Shengping Hou - Publications

Affiliations: 
Gladstone and UCSF, San Francisco, CA, United States 

91 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Mei S, Huang Y, Li N, Xu Z, Xu J, Dai Q, Wu J, Kijlstra A, Yang P, Hou S. Aminooxy-acetic acid inhibits experimental autoimmune uveitis by modulating the balance between effector and regulatory lymphocyte subsets. Current Molecular Medicine. PMID 32072910 DOI: 10.2174/1566524020666200211112219  0.44
2019 Xu L, Zhao T, Yuan G, Hou S, Zeng W, Chen F. rs4750316 is associated with Vogt-Koyanagi-Harada syndrome in a Han Chinese population. Molecular Vision. 25: 834-842. PMID 31908401  0.36
2019 Qi J, Du L, Deng J, Qin Y, Su G, Hou S, Lv M, Zhang Q, Kijlstra A, Yang P. Replication of Genome-Wide Association Analysis Identifies New Susceptibility Loci at Long Noncoding RNA Regions for Vogt-Koyanagi-Harada Disease. Investigative Ophthalmology & Visual Science. 60: 4820-4829. PMID 31747682 DOI: 10.1167/iovs.19-27708  0.44
2019 Tang Z, Li D, Hou S, Zhu X. The cancer exosomes: clinical implications, applications and challenges. International Journal of Cancer. PMID 31671207 DOI: 10.1002/ijc.32762  0.52
2019 Hou S, Li N, Liao X, Kijlstra A, Yang P. Uveitis genetics. Experimental Eye Research. 107853. PMID 31669406 DOI: 10.1016/j.exer.2019.107853  0.44
2019 Wang Q, Su G, Tan X, Deng J, Du L, Huang X, Lv M, Yi S, Hou S, Kijlstra A, Yang P. UVEOGENE: An SNP database for investigations on genetic factors associated with uveitis and their relationship with other systemic autoimmune diseases. Human Mutation. PMID 30614601 DOI: 10.1002/humu.23702  0.44
2018 Sun M, Chen C, Hou S, Li X, Wang H, Zhou J, Chen X, Liu P, Kijlstra A, Lin S, Ye J. A novel mutation of PANK4 causes autosomal dominant congenital posterior cataract. Human Mutation. PMID 30585370 DOI: 10.1002/humu.23696  0.44
2018 Huang Y, He J, Liang H, Hu K, Jiang S, Yang L, Mei S, Zhu X, Yu J, Kijlstra A, Yang P, Hou S. Aryl Hydrocarbon Receptor Regulates Apoptosis and Inflammation in a Murine Model of Experimental Autoimmune Uveitis. Frontiers in Immunology. 9: 1713. PMID 30090104 DOI: 10.3389/fimmu.2018.01713  0.52
2018 Ye Z, Zhang N, Wu C, Zhang X, Wang Q, Huang X, Du L, Cao Q, Tang J, Zhou C, Hou S, He Y, Xu Q, Xiong X, Kijlstra A, et al. A metagenomic study of the gut microbiome in Behcet's disease. Microbiome. 6: 135. PMID 30077182 DOI: 10.1186/s40168-018-0520-6  0.44
2018 Wu P, Du L, Hou S, Su G, Yang L, Hu J, Deng J, Cao Q, Yuan G, Zhou C, Kijlstra A, Yang P. Association of and with ocular Behcet's disease in a Chinese Han population. The British Journal of Ophthalmology. PMID 29907633 DOI: 10.1136/bjophthalmol-2017-311753  0.44
2018 Zhang Q, Li H, Hou S, Yu H, Su G, Deng B, Qi J, Zhou C, Kijlstra A, Yang P. Association of genetic variations in PTPN2 and CD122 with ocular Behcet's disease. The British Journal of Ophthalmology. PMID 29502070 DOI: 10.1136/bjophthalmol-2017-310820  0.44
2018 Yue Y, Zhang J, Yang L, Liu S, Qi J, Cao Q, Zhou C, Wang Y, Kijlstra A, Yang P, Hou S. Association of Long Noncoding RNAs Polymorphisms With Ankylosing Spondylitis, Vogt-Koyanagi-Harada Disease, and Behcet's Disease. Investigative Ophthalmology & Visual Science. 59: 1158-1166. PMID 29490353 DOI: 10.1167/iovs.17-23247  0.44
