Ikuyo Miyanohara

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 et al. · PLoS ONE · 2018 · 53 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Comprehensive analysis of syndromic hearing loss patients in Japan

Michie Ideura, Shin‐ya Nishio, Hideaki Moteki et al. · Scientific Reports · 2019 · 45 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B

Kizuki Watanabe, Shin‐ya Nishio, Shin‐ichi Usami et al. · Scientific Reports · 2024 · 22 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A Case of Cochlear Nerve Deficiency Without Profound Sensorineural Hearing Loss

Ikuyo Miyanohara, Keiichi Miyashita, Koji Takumi et al. · Otology & Neurotology · 2011 · 14 citations

Medicine, Audiology, Otolaryngology +15

Novel Mutations in <i>GRXCR1</i> at DFNB25 Lead to Progressive Hearing Loss and Dizziness

Kentaro Mori, Ikuyo Miyanohara, Hideaki Moteki et al. · Annals of Otology Rhinology & Laryngology · 2015 · 11 citations

Life Sciences, Genetics, Molecular Genetics +16