Takehiko Naito

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

Maiko Miyagawa, Takehiko Naito, Shin‐ya Nishio et al. · PLoS ONE · 2013 · 102 citations · Full text

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

Prevalence of level V metastasis in head and neck squamous cell carcinoma

Kazuyuki Kainuma, Takuya Yano, Ryosuke Kitoh et al. · Acta Oto-Laryngologica · 2012 · 15 citations

A Japanese family showing high-frequency hearing loss with<i>KCNQ4</i>and<i>TECTA</i>mutations

Kotaro Ishikawa, Takehiko Naito, Shin‐ya Nishio et al. · Acta Oto-Laryngologica · 2014 · 10 citations