Sha Y - Search Results

1

Novel bi-allelic DNAH3 variants cause oligoasthenoteratozoospermia.

Li S, Zhang Z, Xie L, Zhao Y, Chen H, Zhang S, Cai Y, Ren B, Liu W, Tang S, Sha Y. Li S, et al. Among authors: sha y. Front Endocrinol (Lausanne). 2024 Oct 28;15:1462509. doi: 10.3389/fendo.2024.1462509. eCollection 2024. Front Endocrinol (Lausanne). 2024. PMID: 39588341 Free PMC article.

2

Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF).

Sha YW, Wang X, Xu X, Su ZY, Cui Y, Mei LB, Huang XJ, Chen J, He XM, Ji ZY, Bao H, Yang X, Li P, Li L. Sha YW, et al. Reprod Sci. 2019 Jan;26(1):26-34. doi: 10.1177/1933719117749756. Epub 2017 Dec 25. Reprod Sci. 2019. PMID: 29277146

3

TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family.

Sha YW, Wang X, Su ZY, Wang C, Ji ZY, Mei LB, Zhang L, Deng BB, Huang XJ, Yan W, Chen J, Li P, Cui YQ, Qu QL, Yin C, He XM. Sha YW, et al. Gene. 2018 Jun 15;659:84-88. doi: 10.1016/j.gene.2018.03.040. Epub 2018 Mar 15. Gene. 2018. PMID: 29551503

4

Biallelic mutations in PMFBP1 cause acephalic spermatozoa.

Sha YW, Wang X, Xu X, Ding L, Liu WS, Li P, Su ZY, Chen J, Mei LB, Zheng LK, Wang HL, Kong SB, You M, Wu JF. Sha YW, et al. Clin Genet. 2019 Feb;95(2):277-286. doi: 10.1111/cge.13461. Epub 2018 Nov 27. Clin Genet. 2019. PMID: 30298696

5

DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella.

Li Y, Sha Y, Wang X, Ding L, Liu W, Ji Z, Mei L, Huang X, Lin S, Kong S, Lu J, Qin W, Zhang X, Zhuang J, Tang Y, Lu Z. Li Y, et al. Among authors: sha y. Clin Genet. 2019 May;95(5):590-600. doi: 10.1111/cge.13525. Epub 2019 Mar 25. Clin Genet. 2019. PMID: 30811583

6

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. Among authors: sha y. 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

7

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. 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.

8

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

9

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. 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.

10

Novel IFT140 variants cause spermatogenic dysfunction in humans.

Wang X, Sha YW, Wang WT, Cui YQ, Chen J, Yan W, Hou XT, Mei LB, Yu CC, Wang J. Wang X, et al. Mol Genet Genomic Med. 2019 Sep;7(9):e920. doi: 10.1002/mgg3.920. Epub 2019 Aug 8. Mol Genet Genomic Med. 2019. PMID: 31397098 Free PMC article. Clinical Trial.

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