GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, +60

The American Journal of Human Genetics

Genetic DisorderGeneticsAudiologyGenetic EpidemiologyGjb2 Mutations +7

Occupational Noise, Smoking, and a High Body Mass Index are Risk Factors for Age-related Hearing Impairment and Moderate Alcohol Consumption is Protective: A European Population-based Multicenter Study

Erik Fransén, Vedat Topsakal, Jan Hendrickx, +32

Journal of the Association for Research in Otolaryngology

Health EffectHealth SciencesOccupational NoiseEnvironmental HealthAudiology +12

GRM7 variants confer susceptibility to age-related hearing impairment

Rick A. Friedman, Lut Van Laer, Matthew J. Huentelman, +29

Human Molecular Genetics

Deletion of the Ca²+-activated potassium (BK) α-subunit but not the BKβ1-subunit leads to progressive hearing loss

Lukas Rüttiger, Matthias Sausbier, Ulrike Zimmermann, +16

Proceedings of the National Academy of Sciences

Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

Francesca Donaudy, Rik L. Snoeckx, Markus Pfister, +16

The American Journal of Human Genetics

Patients AffectedGenetic DisorderGeneticsAudiologyAuditory Physiology +6

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

Lut Van Laer, Els Van Eyken, Erik Fransén, +32

Human Molecular Genetics

GeneticsGenetic EpidemiologyHuman PolymorphismNeurotologyClinical Genetics +22

Feasibility of simultaneous PET/MR imaging in the head and upper neck area

Andreas Boss, Lars Stegger, Sotirios Bisdas, +6

European Radiology

Positron Emission TomographyEngineeringMedical ImagingPet-mriBiomedical Imaging +9

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell

P. Heidrych, Ulrike Zimmermann, Stephanie Kuhn, +10

Human Molecular Genetics

The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells

Kim Cryns, Sofie Thys, Lut Van Laer, +6

Histochemistry and Cell Biology

Developmental BiologyWfs1 GeneGenetic DisorderGeneticsAudiology +13

Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients

Susan Kupka, Tímea Tóth, Maciej Wróbel, +9

Human Mutation