Towards a Unified Testing Framework for Single-Sided Deafness Studies: A Consensus Paper

Paul Van de Heyning, Dayse Távora‐Vieira, Griet Mertens, +36

Audiology and Neurotology

RNA Interference Prevents Autosomal-Dominant Hearing Loss

Seiji B. Shibata, Paul T. Ranum, Hideaki Moteki, +6

The American Journal of Human Genetics

Etiology of single-sided deafness and asymmetrical hearing loss

Shin‐ichi Usami, Ryosuke Kitoh, Hideaki Moteki, +7

Acta Oto-Laryngologica

IgG4-related chronic rhinosinusitis: A new clinical entity of nasal disease

Hideaki Moteki, Masanori Yasuo, Hideaki Hamano, +2

Acta Oto-Laryngologica

Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness

Hidekane Yoshimura, Seiji B. Shibata, Paul T. Ranum, +2

Molecular Therapy

In Vivo Gene TherapyGeneticsHearing HealthHuman Tmc1 DeafnessMature Murine Model +21

Frequency and clinical features of hearing loss caused by STRC deletions

Yoh Yokota, Hideaki Moteki, Shin‐ya Nishio, +15

Scientific Reports

Achievement of hearing preservation in the presence of an electrode covering the residual hearing region

Shin‐ichi Usami, Hideaki Moteki, Nobuyoshi Suzuki, +6

Acta Oto-Laryngologica

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

Shin‐ichi Usami, Hideaki Moteki, Keita Tsukada, +9

Acta Oto-Laryngologica

Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord

Sakiko Furutate, Satoshi Iwasaki, Shin‐ya Nishio, +2

Acta Oto-Laryngologica

WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis

Masafumi Kobayashi, Maiko Miyagawa, Shin‐ya Nishio, +18

PLoS ONE

Large SeriesGeneticsPathologyMolecular GeneticsDisease Gene Identification +21