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821 results

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Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
Garcia-Barcelo MM, Tang CS, Ngan ES, Lui VC, Chen Y, So MT, Leon TY, Miao XP, Shum CK, Liu FQ, Yeung MY, Yuan ZW, Guo WH, Liu L, Sun XB, Huang LM, Tou JF, Song YQ, Chan D, Cheung KM, Wong KK, Cherny SS, Sham PC, Tam PK. Garcia-Barcelo MM, et al. Among authors: tang cs. Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2694-9. doi: 10.1073/pnas.0809630105. Epub 2009 Feb 5. Proc Natl Acad Sci U S A. 2009. PMID: 19196962 Free PMC article.
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.
Garcia-Barceló MM, Yeung MY, Miao XP, Tang CS, Cheng G, So MT, Ngan ES, Lui VC, Chen Y, Liu XL, Hui KJ, Li L, Guo WH, Sun XB, Tou JF, Chan KW, Wu XZ, Song YQ, Chan D, Cheung K, Chung PH, Wong KK, Sham PC, Cherny SS, Tam PK. Garcia-Barceló MM, et al. Among authors: tang cs. Hum Mol Genet. 2010 Jul 15;19(14):2917-25. doi: 10.1093/hmg/ddq196. Epub 2010 May 11. Hum Mol Genet. 2010. PMID: 20460270 Free PMC article.
No NRG1 V266L in Chinese patients with schizophrenia.
Garcia-Barceló MM, Miao X, Tang CS, So HC, Tang W, Leon TY, So M, Yip B, Chen RY, Cheung EF, Chen EY, Li T, Tam P, Cherny SS, Sham PC. Garcia-Barceló MM, et al. Among authors: tang w, tang cs. Psychiatr Genet. 2011 Feb;21(1):47-9. doi: 10.1097/YPG.0b013e328341355b. Psychiatr Genet. 2011. PMID: 20978455
Fine mapping of the NRG1 Hirschsprung's disease locus.
Tang CS, Tang WK, So MT, Miao XP, Leung BM, Yip BH, Leon TY, Ngan ES, Lui VC, Chen Y, Chan IH, Chung PH, Liu XL, Wu XZ, Wong KK, Sham PC, Cherny SS, Tam PK, Garcia-Barceló MM. Tang CS, et al. Among authors: tang wk. PLoS One. 2011 Jan 20;6(1):e16181. doi: 10.1371/journal.pone.0016181. PLoS One. 2011. PMID: 21283760 Free PMC article.
Mutations in the NRG1 gene are associated with Hirschsprung disease.
Tang CS, Ngan ES, Tang WK, So MT, Cheng G, Miao XP, Leon TY, Leung BM, Hui KJ, Lui VH, Chen Y, Chan IH, Chung PH, Liu XL, Wong KK, Sham PC, Cherny SS, Tam PK, Garcia-Barcelo MM. Tang CS, et al. Among authors: tang wk. Hum Genet. 2012 Jan;131(1):67-76. doi: 10.1007/s00439-011-1035-4. Epub 2011 Jun 25. Hum Genet. 2012. PMID: 21706185
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.
Tang CS, Zhang H, Cheung CY, Xu M, Ho JC, Zhou W, Cherny SS, Zhang Y, Holmen O, Au KW, Yu H, Xu L, Jia J, Porsch RM, Sun L, Xu W, Zheng H, Wong LY, Mu Y, Dou J, Fong CH, Wang S, Hong X, Dong L, Liao Y, Wang J, Lam LS, Su X, Yan H, Yang ML, Chen J, Siu CW, Xie G, Woo YC, Wu Y, Tan KC, Hveem K, Cheung BM, Zöllner S, Xu A, Eugene Chen Y, Jiang CQ, Zhang Y, Lam TH, Ganesh SK, Huo Y, Sham PC, Lam KS, Willer CJ, Tse HF, Gao W. Tang CS, et al. Nat Commun. 2015 Dec 22;6:10206. doi: 10.1038/ncomms10206. Nat Commun. 2015. PMID: 26690388 Free PMC article.
821 results