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1 Ergebnisse
1
Rare coding variants in ten genes confer substantial risk f..:
Singh, Tarjinder
;
Poterba, Timothy
;
Curtis, David
...
10.1038/s41586-022-04556-w. , 2022
Link:
http://hdl.handle.net/10138/351897
RT Journal T1
Rare coding variants in ten genes confer substantial risk for schizophrenia
UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_351897&Exemplar=1&LAN=DE A1 Singh, Tarjinder A1 Poterba, Timothy A1 Curtis, David A1 Akil, Huda A1 Al Eissa, Mariam A1 Barchas, Jack D A1 Bass, Nicholas A1 Bigdeli, Tim B A1 Breen, Gerome A1 Bromet, Evelyn J A1 Buckley, Peter F A1 Bunney, William E A1 Bybjerg-Grauholm, Jonas A1 Byerley, William F A1 Chapman, Sinead B A1 Chen, Wei J A1 Churchhouse, Claire A1 Craddock, Nicholas A1 Cusick, Caroline M A1 DeLisi, Lynn A1 Dodge, Sheila A1 Escamilla, Michael A A1 Eskelinen, Saana A1 Fanous, Ayman H A1 Faraone, Stephen A1 Fiorentino, Alessia A1 Francioli, Laurent A1 Gabriel, Stacey B A1 Gage, Diane A1 Taliun, Sarah A. Gagliano A1 Ganna, Andrea A1 Genovese, Giulio A1 Glahn, David C A1 Grove, Jakob A1 Hall, Mei-Hua A1 Hämäläinen, Eija A1 Heyne, Henrike O A1 Holi, Matti A1 Hougaard, David M A1 Howrigan, Daniel P A1 Huang, Hailiang A1 Hwu, Hai-Gwo A1 Kahn, Rene S A1 Kang, Hyun Min A1 Karczewski, Konrad J A1 Kirov, George A1 Knowles, James A A1 Lee, Francis S A1 Lehrer, Douglas S A1 Lescai, Francesco A1 Malaspina, Dolores A1 Marder, Stephen R A1 McCarroll, Steven A A1 McIntosh, Andrew M A1 Medeiros, Helena A1 Milani, Lili A1 Morley, Christopher P A1 Morris, Derek W A1 Mortensen, Preben Bo A1 Myers, Richard M A1 Nordentoft, Merete A1 O'Brien, Niamh L A1 Olivares, Ana Maria A1 Ongur, Dost A1 Ouwehand, Willem H A1 Palmer, Duncan S A1 Paunio, Tiina A1 Quested, Digby A1 Rapaport, Mark H A1 Rees, Elliott A1 Rollins, Brandi A1 Satterstrom, F. Kyle A1 Schatzberg, Alan A1 Scolnick, Edward A1 Scott, Laura J A1 Sharp, Sally A1 Sklar, Pamela A1 Smoller, Jordan W A1 Sobell, Janet L A1 Solomonson, Matthew A1 Stahl, Eli A A1 Stevens, Christine R A1 Suvisaari, Jaana A1 Tiao, Grace A1 Watson, Stanley J A1 Watts, Nicholas A A1 Blackwood, Douglas H A1 Borglum, Anders D A1 Cohen, Bruce M A1 Corvin, Aiden P A1 Esko, Tonu A1 Freimer, Nelson B A1 Glatt, Stephen J A1 Hultman, Christina M A1 McQuillin, Andrew A1 Palotie, Aarno A1 Pato, Carlos N A1 Pato, Michele T A1 Pulver, Ann E A1 St Clair, David A1 Tsuang, Ming T A1 Vawter, Marquis P A1 Walters, James T A1 Werge, Thomas M A1 Ophoff, Roel A A1 Sullivan, Patrick F A1 Owen, Michael J A1 Boehnke, Michael A1 O'Donovan, Michael C A1 Neale, Benjamin M A1 Daly, Mark J PB Nature Publishing Group YR 2022 K1 MUTATIONS K1 INDIVIDUALS K1 ASSOCIATION K1 BURDEN K1 3111 Biomedicine K1 3112 Neurosciences JF 10.1038/s41586-022-04556-w LK http://hdl.handle.net/10138/351897 DO http://hdl.handle.net/10138/351897 SF ELIB - SuUB Bremen
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