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

A genome-wide association study identifies novel loci of vertigo in an Asian population-based cohort.

Communications biology - 22 Aug 2024

Chen Shih-Pin, Hsu Chia-Lin, Chen Ting-Huei, Pan Li-Ling Hope, Wang Yen-Feng, Ling Yu-Hsiang, Chang Hsueh-Chen, Chen Yi-Ming, Fann Cathy Shen-Jang, Wang Shuu-Jiun

Abstract excerpt

The contributing genetic factors of vertigo remain poorly characterized, particularly in individuals of non-European ancestries. Here we show the genetic landscape of vertigo in an Asian population-based cohort. In a two-stage genome-wide association study (Ncase = 6199; Ncontrol = 54,587), we identify vertigo-associated genomic loci in DROSHA and ZNF91/LINC01224, with the latter replicating the findings in...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cohort Studies

Share to Genetic Loci

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 39174713
DOI: 10.1038/s42003-024-06603-w
PMCID: PMC11341872

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A genome-wide association study identifies novel loci of vertigo in an Asian population-based cohort.PMID 39174713Read ↗

A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigoSemantic proximity Read ↗

Identification of potential susceptibility genes in patients with Vestibular Migraine through whole exome sequencingSemantic proximity Read ↗

GWAS of Chronic Dizziness in the Elderly Identifies Novel Loci Implicating<i>MLLT10, BPTF, LINC01225</i>, and<i>ROS1</i>Semantic proximity Read ↗

Genome-Wide Association Study of Chronic Dizziness in the Elderly Identifies Loci Implicating MLLT10, BPTF, LINC01224, and ROS1.Semantic proximity Read ↗

Integrated analysis of proteome-wide and transcriptome-wide association studies identified novel genes and chemicals for vertigoSemantic proximity Read ↗

GWAS and multimodal transcriptomic profiling of human otolithic organs characterize the genetic architecture of balance in the elderlySemantic proximity Read ↗

Vestibular migraine as a vestibulo-trigeminal interface phenotype: a triangulation study across genetics, peripheral multiomics and human cell atlasesSemantic proximity Read ↗

Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis.Semantic proximity Read ↗

Genetics of vestibular disorders: pathophysiological insights.Semantic proximity Read ↗

Genome-wide analysis implicates inner ear development in Ménière’s diseaseSemantic proximity Read ↗

Causal Relationship Between Hypertension And Vertigo: A Mendelian Randomization Study.Semantic proximity Read ↗

Genome-wide analysis implicates inner ear development in Ménière disease.Semantic proximity Read ↗

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