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Acta Oto-Laryngologica|March 25, 2014
A Japanese family showing high-frequency hearing loss with KCNQ4 and TECTA mutationsKotaro Ishikawa, Takehiko Naito, Shin-Ya Nishio, et al.
Scientific Reports|March 8, 2023
Prognostic significance of pre- and post-treatment hematological biomarkers in patients with head and neck cancer treated with chemoradiotherapyYoh-Ichiro Iwasa, Moeka Shimizu, Kazuki Matsuura, et al.
BMC Medical Genetics|September 24, 2013
OTOF mutation screening in Japanese severe to profound recessive hearing loss patientsYoh-ichiro Iwasa, Shin-ya Nishio, Hidekane Yoshimura, et al.
International Journal of Pediatric Otorhinolaryngology|December 15, 2012
An Usher syndrome type 1 patient diagnosed before the appearance of visual symptoms by MYO7A mutation analysisHidekane Yoshimura, Satoshi Iwasaki, Yukihiko Kanda, et al.
Oncology|January 18, 2022
Factors Affecting Nivolumab Therapy Outcome in Patients with Head and Neck Cancer: A Single-Center AnalysisYoh-Ichiro Iwasa, Yoh Yokota, Ryosuke Kitoh, et al.
Plos One|May 30, 2013
Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutationTakehiko Naito, Shin-ya Nishio, Yoh-ichiro Iwasa, et al.
The Annals of Otology, Rhinology, and Laryngology|March 28, 2015
Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafnessShin-Ya Nishio, Mitsuru Hattori, Hideaki Moteki, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|November 24, 2022
Impact of Low Skeletal Muscle Mass on the Prognosis of Patients with Head and Neck Cancer Treated NonsurgicallyYoh-Ichiro Iwasa, Ryosuke Kitoh, Ken Hiramatsu, et al.
The Annals of Otology, Rhinology, and Laryngology|July 30, 2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic HybridizationHideaki Moteki, Hela Azaiez, Christina M Sloan-Heggen, 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.
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