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Genetic associations with psychosis and affective disturbance in Alzheimer's disease Antonsdottir, Inga Margret; Creese, Byron; Klei, Lambertus; DeMichele-Sweet, Mary Ann A.; Weamer, Elise A.; Garcia-Gonzalez, Pablo; Marquie, Marta; Boada, Merce; Alarcon-Martin, Emilio; Valero, Sergi; Liu, Yushi; Hooli, Basavaraj; Aarsland, Dag; Selbaek, Geir; Bergh, Sverre; Rongve, Arvid; Saltvedt, Ingvild; Skjellegrind, Havard K.; Engdahl, Bo; Andreassen, Ole A.; Borroni, Barbara; Mecocci, Patrizia; Wedatilake, Yehani; Mayeux, Richard; Foroud, Tatiana; Ruiz, Agustin; Lopez, Oscar L.; Kamboh, M. Ilyas; Ballard, Clive; Devlin, Bernie; Lyketsos, Constantine; Sweet, Robert A. 分享 收藏
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Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk McKinney, Brandon C.; McClain, Lora L.; Hensler, Christopher M.; Wei, Yue; Klei, Lambertus; Lewis, David A.; Devlin, Bernie; Wang, Jiebiao; Ding, Ying; Sweet, Robert A. 分享 收藏
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism 罕见的编码变异提供了对自闭症遗传结构和表型背景的洞察 Fu, Jack M.; Satterstrom, F. Kyle; Peng, Minshi; Brand, Harrison; Collins, Ryan L.; Dong, Shan; Wamsley, Brie; Klei, Lambertus; Wang, Lily; Hao, Stephanie P.; Stevens, Christine R.; Cusick, Caroline; Babadi, Mehrtash; Banks, Eric; Collins, Brett; Dodge, Sheila; Gabriel, Stacey B.; Gauthier, Laura; Lee, Samuel K.; Liang, Lindsay; Ljungdahl, Alicia; Mahjani, Behrang; Sloofman, Laura; Smirnov, Andrey N.; Barbosa, Mafalda; Betancur, Catalina; Brusco, Alfredo; Chung, Brian H. Y.; Cook, Edwin H.; Cuccaro, Michael L.; Domenici, Enrico; Ferrero, Giovanni Battista; Gargus, J. Jay; Herman, Gail E.; Hertz-Picciotto, Irva; Maciel, Patricia; Manoach, Dara S.; Passos-Bueno, Maria Rita; Persico, Antonio M.; Renieri, Alessandra; Sutcliffe, James S.; Tassone, Flora; Trabetti, Elisabetta; Campos, Gabriele; Cardaropoli, Simona; Carli, Diana; Chan, Marcus C. Y.; Fallerini, Chiara; Giorgio, Elisa; Girardi, Ana Cristina; Hansen-Kiss, Emily; Lee, So Lun; Lintas, Carla; Ludena, Yunin; Nguyen, Rachel; Pavinato, Lisa; Pericak-Vance, Margaret; Pessah, Isaac N.; Schmidt, Rebecca J.; Smith, Moyra; Costa, Claudia I. S.; Trajkova, Slavica; Wang, Jaqueline Y. T.; Yu, Mullin H. C.; Cutler, David J.; De Rubeis, Silvia; Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Roeder, Kathryn; Sanders, Stephan J.; Talkowski, Michael E. 分享 收藏
The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum 强迫症的遗传结构: 跨频谱等位基因对强迫症的责任贡献 Mahjani, Behrang; Klei, Lambertus; Mattheisen, Manuel; Halvorsen, Matthew W.; Reichenberg, Abraham; Roeder, Kathryn; Pedersen, Nancy L.; Boberg, Julia; de Schipper, Elles; Bulik, Cynthia M.; Landen, Mikael; Fundin, Bengt; Mataix-Cols, David; Sandin, Sven; Hultman, Christina M.; Crowley, James J.; Buxbaum, Joseph D.; Ruck, Christian; Devlin, Bernie; Grice, Dorothy E. 分享 收藏
How rare and common risk variation jointly affect liability for autism spectrum disorder Klei, Lambertus; McClain, Lora Lee; Mahjani, Behrang; Panayidou, Klea; De Rubeis, Silvia; Grahnat, Anna-Carin Sall; Karlsson, Gun; Lu, Yangyi; Melhem, Nadine; Xu, Xinyi; Reichenberg, Abraham; Sandin, Sven; Hultman, Christina M.; Buxbaum, Joseph D.; Roeder, Kathryn; Devlin, Bernie 分享 收藏
