Atsushi Namba

Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese

Koji Tsukamoto, Hiroaki Suzuki, Daisuke Harada et al. · European Journal of Human Genetics · 2003 · 256 citations

Medicine, Genetics, Molecular Genetics +15

GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation

Akihiro Ohtsuka, Isamu Yuge, Shinobu Kimura et al. · Human Genetics · 2003 · 155 citations

Life Sciences, Genetics, Molecular Genetics +10

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease

Shin‐ichi Usami, Kentaro Takahashi, Isamu Yuge et al. · European Journal of Human Genetics · 2003 · 95 citations

Medicine, Genetics, Molecular Genetics +11

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 · 67 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Hearing impairment and cognitive function among a community-dwelling population in Japan

Norio Sugawara, Akira Sasaki, Norio Yasui‐Furukori et al. · Annals of General Psychiatry · 2011 · 42 citations · Full text

Health Professions, Geriatric Medicine, Health Sciences +14