【researchmap】
https://researchmap.jp/read0045019

１、Shinagawa J, Moteki H, Nishio S, Ohyama K, Otsuki K, Iwasaki S, Masuda S, Oshikawa C, Ohta Y, Arai Y, Takahashi M, Sakuma N, Abe S, Sakurai Y, Sakaguchi H, Ishino T, Uehara N, Usami S: Prevalence and clinical features of hearing loss caused by EYA4 variants. Scientific reports 10:3662 2020
２、Miyajima H, Moteki H, Day T, Nishio SY, Murata T, Ikezono T, Takeda H, Abe S, Iwasaki S, Takahashi M, Naito Y, Yamazaki H, Kanda Y, Kitajiri SI, Usami S: Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss. Sci Rep 10:7056, 2020.
３、Iwasa Y, Nishio S, Sugaya A, Kataoka Y, Kanda Y, Taniguchi M, Nagai K, Naito Y, Ikezono T, Horie R, Sakurai Y, Matsuoka R, Takeda H, Abe S, Kihara C, Ishino T, Morita S, Iwasaki S, Takahashi M, Ito T, Arai Y, Usami S:OTOF mutation analysis with massively parallel DNA sequencing in 2265 Japanese sensorineural hearing loss patients. PLoS One 16;14(5):e0215931, 2019.
４、Takahashi M, Iwasaki S :A postimplant cholesteatoma after modified radical mastoidectomy. International J of Otolaryngology H and N surgery. 10.4236/ijohns.2019.81004, 2019
５、Ideura M, Nishio SY, Moteki H, Takumi Y, Miyagawa M, Sato T, Kobayashi Y, Ohyama K, Oda K, Matsui T, Ito T, Suzumura H, Nagai K, Izumi S, Nishiyama N, Komori M, Kumakawa K, Takeda H, Kishimoto Y, Iwasaki S, Furutate S, Ishikawa K, Fujioka M, Nakanishi H, Nakayama J, Horie R, Ohta Y, Naito Y, Kakudo M, Sakaguchi H, Kataoka Y, Sugahara K, Hato N, Nakagawa T, Tsuchihashi N, Kanda Y, Kihara C, Tono T, Miyanohara I, Ganaha A, Usami SI.: Comprehensive analysis of syndromic hearing loss patients in Japan. Sci Rep 19,9(1):11976, 2019.
６、Maekawa K, Nishio S, Abe S, Goto S, Honkura Y, Iwasaki S, Kanda Y, Kobayashi Y, Oka S, Okami M, Oshikawa C, Sakuma N, Sano H, Shirakura M, Uehara N, Usami S: Mutational spectrum and clinical features of patients with LOXHD1 variants identified in an 8074 hearing loss patient cohort. Genes 10(10), pii: E735.doi:10.3390, 2019