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

Imputation of SNPs associated with presbycusis through linkage disequilibrium analysis in the ILDR1 gene.

Journal of genetics - 1 Jan 2023

Flores Sergio V, Levi-Monsalve Alejandro, Alvarez-Lobo Juan Pablo

Abstract excerpt

The single-nucleotide polymorphisms (SNP) ILDR1 rs2332035 has shown a high statistical association with presbycusis (hearing loss with age or age-related hearing impairment (ARHI)), according to genetic association studies in European populations. However, linked markers have not been surveyed. Here linkage disequilibrium (LD) of markers in ILDR1, in relation to rs2332035, is explored in the 2504 individuals from...

Read the complete abstract on PubMed

Topics

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to Genotype

Share to Linkage Disequilibrium

Share to Polymorphism, Single Nucleotide

Share to Presbycusis

Share to Receptors, Cell Surface

Source

Identifiers

PMID: 36814109

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Imputation of SNPs associated with presbycusis through linkage disequilibrium analysis in the ILDR1 gene.PMID 36814109Read ↗

Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.Semantic proximity Read ↗

Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families.Semantic proximity Read ↗

A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD).Semantic proximity Read ↗

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait.Semantic proximity Read ↗

Genomewide linkage analysis to presbycusis in the Framingham Heart Study.Semantic proximity Read ↗

A Frameshift Variant in ANKRD24 Implicates Its Role in Human Non-Syndromic Hearing Loss.Semantic proximity Read ↗

Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature.Semantic proximity Read ↗

A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records.Semantic proximity Read ↗

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