2017 Li N, Zhang J, Liao D, Yang L, Wang Y, Hou S. Erratum: Corrigendum: Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis. Scientific Reports. 7: 46785. PMID 31748657 DOI: 10.1038/srep46785  0.44
2017 Li N, Zhang J, Liao D, Yang L, Wang Y, Hou S. Corrigendum: Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis. Scientific Reports. 7: 46785. PMID 28467396 DOI: 10.1038/srep46785  0.44
2017 Yang L, Du L, Yue Y, Huang Y, Zhou Q, Cao S, Qi J, Liang L, Wu L, Wang C, Ye Z, Tian Y, Kijlstra A, Hou S, Yang P. miRNA Copy Number Variants Confer Susceptibility to Acute Anterior Uveitis With or Without Ankylosing Spondylitis. Investigative Ophthalmology & Visual Science. 58: 1991-2001. PMID 28384720 DOI: 10.1167/iovs.16-21047  0.48
2017 Li N, Zhang J, Liao D, Yang L, Wang Y, Hou S. Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis. Scientific Reports. 7: 42628. PMID 28205620 DOI: 10.1038/srep42628  0.44
2016 Lu S, Song S, Hou S, Li H, Yang P. Association of TNFSF4 Polymorphisms with Vogt-Koyanagi-Harada and Behcet's Disease in Han Chinese. Scientific Reports. 6: 37257. PMID 27872495 DOI: 10.1038/srep37257  0.44
2016 Zhou Y, Yu H, Hou S, Fang J, Qin J, Yuan G, Kijlstra A, Yang P. Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese. Molecular Vision. 22: 311-8. PMID 27114698  0.44
2016 Zhang J, Liao D, Yang L, Hou S. Association between Functional MICA-TM and Behcet's Disease: A Systematic Review and Meta-analysis. Scientific Reports. 6: 21033. PMID 26875668 DOI: 10.1038/srep21033  0.44
2016 Jiang Y, Wang H, Yu H, Li L, Xu D, Hou S, Kijlstra A, Yang P. Two Genetic Variations in the IRF8 region are associated with Behçet's disease in Han Chinese. Scientific Reports. 6: 19651. PMID 26794091 DOI: 10.1038/srep19651  0.44
2016 Chen F, Xu L, Zhao T, Xiao X, Pan Y, Hou S. Genetic Variation in the REL Gene Increases Risk of Behcet's Disease in a Chinese Han Population but That of PRKCQ Does Not. Plos One. 11: e0147350. PMID 26784953 DOI: 10.1371/journal.pone.0147350  0.44
2015 Cao S, Chee SP, Yu HG, Sukavatcharin S, Wu L, Kijlstra A, Hou S, Yang P. Investigation of the association of Vogt-Koyanagi-Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai. The British Journal of Ophthalmology. PMID 26628628 DOI: 10.1136/bjophthalmol-2015-307366  0.44
2015 Hou S, Kijlstra A, Yang P. Molecular Genetic Advances in Uveitis. Progress in Molecular Biology and Translational Science. 134: 283-98. PMID 26310161 DOI: 10.1016/bs.pmbts.2015.04.009  0.44
2015 Xu D, Hou S, Zhang J, Jiang Y, Kijlstra A, Yang P. Copy number variations and gene polymorphisms of complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome. Scientific Reports. 5: 12989. PMID 26269006 DOI: 10.1038/srep12989  0.44
2015 Xu D, Hou S, Jiang Y, Zhang J, Cao S, Zhang D, Luo L, Kijlstra A, Yang P. Complement C5 Gene Confers Risk for Acute Anterior Uveitis. Investigative Ophthalmology & Visual Science. 56: 4954-60. PMID 26230759 DOI: 10.1167/iovs.15-16645  0.44
2015 Li H, Hou S, Yu H, Zheng M, Zhang L, Zhang J, Zhang Q, Cao Q, Yuan G, Kijlstra A, Yang P. Association of Genetic Variations in TNFSF15 With Acute Anterior Uveitis in Chinese Han. Investigative Ophthalmology & Visual Science. 56: 4605-4610. PMID 26200500 DOI: 10.1167/iovs.15-16896  0.44
