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Genes|September 27, 2019
The Prevalence and Clinical Characteristics of <i>TECTA</i>-Associated Autosomal Dominant Hearing LossRika Yasukawa, Hideaki Moteki, Shin-Ya Nishio, et al.Scientific Reports|March 15, 2019
Frequency and clinical features of hearing loss caused by STRC deletionsYoh Yokota, Hideaki Moteki, Shin-Ya Nishio, et al.Scientific Reports|February 29, 2020
Prevalence and clinical features of hearing loss caused by EYA4 variantsJun Shinagawa, Hideaki Moteki, Shin-Ya Nishio, et al.Acta Oto-Laryngologica|December 15, 2020
Development and validation of an iPad-based Japanese language monosyllable speech perception test (iCI2004 monosyllable)Shin-Ya Nishio, Tetsuya Tono, Takako Iwaki, et al.Genes|January 25, 2025
Novel <i>OTOG</i> Variants and Clinical Features of Hearing Loss in a Large Japanese CohortYasuhiro Arai, Shin-Ya Nishio, Shinichi Goto, et al.Plos One|May 26, 2017
POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing lossTomohiro Kitano, Maiko Miyagawa, Shin-Ya Nishio, et al.Genes|February 27, 2026
The Clinical Details of <i>MYH9</i>-Related Disease and DFNA17 in a Large Japanese Hearing Loss CohortShinichi Goto, Akira Sasaki, Shin-Ya Nishio, et al.Plos One|March 13, 2018
WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysisMasafumi Kobayashi, Maiko Miyagawa, Shin-Ya Nishio, et al.Plos One|May 17, 2019
OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patientsYoh-Ichiro Iwasa, Shin-Ya Nishio, Akiko Sugaya, et al.Acta Oto-Laryngologica|March 25, 2017
The clinical features and prognosis of mumps-associated hearing loss: a retrospective, multi-institutional investigation in JapanShinya Morita, Keishi Fujiwara, Atsushi Fukuda, et al.Pageof 15