Jiongjiong Hu

Shanghai, China

Last Updated: 09/26/2026

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Found 12 publications

Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss.

Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss.

Journal: Clinical genetics

Published: April 09, 2019

Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway.

Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway.

Journal: FEBS letters

Published: April 06, 2019

Identification of ANLN as a new likely pathogenic gene of branchio-otic syndrome in a three-generation Chinese family.

Identification of ANLN as a new likely pathogenic gene of branchio-otic syndrome in a three-generation Chinese family.

Journal: Molecular genetics & genomic medicine

Published: July 06, 2018

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.

Journal: Human molecular genetics

Published: September 02, 2017

New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss.

New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss.

Journal: Human mutation

Published: December 28, 2016

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.

SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss.

Journal: Human molecular genetics

Published: July 29, 2016

Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss.

Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss.

Journal: Journal of translational medicine

Published: May 26, 2015

Grhl1 deficiency affects inner ear development in zebrafish.

Grhl1 deficiency affects inner ear development in zebrafish.

Journal: The International journal of developmental biology

Published: April 22, 2015

Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish.

Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish.

Journal: PloS one

Published: December 29, 2014

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

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

Journal: PloS one

Published: November 20, 2014

The predictive role of dual source CT for esophageal foreign bodies.

The predictive role of dual source CT for esophageal foreign bodies.

Journal: American journal of otolaryngology

Published: September 11, 2013

Delayed repair of facial nerve trauma: an experimental study in guinea pigs.

Delayed repair of facial nerve trauma: an experimental study in guinea pigs.

Journal: Acta oto-laryngologica

Published: June 18, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026