Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic variants of CDH23 associated with noise-induced hearing loss.

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology - 1 Feb 2014

Kowalski Tomasz Jarema, Pawelczyk Malgorzata, Rajkowska Elzbieta, Dudarewicz Adam, Sliwinska-Kowalska Mariola

Abstract excerpt

OBJECTIVES: Noise-induced hearing loss (NIHL) is a complex disease resulting from the interaction between external and intrinsic/genetic factors. Based on mice studies, one of the most interesting candidate gene for NIHL susceptibility is CDH23-encoding cadherin 23, a component of the stereocilia tip links. The aim of this study was to analyze selected CDH23 single nucleotide polymorphisms (SNPs) and to evaluate...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cadherin Related Proteins
Share to Cadherins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to CDH23 gene

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Hearing Loss, Noise-Induced

Share to Occupational Exposure

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 24448297
DOI: 10.1097/MAO.0b013e3182a00332

Genes

CDH23

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variants of CDH23 associated with noise-induced hearing loss.PMID 24448297Read ↗

Association between genetic polymorphisms of cadherin 23 and noise-induced hearing loss: a meta-analysis.Semantic proximity Read ↗

[Association of cadherin CDH23 gene polymorphisms with noise induced hearing loss in Chinese workers].Semantic proximity Read ↗

[Relationship research among CDH23 gene and the risk of noise-induced hearing loss].Semantic proximity Read ↗

Single nucleotide polymorphisms in the cadherin 23 (CDH23) gene in Polish workers exposed to industrial noise.Semantic proximity Read ↗

[Association between CDH23 gene polymorphisms and susceptibility to noise-induced hearing loss in the Chinese population: a meta-analysis].Semantic proximity Read ↗

Association of cadherin23 single nucleotide polymorphism with age-related hearing impairment in Han Chinese.Semantic proximity Read ↗

Identifying genetic risk variants associated with noise-induced hearing loss based on a novel strategy for evaluating individual susceptibility.Semantic proximity Read ↗

Identifying Genetic Variants Associated With Noise-induced Hearing Loss Based on a Novel Strategy for Evaluating Individual SusceptibilitySemantic proximity Read ↗

[Genetic factors in susceptibility to age- and noise-related hearing loss].Semantic proximity Read ↗

Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss.Semantic proximity Read ↗

Variants in CDH23 Cause Broad Spectrum of Hearing Loss: From Non-Syndromic to Syndromic Hearing Loss as Well as From Congenital to Age-Related Hearing LossSemantic proximity Read ↗

Genetic studies on noise-induced hearing loss: a review.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.