamamori, Hidenaga, Bustillo, Juan R., Clark, Vincent P., Agartz, Ingrid, Mueller, Bryon A., Cahn, Wiepke, de Zwarte, Sonja M. C., Hulshoff Pol, Hilleke E., Kahn, René S., Ophoff, Roel A., van Haren, Neeltje E. M., Andreassen, Ole A., Dale, Anders M., Loughland, Carmel, Henskens, Frans A., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Cairns, Murray J., Tooney, Paul A., Rasser, Paul E., Cooper, Gavin. Elsevier; 2018. Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 control subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) consortium.
LeBlanc, Marissa, Zuber, Verena, Thompson, Wesley K., Andreassen, Ole A., Schizophrenia and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium, Frigessi, Arnoldo, Andreassen, Bettina Kulle, Loughland, Carmel J., Schall, Ulrich, Tooney, Paul A., Michie, Paul T., Cairns, Murray J., Henskens, Frans A., Carr, Vaughan. BioMed Central; 2018. A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework.
Holland, Dominic, Wang, Yunpeng, Dale, Anders M., Tooney, Paul A., Thompson, Wesley K., Schork, Andrew, Chen, Chi-Hua, Lo, Min-Tzu, Witoelar, Aree, Werge, Thomas, O'Donovan, Michael, Andreassen, Ole A.. Frontiers Research Foundation; 2016. Estimating effect sizes and expected replication probabilities from GWAS summary statistics.
Schork, Andrew J., Thompson, Wesley K., The Bipolar Disorder Psychiatric Genomics Consortium,, The Schizophrenia Psychiatric Genomics Consortium,, Schork, Nicholas J., Andreassen, Ole A., Dale, Anders M., Pham, Phillip, Torkamani, Ali, Roddey, J. Cooper, Sullivan, Patrick F., Kelsoe, John R., O'Donovan, Michael C., Furberg, Helen, The Tobacco and Genetics Consortium,. Public Library of Science (PLoS); 2013. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs.