Wu-Chou YH - Search Results

1

NOTCH1 mutations as prognostic marker in oral squamous cell carcinoma.

Wu-Chou YH, Hsieh CH, Liao CT, Lin YT, Fan WL, Yang CH. Wu-Chou YH, et al. Pathol Res Pract. 2021 Jul;223:153474. doi: 10.1016/j.prp.2021.153474. Epub 2021 May 10. Pathol Res Pract. 2021. PMID: 33993060

2

Genetic diagnosis of neurofibromatosis type 1: targeted next- generation sequencing with Multiple Ligation-Dependent Probe Amplification analysis.

Wu-Chou YH, Hung TC, Lin YT, Cheng HW, Lin JL, Lin CH, Yu CC, Chen KT, Yeh TH, Chen YR. Wu-Chou YH, et al. J Biomed Sci. 2018 Oct 5;25(1):72. doi: 10.1186/s12929-018-0474-9. J Biomed Sci. 2018. PMID: 30290804 Free PMC article.

3

Association Studies Between Regulatory Regions of IRF6/TP63 Genes and Nonsyndromic Oral Clefts.

Wu-Chou YH, Lu YC, Chen KP, Chang HF, Lin YT, Lo LJ. Wu-Chou YH, et al. Cleft Palate Craniofac J. 2019 Jul;56(6):778-785. doi: 10.1177/1055665618809244. Epub 2018 Nov 12. Cleft Palate Craniofac J. 2019. PMID: 30419764

4

The SNP rs560426 Within ABCA4-ARHGAP29 Locus and the Risk of Nonsyndromic Oral Clefts.

Wu-Chou YH, Chen KP, Lu YC, Lin YT, Chang HF, Lo LJ. Wu-Chou YH, et al. Cleft Palate Craniofac J. 2020 Jun;57(6):671-677. doi: 10.1177/1055665619899764. Epub 2020 Jan 17. Cleft Palate Craniofac J. 2020. PMID: 31950859

5

A combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.

Wu-Chou YH, Lo LJ, Chen KT, Chang CS, Chen YR. Wu-Chou YH, et al. BMC Med Genet. 2013 Mar 20;14:37. doi: 10.1186/1471-2350-14-37. BMC Med Genet. 2013. PMID: 23510002 Free PMC article.

6

PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease.

Lu CS, Lai SC, Wu RM, Weng YH, Huang CL, Chen RS, Chang HC, Wu-Chou YH, Yeh TH. Lu CS, et al. Am J Med Genet B Neuropsychiatr Genet. 2012 Mar;159B(2):183-91. doi: 10.1002/ajmg.b.32012. Epub 2011 Dec 27. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22213678

7

Targeted Next Generation Sequencing for Genetic Mutations of Dilated Cardiomyopathy.

Yeh JK, Liu WH, Wang CY, Lu JJ, Chen CH, Wu-Chou YH, Chang PY, Chang SC, Yang CH, Tsai ML, Ho MY, Hsieh IC, Wen MS. Yeh JK, et al. Among authors: wu chou yh. Acta Cardiol Sin. 2019 Nov;35(6):571-584. doi: 10.6515/ACS.201911_35(6).20190402A. Acta Cardiol Sin. 2019. PMID: 31879508 Free PMC article.

8

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.

Bishop MR, Diaz Perez KK, Sun M, Ho S, Chopra P, Mukhopadhyay N, Hetmanski JB, Taub MA, Moreno-Uribe LM, Valencia-Ramirez LC, Restrepo Muñeton CP, Wehby G, Hecht JT, Deleyiannis F, Weinberg SM, Wu-Chou YH, Chen PK, Brand H, Epstein MP, Ruczinski I, Murray JC, Beaty TH, Feingold E, Lipinski RJ, Cutler DJ, Marazita ML, Leslie EJ. Bishop MR, et al. Among authors: wu chou yh. Am J Hum Genet. 2020 Jul 2;107(1):124-136. doi: 10.1016/j.ajhg.2020.05.018. Epub 2020 Jun 22. Am J Hum Genet. 2020. PMID: 32574564 Free PMC article.

9

Novel PKD1 and PKD2 mutations in Taiwanese patients with autosomal dominant polycystic kidney disease.

Chang MY, Chen HM, Jenq CC, Lee SY, Chen YM, Tian YC, Chen YC, Hung CC, Fang JT, Yang CW, Wu-Chou YH. Chang MY, et al. J Hum Genet. 2013 Nov;58(11):720-7. doi: 10.1038/jhg.2013.91. Epub 2013 Aug 29. J Hum Genet. 2013. PMID: 23985799

10

Influence of age on adenomatous polyposis coli and p53 mutation frequency in sporadic colorectal cancer-rarity of co-occurrence of mutations in APC, K-ras, and p53 genes.

Chiang JM, Wu Chou YH, Ma SC, Chen JR. Chiang JM, et al. Virchows Arch. 2004 Nov;445(5):465-71. doi: 10.1007/s00428-004-1116-z. Epub 2004 Sep 24. Virchows Arch. 2004. PMID: 15449054

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