Liu W - Search Results

1

CCDC9 is identified as a novel candidate gene of severe asthenozoospermia.

Sha Y, Xu Y, Wei X, Liu W, Mei L, Lin S, Ji Z, Wang X, Su Z, Qiu P, Chen J, Wang X. Sha Y, et al. Among authors: liu w. Syst Biol Reprod Med. 2019 Dec;65(6):465-473. doi: 10.1080/19396368.2019.1655812. Epub 2019 Sep 10. Syst Biol Reprod Med. 2019. PMID: 31502483

2

Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF).

Liu W, Sha Y, Li Y, Mei L, Lin S, Huang X, Lu J, Ding L, Kong S, Lu Z. Liu W, et al. J Med Genet. 2019 Oct;56(10):678-684. doi: 10.1136/jmedgenet-2018-105952. Epub 2019 May 31. J Med Genet. 2019. PMID: 31151990

3

EIF4G1 is a novel candidate gene associated with severe asthenozoospermia.

Sha Y, Liu W, Huang X, Li Y, Ji Z, Mei L, Lin S, Kong S, Lu J, Kong L, Zhu X, Lu Z, Ding L. Sha Y, et al. Among authors: liu w. Mol Genet Genomic Med. 2019 Aug;7(8):e807. doi: 10.1002/mgg3.807. Epub 2019 Jul 3. Mol Genet Genomic Med. 2019. PMID: 31268247 Free PMC article.

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. Among authors: liu w. Clin Genet. 2019 Nov;96(5):385-393. doi: 10.1111/cge.13602. Epub 2019 Jul 23. Clin Genet. 2019. PMID: 31278745

5

Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family.

Sha Y, Ma D, Zhang N, Wei X, Liu W, Wang X. Sha Y, et al. Among authors: liu w. BMC Med Genet. 2019 Aug 1;20(1):133. doi: 10.1186/s12881-019-0864-1. BMC Med Genet. 2019. PMID: 31370824 Free PMC article.

6

Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention.

Liu H, Wei X, Sha Y, Liu W, Gao H, Lin J, Li Y, Tang Y, Wang Y, Wang Y, Su Z. Liu H, et al. Among authors: liu w. J Ovarian Res. 2020 Sep 22;13(1):114. doi: 10.1186/s13048-020-00716-6. J Ovarian Res. 2020. PMID: 32962729 Free PMC article.

7

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: liu w. Andrologia. 2021 Feb;53(1):e13867. doi: 10.1111/and.13867. Epub 2020 Nov 3. Andrologia. 2021. PMID: 33141951

8

Mutations in ZP4 are associated with abnormal zona pellucida and female infertility.

Wei X, Li Y, Liu Q, Liu W, Yan X, Zhu X, Zhou D, Tian Y, Zhang F, Li N, Lu Z. Wei X, et al. Among authors: liu q, liu w. J Clin Pathol. 2022 Mar;75(3):201-204. doi: 10.1136/jclinpath-2020-207170. Epub 2021 Jan 18. J Clin Pathol. 2022. PMID: 33461974

9

Mutations in DNAH8 contribute to multiple morphological abnormalities of sperm flagella and male infertility.

Weng M, Sha Y, Zeng YU, Huang N, Liu W, Zhang X, Zhou H. Weng M, et al. Among authors: liu w. Acta Biochim Biophys Sin (Shanghai). 2021 Mar 26;53(4):472-480. doi: 10.1093/abbs/gmab013. Acta Biochim Biophys Sin (Shanghai). 2021. PMID: 33704367 Free article.

10

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. Among authors: liu w. Clin Genet. 2021 Sep;100(3):280-291. doi: 10.1111/cge.13995. Epub 2021 Jun 11. Clin Genet. 2021. PMID: 33988247

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