List of works - Yong Feng

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

scientific article

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

scientific article published on 02 June 2018

A non-coding variant in 5’ untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans

scientific article published in 2022

A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.

scientific article

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

scientific article published on 20 March 2018

A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss

scientific article published on 2 November 2017

Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV.

scientific article published on 26 October 2016

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

scientific article published on 30 April 2018

Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.

scientific article published on 18 August 2016

Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.

scientific article published on 15 June 2017

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

scientific article published on 05 July 2019

Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II.

scientific article published on 9 September 2017

Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2.

scientific article

Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.

scientific article published on 10 January 2018

Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I.

scientific article published on 17 November 2017

Multivariate analysis of prognostic factors for idiopathic sudden sensorineural hearing loss treated with adjuvant hyperbaric oxygen therapy

scientific article published on 25 October 2017

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

scientific article published on 27 February 2019

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

scientific article published on 17 July 2019

Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families

scientific article published on 12 September 2018

Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.

scientific article published on 15 January 2018

The Advances in Hearing Rehabilitation and Cochlear Implants in China

scientific article

The genetic basis of deafness in populations of African descent.

scientific article

Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations.

scientific article published on 12 March 2018

[Molecular pathogenesis of Waardenburg syndrome type II resulting from SOX10 gene mutation]

scientific article published on 01 August 2016

List of works by Yong Feng

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

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

A non-coding variant in 5’ untranslated region drove up-regulation of pseudo-kinase EPHA10 and caused non-syndromic hearing loss in humans

A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.

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

A novel splicing mutation in SMPX is linked to nonsyndromic progressive hearing loss

Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV.

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss.

Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.

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

Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II.

Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2.

Genetic basis of hearing loss in Spanish, Hispanic and Latino populations.

Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I.

Multivariate analysis of prognostic factors for idiopathic sudden sensorineural hearing loss treated with adjuvant hyperbaric oxygen therapy

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

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

Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families

Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.

The Advances in Hearing Rehabilitation and Cochlear Implants in China

The genetic basis of deafness in populations of African descent.

Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations.

[Molecular pathogenesis of Waardenburg syndrome type II resulting from SOX10 gene mutation]