{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,13]],"date-time":"2025-11-13T12:25:16Z","timestamp":1763036716954},"reference-count":29,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2012,9,1]],"date-time":"2012-09-01T00:00:00Z","timestamp":1346457600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neuroscience Letters"],"published-print":{"date-parts":[[2012,9]]},"DOI":"10.1016\/j.neulet.2012.08.013","type":"journal-article","created":{"date-parts":[[2012,8,14]],"date-time":"2012-08-14T15:34:25Z","timestamp":1344958465000},"page":"150-153","source":"Crossref","is-referenced-by-count":9,"title":["Mutation screening of the HTR2B gene in patients with Tourette syndrome"],"prefix":"10.1016","volume":"526","author":[{"given":"Yi","family":"Guo","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiong","family":"Deng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joseph","family":"Jankovic","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Linyan","family":"Su","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jie","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Weidong","family":"Le","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hongbo","family":"Xu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zuocheng","family":"Yang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jinsong","family":"Tang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shoujin","family":"Kuang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hao","family":"Deng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.neulet.2012.08.013_bib0005","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1126\/science.1116502","article-title":"Sequence variants in SLITRK1 are associated with Tourette's syndrome","volume":"310","author":"Abelson","year":"2005","journal-title":"Science"},{"key":"10.1016\/j.neulet.2012.08.013_bib0010","series-title":"Diagnostic and Statistical Manual of Mental Disorders","year":"2000"},{"key":"10.1016\/j.neulet.2012.08.013_bib0015","doi-asserted-by":"crossref","first-page":"711","DOI":"10.1038\/sj.ejhg.5201824","article-title":"Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome","volume":"15","author":"Belloso","year":"2007","journal-title":"European Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0020","doi-asserted-by":"crossref","first-page":"1061","DOI":"10.1038\/nature09629","article-title":"A population-specific HTR2B stop codon predisposes to severe impulsivity","volume":"468","author":"Bevilacqua","year":"2010","journal-title":"Nature"},{"key":"10.1016\/j.neulet.2012.08.013_bib0025","doi-asserted-by":"crossref","first-page":"417","DOI":"10.1007\/s10048-010-0244-7","article-title":"Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred","volume":"11","author":"Breedveld","year":"2010","journal-title":"Neurogenetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0030","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1097\/YPG.0b013e32833511ce","article-title":"A genetic variant of HTR2C may play a role in the manifestation of Tourette syndrome","volume":"20","author":"Dehning","year":"2010","journal-title":"Psychiatric Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0035","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1038\/nrneurol.2012.26","article-title":"The genetics of Tourette syndrome","volume":"8","author":"Deng","year":"2012","journal-title":"Nature Review Neurology"},{"key":"10.1016\/j.neulet.2012.08.013_bib0040","doi-asserted-by":"crossref","first-page":"933","DOI":"10.1002\/ana.20510","article-title":"Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation","volume":"57","author":"Deng","year":"2005","journal-title":"Annals of Neurology"},{"key":"10.1016\/j.neulet.2012.08.013_bib0045","doi-asserted-by":"crossref","first-page":"1456","DOI":"10.1093\/brain\/awm018","article-title":"Genetics of essential tremor","volume":"130","author":"Deng","year":"2007","journal-title":"Brain"},{"key":"10.1016\/j.neulet.2012.08.013_bib0050","doi-asserted-by":"crossref","first-page":"400","DOI":"10.1111\/j.1600-0404.2006.00706.x","article-title":"Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome","volume":"114","author":"Deng","year":"2006","journal-title":"Acta Neurologica Scandinavica"},{"key":"10.1016\/j.neulet.2012.08.013_bib0055","doi-asserted-by":"crossref","first-page":"1901","DOI":"10.1056\/NEJMoa0907006","article-title":"l-Histidine decarboxylase and Tourette's syndrome","volume":"362","author":"Ercan-Sencicek","year":"2010","journal-title":"New England Journal of Medicine"},{"key":"10.1016\/j.neulet.2012.08.013_bib0060","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1016\/j.neulet.2011.05.245","article-title":"HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease","volume":"501","author":"Guo","year":"2011","journal-title":"Neuroscience Letters"},{"key":"10.1016\/j.neulet.2012.08.013_bib0065","doi-asserted-by":"crossref","first-page":"284","DOI":"10.1016\/j.bbrc.2011.10.042","article-title":"Genetic analysis of IREB2, FAM13A and XRCC5 variants in Chinese Han patients with chronic obstructive pulmonary disease","volume":"415","author":"Guo","year":"2011","journal-title":"Biochemical and Biophysical Research Communications"},{"key":"10.1016\/j.neulet.2012.08.013_bib0070","doi-asserted-by":"crossref","first-page":"1184","DOI":"10.1056\/NEJMra010032","article-title":"Tourette's