The Patients Associated With TMPRSS3 Mutations Are Good Candidates for Electric Acoustic Stimulation

The pre- and post-somatic segments of the human type I spiral ganglion neurons – Structural and functional considerations related to cochlear implantation

(2015) W. Liu et al.   NEUROSCIENCE

Hearing preservation and clinical outcome of 32 consecutive electric acoustic stimulation (EAS) surgeries

(2014) Shin-Ichi Usami et al.   ACTA OTO-LARYNGOLOGICA

A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation

(2014) Juyong Chung et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Large-Scale East-Asian eQTL Mapping Reveals Novel Candidate Genes for LD Mapping and the Genomic Landscape of Transcriptional Effects of Sequence Variants

(2014) Maiko Narahara et al.   PLoS One

Targeted Exon Sequencing Successfully Discovers Rare Causative Genes and Clarifies the Molecular Epidemiology of Japanese Deafness Patients

(2013) Maiko Miyagawa et al.   PLoS One

Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS

(2013) Maiko Miyagawa et al.   PLoS One

Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss

(2012) Majida Charif et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Prediction of cochlear implant performance by genetic mutation: The spiral ganglion hypothesis

(2012) Robert W. Eppsteiner et al.   HEARING RESEARCH

wANNOVAR: annotating genetic variants for personal genomes via the web

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

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

Electric-Acoustic Stimulation of the Auditory System: A Review of the First Decade

(2011) Christoph A. von Ilberg et al.   AUDIOLOGY AND NEURO-OTOLOGY

Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment

(2011) K Lee et al.   CLINICAL GENETICS

Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations

(2011) Nicole J. D. Weegerink et al.   JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY

Tmprss3, a Transmembrane Serine Protease Deficient in Human DFNB8/10 Deafness, Is Critical for Cochlear Hair Cell Survival at the Onset of Hearing

(2011) Lydie Fasquelle et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

MutationTaster evaluates disease-causing potential of sequence alterations

(2010) Jana Marie Schwarz et al.   NATURE METHODS

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Identification of deleterious mutations within three human genomes

(2009) S. Chun et al.   GENOME RESEARCH

Detection of nonneutral substitution rates on mammalian phylogenies

(2009) K. S. Pollard et al.   GENOME RESEARCH

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols