Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa von Hübel, Christopher, Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Medland, Sarah E., Giusti-Rodríguez, Paola, Alfredsson, Lars, Berrettini, Wade H., Boni, Claudette, Burghardt, Roland, Cichon, Sven, Cone, Roger D., Courtet, Philippe, Crowley, James J., Davis, Oliver S. P., de Zwaan, Martina, Dikeos, Dimitris, Dina, Christian, Duncan, Laramie E., Egberts, Karin, Estivill, Xavier, Favaro, Angela, Fernández-Aranda, Fernando, Fichter, Manfred M., Forstner, Andreas J., Forzan, Monica, Franklin, Christopher S., Giegling, Ina, Guillaume, Sébastien, Hakonarson, Hakon, Hatzikotoulas, Konstantinos, Hauser, Joanna, Helder, Sietske G., Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Huckins, Laura M., Hudson, James I., Inoko, Hidetoshi, Janout, Vladimir, Julià, Antonio, Kalsi, Gursharan, Kaminská, Deborah, Karhunen, Leila, Keski-Rahkonen, Anna, Kim, Youl-Ri, Knudsen, Gun Peggy S., La Via, Maria C., Levitan, Robert D., Lin, Bochao Danae, Luykx, Jurjen, Marsal, Sara, Marshall, Christian R., McDevitt, Sara, McGuffin, Peter, Metspalu, Andres, Monteleone, Alessio Maria, Monteleone, Palmiero, Munn-Chernoff, Melissa A., Navratilova, Marie, O’Toole, Julie K., Palotie, Aarno, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ritschel, Franziska, Roberts, Marion, Rotondo, Alessandro, Rujescu, Dan, Rybakowski, Filip, Santonastaso, Paolo, Scherer, Stephen W., Schmidt, Ulrike, Schosser, Alexandra, Slagboom, P. Eline, Sorbi, Sandro, Szatkiewicz, Jin P., Tenconi, Elena, Tortorella, Alfonso, Treasure, Janet, Tziouvas, Konstantinos, van Elburg, Annemarie A., van Furth, Eric F., Zipfel, Stephan, Bergen, Andrew W., Boden, Joseph M., Johnson, Craig, Kaye, Walter H., Mitchell, James E., Olsen, Catherine M., Woodside, D. Blake, Stuber, Garret D., Gordon, Scott, Henders, Anjali K., Juréus, Anders, Petersen, Liselotte, Wade, Tracey D., Landén, Mikael, Sullivan, Patrick F., Breen, Gerome

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Mapping genomic loci implicates genes and synaptic biology in schizophrenia von Trubetskoy, Vassily, Qi, Ting, Bryois, Julien, Chen, Chia-Yen, Magnusson, Sigurdur, Kim, Minsoo, Adams, Mark, Agartz, Ingrid, Agerbo, Esben, Athanasiu, Lavinia, Bacanu, Silviu A., Calkins, Monica E., Carr, Vaughan J., Consoli, Angèle, Costas, Javier, Davis, Kenneth L., Degenhardt, Franziska, Dickerson, Faith, Frustaci, Alessandra, Giegling, Ina, Goldstein, Jacqueline I., González Peñas, Javier, Hayward, Caroline, Howrigan, Daniel P., Ikeda, Masashi, Kam-Thong, Tony, Kamatani, Yoichiro, Khrunin, Andrey, Kim, Sung-Wan, Klovins, Janis, Kubo, Michiaki, Lazzeroni, Laura C., Lehrer, Douglas S., Li, Miaoxin, Liu, Chih-Min, Loughland, Carmel M., Mallet, Jacques, Mattheisen, Manuel, McCarley, Robert W., Meier, Sandra, Milani, Lili, Milanova, Vihra, Morley, Christopher P., Muntané, Gerard, Murphy, Kieran C., Olincy, Ann, Papadimitriou, George N., Parellada, Mara, Paunio, Tiina, Pellegrino, Renata, Radant, Allen D., Saker-Delye, Safaa, Sanjuan, Julio, Savitz, Adam, Seidman, Larry J., Sim, Kang, Stain, Helen J., Streit, Fabian, Strengman, Eric, Ta, Thi Minh Tam, Terao, Chikashi, Toncheva, Draga, Veijola, Juha, Waddington, John, Walter, Henrik, Webb, Bradley T., Wu, Jing Qin, Xu, Zhida, Ayub, Muhammad, Bertolino, Alessandro, Buccola, Nancy G., Byerley, William F., Hwu, Hai-Gwo, McCarroll, Steven A., Neil, Amanda L., Smoller, Jordan W., Vilella, Elisabet, Xu, Shuhua, Braff, David, Buxbaum, Joseph D., Cichon, Sven, Ehrenreich, Hannelore, Escott-Price, Valentina, Esko, Tõnu, Iwata, Nakao, Kirov, George, Lee, Jimmy, Li, Qingqin S., Malhotra, Anil K., Malhotra, Dheeraj, McQuillin, Andrew, Morgan, Vera A., Nöthen, Markus M., Saka, Meram C., Sanders, Alan R., Serretti, Alessandro, van Os, Jim, Yu, Xin, Neale, Benjamin M., Ripke, Stephan