2015 Hu J, Hou S, Zhu X, Fang J, Zhou Y, Liu Y, Bai L, Kijlstra A, Yang P. Interleukin-10 gene polymorphisms are associated with Behcet's disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population. Molecular Vision. 21: 589-603. PMID 26015771  0.52
2015 Li JJ, Bai ML, Chen ZB, Zhou XS, Shi Z, Zhang M, Ding SY, Hou SM, Schwarzacher W, Nichols RJ, Mao BW. Giant single-molecule anisotropic magnetoresistance at room temperature. Journal of the American Chemical Society. 137: 5923-9. PMID 25894840 DOI: 10.1021/ja512483y  0.36
2015 Gao X, Tan X, Qin J, Lv S, Hou S, Kijlstra A, Yang P. No association between Bach2 gene polymorphisms with Vogt-Koyanagi-Harada syndrome (VKH) and Behcet's disease (BD) in a Chinese Han population. The British Journal of Ophthalmology. 99: 1150-4. PMID 25873652 DOI: 10.1136/bjophthalmol-2014-306163  0.44
2015 Liao D, Hou S, Zhang J, Fang J, Liu Y, Bai L, Cao Q, Kijlstra A, Yang P. Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome. Scientific Reports. 5: 9511. PMID 25873156 DOI: 10.1038/srep09511  0.44
2015 Fang J, Chen L, Tang J, Hou S, Liao D, Ye Z, Wang C, Cao Q, Kijlstra A, Yang P. Association Between Copy Number Variations of TLR7 and Ocular Behçet's Disease in a Chinese Han Population. Investigative Ophthalmology & Visual Science. 56: 1517-23. PMID 25650422 DOI: 10.1167/iovs.14-15030  0.44
2015 Li K, Hou S, Qi J, Kijlstra A, Yang P. A variant of CLEC16A gene confers protection for Vogt-Koyanagi-Harada syndrome but not for Behcet's disease in a Chinese Han population. Experimental Eye Research. 132: 225-30. PMID 25576669 DOI: 10.1016/j.exer.2015.01.004  0.44
2015 Hou S, Liao D, Zhang J, Fang J, Chen L, Qi J, Zhang Q, Liu Y, Bai L, Zhou Y, Kijlstra A, Yang P. Genetic variations of IL17F and IL23A show associations with Behçet's disease and Vogt-Koyanagi-Harada syndrome. Ophthalmology. 122: 518-23. PMID 25439430 DOI: 10.1016/j.ophtha.2014.09.025  0.44
2014 Hou S, Qi J, Liao D, Fang J, Chen L, Kijlstra A, Yang P. High C4 gene copy numbers protects against Vogt-Koyanagi-Harada syndrome in Chinese Han. The British Journal of Ophthalmology. 98: 1733-7. PMID 25185257 DOI: 10.1136/bjophthalmol-2014-305596  0.44
2014 Hou S, Du L, Lei B, Pang CP, Zhang M, Zhuang W, Zhang M, Huang L, Gong B, Wang M, Zhang Q, Hu K, Zhou Q, Qi J, Wang C, et al. Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3. Nature Genetics. 46: 1007-11. PMID 25108386 DOI: 10.1038/ng.3061  0.44
2014 Li X, Bai L, Fang J, Hou S, Zhou Q, Yu H, Kijlstra A, Yang P. Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndrome. Plos One. 9: e98373. PMID 24859272 DOI: 10.1371/journal.pone.0098373  0.44
2014 Zhang Q, Qi J, Hou S, Du L, Yu H, Cao Q, Zhou Y, Liao D, Kijlstra A, Yang P. A functional variant of PTPN22 confers risk for Vogt-Koyanagi-Harada syndrome but not for ankylosing spondylitis. Plos One. 9: e96943. PMID 24816862 DOI: 10.1371/journal.pone.0096943  0.44
2014 Shi Y, Jia Y, Hou S, Fang J, Zhou Y, Kijlstra A, Yang P. Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese. Plos One. 9: e95573. PMID 24788730 DOI: 10.1371/journal.pone.0095573  0.44
