E
Edwin H. Cook
Researcher at University of Illinois at Chicago
Publications - 339
Citations - 61045
Edwin H. Cook is an academic researcher from University of Illinois at Chicago. The author has contributed to research in topics: Autism & Heritability of autism. The author has an hindex of 102, co-authored 337 publications receiving 54518 citations. Previous affiliations of Edwin H. Cook include University of Chicago & University of Illinois at Urbana–Champaign.
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Journal ArticleDOI
Vocabulary comprehension in adults with fragile X syndrome (FXS)
Anne Hoffmann,Sue Ellen Krause,Joanne Wuu,Sue Leurgans,Stephen J. Guter,Sandra S. Block,Jeff Salt,Edwin H. Cook,Dominick M. Maino,Elizabeth Berry-Kravis +9 more
TL;DR: Findings from this investigation strongly suggest that the PPVT-III should not be used as a screening tool for language levels or cognitive function in clinical studies since the scores were not representative of global language or non-verbal cognitive skills in adults with intellectual disabilities.
Journal ArticleDOI
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p
Daniel J. Weiner,Emi Ling,Serkan Erdin,Derek J. C. Tai,Rachita Yadav,Jakob Grove,Jack Fu,Ajay Nadig,Nikolas Baya,Jonas Bybjerg-Grauholm,Preben Bo Mortensen,Thomas Werge,Ditte Demontis,Ole Mors,Merete Nordentoft,Thomas Damm Als,M. Baekvad-Hansen,Anders Rosengren,Alexandra Havdahl,Anne Hedemand,Aarno Palotie,Aravinda Chakravarti,Dan E. Arking,Arvis Sulovari,Anna Starnawska,Bhooma Thiruvahindrapuram,Christiaan de Leeuw,Caitlin E. Carey,Christine Ladd-Acosta,C. van der Merwe,Bernie Devlin,Edwin H. Cook,Evan E. Eichler,Elizabeth Corfield,Gwen C. Dieleman,Gerard D. Schellenberg,Hakon Hakonarson,Hilary Coon,Isabel Dziobek,Jacob A. S. Vorstman,Jessica B. Girault,James S. Sutcliffe,Jinjie Duan,John I. Nurnberger,Joachim Hallmayer,Joseph D. Buxbaum,Joseph Piven,Lauren A. Weiss,Lea K. Davis,Magdalena Janecka,Manuel Mattheisen,Matthew W. State,Michael Gill,Mark J. Daly,Mohammed Uddin,Ole Andreassen,Peter Szatmari,Phil Lee,Richard Anney,Stephan Ripke,F. Kyle Satterstrom,Susan L. Santangelo,Susanna Campbell Kuo,Ludger Tebartz van Elst,Thomas Rolland,T. Bougeron,Tinca J. C. Polderman,Tychele N. Turner,Jacky Underwood,V Manikandan,Vamsee Pillalamarri,Varun Warrier,Alexandra Philipsen,Andreas Reif,Anke Hinney,Bru Cormand,Claiton H.D. Bau,Diego L. Rovaris,Edmund J.S. Sonuga-Barke,Eugenio H. Grevet,Giovanni Abrahão Salum,Henrik Larsson,Jan K. Buitelaar,Jan Haavik,James Cooke McGough,Jonna Kuntsi,Josephine Elia,Klaus-Peter Lesch,Marieke Klein,Mark A. Bellgrove,Martin Tesli,Patrick W. L. Leung,Pedro Mario Pan,Søren Dalsgaard,Sandra K. Loo,Sarah E. Medland,Stephen V. Faraone,Ted Reichborn-Kjennerud,Tobias Banaschewski,Ziarih Hawi,Sabina Berretta,Evan Z. Macosko,Jonathan Sebat,Luke J. O’Connor,David M. Hougaard,Anders D. Børglum,Michael E. Talkowski,Steven A. McCarroll,Elise B. Robinson +108 more
TL;DR: In this article , the authors identify the 33-Mb p-arm of chromosome 16 (16p) as harboring the greatest excess of autism's common polygenic influences, including the mechanistically cryptic and autism-associated 16p11.2 copy number variant.
Journal ArticleDOI
Heterozygous FA2H mutations in autism spectrum disorders
Isabelle Scheid,Isabelle Scheid,Anna Maruani,Anna Maruani,Guillaume Huguet,Guillaume Huguet,Claire S. Leblond,Claire S. Leblond,Gudrun Nygren,Henrik Anckarsäter,Anita Beggiato,Maria Råstam,Frédederique Amsellem,I. Carina Gillberg,Monique Elmaleh,Marion Leboyer,Marion Leboyer,Christopher Gillberg,Christopher Gillberg,Catalina Betancur,Catalina Betancur,Mary Coleman,Hiroko Hama,Edwin H. Cook,Thomas Bourgeron,Thomas Bourgeron,Richard Delorme,Richard Delorme +27 more
TL;DR: The results do not support a major role for FA2H coding variants in ASD, but a screening of other genes related to myelin synthesis would allow us to better understand the role of non-neuronal elements in ASD susceptibility.
Journal ArticleDOI
Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases
Jinong Feng,Nicholas John Craddock,Ian Jones,Edwin H. Cook,David Goldman,Leonard L. Heston,Leena Peltonen,Lynn E. DeLisi,Steve S. Sommer +8 more
TL;DR: It is unlikely that mutations in the coding region and splice junction of the GLRA2 gene are associated with schizophrenia and other psychiatric diseases.
Journal ArticleDOI
Does MAOA increase susceptibility to prenatal stress in young children
Suena H. Massey,Amalia E. Hatcher,Caron A. C. Clark,James L. Burns,Daniel S. Pine,Andrew D. Skol,Daniel K. Mroczek,Kimberly Andrews Espy,David Goldman,Edwin H. Cook,Lauren S. Wakschlag +10 more
TL;DR: Findings underscore complex mechanisms linking genetic susceptibility and early adverse exposures and help elucidate mechanisms that appear to have varying developmental expression.