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 replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies.

International journal of audiology - 1 Nov 2012

Hietikko Elina, Kotimäki Jouko, Okuloff Annaleena, Sorri Martti, Männikkö Minna

Abstract excerpt

OBJECTIVE: Multiple candidate genes have been presented for Ménière's disease (MD), but to date no positive replications have been reported. We review here all the previously proposed candidate genes for MD and report our results on the analysis of six such genes, AQP2, KCNE1, KCNE3, HCFC1, COCH,...

Read the complete abstract on PubMed

Topics

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

Share to Aquaporin 2
Share to Calmodulin-Binding Proteins
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Extracellular Matrix Proteins

Share to Host Cell Factor C1

Share to Meniere Disease

Share to Polymorphism, Single Nucleotide

Share to Potassium Channels, Voltage-Gated

Source

Identifiers

PMID: 22934933
DOI: 10.3109/14992027.2012.705900

Genes

ADD1
AQP2
COCH
HCFC1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22934933-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies.PMID 22934933Read ↗

Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis.Semantic proximity Read ↗

Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian PopulationSemantic proximity Read ↗

Ménière's Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients.Semantic proximity Read ↗

Different contribution of missense and loss-of-function variants to the genetic structure of familial and sporadic Meniere diseaseSemantic proximity Read ↗

Genetic advances in Meniere Disease.Semantic proximity Read ↗

Rare missense variants in MYO7A and OTOP2 genes in a South Korean Meniere's disease cohort.Semantic proximity Read ↗

The Polymorphic Analysis of the Human Potassium Channel KCNE Gene Family in Meniere’s Disease-A Preliminary StudySemantic proximity Read ↗

Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3.Semantic proximity Read ↗

Towards personalized medicine in Ménière’s diseaseSemantic proximity Read ↗

Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière's Disease.Semantic proximity Read ↗

New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière’s DiseaseSemantic proximity Read ↗

The genomic landscape of Ménière's disease: a path to endolymphatic hydropsSemantic proximity Read ↗

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