Tang CS - Search Results

1

Intron length and accelerated 3' gene evolution.

Tang CS, Zhao YZ, Smith DK, Epstein RJ. Tang CS, et al. Genomics. 2006 Dec;88(6):682-689. doi: 10.1016/j.ygeno.2006.06.017. Epub 2006 Aug 22. Genomics. 2006. PMID: 16928427 Free article.

2

A structural split in the human genome.

Tang CS, Epstein RJ. Tang CS, et al. PLoS One. 2007 Jul 11;2(7):e603. doi: 10.1371/journal.pone.0000603. PLoS One. 2007. PMID: 17622348 Free PMC article.

3

Adaptive Evolution Hotspots at the GC-Extremes of the Human Genome: Evidence for Two Functionally Distinct Pathways of Positive Selection.

Tang CS, Epstein RJ. Tang CS, et al. Adv Bioinformatics. 2010;2010:856825. doi: 10.1155/2010/856825. Epub 2010 May 3. Adv Bioinformatics. 2010. PMID: 20454629 Free PMC article.

4

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes.

Wong JK, Campbell D, Ngo ND, Yeung F, Cheng G, Tang CS, Chung PH, Tran NS, So MT, Cherny SS, Sham PC, Tam PK, Garcia-Barcelo MM. Wong JK, et al. Among authors: tang cs. BMC Med Genomics. 2016 Dec 12;9(1):75. doi: 10.1186/s12920-016-0236-z. BMC Med Genomics. 2016. PMID: 27955658 Free PMC article.

5

Fine mapping of the 9q31 Hirschsprung's disease locus.

Tang CS, Sribudiani Y, Miao XP, de Vries AR, Burzynski G, So MT, Leon YY, Yip BH, Osinga J, Hui KJ, Verheij JB, Cherny SS, Tam PK, Sham PC, Hofstra RM, Garcia-Barceló MM. Tang CS, et al. Hum Genet. 2010 Jun;127(6):675-83. doi: 10.1007/s00439-010-0813-8. Epub 2010 Apr 2. Hum Genet. 2010. PMID: 20361209 Free PMC article.

6

Genome-wide copy number variation study in anorectal malformations.

Wong EH, Cui L, Ng CL, Tang CS, Liu XL, So MT, Yip BH, Cheng G, Zhang R, Tang WK, Yang W, Lau YL, Baum L, Kwan P, Sun LD, Zuo XB, Ren YQ, Yin XY, Miao XP, Liu J, Lui VC, Ngan ES, Yuan ZW, Zhang SW, Xia J, Wang H, Sun XB, Wang R, Chang T, Chan IH, Chung PH, Zhang XJ, Wong KK, Cherny SS, Sham PC, Tam PK, Garcia-Barcelo MM. Wong EH, et al. Among authors: tang wk, tang cs. Hum Mol Genet. 2013 Feb 1;22(3):621-31. doi: 10.1093/hmg/dds451. Epub 2012 Oct 29. Hum Mol Genet. 2013. PMID: 23108157

7

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.

Guo Y, Baum LW, Sham PC, Wong V, Ng PW, Lui CH, Sin NC, Tsoi TH, Tang CS, Kwan JS, Yip BH, Xiao SM, Thomas GN, Lau YL, Yang W, Cherny SS, Kwan P. Guo Y, et al. Among authors: tang cs. Hum Mol Genet. 2012 Mar 1;21(5):1184-9. doi: 10.1093/hmg/ddr550. Epub 2011 Nov 24. Hum Mol Genet. 2012. PMID: 22116939

8

Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing.

Tang CS, Zhuang X, Lam WY, Ngan ES, Hsu JS, Michelle YU, Man-Ting SO, Cherny SS, Ngo ND, Sham PC, Tam PK, Garcia-Barcelo MM. Tang CS, et al. Eur J Hum Genet. 2018 Jun;26(6):818-826. doi: 10.1038/s41431-018-0129-z. Epub 2018 Feb 26. Eur J Hum Genet. 2018. PMID: 29483666 Free PMC article.

9

Genome-wide association study of BNT162b2 vaccine-related myocarditis identifies potential predisposing functional areas in Hong Kong adolescents.

She CH, Tsang HW, Yang X, Tsao SS, Tang CS, Chan SH, Kwan MY, Chua GT, Yang W, Ip P. She CH, et al. Among authors: tang cs. BMC Genom Data. 2024 Jun 6;25(1):51. doi: 10.1186/s12863-024-01238-6. BMC Genom Data. 2024. PMID: 38844841 Free PMC article.

10

Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism.

Liu W, Wong JK, He Q, Wong EH, Tang CS, Zhang R, So MT, Wong KK, Nicholls J, Cherny SS, Sham PC, Tam PK, Garcia-Barcelo MM, Xia H. Liu W, et al. Among authors: tang cs. BMC Med Genet. 2015 Jul 16;16:49. doi: 10.1186/s12881-015-0189-7. BMC Med Genet. 2015. PMID: 26179878 Free PMC article.

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