Satoko Abe

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

Shin‐ichi Usami, Satoko Abe, Mike D. Weston et al. · Human Genetics · 1999 · 316 citations

Medicine, Neuroscience, Otolaryngology +14

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 gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss

Satoko Abe, Shin‐ichi Usami, Yusuke Nakamura · Journal of Human Genetics · 2003 · 134 citations

Medicine, Genetics, Molecular Genetics +14

Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues**Nucleotide sequence data reported herein are available in the DDBJ/EMBL/GenBank databases; for details, see the Electronic-Database Information section of this article.

Satoko Abe, Toyomasa Katagiri, Akihiko Saito-Hisaminato et al. · The American Journal of Human Genetics · 2003 · 127 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +14