Meichao Men

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

Wu Li, Lingyun Mei, Hongsheng Chen et al. · Neural Plasticity · 2019 · 32 citations · Full text

Variable DNA methylation of aging-related genes is associated with male COPD

Xizi Du, Lin Yuan, Mengping Wu et al. · Respiratory Research · 2019 · 27 citations · Full text

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family

Honghan Wang, Xinwei Wang, Chufeng He et al. · Journal of Human Genetics · 2015 · 23 citations · Full text

Chinese Family, Developmental Biology, Genetic Disorder +9

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

Meichao Men, Jiayu Wu, Yaguang Zhao et al. · Fertility and Sterility · 2019 · 23 citations · Full text

Infertility, Growth Hormone, Mendelian Disorder +13

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

Wu Li, Jie Sun, Jie Ling et al. · Human Genetics · 2018 · 22 citations

Developmental Biology, Genetic Disorder, Genetics +11