Wang Y - Search Results

1

Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome.

Liu M, Shen Y, Zhang X, Wang X, Li D, Wang Y. Liu M, et al. Among authors: wang x, wang y. J Assist Reprod Genet. 2020 Sep;37(9):2151-2157. doi: 10.1007/s10815-020-01855-x. Epub 2020 Jun 16. J Assist Reprod Genet. 2020. PMID: 32556881 Free PMC article.

2

Novel PMM2 missense mutation in a Chinese family with non-syndromic premature ovarian insufficiency.

Peng T, Lv C, Tan H, Huang J, He H, Wang Y, Zeng M, Yi D, Li J, Deng H, Shi X, Xiao H. Peng T, et al. Among authors: wang y. J Assist Reprod Genet. 2020 Feb;37(2):443-450. doi: 10.1007/s10815-019-01675-8. Epub 2020 Jan 4. J Assist Reprod Genet. 2020. PMID: 31902100 Free PMC article.

3

The growth and development conditions in mouse offspring derived from ovarian tissue cryopreservation and orthotopic transplantation.

Yan Z, Li Q, Zhang L, Kang B, Fan W, Deng T, Zhu J, Wang Y. Yan Z, et al. Among authors: wang y. J Assist Reprod Genet. 2020 Apr;37(4):923-932. doi: 10.1007/s10815-020-01734-5. Epub 2020 Mar 27. J Assist Reprod Genet. 2020. PMID: 32221789 Free PMC article.

4

Zp4 is completely dispensable for fertility in female rats†.

Zeng MH, Wang Y, Huang HL, Quan RP, Yang JT, Guo D, Sun Y, Lv C, Li TY, Wang L, Tan HJ, Long PP, Deng HW, Xiao HM. Zeng MH, et al. Among authors: wang l, wang y. Biol Reprod. 2021 Jun 4;104(6):1282-1291. doi: 10.1093/biolre/ioab047. Biol Reprod. 2021. PMID: 33709118

5

The mutation c.346-1G > A in SOHLH1 impairs sperm production in the homozygous but not in the heterozygous condition.

Liu M, Yang Y, Wang Y, Chen S, Shen Y. Liu M, et al. Among authors: wang y. Hum Mol Genet. 2022 Mar 31;31(7):1013-1021. doi: 10.1093/hmg/ddab242. Hum Mol Genet. 2022. PMID: 34448846 Free PMC article.

6

Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects.

Li Y, Wang Y, Wen Y, Zhang T, Wang X, Jiang C, Zheng R, Zhou F, Chen D, Yang Y, Shen Y. Li Y, et al. Among authors: wang x, wang y. Hum Reprod. 2021 Dec 27;37(1):152-177. doi: 10.1093/humrep/deab229. Hum Reprod. 2021. PMID: 34791246

7

Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice.

Shen Y, Guo J, Zhang X, Wang X, Zhu S, Chen D, Xiong W, Lu G, Liu X, Dai C, Gong F, Wang Y, Lin G, Wang Z, Xu W. Shen Y, et al. Among authors: wang x, wang z, wang y. Hum Reprod. 2022 Apr 1;37(4):859-872. doi: 10.1093/humrep/deac026. Hum Reprod. 2022. PMID: 35211729

8

CEP128 is involved in spermatogenesis in humans and mice.

Zhang X, Wang L, Ma Y, Wang Y, Liu H, Liu M, Qin L, Li J, Jiang C, Zhang X, Shan X, Liu Y, Li J, Li Y, Zheng R, Sun Y, Sun J, Leng X, Liang Y, Zhang F, Jiang X, Yang Y, Shen Y. Zhang X, et al. Among authors: wang l, wang y. Nat Commun. 2022 Mar 16;13(1):1395. doi: 10.1038/s41467-022-29109-7. Nat Commun. 2022. PMID: 35296684 Free PMC article.

9

FSIP2 plays a role in the acrosome development during spermiogenesis.

Zheng R, Wang Y, Li Y, Guo J, Wen Y, Jiang C, Yang Y, Shen Y. Zheng R, et al. Among authors: wang y. J Med Genet. 2023 Mar;60(3):254-264. doi: 10.1136/jmedgenet-2021-108406. Epub 2022 Jun 2. J Med Genet. 2023. PMID: 35654582

10

A loss-of-function variant in SSFA2 causes male infertility with globozoospermia and failed oocyte activation.

Huang G, Zhang X, Yao G, Huang L, Wu S, Li X, Guo J, Wen Y, Wang Y, Shang L, Li N, Xu W. Huang G, et al. Among authors: wang y. Reprod Biol Endocrinol. 2022 Jul 14;20(1):103. doi: 10.1186/s12958-022-00976-5. Reprod Biol Endocrinol. 2022. PMID: 35836265 Free PMC article.

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