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Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease.
Zhou F, Cao H, Zuo X, Zhang T, Zhang X, Liu X, Xu R, Chen G, Zhang Y, Zheng X, Jin X, Gao J, Mei J, Sheng Y, Li Q, Liang B, Shen J, Shen C, Jiang H, Zhu C, Fan X, Xu F, Yue M, Yin X, Ye C, Zhang C, Liu X, Yu L, Wu J, Chen M, Zhuang X, Tang L, Shao H, Wu L, Li J, Xu Y, Zhang Y, Zhao S, Wang Y, Li G, Xu H, Zeng L, Wang J, Bai M, Chen Y, Chen W, Kang T, Wu Y, Xu X, Zhu Z, Cui Y, Wang Z, Yang C, Wang P, Xiang L, Chen X, Zhang A, Gao X, Zhang F, Xu J, Zheng M, Zheng J, Zhang J, Yu X, Li Y, Yang S, Yang H, Wang J, Liu J, Hammarström L, Sun L, Wang J, Zhang X. Zhou F, et al. Among authors: yue m. Nat Genet. 2016 Jul;48(7):740-6. doi: 10.1038/ng.3576. Epub 2016 May 23. Nat Genet. 2016. PMID: 27213287
Epigenome-Wide Association Analysis Identified Nine Skin DNA Methylation Loci for Psoriasis.
Zhou F, Wang W, Shen C, Li H, Zuo X, Zheng X, Yue M, Zhang C, Yu L, Chen M, Zhu C, Yin X, Tang M, Li Y, Chen G, Wang Z, Liu S, Zhou Y, Zhang F, Zhang W, Li C, Yang S, Sun L, Zhang X. Zhou F, et al. Among authors: yue m. J Invest Dermatol. 2016 Apr;136(4):779-787. doi: 10.1016/j.jid.2015.12.029. Epub 2015 Dec 29. J Invest Dermatol. 2016. PMID: 26743604 Free article.
A novel MIP mutation in a Chinese family with congenital cataract.
Yuan C, Han T, Su P, Liu M, Zhou X, Zhang D, Jia W, Wang A, Yue M, Xiang Z, Chen L, Zhang X. Yuan C, et al. Among authors: yue m. Ophthalmic Genet. 2018 Aug;39(4):473-476. doi: 10.1080/13816810.2018.1484930. Ophthalmic Genet. 2018. PMID: 29947569
1,031 results