2014 Wei L, Zhou Q, Hou S, Bai L, Liu Y, Qi J, Xiang Q, Zhou Y, Kijlstra A, Yang P. MicroRNA-146a and Ets-1 gene polymorphisms are associated with pediatric uveitis. Plos One. 9: e91199. PMID 24658012 DOI: 10.1371/journal.pone.0091199  0.44
2014 Qi J, Yang Y, Hou S, Qiao Y, Wang Q, Yu H, Zhang Q, Cai T, Kijlstra A, Yang P. Increased Notch pathway activation in Behçet's disease. Rheumatology (Oxford, England). 53: 810-20. PMID 24446471 DOI: 10.1093/rheumatology/ket438  0.44
2014 Xiang Q, Chen L, Hou S, Fang J, Zhou Y, Bai L, Liu Y, Kijlstra A, Yang P. TRAF5 and TRAF3IP2 gene polymorphisms are associated with Behçet's disease and Vogt-Koyanagi-Harada syndrome: a case-control study. Plos One. 9: e84214. PMID 24416204 DOI: 10.1371/journal.pone.0084214  0.44
2014 Fang J, Hou S, Xiang Q, Qi J, Yu H, Shi Y, Zhou Y, Kijlstra A, Yang P. Polymorphisms in genetics of vitamin D metabolism confer susceptibility to ocular Behçet disease in a Chinese Han population. American Journal of Ophthalmology. 157: 488-494.e6. PMID 24184224 DOI: 10.1016/j.ajo.2013.10.010  0.44
2014 Li H, Hou S, Du L, Zhou Q, Kijlstra A, Liu Q. Polymorphisms of TNFAIP3 gene in a Chinese Han population with fuchs heterochromic iridocyclitis. Ophthalmic Genetics. 35: 63-7. PMID 23463983 DOI: 10.3109/13816810.2013.771674  0.44
2014 Zhou Q, Hou S, Liang L, Li X, Tan X, Wei L, Lei B, Kijlstra A, Yang P. MicroRNA-146a and Ets-1 gene polymorphisms in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome. Annals of the Rheumatic Diseases. 73: 170-6. PMID 23268366 DOI: 10.1136/annrheumdis-2012-201627  0.44
2013 Fang J, Hu R, Hou S, Ye Z, Xiang Q, Qi J, Zhou Y, Kijlstra A, Yang P. Association of TLR2 gene polymorphisms with ocular Behcet's disease in a Chinese Han population. Investigative Ophthalmology & Visual Science. 54: 8384-92. PMID 24255044 DOI: 10.1167/iovs.13-12878  0.44
2013 Zhang C, Liu S, Hou S, Lei B, Zheng X, Xiao X, Kijlstra A, Yang P. MIF gene polymorphisms confer susceptibility to Vogt-Koyanagi-Harada syndrome in a Han Chinese population. Investigative Ophthalmology & Visual Science. 54: 7734-8. PMID 24194192 DOI: 10.1167/iovs.13-12187  0.44
2013 Xiang Q, Chen L, Fang J, Hou S, Wei L, Bai L, Liu Y, Zhou Y, Kijlstra A, Yang P. TNF receptor-associated factor 5 gene confers genetic predisposition to acute anterior uveitis and pediatric uveitis. Arthritis Research & Therapy. 15: R113. PMID 24020968 DOI: 10.1186/ar4293  0.44
2013 Yi X, Du L, Hou S, Li F, Chen Y, Kijlstra A, Yang P. FGFR1OP tagSNP but not CCR6 polymorphisms are associated with Vogt-Koyanagi-Harada syndrome in Chinese Han. Plos One. 8: e69358. PMID 23935994 DOI: 10.1371/journal.pone.0069358  0.44
2013 Qi J, Hou S, Zhang Q, Liao D, Wei L, Fang J, Zhou Y, Kijlstra A, Yang P. 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. Human Genetics. 132: 1395-404. PMID 23928854 DOI: 10.1007/s00439-013-1346-8  0.44
2013 Hou S, Qi J, Liao D, Zhang Q, Fang J, Zhou Y, Liu Y, Bai L, Zhang M, Kijlstra A, Yang P. Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis. Arthritis and Rheumatism. 65: 2963-70. PMID 23918728 DOI: 10.1002/art.38116  0.44
