Genome-Wide Association Analysis of Neonatal White Matter Microstructure by 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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Genome-wide association analysis identifies common variants influencing infant brain volumes by Xia, K, Zhang, J, Ahn, M, Jha, S, Crowley, J J, Szatkiewicz, J, Li, T, Zou, F, Zhu, H, Hibar, D, Thompson, P, Sullivan, P F, Styner, M, Gilmore, J H, Knickmeyer, R C

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Integrative functional genomic analysis of human brain development and neuropsychiatric risks by Li, Mingfeng, Santpere, Gabriel, Imamura Kawasawa, Yuka, Evgrafov, Oleg V, Gulden, Forrest O, Pochareddy, Sirisha, Sunkin, Susan M, Li, Zhen, Shin, Yurae, Zhu, Ying, Sousa, André M M, Werling, Donna M, Kitchen, Robert R, Kang, Hyo Jung, Pletikos, Mihovil, Choi, Jinmyung, Muchnik, Sydney, Xu, Xuming, Wang, Daifeng, Lorente-Galdos, Belen, Liu, Shuang, Giusti-Rodríguez, Paola, Won, Hyejung, de Leeuw, Christiaan A, Pardiñas, Antonio F, Hu, Ming, Jin, Fulai, Li, Yun, Owen, Michael J, O'Donovan, Michael C, Walters, James T R, Posthuma, Danielle, Reimers, Mark A, Levitt, Pat, Weinberger, Daniel R, Hyde, Thomas M, Kleinman, Joel E, Geschwind, Daniel H, Hawrylycz, Michael J, State, Matthew W, Sanders, Stephan J, Sullivan, Patrick F, Gerstein, Mark B, Lein, Ed S, Knowles, James A, Sestan, Nenad

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Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa by Yilmaz, Zeynep, Walters, Raymond, Goldstein, Jackie, Ripke, Stephan, Thornton, Laura, Hinney, Anke, Daly, Mark, Sullivan, Patrick F, Zeggini, Eleftheria, Breen, Gerome, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, Aschauer, Harald, Baker, Jessica, Barrett, Jeffrey, Bencko, Vladimir, Boni, Claudette, Perica, Vesna Boraska, Burghardt, Roland, Cassina, Matteo, Cichon, Sven, Crow, Scott, Davis, Oliver, de Zwaan, Martina, Dedoussis, George, Degortes, Daniela, DeSocio, Janiece, Dick, Danielle, Ding, Bo, Egberts, Karin, Escaramís, Geòrgia, Esko, Tõnu, Fichter, Manfred, Finan, Chris, Fischer, Krista, Floyd, James, Föcker, Manuel, Forzan, Monica, Gaborieau, Valerie, Gambaro, Giovanni, Giegling, Ina, Guillaume, Sébastien, Guo, Yiran, Hauser, Joanna, Helder, Sietske, Hendriks, Judith, Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Hudson, James, Inoko, Hidetoshi, Jall, Sigrid, Jamain, Stephane, Johnson, Craig, Julià, Antonio, Kennedy, Martin, Kennedy, James, Keski-Rahkonen, Anna, Klareskog, Lars, Klump, Kelly, Leboyer, Marion, Levitan, Robert, Lissowska, Jolanta, Maj, Mario, Marsal, Sara, Metspalu, Andres, Micali, Nadia, Monteleone, Palmiero, Monteleone, Alessio Maria, Mortensen, Preben, Munn-Chernoff, Melissa, Müller, Timo, Ophoff, Roel, O’Toole, Julie, Pantel, Jacques, Pinto, Dalila, Rabionet, Raquel, Reichborn-Kjennerud, Ted, Ricca, Valdo, Ripatti, Samuli, Ritschel, Franziska, Roberts, Marion, Rotondo, Alessandro, Rybakowski, Filip, Santonastaso, Paolo, Scherag, André, Schork, Nicholas, Scott, Laura, Slachtova, Lenka, Sladek, Robert, Szatkiewicz, Jin, Szeszenia-Dabrowska, Neonila, Tachmazidou, Ioanna, Tortorella, Alfonso, Treasure, Janet, Tsitsika, Artemis, van Furth, Eric, Wade, Tracey, Wagner, Gudrun

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Mapping genomic loci implicates genes and synaptic biology in schizophrenia by 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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Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndrome by Harner, Matthew K., Lichtenstein, Maya, Farrell, Martilias, Dietterich, Tyler E., Filmyer, Dawn M., Bruno, Lisa M., Biondi, Tamara F., Crowley, James J., Lázaro-Muñoz, Gabriel, Stowe, Robert, Shaughnessy, Rita A., Berg, Jonathan S., Szatkiewicz, Jin, Sullivan, Patrick F., Josiassen, Richard C.

