Chen CH - Search Results

1

A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.

Tsai FJ, Yang CF, Chen CC, Chuang LM, Lu CH, Chang CT, Wang TY, Chen RH, Shiu CF, Liu YM, Chang CC, Chen P, Chen CH, Fann CS, Chen YT, Wu JY. Tsai FJ, et al. Among authors: chen cc, chen ch, chen p, chen rh, chen yt. PLoS Genet. 2010 Feb 19;6(2):e1000847. doi: 10.1371/journal.pgen.1000847. PLoS Genet. 2010. PMID: 20174558 Free PMC article.

2

A genome-wide scan using tree-based association analysis for candidate loci related to fasting plasma glucose levels.

Chen CH, Chang CJ, Yang WS, Chen CL, Fann CS. Chen CH, et al. Among authors: chen cl. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S65. doi: 10.1186/1471-2156-4-S1-S65. BMC Genet. 2003. PMID: 14975133 Free PMC article.

3

Association between transforming growth factor-beta1 gene C-509T and T869C polymorphisms and rheumatic heart disease.

Chou HT, Chen CH, Tsai CH, Tsai FJ. Chou HT, et al. Among authors: chen ch. Am Heart J. 2004 Jul;148(1):181-6. doi: 10.1016/j.ahj.2004.03.032. Am Heart J. 2004. PMID: 15215809

4

HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol.

Hung SI, Chung WH, Liou LB, Chu CC, Lin M, Huang HP, Lin YL, Lan JL, Yang LC, Hong HS, Chen MJ, Lai PC, Wu MS, Chu CY, Wang KH, Chen CH, Fann CS, Wu JY, Chen YT. Hung SI, et al. Among authors: chen ch, chen mj, chen yt. Proc Natl Acad Sci U S A. 2005 Mar 15;102(11):4134-9. doi: 10.1073/pnas.0409500102. Epub 2005 Mar 2. Proc Natl Acad Sci U S A. 2005. PMID: 15743917 Free PMC article.

5

A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity.

Yuan HY, Chen JJ, Lee MT, Wung JC, Chen YF, Charng MJ, Lu MJ, Hung CR, Wei CY, Chen CH, Wu JY, Chen YT. Yuan HY, et al. Among authors: chen jj, chen ch, chen yf, chen yt. Hum Mol Genet. 2005 Jul 1;14(13):1745-51. doi: 10.1093/hmg/ddi180. Epub 2005 May 11. Hum Mol Genet. 2005. PMID: 15888487

6

Construction of endophenotypes for complex diseases in the presence of heterogeneity.

Chen CH, Kuo CL, Lin MC, Liang YJ, Fann CS. Chen CH, et al. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S139. doi: 10.1186/1471-2156-6-S1-S139. BMC Genet. 2005. PMID: 16451598 Free PMC article.

7

Long contiguous stretches of homozygosity in the human genome.

Li LH, Ho SF, Chen CH, Wei CY, Wong WC, Li LY, Hung SI, Chung WH, Pan WH, Lee MT, Tsai FJ, Chang CF, Wu JY, Chen YT. Li LH, et al. Among authors: chen ch, chen yt. Hum Mutat. 2006 Nov;27(11):1115-21. doi: 10.1002/humu.20399. Hum Mutat. 2006. PMID: 16955415

8

VKORC1 haplotypes in five East-Asian populations and Indians.

Lee MT, Chen CH, Chuang HP, Lu LS, Chou CH, Chen YT, Liu CY, Wen MS, Lu JJ, Chang CF, Wu JY, Chen YT. Lee MT, et al. Among authors: chen ch, chen yt. Pharmacogenomics. 2009 Oct;10(10):1609-16. doi: 10.2217/pgs.09.80. Pharmacogenomics. 2009. PMID: 19842934

9

Genetic determinants of warfarin dosing in the Han-Chinese population.

Lee MT, Chen CH, Chou CH, Lu LS, Chuang HP, Chen YT, Saleem AN, Wen MS, Chen JJ, Wu JY, Chen YT. Lee MT, et al. Among authors: chen jj, chen ch, chen yt. Pharmacogenomics. 2009 Dec;10(12):1905-13. doi: 10.2217/pgs.09.106. Pharmacogenomics. 2009. PMID: 19958090

10

Common risk allele in aromatic antiepileptic-drug induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Han Chinese.

Hung SI, Chung WH, Liu ZS, Chen CH, Hsih MS, Hui RC, Chu CY, Chen YT. Hung SI, et al. Among authors: chen ch, chen yt. Pharmacogenomics. 2010 Mar;11(3):349-56. doi: 10.2217/pgs.09.162. Pharmacogenomics. 2010. PMID: 20235791

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