syndrome","volume":"345","author":"Jankovic","year":"2001","journal-title":"New England Journal of Medicine"},{"key":"10.1016\/j.neulet.2012.08.013_bib0075","doi-asserted-by":"crossref","first-page":"70","DOI":"10.1016\/j.pediatrneurol.2007.02.015","article-title":"Candidate locus for chorea and tic disorders at 15q","volume":"37","author":"Jankovic","year":"2007","journal-title":"Pediatric Neurology"},{"key":"10.1016\/j.neulet.2012.08.013_bib0080","doi-asserted-by":"crossref","first-page":"1149","DOI":"10.1002\/mds.23618","article-title":"Tourette syndrome: evolving concepts","volume":"26","author":"Jankovic","year":"2011","journal-title":"Movement Disorders"},{"key":"10.1016\/j.neulet.2012.08.013_bib0085","doi-asserted-by":"crossref","first-page":"86","DOI":"10.1176\/appi.neuropsych.18.1.86","article-title":"Tourette syndrome and the law","volume":"18","author":"Jankovic","year":"2006","journal-title":"Journal of Neuropsychiatry and Clinical Neurosciences"},{"key":"10.1016\/j.neulet.2012.08.013_bib0090","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1006\/mcpr.1999.0281","article-title":"Mutation screening of human 5-HT(2B) receptor gene in early-onset obsessive\u2013compulsive disorder","volume":"14","author":"Kim","year":"2000","journal-title":"Molecular and Cellular Probes"},{"key":"10.1016\/j.neulet.2012.08.013_bib0095","doi-asserted-by":"crossref","first-page":"656","DOI":"10.1002\/ajmg.b.31035","article-title":"Linkage analysis of Tourette syndrome in a large Utah pedigree","volume":"153B","author":"Knight","year":"2010","journal-title":"American Journal of Medical Genetics B: Neuropsychiatric Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0100","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1002\/ajmg.b.30779","article-title":"Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region","volume":"150B","author":"Laurin","year":"2009","journal-title":"American Journal of Medical Genetics B: Neuropsychiatric Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0105","doi-asserted-by":"crossref","first-page":"614","DOI":"10.1038\/sj.ejhg.5202006","article-title":"Familial deletion within NLGN4 associated with autism and Tourette syndrome","volume":"16","author":"Lawson-Yuen","year":"2008","journal-title":"European Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0110","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1002\/ajmg.b.32003","article-title":"Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome","volume":"159B","author":"Lei","year":"2012","journal-title":"American Journal of Medical Genetics B: Neuropsychiatric Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0115","doi-asserted-by":"crossref","first-page":"1008","DOI":"10.1086\/303093","article-title":"Significant linkage for Tourette syndrome in a large French Canadian family","volume":"67","author":"Merette","year":"2000","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0120","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1086\/424389","article-title":"Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region","volume":"75","author":"Paschou","year":"2004","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0125","doi-asserted-by":"crossref","first-page":"848","DOI":"10.1086\/319523","article-title":"Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome","volume":"68","author":"Petek","year":"2001","journal-title":"American Journal of Human Genetics"},{"key":"10.1016\/j.neulet.2012.08.013_bib0130","doi-asserted-by":"crossref","first-page":"1267","DOI":"10.1001\/archneurol.2009.213","article-title":"Association of intronic variants of the BTBD9 gene with Tourette syndrome","volume":"66","author":"Riviere","year":"2009","journal-title":"Archives of Neurology"},{"key":"10.1016\/j.neulet.2012.08.013_bib0135","doi-asserted-by":"crossref","first-page":"1495","DOI":"10.1212\/01.wnl.0000296833.25484.bb","article-title":"Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample","volume":"70","author":"Scharf","year":"2008","journal-title":"Neurology"},{"key":"10.1016\/j.neulet.2012.08.013_bib0140","doi-asserted-by":"crossref","first-page":"901","DOI":"10.1002\/ana.22398","article-title":"Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder","volume":"69","author":"Sundaram","year":"2011","journal-title":"Annals of Neurology"},{"key":"10.1016\/j.neulet.2012.08.013_bib0145","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/S0888-7543(03)00097-1","article-title":"CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder","volume":"82","author":"Verkerk","year":"2003","journal-title":"Genomics"}],"container-title":["Neuroscience Letters"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0304394012010658?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0304394012010658?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,7,2]],"date-time":"2019-07-02T21:09:57Z","timestamp":1562101797000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0304394012010658"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,9]]},"references-count":29,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2012,9]]}},"alternative-id":["S0304394012010658"],"URL":"https:\/\/doi.org\/10.1016\/j.neulet.2012.08.013","relation":{},"ISSN":["0304-3940"],"issn-type":[{"value":"0304-3940","type":"print"}],"subject":[],"published":{"date-parts":[[2012,9]]}}}