A novel missense variant inPRKCBsegregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease

Impact of Bilaterality and Headache on Health-Related Quality of Life in Meniere's Disease

(2017) Jose A. Lopez-Escamez et al.   ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY

A comprehensive catalogue of the coding and non-coding transcripts of the human inner ear

(2016) Isabelle Schrauwen et al.   HEARING RESEARCH

Genetic aspects and clinical characteristics of familial meniere's disease in a South Korean population

(2015) Jeon Mi Lee et al.   LARYNGOSCOPE

Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR

(2015) Hui Yang et al.   Nature Protocols

Conserved role of Sonic Hedgehog in tonotopic organization of the avian basilar papilla and mammalian cochlea

(2015) Eun Jin Son et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Utilizing Ethnic-Specific Differences in Minor Allele Frequency to Recategorize Reported Pathogenic Deafness Variants

(2014) A. Eliot Shearer et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Phevor Combines Multiple Biomedical Ontologies for Accurate Identification of Disease-Causing Alleles in Single Individuals and Small Nuclear Families

(2014) Marc V. Singleton et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease

(2014) T. Requena et al.   HUMAN MOLECULAR GENETICS

Genomewide RNAi screen identifies protein kinase Cβ and new members of mitogen-activated protein kinase pathway as regulators of melanoma cell growth and metastasis

(2014) Madeleine Schönherr et al.   Pigment Cell & Melanoma Research

Deafness Gene Expression Patterns in the Mouse Cochlea Found by Microarray Analysis

(2014) Hidekane Yoshimura et al.   PLoS One

Meniere's disease

(2014) J. Harcourt et al.   BMJ-British Medical Journal

Accompanying Symptoms Overlap during Attacks in Menière’s Disease and Vestibular Migraine

(2014) Jose Antonio Lopez-Escamez et al.   Frontiers in Neurology

Hyperglycaemia promotes human brain microvascular endothelial cell apoptosis via induction of protein kinase C-βI and prooxidant enzyme NADPH oxidase

(2014) Beili Shao et al.   Redox Biology

Familial clustering and genetic heterogeneity in Meniere's disease

(2013) T. Requena et al.   CLINICAL GENETICS

High incidence of Meniere-like symptoms in relatives of Meniere patients in the areas of Oulu University Hospital and Kainuu Central Hospital in Finland

(2013) Elina Hietikko et al.   European Journal of Medical Genetics

Improved exome prioritization of disease genes through cross-species phenotype comparison

(2013) P. N. Robinson et al.   GENOME RESEARCH

Immunohistochemical Localization of α2-Adrenergic Receptors in the Neonatal Rat Cochlea and the Vestibular Labyrinth

(2013) Jing Cai et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

Genetic Evidence for an Ethnic Diversity in the Susceptibility to Ménière’s Disease

(2013) Jeffrey Douglass Ohmen et al.   OTOLOGY & NEUROTOLOGY

wANNOVAR: annotating genetic variants for personal genomes via the web

(2012) Xiao Chang et al.   JOURNAL OF MEDICAL GENETICS

A probabilistic disease-gene finder for personal genomes

(2011) M. Yandell et al.   GENOME RESEARCH

Regulation of sodium transport in the inner ear

(2011) Sung Huhn Kim et al.   HEARING RESEARCH

Development of tonotopy in the auditory periphery

(2011) Zoe F. Mann et al.   HEARING RESEARCH

Gene Expression Gradients along the Tonotopic Axis of the Chicken Auditory Epithelium

(2011) Corey S. Frucht et al.   JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY

Molecular Microdomains in a Sensory Terminal, the Vestibular Calyx Ending

(2011) A. Lysakowski et al.   JOURNAL OF NEUROSCIENCE

Hearing assessment in Menière's disease

(2011) Antonio Belinchon et al.   LARYNGOSCOPE

Genetic Aspects of Familial Ménière's Disease

(2011) Diana Arweiler-Harbeck et al.   OTOLOGY & NEUROTOLOGY

Genetic Investigations of Meniere‘s Disease

(2010) Jeffrey T. Vrabec   OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA

Familial Ménière's disease: clinical and genetic aspects

(2008) A W Morrison et al.   JOURNAL OF LARYNGOLOGY AND OTOLOGY