Zhang H - Search Results

1

An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.

Tu C, Wang Y, Nie H, Meng L, Wang W, Li Y, Li D, Zhang H, Lu G, Lin G, Tan YQ, Du J. Tu C, et al. Among authors: zhang h. Clin Genet. 2020 May;97(5):741-746. doi: 10.1111/cge.13712. Epub 2020 Feb 10. Clin Genet. 2020. PMID: 32017041

2

A homozygous FANCM frameshift pathogenic variant causes male infertility.

Yin H, Ma H, Hussain S, Zhang H, Xie X, Jiang L, Jiang X, Iqbal F, Bukhari I, Jiang H, Ali A, Zhong L, Li T, Fan S, Zhang B, Gao J, Li Y, Nazish J, Khan T, Khan M, Zubair M, Hao Q, Fang H, Huang J, Huleihel M, Sha J, Pandita TK, Zhang Y, Shi Q. Yin H, et al. Among authors: zhang b, zhang h, zhang y. Genet Med. 2019 Jan;21(1):62-70. doi: 10.1038/s41436-018-0015-7. Epub 2018 Jun 12. Genet Med. 2019. PMID: 29895858 Free PMC article.

3

Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.

Wang Y, Tu C, Nie H, Meng L, Li D, Wang W, Zhang H, Lu G, Lin G, Tan YQ, Du J. Wang Y, et al. Among authors: zhang h. J Assist Reprod Genet. 2020 Apr;37(4):811-820. doi: 10.1007/s10815-020-01735-4. Epub 2020 Mar 13. J Assist Reprod Genet. 2020. PMID: 32170493 Free PMC article.

4

Novel mutations in PMFBP1, TSGA10 and SUN5: Expanding the spectrum of mutations that may cause acephalic spermatozoa.

Liu G, Wang N, Zhang H, Yin S, Dai H, Lin G, Li W. Liu G, et al. Among authors: zhang h. Clin Genet. 2020 Jun;97(6):938-939. doi: 10.1111/cge.13747. Epub 2020 Apr 13. Clin Genet. 2020. PMID: 32285443 No abstract available.

5

Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice.

Zhang B, Khan I, Liu C, Ma A, Khan A, Zhang Y, Zhang H, Kakakhel MBS, Zhou J, Zhang W, Li Y, Ali A, Jiang X, Murtaza G, Khan R, Zubair M, Yuan L, Khan M, Wang L, Zhang F, Wang X, Ma H, Shi Q. Zhang B, et al. Among authors: zhang f, zhang w, zhang h, zhang y. Clin Genet. 2021 Jan;99(1):176-186. doi: 10.1111/cge.13866. Epub 2020 Nov 2. Clin Genet. 2021. PMID: 33070343

6

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility.

Hu TY, Zhang H, Meng LL, Yuan SM, Tu CF, Du J, Lu GX, Lin G, Nie HC, Tan YQ. Hu TY, et al. Among authors: zhang h. Hum Mutat. 2021 Jan;42(1):31-36. doi: 10.1002/humu.24138. Epub 2020 Nov 15. Hum Mutat. 2021. PMID: 33169450

7

Trace the profile and function of circular RNAs in Sertoli cell only syndrome.

Zhu F, Luo Y, Bo H, Gong G, Tang R, Fan J, Zhang H, Liu G, Zhu W, Tan Y, He Z, Fan L. Zhu F, et al. Among authors: zhang h. Genomics. 2021 Jul;113(4):1845-1854. doi: 10.1016/j.ygeno.2021.04.022. Epub 2021 Apr 15. Genomics. 2021. PMID: 33865957 Free article.

8

Patients with acephalic spermatozoa syndrome linked to novel TSGA10/PMFBP1 variants have favorable pregnancy outcomes from intracytoplasmic sperm injection.

Liu G, Xing X, Zhang H, Zhu W, Lin G, Lu G, Li W. Liu G, et al. Among authors: zhang h. Clin Genet. 2021 Sep;100(3):334-339. doi: 10.1111/cge.14007. Epub 2021 Jun 21. Clin Genet. 2021. PMID: 34089195

9

Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella.

Ma H, Zhang B, Khan A, Zhao D, Ma A, Zhou J, Khan I, Khan K, Zhang H, Zhang Y, Jiang X, Dil S, Zeb A, Rahim F, Shi Q. Ma H, et al. Among authors: zhang b, zhang h, zhang y. Hum Mol Genet. 2021 Oct 13;30(21):1977-1984. doi: 10.1093/hmg/ddab165. Hum Mol Genet. 2021. PMID: 34155512

10

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.

Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, Lu S, Liu C, Tian S, Meng L, Wang W, Tan C, Nie H, Li D, Zhang H, Gong F, Hu L, Lu G, Xu W, Lin G, Zhang F, Cao Y, Tan YQ. Tu C, et al. Among authors: zhang q, zhang f, zhang h. Am J Hum Genet. 2021 Aug 5;108(8):1466-1477. doi: 10.1016/j.ajhg.2021.06.010. Epub 2021 Jul 7. Am J Hum Genet. 2021. PMID: 34237282 Free PMC article.

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