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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes von Ruderfer, Douglas M., Boocock, James, Stahl, Eli A., Charney, Alexander W., Ori, Anil P.S., Alliey-Rodriguez, Ney, Anjorin, Adebayo, Badner, Judith A., Band, Gavin, Bruggeman, Richard, Buccola, Nancy G., Bumpstead, Suzannah J., Casas, Juan P., Chan, Raymond C.K., Chen, Ronald Y.L., Collier, David A., Cormican, Paul, Craddock, Nicholas, Crowley, James J., Curtis, David, Dannlowski, Udo, Davidson, Michael, Demontis, Ditte, Dronov, Serge, Elvsashagen, Torbjorn, Etain, Bruno, Fan, Chun Chieh, Forty, Liz, Fraser, Christine, Garnham, Julie, Gill, Michael, Gillman, Matthew, Gratten, Jacob, Gwilliam, Rhian, Hammer, Christian, Hansen, Thomas, Henskens, Frans A., Jamain, Stephane, Jankowski, Janusz, Joa, Inge, Julia, Antonio, Kandaswamy, Radhika, Kavanagh, David, Keller, Matthew C., Khrunin, Andrey, Lee, Phil H., Legge, Sophie E., Lencz, Todd, Levinson, Douglas F., Levy, Shawn E., Li, Tao, Lin, Kuang, Macek, Milan, McCarley, Robert W., McGuffin, Peter, McInnis, Melvin G., Meijer, Carin J., Melegh, Bela, Mesholam-Gately, Raquelle I., Myin-Germeys, Inez, Nicodemus, Kristin K., Nimgaonkar, Vishwajit, Nordin, Annelie, Nöthen, Markus M., Van Os, Jim, Owen, Michael J., Palmer, Colin N.A., Palotie, Aarno, Papadimitriou, George N., Pato, Michele T., Perlis, Roy H., Petryshen, Tracey L., Plomin, Robert, Potash, James B., Powell, John, Ramos-Quiroga, Josep Antoni, Rautanen, Anna, Reichenberg, Abraham, Ribases, Marta, Rice, John P., Richards, Alexander L., Ricketts, Michelle, Sanchez-Mora, Cristina, Sanders, Alan R., Schall, Ulrich, Serretti, Alessandro, Sham, Pak C., Straub, Richard E., Strauss, John S., Szatkiewicz, Jin P., Thompson, Robert C., Thorgeirsson, Thorgeir E., Treutlein, Jens, Vedder, Helmut, Wang, Qiang, Wu, Jing Qin, Sullivan, Patrick F., Wray, Naomi R., Sklar, Pamela, Kendler, Kenneth S.

