Yang WS - Search Results

1

Genotype-phenotype correlation in Taiwanese children with diazoxide-unresponsive congenital hyperinsulinism.

Lee CT, Tsai WH, Chang CC, Chen PC, Fann CS, Chang HK, Liu SY, Wu MZ, Chiu PC, Hsu WM, Yang WS, Lai LP, Tsai WY, Yang SB, Chen PL. Lee CT, et al. Among authors: yang sb, yang ws. Front Endocrinol (Lausanne). 2023 Nov 16;14:1283907. doi: 10.3389/fendo.2023.1283907. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 38033998 Free PMC article.

2

Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in Taiwan.

Chen PL, Fann CS, Chang CC, Wu IL, Chiu WY, Lin CY, Yang WS, Chang TC. Chen PL, et al. Among authors: yang ws. Clin Endocrinol (Oxf). 2007 May;66(5):646-51. doi: 10.1111/j.1365-2265.2007.02787.x. Clin Endocrinol (Oxf). 2007. PMID: 17492952

3

Human genetics of diabetes mellitus in Taiwan.

Chen PL, Yang WS. Chen PL, et al. Among authors: yang ws. Front Biosci (Landmark Ed). 2009 Jan 1;14(12):4535-45. doi: 10.2741/3546. Front Biosci (Landmark Ed). 2009. PMID: 19273368 Free article. Review.

4

The clinical implications of blood adiponectin in cardiometabolic disorders.

Chang LC, Huang KC, Wu YW, Kao HL, Chen CL, Lai LP, Hwang JJ, Yang WS. Chang LC, et al. Among authors: yang ws. J Formos Med Assoc. 2009 May;108(5):353-66. doi: 10.1016/S0929-6646(09)60079-6. J Formos Med Assoc. 2009. PMID: 19443289 Free article. Review.

5

Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles.

Chen PL, Fann CS, Chu CC, Chang CC, Chang SW, Hsieh HY, Lin M, Yang WS, Chang TC. Chen PL, et al. Among authors: yang ws. PLoS One. 2011 Jan 28;6(1):e16635. doi: 10.1371/journal.pone.0016635. PLoS One. 2011. PMID: 21307958 Free PMC article.

6

Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment.

Wu CC, Lin YH, Lu YC, Chen PJ, Yang WS, Hsu CJ, Chen PL. Wu CC, et al. Among authors: yang ws. PLoS One. 2013;8(2):e57369. doi: 10.1371/journal.pone.0057369. Epub 2013 Feb 22. PLoS One. 2013. PMID: 23451214 Free PMC article.

7

A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease.

Lin MT, Hsu CL; Taiwan Pediatric CV Group; Chen PL, Yang WS, Wang JK, Fann CS, Wu MH. Lin MT, et al. Among authors: yang ws. Transl Res. 2013 Jun;161(6):513-5. doi: 10.1016/j.trsl.2013.02.002. Epub 2013 Feb 27. Transl Res. 2013. PMID: 23454411 No abstract available.

8

Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population.

Hsieh AR, Chang SW, Chen PL, Chu CC, Hsiao CL, Yang WS, Chang CC, Wu JY, Chen YT, Chang TC, Fann CS. Hsieh AR, et al. Among authors: yang ws. BMC Genomics. 2014 Jan 29;15:81. doi: 10.1186/1471-2164-15-81. BMC Genomics. 2014. PMID: 24476119 Free PMC article.

9

A fault-tolerant method for HLA typing with PacBio data.

Chang CJ, Chen PL, Yang WS, Chao KM. Chang CJ, et al. Among authors: yang ws. BMC Bioinformatics. 2014 Sep 3;15(1):296. doi: 10.1186/1471-2105-15-296. BMC Bioinformatics. 2014. PMID: 25183223 Free PMC article.

10

Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.

Chen MJ, Wei SY, Yang WS, Wu TT, Li HY, Ho HN, Yang YS, Chen PL. Chen MJ, et al. Among authors: yang ys, yang ws. Hum Reprod. 2015 Jul;30(7):1732-42. doi: 10.1093/humrep/dev095. Epub 2015 Apr 29. Hum Reprod. 2015. PMID: 25924657

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