Genome-wide association study of Tourette's syndrome.

Genome-wide association study of Tourette's syndrome.
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DOI:
10.1038/mp.2012.69
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发表时间:
2013-06
影响因子:
11
通讯作者:
Pauls, D. L.
Pauls, D. L.
中科院分区:
医学1区
文献类型:
--
作者:
Scharf, J. M.;Yu, D.;Mathews, C. A.;Neale, B. M.;Stewart, S. E.;Fagerness, J. A.;Evans, P.;Gamazon, E.;Edlund, C. K.;Service, S. K.;Tikhomirov, A.;Osiecki, L.;Illmann, C.;Pluzhnikov, A.;Konkashbaev, A.;Davis, L. K.;Han, B.;Crane, J.;Moorjani, P.;Crenshaw, A. T.;Parkin, M. A.;Reus, V. I.;Lowe, T. L.;Rangel-Lugo, M.;Chouinard, S.;Dion, Y.;Girard, S.;Cath, D. C.;Smit, J. H.;King, R. A.;Fernandez, T. V.;Leckman, J. F.;Kidd, K. K.;Kidd, J. R.;Pakstis, A. J.;State, M. W.;Herrera, L. D.;Romero, R.;Fournier, E.;Sandor, P.;Barr, C. L.;Phan, N.;Gross-Tsur, V.;Benarroch, F.;Pollak, Y.;Budman, C. L.;Bruun, R. D.;Erenberg, G.;Naarden, A. L.;Lee, P. C.;Weiss, N.;Kremeyer, B.;Berrio, G. B.;Campbell, D. D.;Cardona Silgado, J. C.;Ochoa, W. C.;Mesa Restrepo, S. C.;Muller, H.;Valencia Duarte, A. V.;Lyon, G. J.;Leppert, M.;Morgan, J.;Weiss, R.;Grados, M. A.;Anderson, K.;Davarya, S.;Singer, H.;Walkup, J.;Jankovic, J.;Tischfield, J. A.;Heiman, G. A.;Gilbert, D. L.;Hoekstra, P. J.;Robertson, M. M.;Kurlan, R.;Liu, C.;Gibbs, J. R.;Singleton, A.;Hardy, J.;Strengman, E.;Ophoff, R. A.;Wagner, M.;Moessner, R.;Mirel, D. B.;Posthuma, D.;Sabatti, C.;Eskin, E.;Conti, D. V.;Knowles, J. A.;Ruiz-Linares, A.;Rouleau, G. A.;Purcell, S.;Heutink, P.;Oostra, B. A.;McMahon, W. M.;Freimer, N. B.;Cox, N. J.;Pauls, D. L.

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多发性抽动症(TS)是一种具有复杂遗传的神经精神疾病中家族复发率最高的发育障碍。然而,明确的TS易感基因的鉴定仍然难以捉摸。在这里,我们报告了首次对欧洲血统的1285例TS和4964名血统匹配的对照进行的全基因组关联研究,其中包括来自北美和以色列的德系犹太人和来自加拿大魁北克的法裔加拿大人这两个欧洲派生的群体隔离株。在对这些欧洲血统样本的GWAs数据的初步荟萃分析中,没有标记达到全基因组的显著阈值(p<5×10−8);在COL27A1内染色体9q32的rs7868992上发现了最高信号(p=1.85×10−6)。二次分析包括来自哥斯达黎加中央山谷和安蒂奥基亚省两个密切相关的拉丁美洲人口分离株的另外211个病例和285个对照,哥伦比亚也将rs7868992确定为最高信号(1,496个病例和5,249个对照的组合样本在1,000个基因组数据的补充后,p=3.6x10−7)。这项研究为最终在更大的队列中识别常见的TS易感变异奠定了基础,并有助于提供对这种疾病的完整遗传结构的更完整的了解。
Tourette Syndrome (TS) is a developmental disorder that has one of the highest familial recurrence rates among neuropsychiatric diseases with complex inheritance. However, the identification of definitive TS susceptibility genes remains elusive. Here, we report the first genome-wide association study (GWAS) of TS in 1285 cases and 4964 ancestry-matched controls of European ancestry, including two European-derived population isolates, Ashkenazi Jews from North America and Israel, and French Canadians from Quebec, Canada. In a primary meta-analysis of GWAS data from these European ancestry samples, no markers achieved a genome-wide threshold of significance (p<5 × 10−8); the top signal was found in rs7868992 on chromosome 9q32 within COL27A1 (p=1.85 × 10−6). A secondary analysis including an additional 211 cases and 285 controls from two closely-related Latin-American population isolates from the Central Valley of Costa Rica and Antioquia, Colombia also identified rs7868992 as the top signal (p=3.6 × 10−7 for the combined sample of 1496 cases and 5249 controls following imputation with 1000 Genomes data). This study lays the groundwork for the eventual identification of common TS susceptibility variants in larger cohorts and helps to provide a more complete understanding of the full genetic architecture of this disorder.
DOI: 10.1016/j.drugalcdep.2007.11.023
发表时间: 2008-05-01
影响因子: 4.2
作者:
Bierut, Laura Jean;Strickland, Jaime R.;Cottler, Linda B.
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发表时间: 2000-07-01
影响因子: 3.8
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通讯作者: Sandor, P
DOI: 10.1371/journal.pgen.1001292
发表时间: 2011-02-03
期刊: PLoS genetics
影响因子: 4.5
作者:
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通讯作者: Cox NJ
DOI: 10.1007/s00439-002-0899-8
发表时间: 2003-05-01
期刊: HUMAN GENETICS
影响因子: 5.3
作者:
Carvajal-Carmona, LG;Ophoff, R;Ruiz-Linares, A
通讯作者: Ruiz-Linares, A
DOI: 10.1038/nature09534
发表时间: 2010-10-28
期刊: NATURE
影响因子: 64.8
作者:
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通讯作者: McVean, Gil A.