Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

Author:

Huang Alden Y.,Yu Dongmei,Davis Lea K.,Sul Jae Hoon,Tsetsos Fotis,Ramensky Vasily,Zelaya Ivette,Ramos Eliana Marisa,Osiecki Lisa,Chen Jason A.,McGrath Lauren M.,Illmann Cornelia,Sandor Paul,Barr Cathy L.,Grados Marco,Singer Harvey S.,Nöthen Markus M.,Hebebrand Johannes,King Robert A.,Dion Yves,Rouleau Guy,Budman Cathy L.,Depienne Christel,Worbe Yulia,Hartmann Andreas,Müller-Vahl Kirsten R.,Stuhrmann Manfred,Aschauer Harald,Stamenkovic Mara,Schloegelhofer Monika,Konstantinidis Anastasios,Lyon Gholson J.,McMahon William M.,Barta Csaba,Tarnok Zsanett,Nagy Peter,Batterson James R.,Rizzo Renata,Cath Danielle C.,Wolanczyk Tomasz,Berlin Cheston,Malaty Irene A.,Okun Michael S.,Woods Douglas W.,Rees Elliott,Pato Carlos N.,Pato Michele T.,Knowles James A.,Posthuma Danielle,Pauls David L.,Cox Nancy J.,Neale Benjamin M.,Freimer Nelson B.,Paschou Peristera,Mathews Carol A.,Scharf Jeremiah M.,Coppola Giovanni,Bruun Ruth D.,Chouinard Sylvain,Darrow Sabrina,Greenberg Erica,Hirschtritt Matthew E.,Kurlan Roger,Leckman James F.,Robertson Mary M.,Smit Jan

Funder

US NIH

NIH ARRA

NIH

NINDS Informatics Center for Neurogenetics and Neurogenomics

Tourette Association of America

German Research Society

Publisher

Elsevier BV

Subject

General Neuroscience

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