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

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

The Effect of Differential Listening Experience on the Development of Expressive and Receptive Language in Children With Bilateral Cochlear Implants

(2014) Christi Hess et al.   EAR AND HEARING

Exome sequencing greatly expedites the progressive research of Mendelian diseases

(2014) Xuejun Zhang   Frontiers of Medicine

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

The promise of whole-exome sequencing in medical genetics

(2013) Bahareh Rabbani et al.   JOURNAL OF HUMAN GENETICS

eXtasy: variant prioritization by genomic data fusion

(2013) Alejandro Sifrim et al.   NATURE METHODS

Genetic and clinical heterogeneity in Meniere's disease

(2012) Irene Gazquez et al.   AUTOIMMUNITY REVIEWS

Copy number variation detection and genotyping from exome sequence data

(2012) N. Krumm et al.   GENOME RESEARCH

Exome sequencing and complex disease: practical aspects of rare variant association studies

(2012) R. Do et al.   HUMAN MOLECULAR GENETICS

Altered Phenotype of the Vestibular Organ in GLAST-1 Null Mice

(2012) Sebastian P. Schraven et al.   JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY

Absence of Glial α-Dystrobrevin Causes Abnormalities of the Blood-Brain Barrier and Progressive Brain Edema

(2012) Chun Fu Lien et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

NIH Image to ImageJ: 25 years of image analysis

(2012) Caroline A Schneider et al.   NATURE METHODS

De novo mutations in human genetic disease

(2012) Joris A. Veltman et al.   NATURE REVIEWS GENETICS

Characteristics of Patients With Unilateral and Bilateral Ménière’s Disease

(2012) Clarice Clemmens et al.   OTOLOGY & NEUROTOLOGY

A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes

(2012) D. G. MacArthur et al.   SCIENCE

EuroQol 5D quality of life in Menière’s disorder can be explained with symptoms and disabilities

(2012) Hilla Levo et al.   INTERNATIONAL JOURNAL OF REHABILITATION RESEARCH

Molecular Microdomains in a Sensory Terminal, the Vestibular Calyx Ending

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

Genetic Aspects of Familial Ménière's Disease

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

Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association

(2010) Dana Gabriková et al.   JOURNAL OF HUMAN GENETICS

Genetic Investigations of Meniere‘s Disease

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

Current Epidemiology of Meniere's Syndrome

(2010) Thomas H. Alexander et al.   OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA

Familial Ménière's disease: clinical and genetic aspects

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