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COLLABORATIVE STUDY OF THE COMBINED EFFECTS OF RARE CNVS AND POLYGENIC RISK ON PSYCHIATRIC TRAITS Sacks, Molly; Klein, Marieke; Shanta, Omar; Ahangari, Mohammad; Hong, Oanh; MacDonald, Jeff; Thiruvahindrapuram, Bhooma; Jacquemont, Sebastien; Bigdeli, Tim; Oetjens, Matthew; Kals, Mart; Scherer, Stephen H.; Sebat, Jonathan 分享 收藏
META-ANALYSIS OF RARE CNV GENOME-WIDE ASSOCIATION STUDIES ACROSS MAJOR PSYCHIATRIC DISORDERS IN EUR, AFR/AFAM, AND ASN/ASAM POPULATIONS Shanta, Omar; Engchuan, Worrawat; MacDonald, Jeff; Klein, Marieke; Thiruvahindrapuram, Bhooma; Maihofer, Adam; Sacks, Molly; Ahangari, Mohammad; Jacquemont, Sebastien; Kendall, Kimberley; Sonderby, Ida; Huguet, Guillaume; Scherer, Steven H.; Sebat, Jonathan 分享 收藏
FUNCTIONAL-BASED ASSOCIATION STUDY OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IN EUROPEAN, AFRICAN, AND EAST ASIAN POPULATIONS Engchuan, Worrawat; Shanta, Omar; Macdonald, Jeffrey R.; Thiruvahindrapuram, Bhooma; Kumar, Kuldeep; Huguet, Guillaume; Wang, Zhuozhi; Pellecchia, Giovanna; Yuen, Ryan K. C.; Merico, Daniele; Jacquemont, Sebastien; Scherer, Stephen W.; Sebat, Jonathan 分享 收藏
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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications 22 q11.2和16 p11.2缺失和重复的神经认知特征 Gur, Ruben C.; Bearden, Carrie E.; Jacquemont, Sebastien; Swillen, Ann; van Amelsvoort, Therese; van den Bree, Marianne; Vorstman, Jacob; Sebat, Jonathan; Ruparel, Kosha; Gallagher, Robert Sean; Mcclellan, Emily; White, Lauren; Crowley, Terrence Blaine; Giunta, Victoria; Kushan, Leila; O'Hora, Kathleen; Verbesselt, Jente; Vandensande, Ans; Vingerhoets, Claudia; van Haelst, Mieke; Hall, Jessica; Harwood, Janet; Chawner, Samuel J. R. A.; Patel, Nishi; Palad, Katrina; Hong, Oanh; Guevara, James; Martin, Charles Olivier; Jizi, Khadije; Belanger, Anne-Marie; Scherer, Stephen W.; Bassett, Anne S.; McDonald-McGinn, Donna M.; Gur, Raquel E. 分享 收藏
A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats de Jong, Tristan V.; Pan, Yanchao; Rastas, Pasi; Munro, Daniel; Tutaj, Monika; Akil, Huda; Benner, Chris; Chen, Denghui; Chitre, Apurva S.; Chow, William; Colonna, Vincenza; Dalgard, Clifton L.; Demos, Wendy M.; Doris, Peter A.; Garrison, Erik; Geurts, Aron M.; Gunturkun, Hakan M.; Guryev, Victor; Hourlier, Thibaut; Howe, Kerstin; Huang, Jun; Kalbfleisch, Ted; Kim, Panjun; Li, Ling; Mahaffey, Spencer; Martin, Fergal J.; Mohammadi, Pejman; Ozel, Ayse Bilge; Polesskaya, Oksana; Pravenec, Michal; Prins, Pjotr; Sebat, Jonathan; Smith, Jennifer R.; Woods, Leah C. Solberg; Tabakoff, Boris; Tracey, Alan; Uliano-Silva, Marcela; Villani, Flavia; Wang, Hongyang; Sharp, Burt M.; Telese, Francesca; Jiang, Zhihua; Saba, Laura; Wang, Xusheng; Murphy, Terence D.; Palmer, Abraham A.; Kwitek, Anne E.; Dwinell, Melinda R.; Williams, Robert W.; Li, Jun Z.; Chen, Hao 分享 收藏
GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA Engchuan, Worrawat; Thiruvahindrapuram, Bhooma; MacDonald, Jeffrey R.; Shanta, Omar; Kumar, Kuldeep; Klein, Marieke; Huguet, Guillaume; Wang, Zhuozhi; Pellecchia, Giovanna; Yuen, Ryan K. C.; Merico, Daniele; Jacquemont, Sebastien; Scherer, Stephen W.; Sebat, Jonathan 分享 收藏
GENOME-WIDE ASSOCIATION OF COPY NUMBER VARIANTS ACROSS SIX MAJOR PSYCHIATRIC DISORDERS REVEALS GENOTYPE-PHENOTYPE RELATIONSHIPS OF RARE VARIANTS Shanta, Omar; Enghuan, Worrawat; MacDonald, Jeffrey Jeffrey; Thiruvahindrapuram, Bhooma; Klein, Marieke; Maihofer, Adam; Jacquemont, Sebastien; Kendall, Kimberley; Sonderby, Ida; Huguet, Guillaume; Kumar, Kuldeep; Schmilovich, Zoe; Scherer, Stephen; Sebat, Jonathan 分享 收藏
UNRAVELING THE IMPACT OF GENOMIC VARIATIONS ON COGNITIVE ABILITY ACROSS THE HUMAN CORTEX: INSIGHTS FROM GENE EXPRESSION AND COPY NUMBER VARIANTS Kumar, Kuldeep; Kazem, Sayeh; Huguet, Guillaume; Renne, Thomas; Engchuan, Bank; Shanta, Omar; Thiruvahindrapuram, Bhooma; MacDonald, Jeff; Klein, Marieke; Scherer, Stephen; Almasy, Laura; Sebat, Jonathan; Glahn, David; Dumas, Guillaume; Jacquemont, Sebastien 分享 收藏
Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism (vol 11, 3650, 2014) Corominas, Roser; Yang, Xinping; Lin, Guan Ning; Kang, Shuli; Shen, Yun; Ghamsari, Lila; Broly, Martin; Rodriguez, Maria; Tam, Stanley; Wanamaker, Shelly A.; Fan, Changyu; Yi, Song; Tasan, Murat; Lemmens, Irma; Kuang, Xingyan; Zhao, Nan; Malhotra, Dheeraj; Michaelson, Jacob J.; Vacic, Vladimir; Calderwood, Michael A.; Roth, Frederick P.; Tavernier, Jan; Horvath, Steve; Salehi-Ashtiani, Kourosh; Korkin, Dmitry; Sebat, Jonathan; Hill, David E.; Hao, Tong; Vidal, Marc; Iakoucheva, Lilia M. 分享 收藏
Control-independent mosaic single nucleotide variant detection with DeepMosaic Yang, Xiaoxu; Xu, Xin; Breuss, Martin W.; Antaki, Danny; Ball, Laurel L. V.; Chung, Changuk; Shen, Jiawei; Li, Chen; George, Renee D.; Wang, Yifan; Bae, Taejeong; Cheng, Yuhe; Abyzov, Alexej M.; Wei, Liping; Alexandrov, Ludmil B.; Sebat, Jonathan L.; Gleeson, Joseph G. 分享 收藏
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p Weiner, Daniel J.; Ling, Emi; Erdin, Serkan; Tai, Derek J. C.; Yadav, Rachita; Grove, Jakob; Fu, Jack M.; Nadig, Ajay; Carey, Caitlin E.; Baya, Nikolas; Bybjerg-Grauholm, Jonas; Berretta, Sabina; Macosko, Evan Z.; Sebat, Jonathan; O'Connor, Luke J.; Hougaard, David M.; Borglum, Anders D.; Talkowski, Michael E.; McCarroll, Steven A.; Robinson, Elise B. 分享 收藏
