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1 Ergebnisse
1
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk ..:
Huang, Alden Y
;
Yu, Dongmei
;
Davis, Lea K
...
qt5fg5q9h1. , 2017
Link:
https://escholarship.org/uc/item/5fg5q9h1
RT Journal T1
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt5fg5q9h1&Exemplar=1&LAN=DE A1 Huang, Alden Y A1 Yu, Dongmei A1 Davis, Lea K A1 Sul, Jae Hoon A1 Tsetsos, Fotis A1 Ramensky, Vasily A1 Zelaya, Ivette A1 Ramos, Eliana Marisa A1 Osiecki, Lisa A1 Chen, Jason A A1 McGrath, Lauren M A1 Illmann, Cornelia A1 Sandor, Paul A1 Barr, Cathy L A1 Grados, Marco A1 Singer, Harvey S A1 Nöthen, Markus M A1 Hebebrand, Johannes A1 King, Robert A A1 Dion, Yves A1 Rouleau, Guy A1 Budman, Cathy L A1 Depienne, Christel A1 Worbe, Yulia A1 Hartmann, Andreas A1 Müller-Vahl, Kirsten R A1 Stuhrmann, Manfred A1 Aschauer, Harald A1 Stamenkovic, Mara A1 Schloegelhofer, Monika A1 Konstantinidis, Anastasios A1 Lyon, Gholson J A1 McMahon, William M A1 Barta, Csaba A1 Tarnok, Zsanett A1 Nagy, Peter A1 Batterson, James R A1 Rizzo, Renata A1 Cath, Danielle C A1 Wolanczyk, Tomasz A1 Berlin, Cheston A1 Malaty, Irene A A1 Okun, Michael S A1 Woods, Douglas W A1 Rees, Elliott A1 Pato, Carlos N A1 Pato, Michele T A1 Knowles, James A A1 Posthuma, Danielle A1 Pauls, David L A1 Cox, Nancy J A1 Neale, Benjamin M A1 Freimer, Nelson B A1 Paschou, Peristera A1 Mathews, Carol A A1 Scharf, Jeremiah M A1 Coppola, Giovanni A1 Tourette Syndrome Association International Consortium for Genetics (TSAICG) A1 Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI) PB eScholarship, University of California YR 2017 K1 Tourette Syndrome Association International Consortium for Genetics K1 Gilles de la Tourette Syndrome GWAS Replication Initiative K1 Humans K1 Tourette Syndrome K1 Genetic Predisposition to Disease K1 Calcium-Binding Proteins K1 Cell Adhesion Molecules K1 Neuronal K1 Neural Cell Adhesion Molecules K1 Nerve Tissue Proteins K1 Odds Ratio K1 Case-Control Studies K1 Genotype K1 Adolescent K1 Adult K1 Child K1 Female K1 Male K1 Genome-Wide Association Study K1 Young Adult K1 DNA Copy Number Variations K1 Contactins K1 White People K1 CNTN6 K1 NRXN1 K1 copy number variation K1 genetics K1 neurodevelopmental disorders K1 structural variation K1 tic disorders K1 Prevention K1 Human Genome K1 Brain Disorders K1 Neurodegenerative K1 Neurosciences K1 Mental Health K1 2.1 Biological and endogenous factors K1 Aetiology K1 Psychology K1 Cognitive Sciences K1 Neurology & Neurosurgery JF qt5fg5q9h1 LK http://dx.doi.org/https://escholarship.org/uc/item/5fg5q9h1 DO https://escholarship.org/uc/item/5fg5q9h1 SF ELIB - SuUB Bremen
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