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Meichao Men
Observed name:
Mei-Chao Men
Institutions:
Central South University,
Xiangya Hospital Central South University
Observed institutions:
Central South University,
Xiangya Hospital Central South University
ORCID:
0000-0003-2558-739X
Observed ORCID:
0000-0003-2558-739X
OpenAlex ID:
A5013820854
New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing
2019
·
Wu Li
, Lingyun Mei
, et al.
·
Neural Plasticity
·
31
PDF
Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism
2019
·
Meichao Men
, Jiayu Wu
, et al.
·
Fertility and Sterility
·
26
PDF
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family
2015
·
Honghan Wang
, Xinwei Wang
, et al.
·
Journal of Human Genetics
·
23
PDF
Identification of a Novel CNV at 8q13 in a Family With Branchio‐Oto‐Renal Syndrome and Epilepsy
2019
·
Meichao Men
, Wu Li
, et al.
·
The Laryngoscope
·
22
Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort
2019
·
Jia-Da Li
, Jiayu Wu
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
21
Variable DNA methylation of aging-related genes is associated with male COPD
2019
·
Xizi Du
, Lin Yuan
, et al.
·
Respiratory Research
·
21
PDF
A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review
2019
·
Taoxi Li
, Yong Feng
, et al.
·
Gene
·
21
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss
2018
·
Wu Li
, Jie Sun
, et al.
·
Human Genetics
·
21
Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IV
2014
·
Hong-Han Wang
, Hong-Sheng Chen
, et al.
·
Gene
·
19
Functional analysis of SOX10 mutations identified in Chinese patients with Kallmann syndrome
2019
·
Wenting Dai
, Jiayu Wu
, et al.
·
Gene
·
17
Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism
2020
·
Wenting Dai
, Jia‐Da Li
, et al.
·
Clinical Genetics
·
15
Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism
2020
·
Qiao Hou
, Jiayu Wu
, et al.
·
European Journal of Endocrinology
·
12
Cross-sectional and longitudinal associations between lipid accumulation product and hyperuricemia
2022
·
Wei Zhou
, Nianchun Shan
, et al.
·
Nutrition Metabolism and Cardiovascular Diseases
·
10
SLIT2 Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic Hypogonadism
2022
·
Jiayu Wu
, Zhenghuan Fang
, et al.
·
Hormone Research in Paediatrics
·
10
Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism
2020
·
Meichao Men
, Xinying Wang
, et al.
·
Journal of Medical Genetics
·
9
Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism
2021
·
Meichao Men
, Dan‐Na Chen
, et al.
·
Molecular Genetics & Genomic Medicine
·
7
Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation
2011
·
Meichao Men
, Lu Jiang
, et al.
·
Acta Oto-Laryngologica
·
5
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism
2023
·
Xinying Wang
, Danna Chen
, et al.
·
Human Molecular Genetics
·
4
PDF
ANOS1 variants in a large cohort of Chinese patients with congenital hypogonadotropic hypogonadism.
2022
·
Wang Zeng
, Jiada Li
, et al.
·
PubMed Central
·
3
PDF
MITF Is Mutated in Type 1 Waardenburg Syndrome With Unusual Phenotype
2020
·
Wu Li
, Yong Feng
, et al.
·
Otology & Neurotology
·
2
Novel multiplex primer extension and denaturing high-performance liquid chromatography for genotyping of the deafness gene mutations.
2011
·
Meichao Men
, Jinjie Xue
, et al.
·
PubMed
·
2
Altered spontaneous brain activity is associated with cognitive impairment in patients with Kallmann syndrome
2026
·
Yan Fu
, Xueying Wang
, et al.
·
Reproductive Biology and Endocrinology
·
1
A novel CLPP variant in a Pakistani family with Perrault syndrome associated with recurrent fevers
2026
·
Nisar Ahmad
, Pingchuan Zhang
, et al.
·
Clinica Chimica Acta
·
1
Establishing the role of ZBTB20 mutations in GnRH deficiency and impaired neurogenesis in the subventricular zone: a human cohort and animal model study
2026
·
Jun Guan
, Jingtan Zhu
, et al.
·
EBioMedicine
Association of increased cortical thickness and cognitive impairment in patients with Kallmann syndrome
2026
·
Yan Fu
, Xueying Wang
, et al.
·
European Journal of Endocrinology
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Works count:
30
Citation count:
303
H-index:
12
I10-index:
14
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