2013 Hou S, Qi J, Zhang Q, Liao D, Li Q, Hu K, Zhou Y, Kijlstra A, Yang P. Genetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese. Human Genetics. 132: 1049-58. PMID 23674219 DOI: 10.1007/s00439-013-1312-5  0.44
2013 Hu K, Hou S, Li F, Xiang Q, Kijlstra A, Yang P. JAK1, but not JAK2 and STAT3, confers susceptibility to Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population. Investigative Ophthalmology & Visual Science. 54: 3360-5. PMID 23611997 DOI: 10.1167/iovs.13-11615  0.44
2013 Li H, Liu Q, Hou S, Du L, Zhou Q, Zhou Y, Kijlstra A, Yang P. TNFAIP3 gene polymorphisms in a Chinese Han population with Vogt-Koyanagi-Harada syndrome. Plos One. 8: e59515. PMID 23555688 DOI: 10.1371/journal.pone.0059515  0.44
2013 Cai T, Wang Q, Zhou Q, Wang C, Hou S, Qi J, Kijlstra A, Yang P. Increased expression of IL-22 is associated with disease activity in Behcet's disease. Plos One. 8: e59009. PMID 23527071 DOI: 10.1371/journal.pone.0059009  0.44
2013 Zhu X, Zhang J, Fan W, Wang F, Yao H, Wang Z, Hou S, Tian Y, Fu W, Xie D, Zhu W, Long J, Wu L, Zheng X, Kung H, et al. The rs391957 variant cis-regulating oncogene GRP78 expression contributes to the risk of hepatocellular carcinoma. Carcinogenesis. 34: 1273-80. PMID 23416888 DOI: 10.1093/carcin/bgt061  0.52
2013 Li H, Liu Q, Hou S, Du L, Zhou Q, Zhou Y, Kijlstra A, Li Z, Yang P. TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population. Human Genetics. 132: 293-300. PMID 23161053 DOI: 10.1007/s00439-012-1250-7  0.44
2013 Hou S, Xiao X, Zhou Y, Zhu X, Li F, Kijlstra A, Yang P. Genetic variant on PDGFRL associated with Behçet disease in Chinese Han populations. Human Mutation. 34: 74-8. PMID 22926996 DOI: 10.1002/humu.22208  0.52
2012 Hou S, Kijlstra A, Yang P. The genetics of Behçet's disease in a Chinese population. Frontiers of Medicine. 6: 354-9. PMID 23161479 DOI: 10.1007/s11684-012-0234-2  0.44
2012 Hou S, Yang Z, Du L, Jiang Z, Shu Q, Chen Y, Li F, Zhou Q, Ohno S, Chen R, Kijlstra A, Rosenbaum JT, Yang P. Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. Arthritis and Rheumatism. 64: 4104-13. PMID 23001997 DOI: 10.1002/art.37708  0.44
2012 Zheng X, Wang D, Hou S, Zhang C, Lei B, Xiao X, Kijlstra A, Yang P. Association of macrophage migration inhibitory factor gene polymorphisms with Behçet's disease in a Han Chinese population. Ophthalmology. 119: 2514-8. PMID 22939113 DOI: 10.1016/j.ophtha.2012.06.039  0.44
2012 Hou S, Xiao X, Li F, Jiang Z, Kijlstra A, Yang P. Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility. Human Genetics. 131: 1841-50. PMID 22829007 DOI: 10.1007/s00439-012-1200-4  0.44
2012 Hou S, Shu Q, Jiang Z, Chen Y, Li F, Chen F, Kijlstra A, Yang P. Replication study confirms the association between UBAC2 and Behçet's disease in two independent Chinese sets of patients and controls. Arthritis Research & Therapy. 14: R70. PMID 22455605 DOI: 10.1186/ar3789  0.44
2012 Chen Y, Yang P, Li F, Hou S, Jiang Z, Shu Q, Kijlstra A. Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population. Current Eye Research. 37: 312-7. PMID 22440163 DOI: 10.3109/02713683.2011.635398  0.44
2012 Zhang Q, Hou S, Jiang Z, Du L, Li F, Xiao X, Kijlstra A, Yang P. No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations. Plos One. 7: e31230. PMID 22396730 DOI: 10.1371/journal.pone.0031230  0.44
