Chen YT - Search Results

1

Over-expression of AURKA, SKA3 and DSN1 contributes to colorectal adenoma to carcinoma progression.

Chuang TP, Wang JY, Jao SW, Wu CC, Chen JH, Hsiao KH, Lin CY, Chen SH, Su SY, Chen YJ, Chen YT, Wu DC, Li LH. Chuang TP, et al. Among authors: chen yj, chen jh, chen sh, chen yt. Oncotarget. 2016 Jul 19;7(29):45803-45818. doi: 10.18632/oncotarget.9960. Oncotarget. 2016. PMID: 27329586 Free PMC article.

2

Type II collagen gene variants and inherited osteonecrosis of the femoral head.

Liu YF, Chen WM, Lin YF, Yang RC, Lin MW, Li LH, Chang YH, Jou YS, Lin PY, Su JS, Huang SF, Hsiao KJ, Fann CS, Hwang HW, Chen YT, Tsai SF. Liu YF, et al. Among authors: chen wm, chen yt. N Engl J Med. 2005 Jun 2;352(22):2294-301. doi: 10.1056/NEJMoa042480. N Engl J Med. 2005. PMID: 15930420 Free article.

3

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

4

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: chen yt. BMC Bioinformatics. 2008 Apr 15;9:196. doi: 10.1186/1471-2105-9-196. BMC Bioinformatics. 2008. PMID: 18412951 Free PMC article.

5

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: chen yt. Hum Mutat. 2008 Aug;29(8):1055-62. doi: 10.1002/humu.20760. Hum Mutat. 2008. PMID: 18470944

6

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: chen yt. BMC Genet. 2008 Dec 24;9:92. doi: 10.1186/1471-2156-9-92. BMC Genet. 2008. PMID: 19108714 Free PMC article.

7

Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease.

Kishnani PS, Chuang TP, Bali D, Koeberl D, Austin S, Weinstein DA, Murphy E, Chen YT, Boyette K, Liu CH, Chen YT, Li LH. Kishnani PS, et al. Among authors: chen yt. Hum Mol Genet. 2009 Dec 15;18(24):4781-90. doi: 10.1093/hmg/ddp441. Epub 2009 Sep 16. Hum Mol Genet. 2009. PMID: 19762333

8

A new analysis tool for individual-level allele frequency for genomic studies.

Yang HC, Lin HC, Huang MC, Li LH, Pan WH, Wu JY, Chen YT. Yang HC, et al. Among authors: chen yt. BMC Genomics. 2010 Jul 5;11:415. doi: 10.1186/1471-2164-11-415. BMC Genomics. 2010. PMID: 20602748 Free PMC article.

9

Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome.

Chang CF, Li LH, Wang CH, Tsai FJ, Chen TC, Wu JY, Chen YT, Tsai AC. Chang CF, et al. Among authors: chen tc, chen yt. Am J Med Genet A. 2010 Sep;152A(9):2365-71. doi: 10.1002/ajmg.a.33580. Am J Med Genet A. 2010. PMID: 20803649

10

SAQC: SNP array quality control.

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

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