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Acta Oto-Laryngologica|April 28, 2022
Etiology of hearing loss affects auditory skill development and vocabulary development in pediatric cochlear implantation casesShin-Ya Nishio, Hideaki Moteki, Maiko Miyagawa, et al.
Stem Cell Research|June 15, 2024
Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23Daisuke Arai, Mikako Takahashi-Shibata, Takao Ukaji, et al.
Acta Oto-Laryngologica|February 17, 2016
SOD1 gene polymorphisms in sudden sensorineural hearing lossRyosuke Kitoh, Shin-Ya Nishio, Kaoru Ogawa, et al.
Human Genetics|July 7, 2021
Human deafness-associated variants alter the dynamics of key molecules in hair cell stereocilia F-actin coresTakushi Miyoshi, Inna A Belyantseva, Shin-Ichiro Kitajiri, et al.
EMBO Molecular Medicine|October 7, 2016
Constitutive activation of DIA1 (DIAPH1) via C-terminal truncation causes human sensorineural hearing lossTakehiko Ueyama, Yuzuru Ninoyu, Shin-Ya Nishio, et al.
Medicine|May 9, 2020
A phase I/IIa double blind single institute trial of low dose sirolimus for Pendred syndrome/DFNB4Masato Fujioka, Takumi Akiyama, Makoto Hosoya, et al.
Genes|September 19, 2019
Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of <i>OTOA</i>-Associated Hearing LossKenjiro Sugiyama, Hideaki Moteki, Shin-Ichiro Kitajiri, et al.
Scientific Reports|April 29, 2020
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing lossHiroki Miyajima, Hideaki Moteki, Timothy Day, et al.
Genes|January 25, 2025
The Heterozygous p.A684V Variant in the <i>WFS1</i> Gene Is a Mutational Hotspot Causing a Severe Hearing Loss PhenotypeShintaro Otsuka, Chihiro Morimoto, Shin-Ya Nishio, et al.
Plos One|March 13, 2014
Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1Hidekane Yoshimura, Satoshi Iwasaki, Shin-Ya Nishio, et al.
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