Rammos, Alexandros, Gonzalez, Lara A. Neira, Weinberger, Daniel R., Mitchell, Kevin J., Nicodemus, Kristin K., Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David, Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu, Begemann, Martin, Belliveau, Richard, Bene, Judit, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin. Nature Publishing Group; 2019. The role of polygenic risk score gene-set analysis in the context of the omnigenic model of schizophrenia.

Marshall, Christian R., , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Howrigan, Daniel P., Gujral, Madhusudan, Brandler, William M., Malhotra, Dheeraj, Wang, Zhouzhi, Fuentes Fajarado, Karin V., Maile, Michelle S., Ripke, Stephan, Agartz, Ingrud, Albus, Margot, Alexander, Madeline, Merico, Daniele, Atkins, Joshua, Cairns, Murray J., Carr, Vaughan J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel L., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Thiruvahindrapuram, Bhooma, Wu, Jing Qin, Wu, Wenting, Greer, Douglas S., Antaki, Douglas, Shetty, Aniket, Holmans, Peter A., Pinto, Dalila. Nature Publishing Group; 2017. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.

Gusev, Alexander, Lee, S. Hong, Kähler, 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, Trynka, Gosia, Price, Alkes L., Finucane, Hilary, Vilhjálmsson, Bjarni J., Xu, Han, Zang, Chongzhi, Ripke, Stephan, Bulik-Sullivan, Brendan, Stahl, Eli. Cell Press; 2014. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.

Bulik-Sullivan, Brendan K., Albus, M, Alexander, M, Amin, F, Bacanu, SA, Begemann, M, Belliveau, RA, Bene, J, Bergen, SE, Bruggeman, R, Bevilacqua, E, Bigdeli, TB, Black, DW, Buccola, NG, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Cairns, MJ, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Chan, RCK, Chen, RYL, Cohen, D, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, N, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Loh, Po-Ru, Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Patterson, Nick, Daly, Mark J., Price, Alkes L., Neale, Benjamin M., Finucane, Hilary K., Ripke, Stephan, Yang, Jian, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M.. Nature Publishing Group; 2015. LD score regression distinguishes confounding from polygenicity in genome-wide association studies.

Goris, An, van Setten, Jessica, Diekstra, Frank, Ripke, Stephan, Patsopoulos, Nikolaos A., Sawcer, Stephen J., The International Multiple Sclerosis Genetics Consortium, van Es, Michael, The Australia and New Zealand MS Genetics Consortium, Andersen, Peter M., Melki, Judith, Meininger, Vincent, Hardiman, Orla, Landers, John E., Brown, Robert H., Shatunov, Aleksey, Leigh, Nigel, Al-Chalabi, Ammar, Shaw, Christopher E., Traynor, Bryan J., Chio, Adriano, Restagno, Gabriella, Mora, Gabriele, Ophoff, Roel A., Oksenberg, Jorge R., Van Damme, Philip, Compston, Alastair, Robberecht, Wim, Dubois, Bénédicte, van den Berg, Leonard H., De Jager, Philip L., Veldink, Jan H., de Bakker, Paul I. W.. Oxford University Press; 2014. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.

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.

Vilhjálmsson, Bjarni J., Yang, Jian, Hayeck, Tristan, Won, Hong-Hee, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) study,, Finucane, Hilary K., Gusev, Alexander, Lindström, Sara, Ripke, Stephan, Genovese, Giulio, Loh, Po-Ru, Bhatia, Gaurav, Do, Ron. Cell Press; 2015. Modeling linkage disequilibrium increases accuracy of polygenic risk scores.

