Fang J - Search Results

1

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. Liao D, et al. Among authors: fang j. Sci Rep. 2015 Apr 15;5:9511. doi: 10.1038/srep09511. Sci Rep. 2015. PMID: 25873156 Free PMC article.

2

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. Hou S, et al. Among authors: fang j. Arthritis Rheum. 2013 Nov;65(11):2963-70. doi: 10.1002/art.38116. Arthritis Rheum. 2013. PMID: 23918728 Free article.

3

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. Qi J, et al. Among authors: fang j. Hum Genet. 2013 Dec;132(12):1395-404. doi: 10.1007/s00439-013-1346-8. Epub 2013 Aug 9. Hum Genet. 2013. PMID: 23928854

4

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. Fang J, et al. Am J Ophthalmol. 2014 Feb;157(2):488-494.e6. doi: 10.1016/j.ajo.2013.10.010. Epub 2013 Nov 1. Am J Ophthalmol. 2014. PMID: 24184224

5

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. Fang J, et al. Invest Ophthalmol Vis Sci. 2013 Dec 30;54(13):8384-92. doi: 10.1167/iovs.13-12878. Invest Ophthalmol Vis Sci. 2013. PMID: 24255044

6

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. Xiang Q, et al. Among authors: fang j. PLoS One. 2014 Jan 8;9(1):e84214. doi: 10.1371/journal.pone.0084214. eCollection 2014. PLoS One. 2014. PMID: 24416204 Free PMC article.

7

Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese.

Shi Y, Jia Y, Hou S, Fang J, Zhou Y, Kijlstra A, Yang P. Shi Y, et al. Among authors: fang j. PLoS One. 2014 May 2;9(5):e95573. doi: 10.1371/journal.pone.0095573. eCollection 2014. PLoS One. 2014. PMID: 24788730 Free PMC article.

8

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. Li X, et al. Among authors: fang j. PLoS One. 2014 May 23;9(5):e98373. doi: 10.1371/journal.pone.0098373. eCollection 2014. PLoS One. 2014. PMID: 24859272 Free PMC article. Clinical Trial.

9

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. Hou S, et al. Among authors: fang j. Br J Ophthalmol. 2014 Dec;98(12):1733-7. doi: 10.1136/bjophthalmol-2014-305596. Epub 2014 Sep 2. Br J Ophthalmol. 2014. PMID: 25185257

10

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. Hou S, et al. Among authors: fang j. Ophthalmology. 2015 Mar;122(3):518-23. doi: 10.1016/j.ophtha.2014.09.025. Epub 2014 Nov 15. Ophthalmology. 2015. PMID: 25439430

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