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder Mahjani, Behrang; De Rubeis, Silvia; Gustavsson Mahjani, Christina; Mulhern, Maureen; Xu, Xinyi; Klei, Lambertus; Satterstrom, F. Kyle; Fu, Jack; Talkowski, Michael E.; Reichenberg, Abraham; Sandin, Sven; Hultman, Christina M.; Grice, Dorothy E.; Roeder, Kathryn; Devlin, Bernie; Buxbaum, Joseph D. 分享 收藏
Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease DeMichele-Sweet, Mary Ann A.; Klei, Lambertus; Creese, Byron; Harwood, Janet C.; Weamer, Elise A.; McClain, Lora; Sims, Rebecca; Hernandez, Isabel; Moreno-Grau, Sonia; Tarraga, Lluis; Boada, Merce; Alarcon-Martin, Emilio; Valero, Sergi; Liu, Yushi; Hooli, Basavaraj; Aarsland, Dag; Selbaek, Geir; Bergh, Sverre; Rongve, Arvid; Saltvedt, Ingvild; Skjellegrind, Havard K.; Engdahl, Bo; Stordal, Eystein; Andreassen, Ole A.; Djurovic, Srdjan; Athanasiu, Lavinia; Seripa, Davide; Borroni, Barbara; Albani, Diego; Forloni, Gianluigi; Mecocci, Patrizia; Serretti, Alessandro; De Ronchi, Diana; Politis, Antonis; Williams, Julie; Mayeux, Richard; Foroud, Tatiana; Ruiz, Agustin; Ballard, Clive; Holmans, Peter; Lopez, Oscar L.; Kamboh, M. Ilyas; Devlin, Bernie; Sweet, Robert A. 分享 收藏
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Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex Werling, Donna M.; Pochareddy, Sirisha; Choi, Jinmyung; An, Joon-Yong; Sheppard, Brooke; Peng, Minshi; Li, Zhen; Dastmalchi, Claudia; Santpere, Gabriel; Sousa, Andre M. M.; Tebbenkamp, Andrew T. N.; Kaur, Navjot; Gulden, Forrest O.; Breen, Michael S.; Liang, Lindsay; Gilson, Michael C.; Zhao, Xuefang; Dong, Shan; Klei, Lambertus; Cicek, A. Ercument; Buxbaum, Joseph D.; Adle-Biassette, Homa; Thomas, Jean-Leon; Aldinger, Kimberly A.; O'Day, Diana R.; Glass, Ian A.; Zaitlen, Noah A.; Talkowski, Michael E.; Roeder, Kathryn; State, Matthew W.; Devlin, Bernie; Sanders, Stephan J.; Sestan, Nenad 分享 收藏
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism 大规模外显子组测序研究暗示自闭症神经生物学的发育和功能变化 Satterstrom, F. Kyle; Kosmicki, Jack A.; Wang, Jiebiao; Breen, Michael S.; De Rubeis, Silvia; An, Joon-Yong; Peng, Minshi; Collins, Ryan; Grove, Jakob; Klei, Lambertus; Stevens, Christine; Reichert, Jennifer; Mulhern, Maureen S.; Artomov, Mykyta; Gerges, Sherif; Sheppard, Brooke; Xu, Xinyi; Bhaduri, Aparna; Norman, Utku; Brand, Harrison; Schwartz, Grace; Nguyen, Rachel; Guerrero, Elizabeth E.; Dias, Caroline; Betancur, Catalina; Cook, Edwin H.; Gallagher, Louise; Gill, Michael; Sutcliffe, James S.; Thurm, Audrey; Zwick, Michael E.; Borglum, Anders D.; State, Matthew W.; Cicek, A. Ercument; Talkowski, Michael E.; Cutler, David J.; Devlin, Bernie; Sanders, Stephan J.; Roeder, Kathryn; Daly, Mark J.; Buxbaum, Joseph D.; Aleksic, Branko; Anney, Richard; Barbosa, Mafalda; Bishop, Somer; Brusco, Alfredo; Bybjerg-Grauholm, Jonas; Carracedo, Angel; Chan, Marcus C. Y.; Chiocchetti, Andreas G.; Chung, Brian H. Y.; Coon, Hilary; Cuccaro, Michael L.; Curro, Aurora; Dalla Bernardina, Bernardo; Doan, Ryan; Domenici, Enrico; Dong, Shan; Fallerini, Chiara; Fernandez-Prieto, Montserrat; Ferrero, Giovanni Battista; Freitag, Christine