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Journal of Human Genetics|January 10, 2014
Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screeningTakuya Yano, Shin-ya Nishio, Shin-ichi Usami, et al.Scientific Reports|December 22, 2025
Targeted long-read nanopore sequencing as a complementary approach for detecting STRC variants and distinguishing the STRCP1 pseudogeneHideaki Moteki, Shin-Ya Nishio, Shin-Ichi UsamiAuris, Nasus, Larynx|February 10, 2007
Meningioma of the paranasal sinus: a case reportKazuyuki Kainuma, Yutaka Takumi, Takeshi Uehara, et al.Auris, Nasus, Larynx|March 13, 2013
Long term speech perception after cochlear implant in pediatric patients with GJB2 mutationsHaruo Yoshida, Haruo Takahashi, Yukihiko Kanda, et al.Acta Oto-Laryngologica|March 17, 2007
Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the gene EYA1Tatsuo Matsunaga, Michiyo Okada, Shin-Ichi Usami, et al.Auris, Nasus, Larynx|April 23, 2018
Pneumolabyrinth, intracochlear and vestibular fluid loss after cochlear implantationHideaki Moteki, Yasunari Fujinaga, Tetsuya Goto, et al.Auris, Nasus, Larynx|October 24, 2002
Identification of 605ins46, a novel GJB2 mutation in a Japanese familyIsamu Yuge, Akihiro Ohtsuka, Tatsuo Matsunaga, et al.Plos One|December 3, 2016
Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss PatientsYoh-Ichiro Iwasa, Shin-Ya Nishio, Shin-Ichi UsamiJournal of Human Genetics|March 8, 2003
Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplificationSatoko Abe, Kumiko Koyama, Shin-ichi Usami, et al.Journal of Human Genetics|May 12, 2007
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in JapaneseHisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta, et al.Pageof 26