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Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant Psychosis by Farrell, Martilias, Dietterich, Tyler E, Harner, Matthew K, Bruno, Lisa M, Filmyer, Dawn M, Shaughnessy, Rita A, Lichtenstein, Maya L, Britt, Allison M, Biondi, Tamara F, Crowley, James J, Lázaro-Muñoz, Gabriel, Forsingdal, Annika E, Nielsen, Jacob, Didriksen, Michael, Berg, Jonathan S, Wen, Jia, Szatkiewicz, Jin, Mary Xavier, Rose, Sullivan, Patrick F, Josiassen, Richard C

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Leveraging base-pair mammalian constraint to understand genetic variation and human disease by Sullivan, Patrick F, Meadows, Jennifer R S, Gazal, Steven, Phan, BaDoi N, Li, Xue, Genereux, Diane P, Dong, Michael X, Bianchi, Matteo, Andrews, Gregory, Sakthikumar, Sharadha, Nordin, Jessika, Roy, Ananya, Christmas, Matthew J, Marinescu, Voichita D, Wang, Chao, Wallerman, Ola, Xue, James, Yao, Shuyang, Sun, Quan, Szatkiewicz, Jin, Wen, Jia, Huckins, Laura M, Lawler, Alyssa, Keough, Kathleen C, Zheng, Zhili, Zeng, Jian, Wray, Naomi R, Li, Yun, Johnson, Jessica, Chen, Jiawen, Paten, Benedict, Reilly, Steven K, Hughes, Graham M, Weng, Zhiping, Pollard, Katherine S, Pfenning, Andreas R, Forsberg-Nilsson, Karin, Karlsson, Elinor K, Lindblad-Toh, Kerstin

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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes by 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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Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia by 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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Biological insights from 108 schizophrenia-associated genetic loci by 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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Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches by Yao, Shuyang, Kuja-Halkola, Ralf, Lu, Yi, Birgegård, Andreas, Yilmaz, Zeynep, Coleman, Joni, Courtet, Philippe, Crawford, Steven, Crow, Scott, Crowley, James, Danner, Unna, Dikeos, Dimitris, Docampo, Elisa, Ehrlich, Stefan, Estivill, Xavier, Favaro, Angela, Fichter, Manfred, Foretova, Lenka, Forzan, Monica, Franklin, Christopher, Gaspar, Héléna, Gonidakis, Fragiskos, Gorwood, Philip, Guo, Yiran, Hakonarson, Hakon, Hatzikotoulas, Konstantinos, Hebebrand, Johannes, Hendriks, Judith, Hilliard, Christopher, Hinney, Anke, Huckins, Laura, Hudson, James, Huemer, Julia, Imgart, Hartmut, Inoko, Hidetoshi, Johnson, Craig, Jordan, Jenny, Juréus, Anders, Kalsi, Gursharan, Karhunen, Leila, Karwautz, Andreas, Kas, Martien, Kennedy, James, Keski-Rahkonen, Anna, Koubek, Doris, Levitan, Robert, Lichtenstein, Paul, Mannik, Katrin, Martin, Nicholas, Merl, Elisabeth, Metspalu, Andres, Meulenbelt, Ingrid, Mitchell, James, Monteleone, Palmiero, Munn-Chernoff, Melissa, Nilsson, Ida, Norring, Claes, Ntalla, Ioanna, Parker, Richard, Rabionet, Raquel, Raevuori, Anu, Rajewski, Andrzej, Reichborn-Kjennerud, Ted, Ritschel, Franziska, Scherag, André, Schmidt, Ulrike, Seitz, Jochen, Slachtova, Lenka, Slopien, Agnieszka, Strober, Michael, Sullivan, Patrick, Szatkiewicz, Jin, Tenconi, Elena, Thornton, Laura, Treasure, Janet, Wagner, Gudrun, Walton, Esther, Woodside, D. Blake, Zeggini, Eleftheria, Zerwas, Stephanie, Andreassen, Ole, Aschauer, Harald, Barrett, Jeffrey, Bencko, Vladimir, Espeseth, Thomas, Floyd, James, Gallinger, Steven, Gambaro, Giovanni, Giegling, Ina, Herms, Stefan, Julià, Antonio, Klareskog, Lars, Le Hellard, Stephanie, Navratilova, Marie, Ophoff, Roel, Pinto, Dalila, Rujescu, Dan, Sladek, Robert, Wichmann, H-Erich, Magnusson, Patrik K.

