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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, Singer HS, Nöthen MM, Hebebrand J, King RA, Dion Y, Rouleau G, Budman CL, Depienne C, Worbe Y, Hartmann A, Müller-Vahl KR, Stuhrmann M, Aschauer H, Stamenkovic M, Schloegelhofer M, Konstantinidis A, Lyon GJ, McMahon WM, Barta C, Tarnok Z, Nagy P, Batterson JR, Rizzo R, Cath DC, Wolanczyk T, Berlin C, Malaty IA, Okun MS, Woods DW, Rees E, Pato CN, Pato MT, Knowles JA, Posthuma D, Pauls DL, Cox NJ, Neale BM, Freimer NB, Paschou P, Mathews CA, Scharf JM, Coppola G; Tourette Syndrome Association International Consortium for Genetics (TSAICG); Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI). Huang AY, et al. Among authors: dion y. Neuron. 2017 Jun 21;94(6):1101-1111.e7. doi: 10.1016/j.neuron.2017.06.010. Neuron. 2017. PMID: 28641109 Free PMC article.
Association between 7q31 markers and Tourette syndrome.
Díaz-Anzaldúa A, Joober R, Rivière JB, Dion Y, Lespérance P, Chouinard S, Richer F, Rouleau GA; Montreal Tourette Syndrome Study Group. Díaz-Anzaldúa A, et al. Among authors: dion y. Am J Med Genet A. 2004 May 15;127A(1):17-20. doi: 10.1002/ajmg.a.20631. Am J Med Genet A. 2004. PMID: 15103711
Association of intronic variants of the BTBD9 gene with Tourette syndrome.
Rivière JB, Xiong L, Levchenko A, St-Onge J, Gaspar C, Dion Y, Lespérance P, Tellier G, Richer F, Chouinard S, Rouleau GA; Montreal Tourette Study Group. Rivière JB, et al. Among authors: dion y. Arch Neurol. 2009 Oct;66(10):1267-72. doi: 10.1001/archneurol.2009.213. Arch Neurol. 2009. PMID: 19822783
Genome-wide TDT analysis in French-Canadian families with Tourette syndrome.
Rivière JB, St-Onge J, Gaspar C, Diab S, Dion Y, Lespérance P, Tellier G, Richer F, Chouinard S, Dubé MP, Rouleau GA; Montreal Tourette Study Group. Rivière JB, et al. Among authors: dion y. Can J Neurol Sci. 2010 Jan;37(1):110-2. doi: 10.1017/s0317167100009744. Can J Neurol Sci. 2010. PMID: 20169783 No abstract available.
Family-based genetic association study of DLGAP3 in Tourette Syndrome.
Crane J, Fagerness J, Osiecki L, Gunnell B, Stewart SE, Pauls DL, Scharf JM; Tourette Syndrome International Consortium for Genetics (TSAICG). Crane J, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):108-14. doi: 10.1002/ajmg.b.31134. Epub 2010 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184590 Free PMC article.
96 results