Yang CF - Search Results

1

Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci.

Kelly TN, Takeuchi F, Tabara Y, Edwards TL, Kim YJ, Chen P, Li H, Wu Y, Yang CF, Zhang Y, Gu D, Katsuya T, Ohkubo T, Gao YT, Go MJ, Teo YY, Lu L, Lee NR, Chang LC, Peng H, Zhao Q, Nakashima E, Kita Y, Shu XO, Kim NH, Tai ES, Wang Y, Adair LS, Chen CH, Zhang S, Li C, Nabika T, Umemura S, Cai Q, Cho YS, Wong TY, Zhu J, Wu JY, Gao X, Hixson JE, Cai H, Lee J, Cheng CY, Rao DC, Xiang YB, Cho MC, Han BG, Wang A, Tsai FJ, Mohlke K, Lin X, Ikram MK, Lee JY, Zheng W, Tetsuro M, Kato N, He J. Kelly TN, et al. Among authors: yang cf. Hypertension. 2013 Nov;62(5):853-9. doi: 10.1161/HYPERTENSIONAHA.113.01148. Epub 2013 Sep 3. Hypertension. 2013. PMID: 24001895 Free PMC article.

2

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: yang cf. PLoS Genet. 2010 Feb 19;6(2):e1000847. doi: 10.1371/journal.pgen.1000847. PLoS Genet. 2010. PMID: 20174558 Free PMC article.

3

Three novel beta-galactosidase gene mutations in Han Chinese patients with GM1 gangliosidosis are correlated with disease severity.

Yang CF, Wu JY, Tsai FJ. Yang CF, et al. J Biomed Sci. 2010 Sep 30;17(1):79. doi: 10.1186/1423-0127-17-79. J Biomed Sci. 2010. PMID: 20920281 Free PMC article.

4

Pharmacogenetics of dipeptidyl peptidase 4 inhibitors in a Taiwanese population with type 2 diabetes.

Liao WL, Lee WJ, Chen CC, Lu CH, Chen CH, Chou YC, Lee IT, Sheu WH, Wu JY, Yang CF, Wang CH, Tsai FJ. Liao WL, et al. Among authors: yang cf. Oncotarget. 2017 Mar 14;8(11):18050-18058. doi: 10.18632/oncotarget.14951. Oncotarget. 2017. PMID: 28160554 Free PMC article.

5

Homozygosity Mapping and Whole-Genome Sequencing Links a Missense Mutation in POMGNT1 to Autosomal Recessive Retinitis Pigmentosa.

Wang NH, Chen SJ, Yang CF, Chen HW, Chuang HP, Lu YH, Chen CH, Wu JY, Niu DM, Chen YT. Wang NH, et al. Among authors: yang cf. Invest Ophthalmol Vis Sci. 2016 Jul 1;57(8):3601-9. doi: 10.1167/iovs.16-19463. Invest Ophthalmol Vis Sci. 2016. PMID: 27391550

6

Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.

Yang CF, Wang CH, Siong H'ng W, Chang CP, Lin WD, Chen YT, Wu JY, Tsai FJ. Yang CF, et al. Hum Mutat. 2017 May;38(5):540-547. doi: 10.1002/humu.23186. Epub 2017 Feb 27. Hum Mutat. 2017. PMID: 28145000

7

Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

Yang CF, Lin SP, Chiang CP, Wu YH, H'ng WS, Chang CP, Chen YT, Wu JY. Yang CF, et al. Am J Hum Genet. 2018 Feb 1;102(2):219-232. doi: 10.1016/j.ajhg.2017.12.012. Epub 2018 Jan 11. Am J Hum Genet. 2018. PMID: 29336782 Free PMC article.

8

PSORS2 is due to mutations in CARD14.

Jordan CT, Cao L, Roberson ED, Pierson KC, Yang CF, Joyce CE, Ryan C, Duan S, Helms CA, Liu Y, Chen Y, McBride AA, Hwu WL, Wu JY, Chen YT, Menter A, Goldbach-Mansky R, Lowes MA, Bowcock AM. Jordan CT, et al. Among authors: yang cf. Am J Hum Genet. 2012 May 4;90(5):784-95. doi: 10.1016/j.ajhg.2012.03.012. Epub 2012 Apr 19. Am J Hum Genet. 2012. PMID: 22521418 Free PMC article.

9

Towards a reference genome that captures global genetic diversity.

Wong KHY, Ma W, Wei CY, Yeh EC, Lin WJ, Wang EHF, Su JP, Hsieh FJ, Kao HJ, Chen HH, Chow SK, Young E, Chu C, Poon A, Yang CF, Lin DS, Hu YF, Wu JY, Lee NC, Hwu WL, Boffelli D, Martin D, Xiao M, Kwok PY. Wong KHY, et al. Among authors: yang cf. Nat Commun. 2020 Oct 30;11(1):5482. doi: 10.1038/s41467-020-19311-w. Nat Commun. 2020. PMID: 33127893 Free PMC article.

10

Investigations of In₂O₃ Added SiC Semiconductive Thin Films and Manufacture of a Heterojunction Diode.

Liao CT, Kao CY, Su ZT, Lin YS, Wang YW, Yang CF. Liao CT, et al. Among authors: yang cf. Nanomaterials (Basel). 2024 May 19;14(10):881. doi: 10.3390/nano14100881. Nanomaterials (Basel). 2024. PMID: 38786836 Free PMC article.

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