Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci by Forrest, Marc P., Zhang, Hanwen, Moy, Winton, McGowan, Heather, Leites, Catherine, Dionisio, Leonardo E., Xu, Zihui, Shi, Jianxin, Sanders, Alan R., Greenleaf, William J., Cowan, Chad A., Pang, Zhiping P., Gejman, Pablo V., Penzes, Peter, Duan, Jubao

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Genetics of Schizophrenia: New Findings and Challenges by Gejman, Pablo V, Sanders, Alan R, Kendler, Kenneth S

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Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications by 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., Gejman, Pablo V.

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Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell–Derived Neurons by Parnell, Euan, Culotta, Lorenza, Forrest, Marc P., Jalloul, Hiba A., Eckman, Blair L., Loizzo, Daniel D., Horan, Katherine K.E., Dos Santos, Marc, Piguel, Nicolas H., Tai, Derek J.C., Zhang, Hanwen, Gertler, Tracy S., Simkin, Dina, Sanders, Alan R., Talkowski, Michael E., Gejman, Pablo V., Kiskinis, Evangelos, Duan, Jubao, Penzes, Peter

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent by de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O’Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R., Keller, Matthew C.

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Transcriptome study of differential expression in schizophrenia by Sanders, Alan R, Göring, Harald H H, Duan, Jubao, Drigalenko, Eugene I, Moy, Winton, Freda, Jessica, He, Deli, Shi, Jianxin, Gejman, Pablo V

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Genomewide Association Analysis of Symptoms of Alcohol Dependence in the Molecular Genetics of Schizophrenia (MGS2) Control Sample by Kendler, Kenneth S., Kalsi, Gursharan, Holmans, Peter A., Sanders, Alan R., Aggen, Steven H., Dick, Danielle M., Aliev, Fazil, Shi, Jianxin, Levinson, Douglas F., Gejman, Pablo V.

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Genome-Wide Association Study of Clinical Dimensions of Schizophrenia: Polygenic Effect on Disorganized Symptoms by 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., Ripke, Stephan, Gejman, Pablo V., Kendler, Kenneth S., Levinson, Douglas F.

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Open chromatin dynamics reveals stage-specific transcriptional networks in hiPSC-based neurodevelopmental model by Zhang, Siwei, Moy, Winton, Zhang, Hanwen, Leites, Catherine, McGowan, Heather, Shi, Jianxin, Sanders, Alan R., Pang, Zhiping P., Gejman, Pablo V., Duan, Jubao

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GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores by Mullins, Niamh, Bigdeli, Tim B, Børglum, Anders D, Coleman, Jonathan R.I, Demontis, Ditte, Mehta, Divya, Ripke, Stephan, Stahl, Eli A, Starnawska, Anna, Anjorin, Adebayo, Corvin, Aiden, Sanders, Alan R, Forstner, Andreas J, Reif, Andreas, Koller, Anna C, Świątkowska, Beata, Baune, Bernhard T, Müller-Myhsok, Bertram, Penninx, Brenda W.J.H, Pato, Carlos, Rujescu, Dan, Hougaard, David M, Quested, Digby, Levinson, Douglas F, Binder, Elisabeth B, Byrne, Enda M, Agerbo, Esben, Streit, Fabian, Mayoral, Fermin, Bellivier, Frank, Degenhardt, Franziska, Breen, Gerome, Morken, Gunnar, Turecki, Gustavo, Rouleau, Guy A, Grabe, Hans J, Jones, Ian, Agartz, Ingrid, Lawrence, Jacob, Walters, James T.R, Strohmaier, Jana, Shi, Jianxin, Hauser, Joanna, Biernacka, Joanna M, Vincent, John B, Kelsoe, John, Strauss, John S, Smoller, Jordan W, Guzman-Parra, José, Berger, Klaus, Scott, Laura J, Jones, Lisa A, Azevedo, M. Helena, Trzaskowski, Maciej, Kogevinas, Manolis, Rietschel, Marcella, Boks, Marco, Ising, Marcus, Grigoroiu-Serbanescu, Maria, Hamshere, Marian L, Leboyer, Marion, Nöthen, Markus M, Preisig, Martin, Boehnke, Michael, O’Donovan, Michael C, Owen, Michael J, Pato, Michele T, Renteria, Miguel E, Budde, Monika, Weissman, Myrna M, Wray, Naomi R, Bass, Nicholas, Craddock, Nicholas, Smeland, Olav B, Mors, Ole, Gejman, Pablo V, Sklar, Pamela, McGrath, Patrick, Hoffmann, Per, McGuffin, Peter, Lee, Phil H, Mortensen, Preben Bo, Kahn, René S, Ophoff, Roel A, Adolfsson, Rolf, Van der Auwera, Sandra, Djurovic, Srdjan, Heilmann-Heimbach, Stefanie, Jamain, Stéphane, Hamilton, Steven P, Lucae, Susanne, Schulze, Thomas G, Hansen, Thomas, Werge, Thomas, Air, Tracy M, Nimgaonkar, Vishwajit, Appadurai, Vivek, Cahn, Wiepke, McQuillin, Andrew, Lewis, Cathryn M

