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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: scharf jm. 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 of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder.
Stewart SE, Fagerness JA, Platko J, Smoller JW, Scharf JM, Illmann C, Jenike E, Chabane N, Leboyer M, Delorme R, Jenike MA, Pauls DL. Stewart SE, et al. Among authors: scharf jm. Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 5;144B(8):1027-33. doi: 10.1002/ajmg.b.30533. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17894418
The genetics of Tourette syndrome: a review.
O'Rourke JA, Scharf JM, Yu D, Pauls DL. O'Rourke JA, et al. Among authors: scharf jm. J Psychosom Res. 2009 Dec;67(6):533-45. doi: 10.1016/j.jpsychores.2009.06.006. Epub 2009 Sep 30. J Psychosom Res. 2009. PMID: 19913658 Free PMC article. Review.
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. Among authors: scharf jm. 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.
The familial association of tourette's disorder and ADHD: the impact of OCD symptoms.
O'Rourke JA, Scharf JM, Platko J, Stewart SE, Illmann C, Geller DA, King RA, Leckman JF, Pauls DL. O'Rourke JA, et al. Among authors: scharf jm. Am J Med Genet B Neuropsychiatr Genet. 2011 Jul;156B(5):553-60. doi: 10.1002/ajmg.b.31195. Epub 2011 May 6. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21557467 Free PMC article.
Effectiveness of a web-based protocol for the screening and phenotyping of individuals with Tourette syndrome for genetic studies.
Egan CA, Marakovitz SE, O'Rourke JA, Osiecki L, Illmann C, Barton L, McLaughlin E, Proujansky R, Royal J, Cowley H, Rangel-Lugo M, Pauls DL, Scharf JM, Mathews CA; Tourette Syndrome Association International Consortium for Genetics. Egan CA, et al. Among authors: scharf jm. Am J Med Genet B Neuropsychiatr Genet. 2012 Dec;159B(8):987-96. doi: 10.1002/ajmg.b.32107. Epub 2012 Oct 22. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 23090870 Free PMC article.
CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.
Nag A, Bochukova EG, Kremeyer B, Campbell DD, Muller H, Valencia-Duarte AV, Cardona J, Rivas IC, Mesa SC, Cuartas M, Garcia J, Bedoya G, Cornejo W, Herrera LD, Romero R, Fournier E, Reus VI, Lowe TL, Farooqi IS; Tourette Syndrome Association International Consortium for Genetics; Mathews CA, McGrath LM, Yu D, Cook E, Wang K, Scharf JM, Pauls DL, Freimer NB, Plagnol V, Ruiz-Linares A. Nag A, et al. Among authors: scharf jm. PLoS One. 2013;8(3):e59061. doi: 10.1371/journal.pone.0059061. Epub 2013 Mar 22. PLoS One. 2013. PMID: 23533600 Free PMC article.
123 results