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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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Biological insights from 108 schizophrenia-associated genetic loci von Neale, Benjamin M, Pers, Tune H, Agartz, Ingrid, Agerbo, Esben, Amin, Farooq, Bergen, Sarah E, Bigdeli, Tim B, Buckner, Randy L, Cai, Guiqing, Catts, Stanley V, Chan, Raymond C. K, Chen, Eric Y. H, Cheng, Wei, Cheung, Eric F. C, Ann Chong, Siow, Robert Cloninger, C, Cohen, Nadine, Crowley, James J, Davidson, Michael, Davis, Kenneth L, Del Favero, Jurgen, Demontis, Ditte, Dinan, Timothy, Djurovic, Srdjan, Drapeau, Elodie, Eriksson, Johan, Escott-Price, Valentina, Friedl, Marion, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giusti-Rodriguez, Paola, Gopal, Srihari, Gratten, Jacob, Hammer, Christian, Hofman, Andrea, Hougaard, David M, Julia, Antonio, Klovins, Janis, Ausrele Kucinskiene, Zita, Hong Lee, S, Lerer, Bernard, Limborska, Svetlana, Lubinski, Jan, Macek Jr, Milan, Magnusson, Patrik K. E, Mattheisen, Manuel, McDonald, Colm, Michie, Patricia T, Milanova, Vihra, Mokrab, Younes, Muller-Myhsok, Bertram, Nenadic, Igor, Nordin, Annelie, Van Os, Jim, Endophenotypes International Consortium, Psychosis, Parkhomenko, Elena, Pejovic-Milovancevic, Milica, Pimm, Jonathan, Price, Alkes, Purcell, Shaun M, Quested, Digby, Rasmussen, Henrik B, Roffman, Joshua L, Schubert, Christian R, Schwab, Sibylle G, Scott, Rodney J, Seidman, Larry J, Silverman, Jeremy M, Smoller, Jordan W, Steinberg, Stacy, Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M, Soderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Wolen, Aaron R, Zheng, Xuebin, Wray, Naomi R, Visscher, Peter M, Trust Case-Control Consortium, Wellcome, Andreassen, Ole A, Blackwood, Douglas H. R, Esko, Tonu, Gill, Michael, Jablensky, Assen V, McCarroll, Steven A, Mowry, Bryan J, Owen, Michael J, Pato, Carlos N, Posthuma, Danielle, Rujescu, Dan, Sham, Pak C, Sklar, Pamela, St Clair, David

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Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia von Halvorsen, Matthew, Huh, Ruth, Oskolkov, Nikolay, Wen, Jia, Netotea, Sergiu, Giusti-Rodriguez, Paola, Karlsson, Robert, Bryois, Julien, Nystedt, Björn, Ameur, Adam, Kähler, Anna K., Ancalade, NaEshia, Farrell, Martilias, Crowley, James J., Li, Yun, Magnusson, Patrik K. E., Gyllensten, Ulf, Hultman, Christina M., Sullivan, Patrick F., Szatkiewicz, Jin P.

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Analysis of shared heritability in common disorders of the brain von Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer, Patsopoulos, Nikolaos A, Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H, Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Letenneur, Luc, Hannequin, Didier, Amouyel, Philippe, Boland, Anne, Deleuze, Jean-François, Duron, Emmanuelle, Vardarajan, Badri N, Reitz, Christiane, Goate, Alison M, Huentelman, Matthew J, Kamboh, M Ilyas, Larson, Eric B, Rogaeva, Ekaterina, St George-Hyslop, Peter, Hakonarson, Hakon, Kukull, Walter A, Farrer, Lindsay A, Barnes, Lisa L, Beach, Thomas G, Demirci, F Yesim, Head, Elizabeth, Hulette, Christine M, Jicha, Gregory A, Kauwe, John S K, Kaye, Jeffrey A, Leverenz, James B, Levey, Allan I, Lieberman, Andrew P, Pankratz, Vernon S, Poon, Wayne W, Quinn, Joseph F, Saykin, Andrew J, Schneider, Lon S, Smith, Amanda G, Sonnen, Joshua A, Stern, Robert A, Van Deerlin, Vivianna M, Van Eldik, Linda J, Harold, Denise, Russo, Giancarlo, Rubinsztein, David C, Bayer, Anthony, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C, Hampel, Harald, Owen, Michael J, Mead, Simon, Passmore, Peter, Morgan, Kevin, Nöthen, Markus M, Rossor, Martin, Lupton, Michelle K, Hoffmann, Per, Kornhuber, Johannes, Lawlor, Brian, McQuillin, Andrew, Al-Chalabi, Ammar, Bis, Joshua C, Ruiz, Agustin, Boada, Mercè, Seshadri, Sudha, Beiser, Alexa, Rice, Kenneth, van der Lee, Sven J, De Jager, Philip L, Geschwind, Daniel H, Riemenschneider, Matthias, Riedel-Heller, Steffi, Rotter, Jerome I, Ransmayr, Gerhard, Hyman, Bradley T, Cruchaga, Carlos, Alegret, Montserrat, Winsvold, Bendik, Palta, Priit, Farh, Kai-How, Cuenca-Leon, Ester, Furlotte, Nicholas, Kurth, Tobias

