Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population (Q28268725)

10

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Bruce J Gantz

object named as

Bruce J Gantz

11

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Edwin M. Stone

object named as

Edwin M Stone

6

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author name string

Charley C Della Santina

2

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Nicole C Meyer

3

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Nancy B Smith

4

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Oluwaseun A Myrie

5

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Kuni Fukushima

7

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Joseph Califano

8

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John P Carey

9

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Lloyd B Minor

12

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Richard J H Smith

American Journal of Medical Genetics Part A

13

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language of work or name

English

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publication date

January 2010

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published in

1 reference

A superfamily of small potassium channel subunits: form and function of the MinK-related peptides (MiRPs).

PubMed

volume

152A

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issue

1

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page(s)

67-74

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cites work

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ConSeq: the identification of functionally and structurally important residues in protein sequences.

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Using haplotype blocks to map human complex trait loci

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Replicating genotype-phenotype associations

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

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A simple and efficient non-organic procedure for the isolation of genomic DNA from blood

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Replication validity of genetic association studies

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Trends in the diagnosis and the management of Meniere's disease: results of a survey.

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Association of HLA-DR and type II collagen autoimmunity with Meniere's disease.

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Genetic dissection of complex traits

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History of Meniere's disease and its clinical presentation

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KCNE regulation of KvLQT1 channels: structure-function correlates

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Aquaporin-2 expression in the mammalian cochlea and investigation of its role in Meniere's disease

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KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells

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Etiology, pathophysiology of symptoms, and pathogenesis of Meniere's disease

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Use of unlinked genetic markers to detect population stratification in association studies.

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Medical management of Meniere's disease

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Absence of COCH mutations in patients with Meniere disease.

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From genotypes to genes: doubling the sample size

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Candidate-gene approaches for studying complex genetic traits: practical considerations

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The AAO-HNS Committee on Hearing and Equilibrium guidelines for the diagnosis and evaluation of therapy in Menière's disease: have they been applied in the published literature of the last decade?

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Comparison of three methods to estimate genetic ancestry and control for stratification in genetic association studies among admixed populations.

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Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease

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Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro

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Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies

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Demonstrating stratification in a European American population

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Hardy–Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations and power

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Epidemiological and Clinical Characteristics of Meniere's Disease in Japan

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HLA Associations with Meniere's Disease

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