Sha Y - Search Results

1

Novel mutations of TEX11 are associated with non-obstructive azoospermia.

Song J, Sha Y, Liu X, Zeng X, Zhao X. Song J, et al. Among authors: sha y. Front Endocrinol (Lausanne). 2023 Apr 14;14:1159723. doi: 10.3389/fendo.2023.1159723. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37124723 Free PMC article.

2

[Ring 22 chromosome syndrome induced azoospermia: a case report and literature review].

Sha YW, Ding L, Song YQ, Ge YS, Zeng H, Li P. Sha YW, et al. Zhonghua Nan Ke Xue. 2012 Dec;18(12):1111-4. Zhonghua Nan Ke Xue. 2012. PMID: 23405794 Review. Chinese.

3

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.

Sha Y, Zheng L, Ji Z, Mei L, Ding L, Lin S, Wang X, Yang X, Li P. Sha Y, et al. BMC Med Genet. 2018 Apr 16;19(1):63. doi: 10.1186/s12881-018-0570-4. BMC Med Genet. 2018. PMID: 29661171 Free PMC article. Review.

4

Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype.

Sha Y, Liu W, Wei X, Zhu X, Luo X, Liang L, Guo T. Sha Y, et al. Clin Genet. 2019 Nov;96(5):385-393. doi: 10.1111/cge.13602. Epub 2019 Jul 23. Clin Genet. 2019. PMID: 31278745

5

A familial analysis of two brothers with azoospermia caused by maternal 46,Y, t(X; 1) (q28; q21) chromosomal abnormality.

Li Y, Sha Y, Wei Z, Liu W, Mei L, Hong Y, Jiang L, Ge Y, Xie Y. Li Y, et al. Among authors: sha y. Andrologia. 2021 Feb;53(1):e13867. doi: 10.1111/and.13867. Epub 2020 Nov 3. Andrologia. 2021. PMID: 33141951

6

Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia.

Tang D, Sha Y, Gao Y, Zhang J, Cheng H, Zhang J, Ni X, Wang C, Xu C, Geng H, He X, Cao Y. Tang D, et al. Among authors: sha y. Reprod Biol Endocrinol. 2021 Feb 20;19(1):27. doi: 10.1186/s12958-021-00709-0. Reprod Biol Endocrinol. 2021. PMID: 33610189 Free PMC article.

7

Pathogenic variants of ATG4D in infertile men with non-obstructive azoospermia identified using whole-exome sequencing.

Sha Y, Liu W, Wei X, Zhu X, Tang B, Zhang X, Yang X, Wang Y, Wang X. Sha Y, et al. Clin Genet. 2021 Sep;100(3):280-291. doi: 10.1111/cge.13995. Epub 2021 Jun 11. Clin Genet. 2021. PMID: 33988247

8

Deleterious variants in TAF7L cause human oligoasthenoteratozoospermia and its impairing histone to protamine exchange inducing reduced in vitro fertilization.

Bai H, Sha Y, Tan Y, Li P, Zhang Y, Xu J, Xu S, Ji Z, Wang X, Chen W, Zhang J, Yao C, Li Z, Zhi E. Bai H, et al. Among authors: sha y. Front Endocrinol (Lausanne). 2023 Jan 11;13:1099270. doi: 10.3389/fendo.2022.1099270. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36714566 Free PMC article.

9

Non-chimerism and chimerism pseudo dicentric Y chromosome: two case reports about azoospermia and cytogenetic/molecular genetic analysis in the Chinese population.

Li P, Ding L, Sha YW, Song YQ, Lin J, Werner EF, She M. Li P, et al. J Assist Reprod Genet. 2013 Apr;30(4):539-46. doi: 10.1007/s10815-013-9969-1. Epub 2013 Mar 16. J Assist Reprod Genet. 2013. PMID: 23504399 Free PMC article.

10

A novel mutation in HAUS7 results in severe oligozoospermia in two brothers.

Li L, Sha YW, Su ZY, Mei LB, Ji ZY, Zhang Q, Lin SB, Wang X, Qiu PP, Li P, Yin C. Li L, et al. Gene. 2018 Jan 10;639:106-110. doi: 10.1016/j.gene.2017.10.014. Epub 2017 Oct 7. Gene. 2018. PMID: 29017965

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