Yang W - Search Results

1

Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.

Chau JFT, Yu MHC, Chui MMC, Yeung CCW, Kwok AWC, Zhuang X, Lee R, Fung JLF, Lee M, Mak CCY, Ng NYT, Chung CCY, Chan MCY, Tsang MHY, Chan JCK, Chan KYK, Kan ASY, Chung PHY, Yang W, Lee SL, Chan GCF, Tam PKH, Lau YL, Yeung KS, Chung BHY, Tang CSM. Chau JFT, et al. Among authors: yang w. NPJ Genom Med. 2022 Mar 21;7(1):23. doi: 10.1038/s41525-022-00287-z. NPJ Genom Med. 2022. PMID: 35314707 Free PMC article.

2

Predicting the number and sizes of IBD regions among family members and evaluating the family size requirement for linkage studies.

Yang W, Wang Z, Wang L, Sham PC, Huang P, Lau YL. Yang W, et al. Eur J Hum Genet. 2008 Dec;16(12):1535-43. doi: 10.1038/ejhg.2008.116. Epub 2008 Jun 25. Eur J Hum Genet. 2008. PMID: 18575462

3

Promoter-sharing by different genes in human genome--CPNE1 and RBM12 gene pair as an example.

Yang W, Ng P, Zhao M, Wong TK, Yiu SM, Lau YL. Yang W, et al. BMC Genomics. 2008 Oct 3;9:456. doi: 10.1186/1471-2164-9-456. BMC Genomics. 2008. PMID: 18831769 Free PMC article.

4

ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai.

Yang W, Zhao M, Hirankarn N, Lau CS, Mok CC, Chan TM, Wong RW, Lee KW, Mok MY, Wong SN, Avihingsanon Y, Lin IO, Lee TL, Ho MH, Lee PP, Wong WH, Sham PC, Lau YL. Yang W, et al. Hum Mol Genet. 2009 Jun 1;18(11):2063-70. doi: 10.1093/hmg/ddp118. Epub 2009 Mar 13. Hum Mol Genet. 2009. PMID: 19286673 Free PMC article.

5

Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes.

Chung BH, Lam ST, Tong TM, Li SY, Lun KS, Chan DH, Fok SF, Or JS, Smith DK, Yang W, Lau YL. Chung BH, et al. Among authors: yang w. Am J Med Genet A. 2009 Jul;149A(7):1452-9. doi: 10.1002/ajmg.a.32918. Am J Med Genet A. 2009. PMID: 19533785

6

ELF1 is associated with systemic lupus erythematosus in Asian populations.

Yang J, Yang W, Hirankarn N, Ye DQ, Zhang Y, Pan HF, Mok CC, Chan TM, Wong RW, Mok MY, Lee KW, Wong SN, Leung AM, Li XP, Avihingsanon Y, Rianthavorn P, Deekajorndej T, Suphapeetiporn K, Shotelersuk V, Baum L, Kwan P, Lee TL, Ho MH, Lee PP, Wong WH, Zeng S, Zhang J, Wong CM, Ng IO, Garcia-Barceló MM, Cherny SS, Tam PK, Sham PC, Lau CS, Lau YL. Yang J, et al. Among authors: yang w. Hum Mol Genet. 2011 Feb 1;20(3):601-7. doi: 10.1093/hmg/ddq474. Epub 2010 Nov 2. Hum Mol Genet. 2011. PMID: 21044949

7

Homozygosity mapping on a single patient: identification of homozygous regions of recent common ancestry by using population data.

Zhang L, Yang W, Ying D, Cherny SS, Hildebrandt F, Sham PC, Lau YL. Zhang L, et al. Among authors: yang w. Hum Mutat. 2011 Mar;32(3):345-53. doi: 10.1002/humu.21432. Hum Mutat. 2011. PMID: 21309031 Free PMC article.

8

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.

Guo Y, Baum LW, Sham PC, Wong V, Ng PW, Lui CH, Sin NC, Tsoi TH, Tang CS, Kwan JS, Yip BH, Xiao SM, Thomas GN, Lau YL, Yang W, Cherny SS, Kwan P. Guo Y, et al. Among authors: yang w. Hum Mol Genet. 2012 Mar 1;21(5):1184-9. doi: 10.1093/hmg/ddr550. Epub 2011 Nov 24. Hum Mol Genet. 2012. PMID: 22116939

9

PriVar: a toolkit for prioritizing SNVs and indels from next-generation sequencing data.

Zhang L, Zhang J, Yang J, Ying D, Lau YL, Yang W. Zhang L, et al. Among authors: yang w, yang j. Bioinformatics. 2013 Jan 1;29(1):124-5. doi: 10.1093/bioinformatics/bts627. Epub 2012 Oct 25. Bioinformatics. 2013. PMID: 23104884

10

Genome-wide copy number variation study in anorectal malformations.

Wong EH, Cui L, Ng CL, Tang CS, Liu XL, So MT, Yip BH, Cheng G, Zhang R, Tang WK, Yang W, Lau YL, Baum L, Kwan P, Sun LD, Zuo XB, Ren YQ, Yin XY, Miao XP, Liu J, Lui VC, Ngan ES, Yuan ZW, Zhang SW, Xia J, Wang H, Sun XB, Wang R, Chang T, Chan IH, Chung PH, Zhang XJ, Wong KK, Cherny SS, Sham PC, Tam PK, Garcia-Barcelo MM. Wong EH, et al. Among authors: yang w. Hum Mol Genet. 2013 Feb 1;22(3):621-31. doi: 10.1093/hmg/dds451. Epub 2012 Oct 29. Hum Mol Genet. 2013. PMID: 23108157

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