Yang YM - Search Results

1

Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease.

Liu B, Chen SC, Yang YM, Yan K, Qian YQ, Zhang JY, Hu YT, Dong MY, Jin F, Huang HF, Xu CM. Liu B, et al. Among authors: yang ym. Sci Rep. 2015 Dec 3;5:17468. doi: 10.1038/srep17468. Sci Rep. 2015. PMID: 26632257 Free PMC article.

2

Association between premature ovarian failure, polymorphisms in MTHFR and MTRR genes and serum homocysteine concentration.

Hou N, Chen S, Chen F, Jiang M, Zhang J, Yang Y, Zhu B, Bai X, Hu Y, Huang H, Xu C. Hou N, et al. Reprod Biomed Online. 2016 Apr;32(4):407-13. doi: 10.1016/j.rbmo.2016.01.009. Epub 2016 Jan 29. Reprod Biomed Online. 2016. PMID: 26874989

3

Corrigendum: Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease.

Liu B, Chen SC, Yang YM, Yan K, Qian YQ, Zhang JY, Hu YT, Dong MY, Jin F, Huang HF, Xu CM. Liu B, et al. Among authors: yang ym. Sci Rep. 2016 Feb 23;6:21578. doi: 10.1038/srep21578. Sci Rep. 2016. PMID: 26902268 Free PMC article. No abstract available.

4

A feasible diagnostic approach for the translocation carrier from the indication of products of conception.

Qian YQ, Fu XY, Wang XQ, Luo YQ, Chen M, Yan K, Yang YM, Liu B, Wang LY, Huang YZ, Li HG, Pan HY, Jin F, Dong MY. Qian YQ, et al. Among authors: yang ym. Mol Cytogenet. 2018 Jan 30;11:12. doi: 10.1186/s13039-018-0362-8. eCollection 2018. Mol Cytogenet. 2018. PMID: 29422950 Free PMC article.

5

Detection of fetal subchromosomal aberration with cell-free DNA screening led to diagnosis of parental translocation: Review of 11344 consecutive cases in a university hospital.

Qian YQ, Wang XQ, Chen M, Luo YQ, Yan K, Yang YM, Liu B, Wang LY, Huang YZ, Li HG, Pan HY, Jin F, Dong MY. Qian YQ, et al. Among authors: yang ym. Eur J Med Genet. 2019 Feb;62(2):115-123. doi: 10.1016/j.ejmg.2018.06.012. Epub 2018 Jun 19. Eur J Med Genet. 2019. PMID: 29929010

6

The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies.

Li H, Lei Y, Zhu H, Luo Y, Qian Y, Chen M, Sun Y, Yan K, Yang Y, Liu B, Wang L, Huang Y, Hu J, Xu J, Dong M. Li H, et al. Mol Cytogenet. 2018 Dec 3;11:59. doi: 10.1186/s13039-018-0407-z. eCollection 2018. Mol Cytogenet. 2018. PMID: 30524505 Free PMC article.

7

Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform.

Wang LY, Rao XQ, Luo YQ, Liu B, Peng CF, Chen D, Yan K, Qian YQ, Yang YM, Huang YZ, Chen M, Sun YX, Li HG, Ye YH, Jin F, Liu HL, Dong MY. Wang LY, et al. Among authors: yang ym. Hum Genomics. 2019 Jan 3;13(1):1. doi: 10.1186/s40246-018-0187-x. Hum Genomics. 2019. PMID: 30606250 Free PMC article.

8

Paternal Low-Level Mosaicism-Caused SATB2-Associated Syndrome.

Qian Y, Liu J, Yang Y, Chen M, Jin C, Chen P, Lei Y, Pan H, Dong M. Qian Y, et al. Front Genet. 2019 Jul 2;10:630. doi: 10.3389/fgene.2019.00630. eCollection 2019. Front Genet. 2019. PMID: 31333717 Free PMC article.

9

Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene.

Yang YM, Yan K, Liu B, Chen M, Wang LY, Huang YZ, Qian YQ, Sun YX, Li HG, Dong MY. Yang YM, et al. J Zhejiang Univ Sci B. 2019 Sept.;20(9):753-765. doi: 10.1631/jzus.B1800541. J Zhejiang Univ Sci B. 2019. PMID: 31379145 Free PMC article.

10

[Prenatal diagnosis of a fetus with Phelan-McDermid syndrome].

Luo Y, Qian Y, Wang L, Yang Y, Sun Y, Jin F, Dong M. Luo Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Aug 10;36(8):841-843. doi: 10.3760/cma.j.issn.1003-9406.2019.08.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31400142 Chinese.

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