Zhang Y - Search Results

1

Temporal persistence of residual fetal cell-free DNA from a deceased cotwin after selective fetal reduction in dichorionic diamniotic twin pregnancies.

Chen M, Su F, Wang J, Zhou L, Liu Q, Chai X, Yuan Y, Cen M, Wu Y, Wang Y, Chen F, Zhang Y, Chen D, Gao Y. Chen M, et al. Among authors: zhang y. Prenat Diagn. 2021 Nov;41(12):1602-1610. doi: 10.1002/pd.5898. Epub 2021 Feb 8. Prenat Diagn. 2021. PMID: 33555061

2

Non-invasive fetal sex determination by maternal plasma sequencing and application in X-linked disorder counseling.

Pan X, Zhang C, Li X, Chen S, Ge H, Zhang Y, Chen F, Jiang H, Jiang F, Zhang H, Wang W, Zhang X. Pan X, et al. Among authors: zhang c, zhang h, zhang x, zhang y. J Matern Fetal Neonatal Med. 2014 Dec;27(18):1829-33. doi: 10.3109/14767058.2014.885942. Epub 2014 Feb 20. J Matern Fetal Neonatal Med. 2014. PMID: 24444365

3

Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing.

Ma D, Ge H, Li X, Jiang T, Chen F, Zhang Y, Hu P, Chen S, Zhang J, Ji X, Xu X, Jiang H, Chen M, Wang W, Xu Z. Ma D, et al. Among authors: zhang j, zhang y. Gene. 2014 Jul 10;544(2):252-8. doi: 10.1016/j.gene.2014.04.055. Epub 2014 Apr 24. Gene. 2014. PMID: 24768736

4

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: zhang c, zhang y. 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.

5

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. Among authors: zhang jm, zhang yy. 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.

6

Noninvasive prenatal paternity testing by maternal plasma DNA sequencing in twin pregnancies.

Xie Y, Qu N, Lin S, Jiang H, Zhang Y, Zhang X, Liang H, Chen F, Ou X. Xie Y, et al. Among authors: zhang x, zhang y. Electrophoresis. 2020 Jun;41(12):1095-1102. doi: 10.1002/elps.202000036. Epub 2020 May 14. Electrophoresis. 2020. PMID: 32249439

7

Simultaneous detection of fetal aneuploidy, de novo FGFR3 mutations and paternally derived β-thalassemia by a novel method of noninvasive prenatal testing.

Yang L, Wu Y, Hu Z, Zhang H, Pu D, Yan H, Zhang S, Jiang H, Liu Q, Yuan Y, Zhang Y, Chen F, Lu Y, Pan S, Lin L, Gao Y. Yang L, et al. Among authors: zhang s, zhang h, zhang y. Prenat Diagn. 2021 Mar;41(4):440-448. doi: 10.1002/pd.5879. Epub 2021 Jan 21. Prenat Diagn. 2021. PMID: 33340121 Free PMC article.

8

The Setup and Application of Reference Material in Sequencing-Based Noninvasive Prenatal Testing.

Qu S, Zhang Y, Yang X, Tan Y, Li M, Yang X, Zhou L, Chen D, Chen Y, Yan M, Wang Q, Yu T, Sun N, Jiang H, Su F, Di Y, Lin G, Yuan Y, Chen F, Mu F, Huang J. Qu S, et al. Among authors: zhang y. Gynecol Obstet Invest. 2021;86(1-2):123-131. doi: 10.1159/000513472. Epub 2021 Mar 30. Gynecol Obstet Invest. 2021. PMID: 33784691

9

Non-Invasive Prenatal Diagnosis of Monogenic Disorders Through Bayesian- and Haplotype-Based Prediction of Fetal Genotype.

Li J, Lu J, Su F, Yang J, Ju J, Lin Y, Xu J, Qi Y, Hou Y, Wu J, He W, Yang Z, Wu Y, Tang Z, Huang Y, Zhang G, Yang Y, Long Z, Cheng X, Liu P, Xia J, Zhang Y, Wang Y, Chen F, Zhang J, Zhao L, Jin X, Gao Y, Yin A. Li J, et al. Among authors: zhang g, zhang j, zhang y. Front Genet. 2022 Jul 1;13:911369. doi: 10.3389/fgene.2022.911369. eCollection 2022. Front Genet. 2022. PMID: 35846127 Free PMC article.

10

Simultaneous detection of genomic imbalance in patients receiving preimplantation genetic testing for monogenic diseases (PGT-M).

Yang L, Xu Y, Xia J, Yan H, Ding C, Shi Q, Wu Y, Liu P, Pan J, Zeng Y, Zhang Y, Chen F, Jiang H, Xu Y, Li W, Zhou C, Gao Y. Yang L, et al. Among authors: zhang y. Front Genet. 2022 Sep 29;13:976131. doi: 10.3389/fgene.2022.976131. eCollection 2022. Front Genet. 2022. PMID: 36246639 Free PMC article.

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