Liheng Chen

83 Fen Yang Road
Shanghai, 200031, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 13 publications

Natural history and phenotype-genotype correlations in GJB2-related hearing loss: a systematic and comprehensive review.

Natural history and phenotype-genotype correlations in GJB2-related hearing loss: a systematic and comprehensive review.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: December 18, 2025

Multicentre gene therapy for OTOF-related deafness followed up to 2.5 years.

Multicentre gene therapy for OTOF-related deafness followed up to 2.5 years.

Journal: Nature

Published: September 14, 2025

A Splice-Site Variant in ACY1 Associated with Congenital Hearing Loss: Clinical, Biochemical, and Zebrafish Functional Evidence.

A Splice-Site Variant in ACY1 Associated with Congenital Hearing Loss: Clinical, Biochemical, and Zebrafish Functional Evidence.

Journal: Biochemical genetics

Published: September 07, 2025

Re-administration of AAV-mediated gene therapy for OTOF-related deafness: a single-arm trial.

Re-administration of AAV-mediated gene therapy for OTOF-related deafness: a single-arm trial.

Journal: Nature medicine

Published: August 12, 2025

International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials.

International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials.

Journal: Med (New York, N.Y.)

Published: July 22, 2025

Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital Deafness.

Gene Therapy vs Cochlear Implantation in Restoring Hearing Function and Speech Perception for Individuals With Congenital Deafness.

Journal: JAMA neurology

Published: July 21, 2025

Unraveling the genetic basis of post-infancy diagnosed sensorineural hearing loss using whole exome sequencing.

Unraveling the genetic basis of post-infancy diagnosed sensorineural hearing loss using whole exome sequencing.

Journal: Hearing research

Published: June 17, 2025

Prevalence and spectrum of STRC variants in 1015 sensorineural hearing loss patients: insights from the Chinese population.

Prevalence and spectrum of STRC variants in 1015 sensorineural hearing loss patients: insights from the Chinese population.

Journal: Molecular genetics and genomics : MGG

Published: March 24, 2025

PAM-flexible adenine base editing rescues hearing loss in a humanized MPZL2 mouse model harboring an East Asian founder mutation.

PAM-flexible adenine base editing rescues hearing loss in a humanized MPZL2 mouse model harboring an East Asian founder mutation.

Journal: Nature communications

Published: November 15, 2024

Genetic analysis of patients with low-frequency non-syndromic hearing loss.

Genetic analysis of patients with low-frequency non-syndromic hearing loss.

Journal: Molecular genetics and genomics : MGG

Published: August 05, 2024

The natural history of the relationship between OTOF mutation-related genotypes and audiological phenotypes

The natural history of the relationship between OTOF mutation-related genotypes and audiological phenotypes

Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery

Published: April 13, 2024

Heterozygous deletion of HOXC10-HOXC9 causes lower limb abnormalities in congenital vertical talus.

Heterozygous deletion of HOXC10-HOXC9 causes lower limb abnormalities in congenital vertical talus.

Journal: Journal of medical genetics

Published: September 22, 2023

Showing 1-12 of 13

Last Updated: 09/26/2026