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Shengping Hou - Publications

Affiliations: 
Gladstone and UCSF, San Francisco, CA, United States 
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24 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
2022 Li W, Tan J, He S, Yue Y, Liu H, Li R, Wang X, Wang G, Fan W, Zhao C, Zhou Q, Yang P, Hou S. iPSC-based model of Vogt-Koyanagi-Harada disease for phenotype recapitulation and drug screening. Clinical Immunology (Orlando, Fla.). 246: 109205. PMID 36509389 DOI: 10.1016/j.clim.2022.109205  0.309
2020 Tan J, Liu H, Huang M, Li N, Tang S, Meng J, Tang S, Zhou H, Kijlstra A, Yang P, Hou S. Small molecules targeting RORγt inhibit autoimmune disease by suppressing Th17 cell differentiation. Cell Death & Disease. 11: 697. PMID 32829384 DOI: 10.1038/s41419-020-02891-2  0.382
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  0.304
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  0.305
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  0.305
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  0.311
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  0.331
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  0.325
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  0.335
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  0.33
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  0.333
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  0.3
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  0.325
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  0.339
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  0.303
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  0.312
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  0.301
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  0.369
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  0.347
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  0.308
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  0.327
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  0.312
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  0.353
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  0.345
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