Men M - Search Results

1

A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.

Wang X, Chen D, Zhao Y, Men M, Chen Z, Jiang F, Zheng R, Stamou MI, Plummer L, Balasubramanian R, Li JD. Wang X, et al. Among authors: men m. Hum Mol Genet. 2023 May 5;32(10):1722-1729. doi: 10.1093/hmg/ddad014. Hum Mol Genet. 2023. PMID: 36694982 Free PMC article.

2

Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort.

Li JD, Wu J, Zhao Y, Wang X, Jiang F, Hou Q, Chen DN, Zheng R, Yu R, Zhou W, Men M. Li JD, et al. Among authors: men m. J Clin Endocrinol Metab. 2020 May 1;105(5):dgz182. doi: 10.1210/clinem/dgz182. J Clin Endocrinol Metab. 2020. PMID: 31689711

3

Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism.

Dai W, Li JD, Zhao Y, Wu J, Jiang F, Chen DN, Zheng R, Men M. Dai W, et al. Among authors: men m. Clin Genet. 2020 May;97(5):696-703. doi: 10.1111/cge.13723. Epub 2020 Feb 21. Clin Genet. 2020. PMID: 32060892

4

Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism.

Men M, Wang X, Wu J, Zeng W, Jiang F, Zheng R, Li JD. Men M, et al. J Med Genet. 2021 Jan;58(1):66-72. doi: 10.1136/jmedgenet-2019-106786. Epub 2020 May 10. J Med Genet. 2021. PMID: 32389901

5

Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism.

Men M, Chen DN, Li JD, Wang X, Zeng W, Jiang F, Zheng R, Dai W. Men M, et al. Mol Genet Genomic Med. 2021 Nov;9(11):e1816. doi: 10.1002/mgg3.1816. Epub 2021 Oct 11. Mol Genet Genomic Med. 2021. PMID: 34636164 Free PMC article.

6

SLIT2 Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic Hypogonadism.

Wu J, Fang Z, Wang X, Zeng W, Zhao Y, Jiang F, Chen DN, Zheng R, Li J, Men M, Li JD. Wu J, et al. Among authors: men m. Horm Res Paediatr. 2022;95(4):384-392. doi: 10.1159/000525769. Epub 2022 Jul 7. Horm Res Paediatr. 2022. PMID: 35797970

7

Functional analysis of SOX10 mutations identified in Chinese patients with Kallmann syndrome.

Dai W, Wu J, Zhao Y, Jiang F, Zheng R, Chen DN, Men M, Li JD. Dai W, et al. Among authors: men m. Gene. 2019 Jun 20;702:99-106. doi: 10.1016/j.gene.2019.03.039. Epub 2019 Mar 23. Gene. 2019. PMID: 30914325

8

Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism.

Men M, Wu J, Zhao Y, Xing X, Jiang F, Zheng R, Li JD. Men M, et al. Fertil Steril. 2020 Jan;113(1):158-166. doi: 10.1016/j.fertnstert.2019.08.069. Epub 2019 Nov 17. Fertil Steril. 2020. PMID: 31748124 Free article.

9

Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism.

Hou Q, Wu J, Zhao Y, Wang X, Jiang F, Chen DN, Zheng R, Men M, Li JD. Hou Q, et al. Among authors: men m. Eur J Endocrinol. 2020 Sep;183(3):245-254. doi: 10.1530/EJE-19-1018. Eur J Endocrinol. 2020. PMID: 32520725

10

ANOS1 variants in a large cohort of Chinese patients with congenital hypogonadotropic hypogonadism.

Zeng W, Li J, Wang X, Jiang F, Men M. Zeng W, et al. Among authors: men m. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2022 Jul 28;47(7):847-857. doi: 10.11817/j.issn.1672-7347.2022.220071. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2022. PMID: 36039580 Free PMC article.

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