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Gene expression imputation across multiple brain regions provides insights into schizophrenia risk von Huckins, Laura M., Dobbyn, Amanda, Ruderfer, Douglas M., Hoffman, Gabriel, Wang, Weiqing, Pardiñas, Antonio F., Rajagopal, Veera M., Als, Thomas D., T. Nguyen, Hoang, Girdhar, Kiran, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R., Purcell, Shaun, Demontis, Ditte, Børglum, Anders D., Walters, James T. R., O’Donovan, Michael C., Sullivan, Patrick, Owen, Michael J., Devlin, Bernie, Sieberts, Solveig K., Cox, Nancy J., Im, Hae Kyung, Sklar, Pamela, Stahl, Eli A.

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Copy number variation in schizophrenia in Sweden von Szatkiewicz, J P, O'Dushlaine, C, Chen, G, Chambert, K, Moran, J L, Neale, B M, Fromer, M, Ruderfer, D, Akterin, S, Bergen, S E, Kähler, A, Magnusson, P K E, Kim, Y, Crowley, J J, Rees, E, Kirov, G, O'Donovan, M C, Owen, M J, Walters, J, Scolnick, E, Sklar, P, Purcell, S, Hultman, C M, McCarroll, S A, Sullivan, P F

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The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study von Song, Jie, Yao, Shuyang, Kowalec, Kaarina, Lu, Yi, Sariaslan, Amir, Szatkiewicz, Jin P., Larsson, Henrik, Lichtenstein, Paul, Hultman, Christina M., Sullivan, Patrick F.

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Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles von Goldstein, Jacqueline I., Fredrik Jarskog, L., Hilliard, Chris, Alfirevic, Ana, Duncan, Laramie, Fourches, Denis, Huang, Hailiang, Lek, Monkol, Neale, Benjamin M., Ripke, Stephan, Shianna, Kevin, Szatkiewicz, Jin P., Tropsha, Alexander, van den Oord, Edwin JCG, Cascorbi, Ingolf, Dettling, Michael, Gazit, Ephraim, Goff, Donald C., Holden, Arthur L., Kelly, Deanna L., Malhotra, Anil K., Nielsen, Jimmi, Pirmohamed, Munir, Rujescu, Dan, Werge, Thomas, Levy, Deborah L., Josiassen, Richard C., Kennedy, James L., Lieberman, Jeffrey A., Daly, Mark J., Sullivan, Patrick F.

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Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia von Wen, Jia, Trost, Brett, Engchuan, Worrawat, Halvorsen, Matthew, Pallotto, Linda M., Mitina, Aleksandra, Ancalade, NaEshia, Farrell, Martilias, Backstrom, Ian, Guo, Keyi, Pellecchia, Giovanna, Thiruvahindrapuram, Bhooma, Giusti-Rodriguez, Paola, Rosen, Jonathan David, Li, Yun, Won, Hyejung, Magnusson, Patrik K. E., Gyllensten, Ulf, Bassett, Anne S., Hultman, Christina M., Sullivan, Patrick F., Yuen, Ryan K. C., Szatkiewicz, Jin P.

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Genome-Wide Association Analysis of Neonatal White Matter Microstructure von Zhang, J, Xia, K, Ahn, M, Jha, S C, Blanchett, R, Crowley, J J, Szatkiewicz, J P, Zou, F, Zhu, H, Styner, M, Gilmore, J H, Knickmeyer, R C

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Characterization of Single Gene Copy Number Variants in Schizophrenia von Szatkiewicz, Jin P., Fromer, Menachem, Nonneman, Randal J., Ancalade, NaEshia, Johnson, Jessica S., Stahl, Eli A., Rees, Elliott, Bergen, Sarah E., Hultman, Christina M., Kirov, George, O’Donovan, Michael, Owen, Michael, Holmans, Peter, Sklar, Pamela, Sullivan, Patrick F., Purcell, Shaun M., Crowley, James J., Ruderfer, Douglas M.

