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

Novel GPR156 variants confirm its role in moderate sensorineural hearing loss.

Scientific reports - 9 Oct 2023

Ramzan Memoona, Bozan Nazim, Seyhan Serhat, Zafeer Mohammad Faraz, Ayral Aburrahman, Duman Duygu, Bademci Guney, Tekin Mustafa

Abstract excerpt

Hereditary hearing loss (HL) is a genetically heterogeneous disorder affecting people worldwide. The implementation of advanced sequencing technologies has significantly contributed to the identification of novel genes involved in HL. In this study, probands of two Turkish families with non-syndromic moderate HL were subjected to exome sequencing. The data analysis identified the c.600G > A (p.Thr200Thr) and...

Read the complete abstract on PubMed

Topics

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

Share to Deafness
Share to Ear, Inner
Share to Hearing Loss, Sensorineural

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Pedigree

Share to Phenotype

Share to Receptors, G-Protein-Coupled

Share to RNA Splicing

Source

Open in PubMed Open full text

Identifiers

PMID: 37814107
DOI: 10.1038/s41598-023-44259-4
PMCID: PMC10562426

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 · 12 closest

Novel GPR156 variants confirm its role in moderate sensorineural hearing loss.PMID 37814107Read ↗

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.Semantic proximity Read ↗

Novel GRHL2 Gene Variant Associated with Hearing Loss: A Case Report and Review of the Literature.Semantic proximity Read ↗

Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window.Semantic proximity Read ↗

Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delay.Semantic proximity Read ↗

GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss.Semantic proximity Read ↗

A frameshift mutation in GRXCR2 causes recessively inherited hearing loss.Semantic proximity Read ↗

Functions of G protein‐coupled receptor 56 in health and diseaseSemantic proximity Read ↗

A novel GPR56 mutation causes bilateral frontoparietal polymicrogyria.Semantic proximity Read ↗

Disease-associated mutations prevent GPR56-collagen III interaction.Semantic proximity Read ↗

An alteration in ELMOD3, an Arl2 GTPase-activating protein, is associated with hearing impairment in humans.Semantic proximity Read ↗

A rare variant in GPR156 associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice.Semantic proximity Read ↗

GPR37L1 modulates seizure susceptibility: Evidence from mouse studies and analyses of a human GPR37L1 variant.Semantic proximity Read ↗

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