Wu JY - Search Results

1

Yang HC, Lin HC, Kang M, Chen CH, Lin CW, Li LH, Wu JY, Chen YT, Pan WH. Yang HC, et al. Among authors: wu jy. BMC Bioinformatics. 2011 Apr 18;12:100. doi: 10.1186/1471-2105-12-100. BMC Bioinformatics. 2011. PMID: 21501472 Free PMC article.

2

ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease.

Wu JY, Kao HJ, Li SC, Stevens R, Hillman S, Millington D, Chen YT. Wu JY, et al. J Clin Invest. 2004 Feb;113(3):434-40. doi: 10.1172/JCI19574. J Clin Invest. 2004. PMID: 14755340 Free PMC article.

3

Medical genetics: a marker for Stevens-Johnson syndrome.

Chung WH, Hung SI, Hong HS, Hsih MS, Yang LC, Ho HC, Wu JY, Chen YT. Chung WH, et al. Among authors: wu jy. Nature. 2004 Apr 1;428(6982):486. doi: 10.1038/428486a. Nature. 2004. PMID: 15057820

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: wu jy, wu ms. 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: wu jy. 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

Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations.

Pan WH, Fann CS, Wu JY, Hung YT, Ho MS, Tai TH, Chen YJ, Liao CJ, Yang ML, Cheng AT, Chen YT. Pan WH, et al. Among authors: wu jy. Hum Hered. 2006;61(1):27-30. doi: 10.1159/000091834. Epub 2004 May 28. Hum Hered. 2006. PMID: 16534213 No abstract available.

7

A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect.

Niu DM, Hwang B, Hwang HW, Wang NH, Wu JY, Lee PC, Chien JC, Shieh RC, Chen YT. Niu DM, et al. Among authors: wu jy. J Med Genet. 2006 Oct;43(10):817-21. doi: 10.1136/jmg.2006.042192. Epub 2006 May 17. J Med Genet. 2006. PMID: 16707561 Free PMC article.

8

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: wu jy. Hum Mutat. 2006 Nov;27(11):1115-21. doi: 10.1002/humu.20399. Hum Mutat. 2006. PMID: 16955415

9

A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention.

Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Ouyang WC, Chan HY, Chen JJ, Yang WC, Lin CY, Lee SF, Hwu HG. Liu YL, et al. Among authors: wu jy. Biol Psychiatry. 2006 Sep 15;60(6):554-62. doi: 10.1016/j.biopsych.2006.04.024. Biol Psychiatry. 2006. PMID: 16997000

10

ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein beta-subunit.

Kao HJ, Cheng CF, Chen YH, Hung SI, Huang CC, Millington D, Kikuchi T, Wu JY, Chen YT. Kao HJ, et al. Among authors: wu jy. Hum Mol Genet. 2006 Dec 15;15(24):3569-77. doi: 10.1093/hmg/ddl433. Epub 2006 Nov 20. Hum Mol Genet. 2006. PMID: 17116638

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