De Novo Coding Variants Are Strongly Associated with Tourette Disorder

Author:

Willsey A. Jeremy,Fernandez Thomas V.,Yu Dongmei,King Robert A.,Dietrich Andrea,Xing Jinchuan,Sanders Stephan J.,Mandell Jeffrey D.,Huang Alden Y.,Richer Petra,Smith Louw,Dong Shan,Samocha Kaitlin E.,Neale Benjamin M.,Coppola Giovanni,Mathews Carol A.,Tischfield Jay A.,Scharf Jeremiah M.,State Matthew W.,Heiman Gary A.,Abdulkadir Mohamed,Bohnenpoll Julia,Bromberg Yana,Brown Lawrence W.,Cheon Keun-Ah,Coffey Barbara J.,Deng Li,Dietrich Andrea,Dong Shan,Elzerman Lonneke,Fernandez Thomas V.,Fründt Odette,Garcia-Delgar Blanca,Gedvilaite Erika,Gilbert Donald L.,Grice Dorothy E.,Hagstrøm Julie,Hedderly Tammy,Heiman Gary A.,Heyman Isobel,Hoekstra Pieter J.,Hong Hyun Ju,Huyser Chaim,Ibanez-Gomez Laura,Kim Young Key,Kim Young-Shin,King Robert A.,Koh Yun-Joo,Kook Sodahm,Kuperman Samuel,Lamerz Andreas,Leventhal Bennett,Ludolph Andrea G.,Lühr da Silva Claudia,Madruga-Garrido Marcos,Mandell Jeffrey D.,Maras Athanasios,Mir Pablo,Morer Astrid,Münchau Alexander,Murphy Tara L.,Nasello Cara,Openneer Thaïra J.C.,Plessen Kerstin J.,Richer Petra,Roessner Veit,Sanders Stephan,Shin Eun-Young,Sival Deborah A.,Smith Louw,Song Dong-Ho,Song Jungeun,State Matthew W.,Stolte Anne Marie,Sun Nawei,Tischfield Jay A.,Tübing Jennifer,Visscher Frank,Walker Michael F.,Wanderer Sina,Wang Shuoguo,Willsey A. Jeremy,Woods Martin,Xing Jinchuan,Zhang Yeting,Zhou Anbo,Zinner Samuel H.,Barr Cathy L.,Batterson James R.,Berlin Cheston,Bruun Ruth D.,Budman Cathy L.,Cath Danielle C.,Chouinard Sylvain,Coppola Giovanni,Cox Nancy J.,Darrow Sabrina,Davis Lea K.,Dion Yves,Freimer Nelson B.,Grados Marco A.,Hirschtritt Matthew E.,Huang Alden Y.,Illmann Cornelia,King Robert A.,Kurlan Roger,Leckman James F.,Lyon Gholson J.,Malaty Irene A.,Mathews Carol A.,MaMahon William M.,Neale Benjamin M.,Okun Michael S.,Osiecki Lisa,Pauls David L.,Posthuma Danielle,Ramensky Vasily,Robertson Mary M.,Rouleau Guy A.,Sandor Paul,Scharf Jeremiah M.,Singer Harvey S.,Smit Jan,Sul Jae-Hoon,Yu Dongmei

Funder

NIMH Repository and Genomics Resource

National Institute of Mental Health

National Institute of Neurological Disorders and Stroke

Harvard Clinical and Translational Science Center

Tourette Association of America

New Jersey Center for Tourette Syndrome and Associated Disorders

Overlook International Fund

Instituto de Salud Carlos III

Consejería de Economía, Innovación, Ciencia y Empresa de la Junta de Andalucía

Consejería de Salud y Bienestar Social de la Junta de Andalucía

Sociedad Andaluza de Neurología

Fundación Alicia Koplowitz

Fundación Mutua Madrileña

the Jaques and Gloria Gossweiler Foundation

Deutsche Forschungsgemeinschaft

NIHR Great Ormond Street Hospital Biomedical Research Centre

PhRMA Foundation

Publisher

Elsevier BV

Subject

General Neuroscience

Reference97 articles.

1. Sequence variants in SLITRK1 are associated with Tourette’s syndrome;Abelson;Science,2005

2. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

3. Predicting functional effect of human missense mutations using PolyPhen-2;Adzhubei;Curr. Protoc. Hum. Genet.,2013

4. De novo mutations in epileptic encephalopathies;Allen;Nature,2013

5. Diagnostic and Statistical Manual of Mental Disorders, DSM-IV-TR edn,2000

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