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. R., Bramon, Elvira, Buxbaum, Joseph D., Børglum, Anders D., Cichon, Sven, Darvasi, Ariel, Buckner, Randy L., Domenici, Enrico, Ehrenreich, Hannelore, Esko, Tõnu, Gejman, Pablo V., Gill, Michael, Gurling, Hugh, Hultman, Christina M., Iwata, Nakao, Jablensky, Assen V., Jönsson, Erik G., Byerley, William, 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, Cahn, Wiepke, Moran, Jennifer L., Mortensen, Preben B., Mowry, Bryan J., Nöthen, Markus M., Ophoff, Roel A., Owen, Michael J., Palotie, Aarno, Pato, Carlos N., Petryshen, Tracey L., Posthuma, Danielle, Cai, Guiqing, Rietschel, Marcella, Riley, Brien P., Rujescu, Dan, Sham, Pak C., Sklar, Pamela, St Clair, David, Weinberger, David R., Wendland, Jens R., Werge, Thomas, Daly, Mark J., Walters, James T. R., Campion, Dominique, Sullivan, Patrick F., O'Donovan, Michael C., 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, Farh, Kai-How, Cheung, Eric F. C., Ann Chong, Siow, Robert Cloninger, C., Cohen, David, Cohen, Nadine, Cormican, Paul, Craddock, Nick, Crowley, James J., Curtis, David, Davidson, Michael, Holmans, Peter A., Davis, Kenneth L., Degenhardt, Franziska, Del Favero, Jurgen, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Lee, Phil, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H., Farrell, Martilias S., Frank, Josef, Franke, Lude, Bulik-Sullivan, Brendan, Freedman, Robert, Freimer, Nelson B., Friedl, Marion, Friedman, Joseph I., Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Collier, David A., Goldstein, Jacqueline I., Golimbet, Vera, Gopal, Srihari, Gratten, Jacob, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian L., Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Huang, Hailiang, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Joa, Inge. Nature Publishing Group; 2014. Biological insights from 108 schizophrenia-associated genetic loci.

Ek, Weronica E., Reznichenko, Anna, Holliday, Elizabeth G., Houghton, Lesley, Gazouli, Maria, Karamanolis, George, Rappold, Gudrun, Burwinkel, Barbara, Surowy, Harald, Rafter, Joseph, Assadi, Ghazaleh, Li, Ling, Ripke, Stephan, , , , , , , , , , , Niesler, Beate, , , , , , , , , , , Zucchelli, Marco, , , , , Rivera, Natalia V., Schmidt, Peter T., Pedersen, Nancy L., Magnusson, Patrik, Talley, Nicholas J.. BMJ Group; 2015. Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts.

Terwisscha van Scheltinga, Afke F., Schall, U, Michie, P, Carr, VJ, Scott, RJ, Bakker, Steven C., Kahn, René S., van Haren, Neeltje E. M., Derks, Eske M., Buizer-Voskamp, Jacobine E., Boos, Heleen B. M., Cahn, Wiepke, Hulshoff Pol, Hilleke E., Ripke, Stephan, Ophoff, Roel A.. Elsevier; 2013. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume.

Finucane, Hilary K., Bulik-Sullivan, Brendan, Ripke, Stephan, Day, Felix R., ReproGen Consortium,, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, The RACI Consortium,, Purcell, Shaun, Stahl, Eli, Lindstrom, Sara, Perry, John R. B., Okada, Yukinori, Gusev, Alexander, Raychaudhuri, Soumya, Daly, Mark J., Patterson, Nick, Neale, Benjamin M., Price, Alkes L., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Trynka, Gosia, Tooney, Paul A., Wu, Jing Qin, Reshef, Yakir, Loh, Po-Ru, Anttila, Verneri, Xu, Han, Zang, Chongzhi, Farh, Kyle. Nature Publishing; 2015. Partitioning heritability by functional annotation using genome-wide association summary statistics.

Anttila, Verneri, Bulik-Sullivan, Brendan, Patsopoulos, Nikolaos A., Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H., Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Finucane, Hilary K., Holliday, Elizabeth, Attia, John, Cairns, Murray, Loughland, Carmel, Schall, Ulrich, Henskens, Frans, Scott, Rodney, Reitz, C, Goate, AM, Huentelman, MJ, Walters, Raymond K., Ilyas Kamboh, M, Larson, EB, Rogaeva, E, George-Hyslop, PS, Hakonarson, H, Kukull, WA, Farrer, LA, Barnes, LL, Beach, TG, Yesim Demirci, F, Bras, Jose, Head, E, Hulette, CM, Jicha, GA, Kauwe, JSK, Kaye, JA, Leverenz, JB, Levey, AI, Lieberman, AP, Pankratz, VS, Poon, WW, Duncan, Laramie, Quinn, JF, Saykin, AJ, Schneider, LS, Smith, AG, Escott-Price, Valentina, Falcone, Guido J., Gormley, Padhraig, Malik, Rainer. American Association for the Advancement of Science; 2018. Analysis of shared heritability in common disorders of the brain.

