| A large cohort study of GJB2 mutations in Japanese hearing loss patients K Tsukada, S Nishio, S Usami, Deafness Gene Study Consortium Clinical genetics 78 (5), 464-470, 2010 | 160 | 2010 |
| Ubiquinol-10 supplementation activates mitochondria functions to decelerate senescence in senescence-accelerated mice G Tian, J Sawashita, H Kubo, S Nishio, S Hashimoto, N Suzuki, ... Antioxidants & redox signaling 20 (16), 2606-2620, 2014 | 137 | 2014 |
| Ethnic-Specific Spectrum of GJB2 and SLC26A4 Mutations: Their Origin and a Literature Review K Tsukada, S Nishio, M Hattori, S Usami Annals of Otology, Rhinology & Laryngology 124 (1_suppl), 61S-76S, 2015 | 127 | 2015 |
| Etiology of single-sided deafness and asymmetrical hearing loss S Usami, R Kitoh, H Moteki, S Nishio, T Kitano, M Kobayashi, ... Acta oto-laryngologica 137 (sup565), S2-S7, 2017 | 110 | 2017 |
| Mutation spectrum and genotype–phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study M Miyagawa, S Nishio, S Usami Journal of human genetics 59 (5), 262-268, 2014 | 105 | 2014 |
| Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients M Miyagawa, T Naito, S Nishio, N Kamatani, S Usami PloS one 8 (8), e71381, 2013 | 103 | 2013 |
| Achievement of hearing preservation in the presence of an electrode covering the residual hearing region SI Usami, H Moteki, N Suzuki, H Fukuoka, M Miyagawa, SY Nishio, ... Acta oto-laryngologica 131 (4), 405-412, 2011 | 99 | 2011 |
| Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS M Miyagawa, S Nishio, T Ikeda, K Fukushima, S Usami PLoS One 8 (10), e75793, 2013 | 98 | 2013 |
| Deafness gene variations in a 1120 nonsyndromic hearing loss cohort: molecular epidemiology and deafness mutation spectrum of patients in Japan S Nishio, S Usami Annals of Otology, Rhinology & Laryngology 124 (1_suppl), 49S-60S, 2015 | 92 | 2015 |
| Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study M Miyagawa, S Nishio, S Usami Public Library of Science 7 (8), e40366, 2012 | 90 | 2012 |
| Nationwide epidemiological survey of idiopathic sudden sensorineural hearing loss in Japan R Kitoh, S Nishio, K Ogawa, S Kanzaki, N Hato, M Sone, S Fukuda, ... Acta oto-laryngologica 137 (sup565), S8-S16, 2017 | 86 | 2017 |
| A comprehensive study on the etiology of patients receiving cochlear implantation with special emphasis on genetic epidemiology M Miyagawa, SY Nishio, SI Usami Otology & Neurotology 37 (2), e126-e134, 2016 | 78 | 2016 |
| Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation T Naito, S Nishio, Y Iwasa, T Yano, K Kumakawa, S Abe, K Ishikawa, ... PloS one 8 (5), e63231, 2013 | 78 | 2013 |
| Hearing preservation and clinical outcome of 32 consecutive electric acoustic stimulation (EAS) surgeries SI Usami, H Moteki, K Tsukada, M Miyagawa, SY Nishio, Y Takumi, ... Acta Oto-Laryngologica 134 (7), 717-727, 2014 | 73 | 2014 |
| Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study S Usami, S Nishio, M Nagano, S Abe, T Yamaguchi, ... PloS one 7 (2), e31276, 2012 | 73 | 2012 |
| Frequency and clinical features of hearing loss caused by STRC deletions Y Yokota, H Moteki, S Nishio, T Yamaguchi, K Wakui, Y Kobayashi, ... Scientific Reports 9 (1), 4408, 2019 | 70 | 2019 |
| Constitutive activation of DIA 1 (DIAPH 1) via C‐terminal truncation causes human sensorineural hearing loss T Ueyama, Y Ninoyu, S Nishio, T Miyoshi, H Torii, K Nishimura, ... EMBO molecular medicine 8 (11), 1310-1324, 2016 | 60 | 2016 |
| The responsible genes in Japanese deafness patients and clinical application using Invader assay SI Usami, M Wagatsuma, H Fukuoka, H Suzuki, K Tsukada, S Nishio, ... Acta oto-laryngologica 128 (4), 446-454, 2008 | 60 | 2008 |
| Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord S Furutate, S Iwasaki, S Nishio, H Moteki, S Usami Acta oto-laryngologica 131 (9), 976-982, 2011 | 59 | 2011 |
| Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness S Nishio, M Hattori, H Moteki, K Tsukada, M Miyagawa, T Naito, ... Annals of Otology, Rhinology & Laryngology 124 (1_suppl), 6S-48S, 2015 | 52 | 2015 |