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Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis von Brucker, Amanda, Lu, Wenbin, Marceau West, Rachel, Yu, Qi-You, Hsiao, Chuhsing Kate, Hsiao, Tzu-Hung, Lin, Ching-Heng, Magnusson, Patrik K E, Sullivan, Patrick F, Szatkiewicz, Jin P, Lu, Tzu-Pin, Tzeng, Jung-Ying

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Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia von Halvorsen, Matthew, Huh, Ruth, Oskolkov, Nikolay, Wen, Jia, Netotea, Sergiu, Giusti-Rodriguez, Paola, Karlsson, Robert, Bryois, Julien, Nystedt, Björn, Ameur, Adam, Kähler, Anna K., Ancalade, NaEshia, Farrell, Martilias, Crowley, James J., Li, Yun, Magnusson, Patrik K. E., Gyllensten, Ulf, Hultman, Christina M., Sullivan, Patrick F., Szatkiewicz, Jin P.

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Allele-specific copy-number discovery from whole-genome and whole-exome sequencing von Wang, WeiBo, Wang, Wei, Sun, Wei, Crowley, James J, Szatkiewicz, Jin P

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A New Method for Detecting Associations with Rare Copy-Number Variants von Tzeng, Jung-Ying, Magnusson, Patrik K E, Sullivan, Patrick F, Szatkiewicz, Jin P

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Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies von Baker, Jessica H., Gordon, Scott, Mattheisen, Manuel, Ripke, Stephan, Yao, Shuyang, Adan, Roger A.H., Boraska Perica, Vesna, Cichon, Sven, Cone, Roger D., DeSocio, Janiece E., Docampo, Elisa, Escaramís, Geòrgia, Esko, Tõnu, Favaro, Angela, Fischer, Krista, Föcker, Manuel, Gonidakis, Fragiskos, Guillaume, Sébastien, Guo, Yiran, Hakonarson, Hakon, Hebebrand, Johannes, Helder, Sietske G., Herms, Stefan, Herzog, Wolfgang, Huckins, Laura M., Hudson, James I., Karhunen, Leila, Karwautz, Andreas, Kennedy, James L., Klump, Kelly L., Le Hellard, Stephanie, Lin, Bochao Danae, Meulenbelt, Ingrid, Mitchell, Karen, Monteleone, Alessio Maria, Nacmias, Benedetta, Ophoff, Roel A., Padyukov, Leonid, Palotie, Aarno, Pinto, Dalila, Ricca, Valdo, Ritschel, Franziska, Santonastaso, Paolo, Scherag, André, Seitz, Jochen, Slachtova, Lenka, Slof‐Op't Landt, Margarita C.T., Slopien, Agnieszka, Szatkiewicz, Jin P., Wagner, Gudrun, Walton, Esther, Widen, Elisabeth, Crawford, Steven, Johnson, Craig, Mitchell, James, Whiteman, David C., Birgegård, Andreas, Norring, Claes, Polimanti, Renato, Clarke, Toni‐Kim, Degenhardt, Franziska, Docherty, Anna R., Foo, Jerome C., Fox, Louis, Frank, Josef, Hack, Laura M., Lahti, Jari, Lahti‐Pulkkinen, Marius, Loukola, Anu, Palviainen, Teemu, Saccone, Nancy L., Salvatore, Jessica E., Strohmaier, Jana, Wang, Jen‐Chyong, Wills, Amanda G., Boardman, Jason D., Choi, Doo‐Sup, Culverhouse, Robert C., Dahmen, Norbert, Domingue, Benjamin W., Gäebel, Wolfgang, Ising, Marcus, Keyes, Margaret, Lucae, Susanne, Nurnberger, John I., Preuss, Ulrich, Bierut, Laura J., Brown, Sandra A., Costello, E. Jane, Eriksson, Johan G., Foroud, Tatiana M., Hesselbrock, Victor, Johnson, Eric O., Stallings, Michael C., Vrieze, Scott, Wade, Tracey D., Heath, Andrew C., Martin, Nicholas G., Breen, Gerome, Bulik, Cynthia M.

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Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample von Szatkiewicz, J P, Neale, B M, O'Dushlaine, C, Fromer, M, Goldstein, J I, Moran, J L, Chambert, K, Kähler, A, Magnusson, P K E, Hultman, C M, Sklar, P, Purcell, S, McCarroll, S A, Sullivan, P F

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