Nie H - Search Results

1

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: nie h. 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

2

Long Y chromosome is not a fetal loss risk.

Nie H, Lu G. Nie H, et al. J Assist Reprod Genet. 2011 Feb;28(2):151-6. doi: 10.1007/s10815-010-9497-1. Epub 2010 Nov 17. J Assist Reprod Genet. 2011. PMID: 21082233 Free PMC article.

3

[Karyotype analysis of qualified sperm donors on preliminary screening].

Nie HC, Tan YQ, Lu GX. Nie HC, et al. Zhonghua Nan Ke Xue. 2011 Jan;17(1):13-6. Zhonghua Nan Ke Xue. 2011. PMID: 21351525 Chinese.

4

Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations.

Wang W, Tu C, Nie H, Meng L, Li Y, Yuan S, Zhang Q, Du J, Wang J, Gong F, Fan L, Lu GX, Lin G, Tan YQ. Wang W, et al. Among authors: nie h. J Med Genet. 2019 Nov;56(11):750-757. doi: 10.1136/jmedgenet-2019-106031. Epub 2019 Aug 14. J Med Genet. 2019. PMID: 31413122 Free PMC article.

5

Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella.

Tu C, Nie H, Meng L, Yuan S, He W, Luo A, Li H, Li W, Du J, Lu G, Lin G, Tan YQ. Tu C, et al. Among authors: nie h. Sci Rep. 2019 Nov 1;9(1):15864. doi: 10.1038/s41598-019-52436-7. Sci Rep. 2019. PMID: 31676830 Free PMC article. Clinical Trial.

6

Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD.

Tu C, Nie H, Meng L, Wang W, Li H, Yuan S, Cheng D, He W, Liu G, Du J, Gong F, Lu G, Lin G, Zhang Q, Tan YQ. Tu C, et al. Among authors: nie h. Hum Genet. 2020 Feb;139(2):257-271. doi: 10.1007/s00439-020-02110-0. Epub 2020 Jan 16. Hum Genet. 2020. PMID: 31942643

7

An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.

Tu C, Wang Y, Nie H, Meng L, Wang W, Li Y, Li D, Zhang H, Lu G, Lin G, Tan YQ, Du J. Tu C, et al. Among authors: nie h. Clin Genet. 2020 May;97(5):741-746. doi: 10.1111/cge.13712. Epub 2020 Feb 10. Clin Genet. 2020. PMID: 32017041

8

A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.

Tu C, Meng L, Nie H, Yuan S, Wang W, Du J, Lu G, Lin G, Tan YQ. Tu C, et al. Among authors: nie h. Fertil Steril. 2020 Mar;113(3):561-568. doi: 10.1016/j.fertnstert.2019.10.029. Epub 2020 Feb 25. Fertil Steril. 2020. PMID: 32111475 Free article.

9

Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.

Wang Y, Tu C, Nie H, Meng L, Li D, Wang W, Zhang H, Lu G, Lin G, Tan YQ, Du J. Wang Y, et al. Among authors: nie h. J Assist Reprod Genet. 2020 Apr;37(4):811-820. doi: 10.1007/s10815-020-01735-4. Epub 2020 Mar 13. J Assist Reprod Genet. 2020. PMID: 32170493 Free PMC article.

10

The expression characteristics of FBXW7 in human testis suggest its function is different from that in mice.

Zhou D, Wang X, Liu Z, Huang Z, Nie H, Zhu W, Tan Y, Fan L. Zhou D, et al. Among authors: nie h. Tissue Cell. 2020 Feb;62:101315. doi: 10.1016/j.tice.2019.101315. Epub 2019 Nov 10. Tissue Cell. 2020. PMID: 32433022

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