Xie W - Search Results

1

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing.

Chen S, Lau TK, Zhang C, Xu C, Xu Z, Hu P, Xu J, Huang H, Pan L, Jiang F, Chen F, Pan X, Xie W, Liu P, Li X, Zhang L, Li S, Li Y, Xu X, Wang W, Wang J, Jiang H, Zhang X. Chen S, et al. Among authors: xie w. Prenat Diagn. 2013 Jun;33(6):584-90. doi: 10.1002/pd.4110. Prenat Diagn. 2013. PMID: 23592436

2

Rapid detection of aneuploidies on a benchtop sequencing platform.

Xie W, Tan Y, Li X, Lin G, Jiang H, Chen F, Zhang C, Gong F, Pan X, Chen S, Lu G, Wang W, Zhang X. Xie W, et al. Prenat Diagn. 2013 Mar;33(3):232-7. doi: 10.1002/pd.4049. Epub 2013 Jan 28. Prenat Diagn. 2013. PMID: 23359364

3

Effective noninvasive zygosity determination by maternal plasma target region sequencing.

Zheng J, Xu C, Guo J, Wei Y, Ge H, Li X, Zhang C, Jiang H, Pan L, Tang W, Xie W, Zhang H, Zhao Y, Jiang F, Chen S, Wang W, Xu X, Chen F, Huang H, Jiang H. Zheng J, et al. Among authors: xie w. PLoS One. 2013 Jun 10;8(6):e65050. doi: 10.1371/journal.pone.0065050. Print 2013. PLoS One. 2013. PMID: 23762285 Free PMC article.

4

Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies.

Huang X, Zheng J, Chen M, Zhao Y, Zhang C, Liu L, Xie W, Shi S, Wei Y, Lei D, Xu C, Wu Q, Guo X, Shi X, Zhou Y, Liu Q, Gao Y, Jiang F, Zhang H, Su F, Ge H, Li X, Pan X, Chen S, Chen F, Fang Q, Jiang H, Lau TK, Wang W. Huang X, et al. Among authors: xie w. Prenat Diagn. 2014 Apr;34(4):335-40. doi: 10.1002/pd.4303. Epub 2014 Feb 3. Prenat Diagn. 2014. PMID: 24357023

5

PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing.

Li X, Chen S, Xie W, Vogel I, Choy KW, Chen F, Christensen R, Zhang C, Ge H, Jiang H, Yu C, Huang F, Wang W, Jiang H, Zhang X. Li X, et al. Among authors: xie w. PLoS One. 2014 Jan 21;9(1):e85096. doi: 10.1371/journal.pone.0085096. eCollection 2014. PLoS One. 2014. PMID: 24465483 Free PMC article.

6

Performance comparison between rapid sequencing platforms for ultra-low coverage sequencing strategy.

Chen S, Li S, Xie W, Li X, Zhang C, Jiang H, Zheng J, Pan X, Zheng H, Liu JS, Deng Y, Chen F, Jiang H. Chen S, et al. Among authors: xie w. PLoS One. 2014 Mar 20;9(3):e92192. doi: 10.1371/journal.pone.0092192. eCollection 2014. PLoS One. 2014. PMID: 24651575 Free PMC article.

7

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness.

Meng M, Li X, Ge H, Chen F, Han M, Zhang Y, Kang D, Xie W, Gao Z, Pan X, Dai P, Chi F, Chen S, Liu P, Zhang C, Cao J, Jiang H, Xu X, Wang W, Duan T. Meng M, et al. Among authors: xie w. Genet Med. 2014 Dec;16(12):972-6. doi: 10.1038/gim.2014.51. Epub 2014 May 15. Genet Med. 2014. PMID: 24830326 Free article.

8

Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma.

Xu Y, Li X, Ge HJ, Xiao B, Zhang YY, Ying XM, Pan XY, Wang L, Xie WW, Ni L, Chen SP, Jiang WT, Liu P, Ye H, Cao Y, Zhang JM, Liu Y, Yang ZJ, Chen YW, Chen F, Jiang H, Ji X. Xu Y, et al. Genet Med. 2015 Nov;17(11):889-96. doi: 10.1038/gim.2014.207. Epub 2015 Feb 5. Genet Med. 2015. PMID: 25654318 Free article.

9

Copy-Number Variants Detection by Low-Pass Whole-Genome Sequencing.

Dong Z, Xie W, Chen H, Xu J, Wang H, Li Y, Wang J, Chen F, Choy KW, Jiang H. Dong Z, et al. Among authors: xie w. Curr Protoc Hum Genet. 2017 Jul 11;94:8.17.1-8.17.16. doi: 10.1002/cphg.43. Curr Protoc Hum Genet. 2017. PMID: 28696555

10

An Advanced Model to Precisely Estimate the Cell-Free Fetal DNA Concentration in Maternal Plasma.

Kang X, Xia J, Wang Y, Xu H, Jiang H, Xie W, Chen F, Zeng P, Li X, Xie Y, Liu H, Huang G, Chen D, Liu P, Jiang H, Zhang X. Kang X, et al. Among authors: xie y, xie w. PLoS One. 2016 Sep 23;11(9):e0161928. doi: 10.1371/journal.pone.0161928. eCollection 2016. PLoS One. 2016. PMID: 27662469 Free PMC article.

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