Hearing loss: a common disorder caused by many rare alleles

Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

(2010) Atteeq Ur Rehman et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82

(2010) Tom Walsh et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mechanosensitive Hair Cell-like Cells from Embryonic and Induced Pluripotent Stem Cells

(2010) Kazuo Oshima et al.   CELL

Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids

(2010) Amel Bahloul et al.   HUMAN MOLECULAR GENETICS

Hearing Impairment: A Panoply of Genes and Functions

(2010) Amiel A. Dror et al.   NEURON

Future approaches for inner ear protection and repair

(2010) Seiji B. Shibata et al.   JOURNAL OF COMMUNICATION DISORDERS

Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology

(2009) Amiel A. Dror et al.   Annual Review of Genetics

Mechanotransduction by Hair Cells: Models, Molecules, and Mechanisms

(2009) Peter G. Gillespie et al.   CELL

Origins and Mechanisms of miRNAs and siRNAs

(2009) Richard W. Carthew et al.   CELL

Expression patterns of miR-96, miR-182 and miR-183 in the developing inner ear

(2009) Rosalie Sacheli et al.   GENE EXPRESSION PATTERNS

MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness

(2009) Lilach M. Friedman et al.   MAMMALIAN GENOME

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss

(2009) Ángeles Mencía et al.   NATURE GENETICS

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

(2009) Morag A Lewis et al.   NATURE GENETICS

Linking genes underlying deafness to hair-bundle development and function

(2009) Christine Petit et al.   NATURE NEUROSCIENCE

Deafness Genes in Israel: Implications for Diagnostics in the Clinic

(2009) Zippora Brownstein et al.   PEDIATRIC RESEARCH

A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells

(2009) M. Schwander et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Mutation spectrum ofMYO7Aand evaluation of a novel nonsyndromic deafnessDFNB2allele with residual function

(2008) Saima Riazuddin et al.   HUMAN MUTATION

Functional auditory hair cells produced in the mammalian cochlea by in utero gene transfer

(2008) Samuel P. Gubbels et al.   NATURE

Stereocilin-deficient mice reveal the origin of cochlear waveform distortions

(2008) Elisabeth Verpy et al.   NATURE

Usher syndrome: Animal models, retinal function of Usher proteins, and prospects for gene therapy

(2007) David S. Williams   VISION RESEARCH