2012 Zhou Q, Kijlstra A, Hou S, Yu H, Zhang X, Li X, Xiao X, Yang P. Lack of association of miR-146a and Ets-1 gene polymorphisms with Fuchs uveitis syndrome in Chinese Han patients. Molecular Vision. 18: 426-30. PMID 22355253  0.44
2012 Hu K, Hou S, Jiang Z, Kijlstra A, Yang P. JAK2 and STAT3 polymorphisms in a Han Chinese population with Behçet's disease. Investigative Ophthalmology & Visual Science. 53: 538-41. PMID 22205606 DOI: 10.1167/iovs.11-8440  0.44
2012 Chen F, Hou S, Jiang Z, Chen Y, Kijlstra A, Rosenbaum JT, Yang P. CD40 gene polymorphisms confer risk of Behcet's disease but not of Vogt-Koyanagi-Harada syndrome in a Han Chinese population. Rheumatology (Oxford, England). 51: 47-51. PMID 22087016 DOI: 10.1093/rheumatology/ker345  0.44
2011 Meng Q, Guo H, Hou S, Jiang Z, Kijlstra A, Yang P. Lack of an association of PD-1 and its ligand genes with Behcet's disease in a Chinese Han population. Plos One. 6: e25345. PMID 22039410 DOI: 10.1371/journal.pone.0025345  0.44
2011 Chen F, Hou S, Jiang Z, Li F, Chen Y, Kijlstra A, Yang P. CD40 polymorphisms in Han Chinese patients with Fuch uveitis syndrome. Molecular Vision. 17: 2469-72. PMID 21976957  0.44
2011 Li JF, Ding SY, Yang ZL, Bai ML, Anema JR, Wang X, Wang A, Wu DY, Ren B, Hou SM, Wandlowski T, Tian ZQ. Extraordinary enhancement of Raman scattering from pyridine on single crystal Au and Pt electrodes by shell-isolated Au nanoparticles. Journal of the American Chemical Society. 133: 15922-5. PMID 21899270 DOI: 10.1021/ja2074533  0.44
2011 Chu M, Yang P, Hu R, Hou S, Li F, Chen Y, Kijlstra A. Elevated serum osteopontin levels and genetic polymorphisms of osteopontin are associated with Vogt-Koyanagi-Harada disease. Investigative Ophthalmology & Visual Science. 52: 7084-9. PMID 21810982 DOI: 10.1167/iovs.11-7539  0.44
2011 Tan W, Hou S, Jiang Z, Hu Z, Yang P, Ye J. Association of EPHA2 polymorphisms and age-related cortical cataract in a Han Chinese population. Molecular Vision. 17: 1553-8. PMID 21686326  0.44
2011 Chu M, Yang P, Hou S, Li F, Chen Y, Kijlstra A. Behçet's disease exhibits an increased osteopontin serum level in active stage but no association with osteopontin and its receptor gene polymorphisms. Human Immunology. 72: 525-9. PMID 21513757 DOI: 10.1016/j.humimm.2011.03.016  0.44
2011 Mao L, Yang P, Hou S, Li F, Kijlstra A. Label-free proteomics reveals decreased expression of CD18 and AKNA in peripheral CD4+ T cells from patients with Vogt-Koyanagi-Harada syndrome. Plos One. 6: e14616. PMID 21297967 DOI: 10.1371/journal.pone.0014616  0.44
2010 Zhou H, Jiang Z, Yang P, Hou S, Li F, Shu Q, Chen Y, Chen F. Polymorphisms of IL23R and Fuchs' syndrome in a Chinese Han population. Molecular Vision. 16: 2585-9. PMID 21151597  0.44
2010 Li F, Yang P, Liu X, Wang C, Hou S, Kijlstra A. Upregulation of interleukin 21 and promotion of interleukin 17 production in chronic or recurrent Vogt-Koyanagi-Harada disease. Archives of Ophthalmology (Chicago, Ill. : 1960). 128: 1449-54. PMID 21060047 DOI: 10.1001/archophthalmol.2010.265  0.44
