Wu JY - Search Results

1

Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese.

Wei CY, Yang JH, Yeh EC, Tsai MF, Kao HJ, Lo CZ, Chang LP, Lin WJ, Hsieh FJ, Belsare S, Bhaskar A, Su MW, Lee TC, Lin YL, Liu FT, Shen CY, Li LH, Chen CH, Wall JD, Wu JY, Kwok PY. Wei CY, et al. Among authors: wu jy. NPJ Genom Med. 2021 Feb 11;6(1):10. doi: 10.1038/s41525-021-00178-9. NPJ Genom Med. 2021. PMID: 33574314 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

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.

4

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

5

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

6

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

7

MPDA: microarray pooled DNA analyzer.

Yang HC, Huang MC, Li LH, Lin CH, Yu AL, Diccianni MB, Wu JY, Chen YT, Fann CS. Yang HC, et al. Among authors: wu jy. BMC Bioinformatics. 2008 Apr 15;9:196. doi: 10.1186/1471-2105-9-196. BMC Bioinformatics. 2008. PMID: 18412951 Free PMC article.

8

Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.

Lin CH, Huang MC, Li LH, Wu JY, Chen YT, Fann CS. Lin CH, et al. Among authors: wu jy. Hum Mutat. 2008 Aug;29(8):1055-62. doi: 10.1002/humu.20760. Hum Mutat. 2008. PMID: 18470944

9

Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.

Lee MT, Tsai AC, Chou CH, Sun FM, Huang LC, Yen P, Lin CC, Liu CY, Wu JY, Chen YT, Tsai FJ. Lee MT, et al. Among authors: wu jy. Genomic Med. 2008 Jan;2(1-2):45-9. doi: 10.1007/s11568-008-9024-y. Epub 2008 Aug 12. Genomic Med. 2008. PMID: 18696259 Free PMC article.

10

A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan.

Lin CH, Li LH, Ho SF, Chuang TP, Wu JY, Chen YT, Fann CS. Lin CH, et al. Among authors: wu jy. BMC Genet. 2008 Dec 24;9:92. doi: 10.1186/1471-2156-9-92. BMC Genet. 2008. PMID: 19108714 Free PMC article.

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