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A reliable, high-resolution and high-throughput genotyping method for HLA-DRB1.
Yang F, Jiang F, Chai X, Guo Y, Lan Z, Yuan Y, Huang C, Zhu Z, Li H, Du B, Wang J, Zhou L, Chen Z, Yang L, Zhou M, Zeng H, Xu Y, Wang W. Yang F, et al. Among authors: wang w, wang j. Hum Immunol. 2015 Jun;76(6):397-401. doi: 10.1016/j.humimm.2015.04.003. Epub 2015 Apr 15. Hum Immunol. 2015. PMID: 25890007
A short-read multiplex sequencing method for reliable, cost-effective and high-throughput genotyping in large-scale studies.
Cao H, Wang Y, Zhang W, Chai X, Zhang X, Chen S, Yang F, Zhang C, Guo Y, Liu Y, Tang Z, Chen C, Xue Y, Zhen H, Xu Y, Rao B, Liu T, Zhao M, Zhang W, Li Y, Zhang X, Tellier LC, Krogh A, Kristiansen K, Wang J, Li J. Cao H, et al. Among authors: wang j, wang y. Hum Mutat. 2013 Dec;34(12):1715-20. doi: 10.1002/humu.22439. Epub 2013 Oct 7. Hum Mutat. 2013. PMID: 24014314
Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies.
Jiang F, Ren J, Chen F, Zhou Y, Xie J, Dan S, Su Y, Xie J, Yin B, Su W, Zhang H, Wang W, Chai X, Lin L, Guo H, Li Q, Li P, Yuan Y, Pan X, Li Y, Liu L, Chen H, Xuan Z, Chen S, Zhang C, Zhang H, Tian Z, Zhang Z, Jiang H, Zhao L, Zheng W, Li S, Li Y, Wang J, Wang J, Zhang X. Jiang F, et al. Among authors: wang w, wang j. BMC Med Genomics. 2012 Dec 1;5:57. doi: 10.1186/1755-8794-5-57. BMC Med Genomics. 2012. PMID: 23198897 Free PMC article.
Targeted next-generation sequencing as a comprehensive test for patients with and female carriers of DMD/BMD: a multi-population diagnostic study.
Wei X, Dai Y, Yu P, Qu N, Lan Z, Hong X, Sun Y, Yang G, Xie S, Shi Q, Zhou H, Zhu Q, Chu Y, Yao F, Wang J, He J, Yang Y, Liang Y, Yang Y, Qi M, Yang L, Wang W, Wu H, Duan J, Shen C, Wang J, Cui L, Yi X. Wei X, et al. Among authors: wang w, wang j. Eur J Hum Genet. 2014 Jan;22(1):110-8. doi: 10.1038/ejhg.2013.82. Epub 2013 Jun 12. Eur J Hum Genet. 2014. PMID: 23756440 Free PMC article.
Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors.
Dan S, Wang W, Ren J, Li Y, Hu H, Xu Z, Lau TK, Xie J, Zhao W, Huang H, Xie J, Sun L, Zhang X, Wang W, Liao S, Qiang R, Cao J, Zhang Q, Zhou Y, Zhu H, Zhong M, Guo Y, Lin L, Gao Z, Yao H, Zhang H, Zhao L, Jiang F, Chen F, Jiang H, Li S, Li Y, Wang J, Wang J, Duan T, Su Y, Zhang X. Dan S, et al. Among authors: wang w, wang j. Prenat Diagn. 2012 Dec;32(13):1225-32. doi: 10.1002/pd.4002. Epub 2012 Nov 9. Prenat Diagn. 2012. PMID: 23138752 Clinical Trial.
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