Wu Li

Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families

Shushan Sang, Jie Ling, Xuezhong Liu et al. · Frontiers in Genetics · 2019 · 37 citations · Full text

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

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

Identification of a Novel CNV at 8q13 in a Family With Branchio‐Oto‐Renal Syndrome and Epilepsy

Meichao Men, Wu Li, Hongsheng Chen et al. · The Laryngoscope · 2019 · 22 citations

A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family

Yuyuan Deng, Zhijie Niu, Liang‐Liang Fan et al. · Journal of Human Genetics · 2018 · 19 citations

Novel Mutation, Chinese Family, Developmental Biology +9