Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3-Reference-Cited by-同舟云学术

Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3

Published:2014-09 Issue:9 Volume:46 Page:1007-1011
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Hou Shengping,Du Liping,Lei Bo,Pang Chi Pui,Zhang Meifen,Zhuang Wenjuan,Zhang Minglian,Huang Lulin,Gong Bo,Wang Meilin,Zhang Qi,Hu Ke,Zhou Qingyun,Qi Jian,Wang Chaokui,Tian Yuan,Ye Zi,Liang Liang,Yu Hongsong,Li Hong,Zhou Yan,Cao Qingfeng,Liu Yunjia,Bai Lin,Liao Dan,Kijlstra Aize,Xu Jianfeng,Yang Zhenglin,Yang Peizeng

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.3061.pdf

Reference48 articles.

1. Yang, P. et al. Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients. Ophthalmology 114, 606–614 (2007).

2. Moorthy, R.S., Inomata, H. & Rao, N.A. Vogt-Koyanagi-Harada syndrome. Surv. Ophthalmol. 39, 265–292 (1995).

3. Kim, M.H. et al. Association of HLA with Vogt-Koyanagi-Harada syndrome in Koreans. Am. J. Ophthalmol. 129, 173–177 (2000).

4. Weisz, J.M. et al. Association between Vogt-Koyanagi-Harada syndrome and HLA-DR1 and -DR4 in Hispanic patients living in southern California. Ophthalmology 102, 1012–1015 (1995).

5. Zhao, M., Jiang, Y. & Abrahams, I.W. Association of HLA antigens with Vogt-Koyanagi-Harada syndrome in a Han Chinese population. Arch. Ophthalmol. 109, 368–370 (1991).

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