M.; Fromer, Menachem; Gargus, J. Jay; Geschwind, Daniel; Giorgio, Elisa; Gonzalez-Penas, Javier; Guter, Stephen; Halpern, Danielle; Hansen-Kiss, Emily; He, Xin; Herman, Gail E.; Hertz-Picciotto, Irva; Hougaard, David M.; Hultman, Christina M.; Ionita-Laza, Iuliana; Jacob, Suma; Jamison, Jesslyn; Jugessur, Astanand; Kaartinen, Miia; Knudsen, Gun Peggy; Kolevzon, Alexander; Kushima, Itaru; Lee, So Lun; Lehtimaki, Terho; Lim, Elaine T.; Lintas, Carla; Lipkin, W. Ian; Lopergolo, Diego; Lopes, Fatima; Ludena, Yunin; Maciel, Patricia; Magnus, Per; Mahjani, Behrang; Maltman, Nell; Manoach, Dara S.; Meiri, Gal; Menashe, Idan; Miller, Judith; Minshew, Nancy; Montenegro, Eduarda M. S.; Moreira, Danielle; Morrow, Eric M.; Mors, Ole; Mortensen, Preben Bo; Mosconi, Matthew; Muglia, Pierandrea; Neale, Benjamin M.; Nordentoft, Merete; Ozaki, Norio; Palotie, Aarno; Parellada, Mara; Passos-Bueno, Maria Rita; Pericak-Vance, Margaret; Persico, Antonio M.; Pessah, Isaac; Puura, Kaija; Reichenberg, Abraham; Renieri, Alessandra; Riberi, Evelise; Robinson, Elise B.; Samocha, Kaitlin E.; Sandin, Sven; Santangelo, Susan L.; Schellenberg, Gerry; Scherer, Stephen W.; Schlitt, Sabine; Schmidt, Rebecca; Schmitt, Lauren; Silva, Isabela M. W.; Singh, Tarjinder; Siper, Paige M.; Smith, Moyra; Soares, Gabriela; Stoltenberg, Camilla; Suren, Pal; Susser, Ezra; Sweeney, John; Szatmari, Peter; Tang, Lara; Tassone, Flora; Teufel, Karoline; Trabetti, Elisabetta; Trelles, Maria del Pilar; Walsh, Christopher A.; Weiss, Lauren A.; Werge, Thomas; Werling, Donna M.; Wigdor, Emilie M.; Wilkinson, Emma; Willsey, A. Jeremy; Yu, Timothy W.; Yu, Mullin Hc; Yuen, Ryan; Zachi, Elaine; Agerbo, Esben; Als, Thomas Damm; Appadurai, Vivek; Baekvad-Hansen, Marie; Belliveau, Rich; Buil, Alfonso; Carey, Caitlin E.; Cerrato, Felecia; Chambert, Kimberly; Churchhouse, Claire; Dalsgaard, Soren; Demontis, Ditte; Dumont, Ashley; Goldstein, Jacqueline; Hansen, Christine S.; Hauberg, Mads Engel; Hollegaard, Mads, V; Howrigan, Daniel P.; Huang, Hailiang; Maller, Julian; Martin, Alicia R.; Martin, Joanna; Mattheisen, Manuel; Moran, Jennifer; Pallesen, Jonatan; Palmer, Duncan S.; Pedersen, Carsten Bocker; Pedersen, Marianne Giortz; Poterba, Timothy; Poulsen, Jesper Buchhave; Ripke, Stephan; Schork, Andrew J.; Thompson, Wesley K.; Turley, Patrick; Walters, Raymond K. 分享 收藏
Age dependent association of inbreeding with risk for schizophrenia in Egypt McClain, Lora; Mansour, Hader; Ibrahim, Ibtihal; Klei, Lambertus; Fathi, Warda; Wood, Joel; Kodavali, Chowdari; Maysterchuk, Alina; Wood, Shawn; El-Chennawi, Farha; Ibrahim, Nahed; Eissa, Ahmed; El-Bahaei, Wafaa; El Sayed, Hanan; Yassein, Amal; Tobar, Salwa; El-Boraie, Hala; El-Sheshtawy, Eman; Salah, Hala; Ali, Ahmed; Erdin, Serkan; Devlin, Bernie; Talkowski, Michael; Nimgaonkar, Vishwajit 分享 收藏
Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS) 队列概况: 瑞典强迫症和慢性抽动障碍的流行病学和遗传学 (EGOS) Mahjani, Behrang; Dellenvall, Karin; Grahnat, Anna-Carin Sall; Karlsson, Gun; Tuuliainen, Aki; Reichert, Jennifer; Mahjani, Christina G.; Klei, Lambertus; De Rubeis, Silvia; Reichenberg, Abraham; Devlin, Bernie; Hultman, Christina M.; Buxbaum, Joseph D.; Sandin, Sven; Grice, Dorothy E. 分享 收藏
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