Jiongjiong Hu

Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

Fei Liu, Jiongjiong Hu, Xia Wen-jun et al. · PLoS ONE · 2015 · 29 citations · Full text

Family Members, Exome Sequencing, Genetics +16

Mutations in <i> <scp>TOP</scp> 2B </i> cause autosomal‐dominant hereditary hearing loss <i>via</i> inhibition of the <scp>PI</scp> 3K‐Akt signalling pathway

Wenjun Xia, Jiongjiong Hu, Jing Ma et al. · FEBS Letters · 2019 · 21 citations

Novel TRRAP mutation causes autosomal dominant non‐syndromic hearing loss

Wenjun Xia, Jiongjiong Hu, Jing Ma et al. · Clinical Genetics · 2019 · 21 citations

A novel torsion instrument for miniaturized components based on the flexural pivot

Dabiao Liu, Jianhui Hu, Hao Liu et al. · Measurement · 2022 · 21 citations

Novel Torsion Instrument, Engineering, Micromechanics +10

Grhl1 deficiency affects inner ear development in zebrafish

Fei Liu, Fan Yang, Danping Wen et al. · The International Journal of Developmental Biology · 2015 · 19 citations

Genetics, Molecular Genetics, Grhl1 Deficiency +17