logo
科言猫学术研究的AI总结
language
手机端手机端
  • Phone Feature微信小程序
简体中文简体中文
notice消息通知
博客博客
arrow
E

Edwin H. Cook

University of Illinois Chicago
H指数:120
被引数:7.1万

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Deleterious coding variation associated with autism is shared across ancestries

与自闭症相关的有害编码变异在祖先之间共享

Nature Medicine
IF50
2026-03-300
OAAI
Marina Natividad Avila; Seulgi Jung; F. Kyle Satterstrom; Jack M. Fu; Tess Levy; Laura G. Sloofman; Lambertus Klei; Thariana Pichardo; Dalia Marquez; Christine R. Stevens; Caroline M. Cusick; Jennifer L. Ames; Gabriele S. Campos; Hilda Cerros; Roberto Chaskel; Claudia I. S. Costa; Michael L. Cuccaro; Andrea del Pilar Lopez; Magdalena Fernandez; Eugenio Ferro; Liliana Galeano; Ana Cristina D. E. S. Girardi; Anthony J. Griswold; Luis C. Hernandez; Naila Lourenço; Yunin Ludena; Diana Núñez-Ríos; Rosa Oyama; Katherine P. Peña; Isaac Pessah; Rebecca Schmidt; Holly M. Sweeney; Lizbeth Tolentino; Jaqueline Y. T. Wang; Lilia Albores-Gallo; Lisa A. Croen; Carlos S. Cruz-Fuentes; Irva Hertz-Picciotto; Alexander Kolevzon; Maria Claudia Lattig; Liliana Mayo; Maria Rita Passos-Bueno; Margaret A. Pericak-Vance; Paige M. Siper; Flora Tassone; M. Pilar Trelles; Michael E. Talkowski; Mark J. Daly; Behrang Mahjani; Silvia De Rubeis; Edwin H. Cook; Kathryn Roeder; Catalina Betancur; Bernie Devlin; Joseph D. Buxbaum
Analyses of GWAS and Sub-Threshold Loci Lead to the Discovery of Dendrite Development and Morphology Dysfunction Underlying Schizophrenia Genetic Risk

全基因组关联研究（GWAS）和亚阈值位点的分析揭示了精神分裂症遗传风险下树突发育和形态功能障碍的发现。

Advanced Science
IF14.1
2025-08-290
OAAI
Rui Chen; Benjamin Siciliano; Quan Wang; Chongchong Xu; Qiang Wei; Hai Yang; James S Sutcliffe; Yi Jiang; Ying Ji; Chunyu Liu; Feixiong Cheng; Edwin H Cook; Nancy J Cox; Xue Zhong; Zhexing Wen; Bingshan Li
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

NATURE GENETICS
IF31.8
2022-08-18198
OA
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.
Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability

GNB2的复发性从头错义变异可导致综合征性智力障碍

JOURNAL OF MEDICAL GENETICS
IF3.7
2021-06-286
OA
Tan, Natalie B.; Pagnamenta, Alistair T.; Ferla, Matteo P.; Gadian, Jonathan; Chung, Brian H. Y.; Chan, Marcus C. Y.; Fung, Jasmine L. F.; Cook, Edwin; Guter, Stephen; Boschann, Felix; Heinen, Andre; Schallner, Jens; Mignot, Cyril; Keren, Boris; Whalen, Sandra; Sarret, Catherine; Mittag, Dana; Demmer, Laurie; Stapleton, Rachel; Saida, Ken; Matsumoto, Naomichi; Miyake, Noriko; Sheffer, Ruth; Mor-Shaked, Hagar; Barnett, Christopher P.; Byrne, Alicia B.; Scott, Hamish S.; Kraus, Alison; Cappuccio, Gerarda; Brunetti-Pierri, Nicola; Iorio, Raffaele; Di Dato, Fabiola; Pais, Lynn S.; Yeung, Alison; Tan, Tiong Y.; Taylor, Jenny C.; Christodoulou, John; White, Susan M.
A framework for an evidence-based gene list relevant to autism spectrum disorder
NATURE REVIEWS GENETICS
IF52
2020-04-2186
OAAI
Schaaf, Christian P.; Betancur, Catalina; Yuen, Ryan K. C.; Parr, Jeremy R.; Skuse, David H.; Gallagher, Louise; Bernier, Raphael A.; Buchanan, Janet A.; Buxbaum, Joseph D.; Chen, Chun-An; Dies, Kira A.; Elsabbagh, Mayada; Firth, Helen V.; Frazier, Thomas; Hoang, Ny; Howe, Jennifer; Marshall, Christian R.; Michaud, Jacques L.; Rennie, Olivia; Szatmari, Peter; Chung, Wendy K.; Bolton, Patrick F.; Cook, Edwin H.; Scherer, Stephen W.; Vorstman, Jacob A. S.
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

CELL
IF42.5
2020-02-011.3K
OAAI
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.

研究方向

暂未获取到该数据
J
James S. Sutcliffe
H 指数:76论文数:183被引数:4.9万
J
Jeremy Veenstra‐VanderWeele
H 指数:64论文数:300被引数:1.7万
S
Stephen J. Guter
H 指数:28论文数:57被引数:1.3万
C
Catherine Lord
H 指数:154论文数:1,228被引数:11.1万
J
Joseph D. Buxbaum
H 指数:140论文数:796被引数:11.7万
B
Bernie Devlin
H 指数:102论文数:371被引数:5.8万
S
Suma Jacob
H 指数:39论文数:155被引数:1.0万
D
Daniel H. Geschwind
H 指数:188论文数:983被引数:15.0万
S
Stephen W. Scherer
H 指数:161论文数:1,092被引数:11.9万
H
Hilary Coon
H 指数:73论文数:345被引数:3.6万