Xinzhang Cai

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 · 38 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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 · 33 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A nonsense <i>TMEM43</i> variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder

Minwoo Wendy Jang, Doo‐Yi Oh, Eunyoung Yi et al. · Proceedings of the National Academy of Sciences · 2021 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing

Yalan Liu, Lili Wang, Yong Feng et al. · PLoS ONE · 2016 · 26 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Extrusion pump ABCC1 was first linked with nonsyndromic hearing loss in humans by stepwise genetic analysis

Meng Li, Lingyun Mei, Chufeng He et al. · Genetics in Medicine · 2019 · 26 citations · Full text

Medicine, Genetics, Molecular Genetics +10