Tan C - Search Results

1

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.

Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, Lu S, Liu C, Tian S, Meng L, Wang W, Tan C, Nie H, Li D, Zhang H, Gong F, Hu L, Lu G, Xu W, Lin G, Zhang F, Cao Y, Tan YQ. Tu C, et al. Among authors: tan c, tan yq. Am J Hum Genet. 2021 Aug 5;108(8):1466-1477. doi: 10.1016/j.ajhg.2021.06.010. Epub 2021 Jul 7. Am J Hum Genet. 2021. PMID: 34237282 Free PMC article.

2

Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency.

Zhang YX, He WB, Xiao WJ, Meng LL, Tan C, Du J, Lu GX, Lin G, Tan YQ. Zhang YX, et al. Among authors: tan c, tan yq. Mol Genet Genomic Med. 2020 Apr;8(4):e1165. doi: 10.1002/mgg3.1165. Epub 2020 Feb 11. Mol Genet Genomic Med. 2020. PMID: 32048466 Free PMC article.

3

Homozygous variants in SYCP2L cause premature ovarian insufficiency.

He WB, Tan C, Zhang YX, Meng LL, Gong F, Lu GX, Lin G, Du J, Tan YQ. He WB, et al. Among authors: tan c, tan yq. J Med Genet. 2021 Mar;58(3):168-172. doi: 10.1136/jmedgenet-2019-106789. Epub 2020 Apr 17. J Med Genet. 2021. PMID: 32303603 Free PMC article.

4

A recurrent mutation in TBPL2 causes diminished ovarian reserve and female infertility.

He WB, Zhang YX, Tan C, Meng LL, Liu G, Li Y, Gong F, Wu BL, Lu GX, Lin G, Du J, Tan YQ. He WB, et al. Among authors: tan c, tan yq. J Genet Genomics. 2020 Dec 20;47(12):785-788. doi: 10.1016/j.jgg.2020.09.004. Epub 2020 Nov 18. J Genet Genomics. 2020. PMID: 33541821 No abstract available.

5

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.

Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, Nie H, Zhang H, Du J, Lu G, Fan LQ, Cao Y, Lin G, Tan YQ. Tan C, et al. Among authors: tan y, tan yq. Am J Hum Genet. 2022 Jan 6;109(1):157-171. doi: 10.1016/j.ajhg.2021.11.022. Epub 2021 Dec 20. Am J Hum Genet. 2022. PMID: 34932939 Free PMC article.

6

RNA splicing analysis contributes to reclassifying variants of uncertain significance and improves the diagnosis of monogenic disorders.

He WB, Xiao WJ, Dai CL, Wang YR, Li XR, Gong F, Meng LL, Tan C, Zeng SC, Lu GX, Lin G, Tan YQ, Hu H, Du J. He WB, et al. Among authors: tan c, tan yq. J Med Genet. 2022 Oct;59(10):1010-1016. doi: 10.1136/jmedgenet-2021-108013. Epub 2022 Feb 4. J Med Genet. 2022. PMID: 35121647

7

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia.

Hu T, Meng L, Tan C, Luo C, He WB, Tu C, Zhang H, Du J, Nie H, Lu GX, Lin G, Tan YQ. Hu T, et al. Among authors: tan c, tan yq. J Med Genet. 2023 Feb;60(2):144-153. doi: 10.1136/jmedgenet-2021-108249. Epub 2022 Apr 6. J Med Genet. 2023. PMID: 35387802

8

Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice.

Wang W, Meng L, He J, Su L, Li Y, Tan C, Xu X, Nie H, Zhang H, Du J, Lu G, Luo M, Lin G, Tu C, Tan YQ. Wang W, et al. Among authors: tan c, tan yq. Mol Hum Reprod. 2022 May 27;28(6):gaac015. doi: 10.1093/molehr/gaac015. Mol Hum Reprod. 2022. PMID: 35485979

9

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.

Wang Y, Liu L, Tan C, Meng G, Meng L, Nie H, Du J, Lu GX, Lin G, He WB, Tan YQ. Wang Y, et al. Among authors: tan c, tan yq. Front Genet. 2022 Aug 5;13:936264. doi: 10.3389/fgene.2022.936264. eCollection 2022. Front Genet. 2022. PMID: 35991565 Free PMC article.

10

Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility.

Li Y, Li Y, Wang Y, Meng L, Tan C, Du J, Tan YQ, Nie H, Zhang Q, Lu G, Lin G, Li H, Zhang H, Tu C. Li Y, et al. Among authors: tan c, tan yq. J Assist Reprod Genet. 2023 Jan;40(1):41-51. doi: 10.1007/s10815-022-02681-z. Epub 2022 Dec 14. J Assist Reprod Genet. 2023. PMID: 36515799 Free PMC article.

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