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Common-variant associations with fragile X syndrome (vol 24, pg 338, 2019) by Crowley, JJ, Szatkiewicz, J, Kahler, AK, Giusti-Rodriguez, P, Ancalade, N, Booker, JK, Carr, JL, Giamberardino, SN, Crawford, GE, Losh, M

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Crossover interference underlies sex differences in recombination rates by Petkov, Petko M, Broman, Karl W, Szatkiewicz, Jin P, Paigen, Kenneth

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Correction: Common-variant associations with fragile X syndrome by Crowley, James J., Szatkiewicz, Jin, Kähler, Anna K., Giusti-Rodriguez, Paola, Ancalade, NaEshia, Booker, Jessica K., Carr, Jennifer L., Giamberardino, Stephanie N., Crawford, Greg E., Losh, Molly, Stockmeier, Craig A., Taylor, Annette K., Piven, Joseph, Sullivan, Patrick F.

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The genomics of major psychiatric disorders in a large pedigree from Northern Sweden by Szatkiewicz, Jin, Crowley, James J., Adolfsson, Annelie Nordin, Åberg, Karolina A., Alaerts, Maaike, Genovese, Giulio, McCarroll, Steven, Del-Favero, Jurgen, Adolfsson, Rolf, Sullivan, Patrick F.

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Characterization of human embryonic stem cell lines by the International Stem Cell Initiative by Adewumi, Oluseun, Aflatoonian, Behrouz, Ahrlund-Richter, Lars, Amit, Michal, Andrews, Peter W, Beighton, Gemma, Bello, Paul A, Benvenisty, Nissim, Berry, Lorraine S, Bevan, Simon, Blum, Barak, Brooking, Justin, Chen, Kevin G, Choo, Andre B H, Churchill, Gary A, Corbel, Marie, Damjanov, Ivan, Draper, Jon S, Dvorak, Petr, Emanuelsson, Katarina, Fleck, Roland A, Ford, Angela, Gertow, Karin, Gertsenstein, Marina, Gokhale, Paul J, Hamilton, Rebecca S, Hampl, Ales, Healy, Lyn E, Hovatta, Outi, Hyllner, Johan, Imreh, Marta P, Itskovitz-Eldor, Joseph, Jackson, Jamie, Johnson, Jacqueline L, Jones, Mark, Kee, Kehkooi, King, Benjamin L, Knowles, Barbara B, Lako, Majlinda, Lebrin, Franck, Mallon, Barbara S, Manning, Daisy, Mayshar, Yoav, McKay, Ronald D G, Michalska, Anna E, Mikkola, Milla, Mileikovsky, Masha, Minger, Stephen L, Moore, Harry D, Mummery, Christine L, Nagy, Andras, Nakatsuji, Norio, O'Brien, Carmel M, Oh, Steve K W, Olsson, Cia, Otonkoski, Timo, Park, Kye-Yoon, Passier, Robert, Patel, Hema, Patel, Minal, Pedersen, Roger, Pera, Martin F, Piekarczyk, Marian S, Pera, Renee A Reijo, Reubinoff, Benjamin E, Robins, Allan J, Rossant, Janet, Rugg-Gunn, Peter, Schulz, Thomas C, Semb, Henrik, Sherrer, Eric S, Siemen, Henrike, Stacey, Glyn N, Stojkovic, Miodrag, Suemori, Hirofumi, Szatkiewicz, Jin, Turetsky, Tikva, Tuuri, Timo, van den Brink, Steineke, Vintersten, Kristina, Vuoristo, Sanna, Ward, Dorien, Weaver, Thomas A, Young, Lesley A, Zhang, Weidong

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Common-variant associations with fragile X syndrome by Crowley, James J., Szatkiewicz, Jin, Kähler, Anna K., Giusti-Rodriguez, Paola, Ancalade, NaEshia, Booker, Jessica K., Carr, Jennifer L., Crawford, Greg E., Losh, Molly, Stockmeier, Craig A., Taylor, Annette K., Piven, Joseph, Sullivan, Patrick F.

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The impact of educational attainment, intelligence and intellectual disability on schizophrenia: a Swedish population-based register and genetic study by 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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Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington’s Disease by Farrell, Martilias, Lichtenstein, Maya, Crowley, James J, Filmyer, Dawn M, Lázaro-Muñoz, Gabriel, Shaughnessy, Rita A, Mackenzie, Ian R, Hirsch-Reinshagen, Veronica, Stowe, Robert, Evans, James P, Berg, Jonathan S, Szatkiewicz, Jin, Josiassen, Richard C, Sullivan, Patrick F

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