A GENOME-WIDE ASSOCIATION STUDY OF COPY NUMBER VARIATION ACROSS MAJOR PSYCHIATRIC DISORDERS IN 500,000 INDIVIDUALS Shanta, Omar; Klein, Marieke; Engchuan, Worrawat; MacDonald, Jeffrey; Thiruvahindrapuram, Bhooma; Maihofer, Adam; Jacquemont, Sebastien; Kendall, Kimberley; Sonderby, Ida; Huguet, Guillaume; Schmilovich, Zoe; Poulain, Cecile; Scherer, Stephen; Sebat, Jonathan 分享 收藏
Rare copy number variation in posttraumatic stress disorder 创伤后应激障碍中罕见的拷贝数变异 Maihofer, Adam X.; Engchuan, Worrawat; Huguet, Guillaume; Klein, Marieke; MacDonald, Jeffrey R.; Shanta, Omar; Thiruvahindrapuram, Bhooma; Jean-louis, Martineau; Saci, Zohra; Jacquemont, Sebastien; Scherer, Stephen W.; Ketema, Elizabeth; Aiello, Allison E.; Amstadter, Ananda B.; Avdibegovic, Esmina; Babic, Dragan; Baker, Dewleen G.; Bisson, Jonathan, I; Boks, Marco P.; Bolger, Elizabeth A.; Bryant, Richard A.; Bustamante, Angela C.; Caldas-de-Almeida, Jose Miguel; Cardoso, Graca; Deckert, Jurgen; Delahanty, Douglas L.; Domschke, Katharina; Dunlop, Boadie W.; Dzubur-Kulenovic, Alma; Evans, Alexandra; Feeny, Norah C.; Franz, Carol E.; Gautam, Aarti; Geuze, Elbert; Goci, Aferdita; Hammamieh, Rasha; Jakovljevic, Miro; Jett, Marti; Jones, Ian; Kaufman, Milissa L.; Kessler, Ronald C.; King, Anthony P.; Kremen, William S.; Lawford, Bruce R.; Lebois, Lauren A. M.; Lewis, Catrin; Liberzon, Israel; Linnstaedt, Sarah D.; Lugonja, Bozo; Luykx, Jurjen J.; Lyons, Michael J.; Mavissakalian, Matig R.; McLaughlin, Katie A.; McLean, Samuel A.; Mehta, Divya; Mellor, Rebecca; Morris, Charles Phillip; Muhie, Seid; Orcutt, Holly K.; Peverill, Matthew; Ratanatharathorn, Andrew; Risbrough, Victoria B.; Rizzo, Albert; Roberts, Andrea L.; Rothbaum, Alex O.; Rothbaum, Barbara O.; Roy-Byrne, Peter; Ruggiero, Kenneth J.; Rutten, Bart P. F.; Schijven, Dick; Seng, Julia S.; Sheerin, Christina M.; Sorenson, Michael A.; Teicher, Martin H.; Uddin, Monica; Ursano, Robert J.; Vinkers, Christiaan H.; Voisey, Joanne; Weber, Heike; Winternitz, Sherry; Xavier, Miguel; Yang, Ruoting; Young, Ross McD; Zoellner, Lori A.; Salem, Rany M.; Shaffer, Richard A.; Wu, Tianying; Ressler, Kerry J.; Stein, Murray B.; Koenen, Karestan C.; Sebat, Jonathan; Nievergelt, Caroline M. 分享 收藏
Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes Kimura, Hiroki; Nakatochi, Masahiro; Aleksic, Branko; Guevara, James; Toyama, Miho; Hayashi, Yu; Kato, Hidekazu; Kushima, Itaru; Morikawa, Mako; Ishizuka, Kanako; Okada, Takashi; Tsurusaki, Yoshinori; Fujita, Atsushi; Miyake, Noriko; Ogi, Tomoo; Takata, Atsushi; Matsumoto, Naomichi; Buxbaum, Joseph; Ozaki, Norio; Sebat, Jonathan 分享 收藏
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