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Items: 1 to 20 of 243

1.

Association Between Copy Number Variations of TLR7 and Ocular Behçet's Disease in a Chinese Han Population.

Fang J, Chen L, Tang J, Hou S, Liao D, Ye Z, Wang C, Cao Q, Kijlstra A, Yang P.

Invest Ophthalmol Vis Sci. 2015 Feb 3;56(3):1517-23. doi: 10.1167/iovs.14-15030.

PMID:
25650422
2.

Association of TLR2 gene polymorphisms with ocular Behcet's disease in a Chinese Han population.

Fang J, Hu R, Hou S, Ye Z, Xiang Q, Qi J, Zhou Y, Kijlstra A, Yang P.

Invest Ophthalmol Vis Sci. 2013 Dec 30;54(13):8384-92. doi: 10.1167/iovs.13-12878.

PMID:
24255044
3.

Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis.

Hou S, Qi J, Liao D, Zhang Q, Fang J, Zhou Y, Liu Y, Bai L, Zhang M, Kijlstra A, Yang P.

Arthritis Rheum. 2013 Nov;65(11):2963-70. doi: 10.1002/art.38116.

4.

A variant of CLEC16A gene confers protection for Vogt-Koyanagi-Harada syndrome but not for Behcet's disease in a Chinese Han population.

Li K, Hou S, Qi J, Kijlstra A, Yang P.

Exp Eye Res. 2015 Mar;132:225-30. doi: 10.1016/j.exer.2015.01.004. Epub 2015 Jan 7.

PMID:
25576669
5.

No association between Bach2 gene polymorphisms with Vogt-Koyanagi-Harada syndrome (VKH) and Behcet's disease (BD) in a Chinese Han population.

Gao X, Tan X, Qin J, Lv S, Hou S, Kijlstra A, Yang P.

Br J Ophthalmol. 2015 Aug;99(8):1150-4. doi: 10.1136/bjophthalmol-2014-306163. Epub 2015 Apr 14.

PMID:
25873652
6.

A functional variant of pre-miRNA-196a2 confers risk for Behcet's disease but not for Vogt-Koyanagi-Harada syndrome or AAU in ankylosing spondylitis.

Qi J, Hou S, Zhang Q, Liao D, Wei L, Fang J, Zhou Y, Kijlstra A, Yang P.

Hum Genet. 2013 Dec;132(12):1395-404. doi: 10.1007/s00439-013-1346-8. Epub 2013 Aug 9.

PMID:
23928854
7.

Copy number variations and gene polymorphisms of complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome.

Xu D, Hou S, Zhang J, Jiang Y, Kijlstra A, Yang P.

Sci Rep. 2015 Aug 13;5:12989. doi: 10.1038/srep12989.

8.

Genetic variations of IL17F and IL23A show associations with Behçet's disease and Vogt-Koyanagi-Harada syndrome.

Hou S, Liao D, Zhang J, Fang J, Chen L, Qi J, Zhang Q, Liu Y, Bai L, Zhou Y, Kijlstra A, Yang P.

Ophthalmology. 2015 Mar;122(3):518-23. doi: 10.1016/j.ophtha.2014.09.025. Epub 2014 Nov 15.

PMID:
25439430
9.

Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome.

Liao D, Hou S, Zhang J, Fang J, Liu Y, Bai L, Cao Q, Kijlstra A, Yang P.

Sci Rep. 2015 Apr 15;5:9511. doi: 10.1038/srep09511.

10.

Interleukin-10 gene polymorphisms are associated with Behcet's disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population.

Hu J, Hou S, Zhu X, Fang J, Zhou Y, Liu Y, Bai L, Kijlstra A, Yang P.

Mol Vis. 2015 May 22;21:589-603. eCollection 2015.

11.

Polymorphisms in genetics of vitamin D metabolism confer susceptibility to ocular Behçet disease in a Chinese Han population.

Fang J, Hou S, Xiang Q, Qi J, Yu H, Shi Y, Zhou Y, Kijlstra A, Yang P.

Am J Ophthalmol. 2014 Feb;157(2):488-494.e6. doi: 10.1016/j.ajo.2013.10.010. Epub 2013 Nov 1.

PMID:
24184224
12.

Association of Long Noncoding RNAs Polymorphisms With Ankylosing Spondylitis, Vogt-Koyanagi-Harada Disease, and Behcet's Disease.

Yue Y, Zhang J, Yang L, Liu S, Qi J, Cao Q, Zhou C, Wang Y, Kijlstra A, Yang P, Hou S.

Invest Ophthalmol Vis Sci. 2018 Feb 1;59(2):1158-1166. doi: 10.1167/iovs.17-23247.

PMID:
29490353
13.

TRAF5 and TRAF3IP2 gene polymorphisms are associated with Behçet's disease and Vogt-Koyanagi-Harada syndrome: a case-control study.

Xiang Q, Chen L, Hou S, Fang J, Zhou Y, Bai L, Liu Y, Kijlstra A, Yang P.

PLoS One. 2014 Jan 8;9(1):e84214. doi: 10.1371/journal.pone.0084214. eCollection 2014.

14.

MicroRNA-146a and Ets-1 gene polymorphisms in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome.

Zhou Q, Hou S, Liang L, Li X, Tan X, Wei L, Lei B, Kijlstra A, Yang P.

Ann Rheum Dis. 2014 Jan;73(1):170-6. doi: 10.1136/annrheumdis-2012-201627. Epub 2012 Dec 25.

PMID:
23268366
15.

FAS Gene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese.

Yu H, Luo L, Wu L, Zheng M, Zhang L, Liu Y, Li H, Cao Q, Kijlstra A, Yang P.

Hum Mutat. 2015 Nov;36(11):1064-9. doi: 10.1002/humu.22829. Epub 2015 Aug 3.

PMID:
26136352
16.

Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population.

Chen Y, Yang P, Li F, Hou S, Jiang Z, Shu Q, Kijlstra A.

Curr Eye Res. 2012 Apr;37(4):312-7. doi: 10.3109/02713683.2011.635398.

PMID:
22440163
17.

Association of T-Bet, GATA-3, RORC, and FOXP3 Copy Number Variations With Acute Anterior Uveitis With or Without Ankylosing Spondylitis in Chinese Han.

Bai L, Liu Y, Hou S, Liao D, Kijlstra A, Yang P.

Invest Ophthalmol Vis Sci. 2016 Apr;57(4):1847-52. doi: 10.1167/iovs.15-17960.

PMID:
27082299
18.

Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndrome.

Li X, Bai L, Fang J, Hou S, Zhou Q, Yu H, Kijlstra A, Yang P.

PLoS One. 2014 May 23;9(5):e98373. doi: 10.1371/journal.pone.0098373. eCollection 2014.

19.

High C4 gene copy numbers protects against Vogt-Koyanagi-Harada syndrome in Chinese Han.

Hou S, Qi J, Liao D, Fang J, Chen L, Kijlstra A, Yang P.

Br J Ophthalmol. 2014 Dec;98(12):1733-7. doi: 10.1136/bjophthalmol-2014-305596. Epub 2014 Sep 2.

PMID:
25185257
20.

Association of TLR7 gene copy number variations with ankylosing spondylitis in a Chinese population: a case control study.

Wang M, Xu S, Zhang X, Chen M, Han R, Hu X, Yuan Y, Ma Y, Yang J, Wu M, Liu R, Jiang G, Pan F.

Clin Exp Rheumatol. 2018 Sep-Oct;36(5):814-819. Epub 2018 Feb 28.

PMID:
29533758

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