Yoh-ichiro Iwasa

Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation

Takehiko Naito, Shin‐ya Nishio, Yoh-ichiro Iwasa et al. · PLoS ONE · 2013 · 66 citations · Full text

Founder Mutation, Genotype-phenotype Correlations, Deafness Gene +14

OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients

Yoh-ichiro Iwasa, Shin‐ya Nishio, Akiko Sugaya et al. · PLoS ONE · 2019 · 47 citations · Full text

Genetics, Pathology, Molecular Genetics +19

Deafness Gene Expression Patterns in the Mouse Cochlea Found by Microarray Analysis

Hidekane Yoshimura, Yutaka Takumi, Shin‐ya Nishio et al. · PLoS ONE · 2014 · 44 citations · Full text

OTOF mutation screening in Japanese severe to profound recessive hearing loss patients

Yoh-ichiro Iwasa, Shin‐ya Nishio, Hidekane Yoshimura et al. · BMC Medical Genetics · 2013 · 43 citations · Full text

Detection and Confirmation of Deafness-Causing Copy Number Variations in the <i>STRC</i> Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization

Hideaki Moteki, Héla Azaiez, Christina Sloan-Heggen et al. · Annals of Otology Rhinology & Laryngology · 2016 · 40 citations · Full text