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Genome-wide association study identifies 74 loci associated with educational attainment by Turley, Patrick, Chen, Guo-Bo, Emilsson, Valur, Meddens, S. Fleur W., Thom, Kevin, Timshel, Pascal, Bacelis, Jonas, Baumbach, Clemens, Girotto, Giorgia, Gupta, Richa, Hofer, Edith, Horikoshi, Momoko, Lind, Penelope A., Mangino, Massimo, Marten, Jonathan, Pervjakova, Natalia, Peyrot, Wouter J., Qian, Yong, Schmidt, Börge, Schraut, Katharina E., Teumer, Alexander, Westra, Harm-Jan, Alizadeh, Behrooz Z., Bakshi, Andrew, Baumeister, Sebastian E., Bønnelykke, Klaus, Boyle, Patricia A., Davies, Gail, De Neve, Jan-Emmanuel, Demuth, Ilja, Ding, Jun, Eisele, Lewin, Eklund, Niina, Faul, Jessica D., Forstner, Andreas J., Gunnarsson, Bjarni, Halldórsson, Bjarni V., Heath, Andrew C., Hocking, Lynne J., Hottenga, Jouke-Jan, de Jager, Philip L., Joshi, Peter K., Kaakinen, Marika A., Kiemeney, Lambertus A. L. M., Koskinen, Seppo, Kraja, Aldi T., Kroh, Martin, Lichtenstein, Paul, Lichtner, Peter, Liewald, David C. M., Loukola, Anu, Madden, Pamela A., Mäki-Opas, Tomi, Marioni, Riccardo E., Marques-Vidal, Pedro, Meddens, Gerardus A., Meisinger, Christa, Montgomery, Grant W., Nyholt, Dale R., Ollier, William E. R., Pedersen, Nancy L., Robino, Antonietta, Rostapshova, Olga, Sanders, Alan R., Sarin, Antti-Pekka, Terracciano, Antonio, Tobin, Martin D., Ulivi, Sheila, van Rooij, Frank J. A., Venturini, Cristina, Vinkhuyzen, Anna A. E., Vonk, Judith M., Vozzi, Diego, Ware, Erin B., Berger, Klaus, Chabris, Christopher F., Cucca, Francesco, Deary, Ian J., Dedoussis, George V., Groenen, Patrick J. F., Hinds, David A., Kaprio, Jaakko, Magnusson, Patrik K. E., Metspalu, Andres, Perola, Markus, Samani, Nilesh J., Schlessinger, David, Schmidt, Reinhold, Sørensen, Thorkild I. A., Spector, Tim D., Stefansson, Kari, Thorsteinsdottir, Unnur, Tiemeier, Henning, Weir, David R., Krueger, Robert F., Hofman, Albert, Meyer, Michelle N., Visscher, Peter M., Esko, Tõnu, Koellinger, Philipp D.

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Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants by Zhang, Siwei, Zhang, Hanwen, Zhou, Yifan, Qiao, Min, Zhao, Siming, Kozlova, Alena, Shi, Jianxin, Sanders, Alan R, Wang, Gao, Luo, Kaixuan, Sengupta, Subhajit, West, Siobhan, Qian, Sheng, Streit, Michael, Avramopoulos, Dimitrios, Cowan, Chad A, Chen, Mengjie, Pang, Zhiping P, Gejman, Pablo V, He, Xin, Duan, Jubao

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Clinotator: analyzing ClinVar variation reports to prioritize reclassification efforts by Butler Iii, Robert R, Gejman, Pablo V

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Common variants on chromosome 6p22.1 are associated with schizophrenia by Shi, Jianxin, Levinson, Douglas F., Duan, Jubao, Sanders, Alan R., Zheng, Yonglan, Pe’er, Itsik, Dudbridge, Frank, Holmans, Peter A., Whittemore, Alice S., Mowry, Bryan J., Olincy, Ann, 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, Gejman, Pablo V.

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Clinotator: analyzing ClinVar variation reports to prioritize reclassification efforts [version 2; peer review: 2 approved] by Butler III, Robert R, Gejman, Pablo V

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Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons by Kozlova, Alena, Zhang, Siwei, Kotlar, Alex V., Jamison, Brendan, Zhang, Hanwen, Shi, Serena, Forrest, Marc P., McDaid, John, Cutler, David J., Epstein, Michael P., Zwick, Michael E., Pang, Zhiping P., Sanders, Alan R., Warren, Stephen T., Gejman, Pablo V., Mulle, Jennifer G., Duan, Jubao

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The Genetic Relevance of Human Induced Pluripotent Stem Cell-Derived Microglia to Alzheimer’s Disease and Major Neuropsychiatric Disorders by Butler III, Robert R., Kozlova, Alena, Zhang, Hanwen, Zhang, Siwei, Streit, Michael, Sanders, Alan R., Laudanski, Krzysztof, Pang, Zhiping P., Gejman, Pablo V., Duan, Jubao

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Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines by Duan, Jubao, Shi, Jianxin, Ge, Xijin, Dölken, Lars, Moy, Winton, He, Deli, Shi, Sandra, Sanders, Alan R., Ross, Jeff, Gejman, Pablo V.

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Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples by Gladwin, Thomas E, Derks, Eske M, Rietschel, Marcella, Mattheisen, Manuel, Breuer, René, Schulze, Thomas G, Nöthen, Markus M, Levinson, Douglas, Shi, Jianxin, Gejman, Pablo V, Cichon, Sven, Ophoff, Roel A

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Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders by Cichon, Sven, Craddock, Nick, Daly, Mark, Faraone, Stephen V, Gejman, Pablo V, Kelsoe, John, Lehner, Thomas, Levinson, Douglas F, Moran, Audra, Sklar, Pamela, Sullivan, Patrick F

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