Gao Y - Search Results

1

Novel mutations in DNAH17 cause sperm flagellum defects and their influence on ICSI outcome.

Song B, Yang T, Shen Q, Liu Y, Wang C, Li G, Gao Y, Cao Y, He X. Song B, et al. Among authors: gao y. J Assist Reprod Genet. 2023 Oct;40(10):2485-2492. doi: 10.1007/s10815-023-02897-7. Epub 2023 Aug 14. J Assist Reprod Genet. 2023. PMID: 37574497 Review.

2

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA.

Tian S, Tu C, He X, Meng L, Wang J, Tang S, Gao Y, Liu C, Wu H, Zhou Y, Lv M, Lin G, Jin L, Cao Y, Tang D, Zhang F, Tan YQ. Tian S, et al. Among authors: gao y. J Med Genet. 2023 Aug;60(8):827-834. doi: 10.1136/jmg-2022-108887. Epub 2023 Jan 2. J Med Genet. 2023. PMID: 36593121

3

Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans.

Lv M, Tang D, Yu H, Geng H, Zhou Y, Shao Z, Li K, Gao Y, Guo S, Xu C, Tan Q, Liu C, Guo R, Wu H, Duan Z, Zhang J, Wang G, Hua R, Fu F, Wang K, Xu Y, Zhou P, Wei Z, Zhang F, Cao Y, He X. Lv M, et al. Among authors: gao y. Int J Biol Sci. 2023 Jan 1;19(2):393-411. doi: 10.7150/ijbs.76051. eCollection 2023. Int J Biol Sci. 2023. PMID: 36632462 Free PMC article.

4

Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility.

Liu Y, Li Y, Meng L, Li K, Gao Y, Lv M, Guo R, Xu Y, Zhou P, Wei Z, He X, Cao Y, Wu H, Tan Y, Hua R. Liu Y, et al. Among authors: gao y. Hum Mol Genet. 2023 May 5;32(10):1730-1740. doi: 10.1093/hmg/ddad013. Hum Mol Genet. 2023. PMID: 36708031

5

Novel HYDIN variants associated with male infertility in two Chinese families.

Yu H, Shi X, Shao Z, Geng H, Guo S, Li K, Gu M, Xu C, Gao Y, Tan Q, Duan Z, Wu H, Hua R, Guo R, Wei Z, Zhou P, Cao Y, He X, Li L, Zhang X, Lv M. Yu H, et al. Among authors: gao y. Front Endocrinol (Lausanne). 2023 Jan 18;14:1118841. doi: 10.3389/fendo.2023.1118841. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 36742411 Free PMC article.

6

DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath.

Wu H, Liu Y, Li Y, Li K, Xu C, Gao Y, Lv M, Guo R, Xu Y, Zhou P, Wei Z, Hua R, He X, Cao Y. Wu H, et al. Among authors: gao y. Cell Death Dis. 2023 Feb 15;14(2):127. doi: 10.1038/s41419-023-05653-y. Cell Death Dis. 2023. PMID: 36792588 Free PMC article.

7

Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos.

Tang F, Gao Y, Li K, Tang D, Hao Y, Lv M, Wu H, Cheng H, Fei J, Jin Z, Wang C, Xu Y, Wei Z, Zhou P, Zhang Z, He X, Cao Y. Tang F, et al. Among authors: gao y. J Assist Reprod Genet. 2023 Jul;40(7):1689-1702. doi: 10.1007/s10815-023-02761-8. Epub 2023 Mar 3. J Assist Reprod Genet. 2023. PMID: 36864181

8

[Genetic analysis of a patient with familial hypercholesterolemia due to variant of LDLR gene].

Wang G, Liu L, Gao Y, Lyu M, Wu H, He X. Wang G, et al. Among authors: gao y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Apr 10;40(4):458-461. doi: 10.3760/cma.j.cn511374-20210109-00022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 36972942 Chinese.

9

ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.

Hua R, Xue R, Liu Y, Li Y, Sha X, Li K, Gao Y, Shen Q, Lv M, Xu Y, Zhang Z, He X, Cao Y, Wu H. Hua R, et al. Among authors: gao y. Hum Reprod. 2023 Jun 1;38(6):1213-1223. doi: 10.1093/humrep/dead059. Hum Reprod. 2023. PMID: 37004249

10

Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans.

Guo R, Wu H, Zhu X, Wang G, Hu K, Li K, Geng H, Xu C, Zu C, Gao Y, Tang D, Cao Y, He X. Guo R, et al. Among authors: gao y. J Med Genet. 2024 May 21;61(6):553-565. doi: 10.1136/jmg-2023-109766. J Med Genet. 2024. PMID: 38341271

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