Trastulla, Lucia, Dolgalev, Georgii, Domenici, Enrico, Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Ronald J., Adolfsson, Rolf, Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau, Richard A., Moser, Sylvain, Bene, Judit, Bergen, SE, Bevilacqua, E, Bigdeli, TB, Black, DW, Blackwood, DHR, Borglum, AD, Bramon, E, Bruggeman, R, Buccola, NG, Jiménez-Barrón, Laura T., Buckner, RL, Bulik-Sullivan, B, Buxbaum, JD, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Andlauer, Till F. M., Catts, SV, Chambert, KD, Chan, RCK, Chen, EYH, Chen, RYL, Cheng, W, Cheung, EFC, Chong, SA, Cichon, S, Cloninger, CR, von Scheidt, Moritz, Cohen, D, Cohen, N, Collier, DA, Cormican, P, Craddock, N, Crowley, JJ, Daly, MJ, Darvasi, A, Davidson, M, Davis, KL, Ruderfer, Douglas M., Degenhardt, F, Del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Ripke, Stephan, Ehrenreich, H, Eichhammer, P, Eriksson, J, Escott-Price, V, Esko, T, Essioux, L, Farh, KH, Farrell, MS, Frank, J, Franke, L, McQuillin, Andrew, Freedman, R, Freimer, NB, Friedman, JI, Fromer, M, Gejman, PV, Genovese, G, Georgieva, L, Giegling, I, Gill, M, Giusti-Rodriguez, P, Stahl, Eli A., Godard, S, Goldstein, JI, Gopal, S, Gratten, J, Gurling, H, de Haan, L, Hammer, C, Hamshere, ML, Hansen, M, Hansen, T. Nature Publishing Group; 2024. Distinct genetic liability profiles define clinically relevant patient strata across common diseases.

Ni, Guiyan, Gratten, Jacob, Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Wray, Naomi R., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Bevilacqua, E, Bigdeli, TB, Black, DW, Bruggeman, R, Buccola, NG, Lee, Sang Hong, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Ripke, Stephan, Chan, RCK, Chen, RYL, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, D, Cohen, N, Cormican, P, Neale, Benjamin M., Craddock, N, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Corvin, Aiden, Djurovic, S, Donohoe, G, Drapeau, E, Walters, James T. R., Farh, Kai-How, Holmans, Peter A.. Springer; 2018. Age at first birth in women is genetically associated with increased risk of schizophrenia.

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.

Li, Wen, Fan, Chun Chieh, Mäki-Marttunen, Tuomo, Thompson, Wesley K., Schork, Andrew J., Bettella, Francesco, Ripke, Stephan, Neal, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Djurovic, Srdjan, Dale, Andrew M., Andreassen, Ole A., Wang, Yunpeng. Wiley; 2018. A molecule-based genetic association approach implicates a range of voltage-gated calcium channels associated with schizophrenia.

Ni, Guiyan, Moser, Gerhard, 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., Henskens, Frans A., Loughland, Carmel A., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Wray, Naomi R., Lee, S. Hong. Cell Press; 2018. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood.

Ruderfer, Douglas M., Ripke, Stephan, McQuillin, Andrew, Boocock, James, Stahl, Eli A., Pavlides, Jennifer M. Whitehead, Mullins, Niamh, Charney, Alexander W., Ori, Anil P. S., Loohuis, Loes M. Olde, Domenici, Enrico, Di Florio, Arianna, Papiol, Sergi, Kalman, Janos L., Trubetskoy, Vassily, Adolfsson, Rolf, Agartz, Ingrid, Agerbo, Esben, Akil, Huda, Albani, Diego, Albus, Margot, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin. Cell Press; 2018. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.