2010 Shu Q, Yang P, Hou S, Li F, Chen Y, Du L, Jiang Z. Interleukin-17 gene polymorphism is associated with Vogt-Koyanagi-Harada syndrome but not with Behçet's disease in a Chinese Han population. Human Immunology. 71: 988-91. PMID 20620187 DOI: 10.1016/j.humimm.2010.06.020  0.44
2010 Hou S, Chen Y, Liang J, Li L, Wu T, Tian XC, Zhang S. Developmental stage-specific imprinting of IPL in domestic pigs (Sus scrofa). Journal of Biomedicine & Biotechnology. 2010: 527539. PMID 20589073 DOI: 10.1155/2010/527539  0.36
2010 Hu K, Yang P, Jiang Z, Hou S, Du L, Li F. STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behçet's disease. Human Immunology. 71: 723-6. PMID 20438790 DOI: 10.1016/j.humimm.2010.04.007  0.44
2010 Jiang Z, Yang P, Hou S, Du L, Xie L, Zhou H, Kijlstra A. IL-23R gene confers susceptibility to Behcet's disease in a Chinese Han population. Annals of the Rheumatic Diseases. 69: 1325-8. PMID 20375120 DOI: 10.1136/ard.2009.119420  0.44
2010 Jiang Z, Yang P, Hou S, Li F, Zhou H. Polymorphisms of IL23R and Vogt-Koyanagi-Harada syndrome in a Chinese Han population. Human Immunology. 71: 414-7. PMID 20116410 DOI: 10.1016/j.humimm.2010.01.026  0.44
2010 Hou S, Yang P, Du L, Jiang Z, Mao L, Shu Q, Zhou H, Kijlstra A. Monocyte chemoattractant protein-1 -2518 A/G single nucleotide polymorphism in Chinese Han patients with ocular Behçet's disease. Human Immunology. 71: 79-82. PMID 19782713 DOI: 10.1016/j.humimm.2009.09.354  0.44
2009 Li H, Yang P, Jiang Z, Hou S, Xie L. Lack of association of two polymorphisms of IRF5 with Behcet's disease. Molecular Vision. 15: 2018-21. PMID 19816589  0.44
2009 Hou S, Yang P, Xie L, Du L, Zhou H, Jiang Z. Monocyte chemoattractant protein (MCP)-1 -2518 A/G SNP in Chinese Han patients with VKH syndrome. Molecular Vision. 15: 1537-41. PMID 19668598  0.44
2009 Li K, Yang P, Zhao M, Hou S, Du L, Zhou H, Kijlstra A. Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome. Molecular Vision. 15: 955-61. PMID 19452015  0.44
2009 Meng Q, Liu X, Yang P, Hou S, Du L, Zhou H, Kijlstra A. PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome. Molecular Vision. 15: 386-92. PMID 19234630  0.44
2008 Hou S, Yang P, Du L, Zhou H, Lin X, Liu X, Kijlstra A. Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population. Molecular Vision. 14: 2597-603. PMID 19122825  0.44
2008 Li K, Zhao M, Hou S, Du L, Kijlstra A, Yang P. Association between polymorphisms of FCRL3, a non-HLA gene, and Behçet's disease in a Chinese population with ophthalmic manifestations. Molecular Vision. 14: 2136-42. PMID 19050767  0.44
2008 Hou S, Yang P, Du L, Zhou H, Lin X, Liu X, Kijlstra A. SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease. Clinical Immunology (Orlando, Fla.). 129: 170-5. PMID 18657476 DOI: 10.1016/j.clim.2008.06.006  0.44
2008 Du L, Yang P, Hou S, Lin X, Zhou H, Huang X, Wang L, Kijlstra A. Association of the CTLA-4 gene with Vogt-Koyanagi-Harada syndrome. Clinical Immunology (Orlando, Fla.). 127: 43-8. PMID 18282809 DOI: 10.1016/j.clim.2008.01.004  0.44
2007 Jiang L, Yang P, He H, Li B, Lin X, Hou S, Zhou H, Huang X, Aize K. Increased expression of Foxp3 in splenic CD8+ T cells from mice with anterior chamber-associated immune deviation. Molecular Vision. 13: 968-74. PMID 17653037  0.44
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