Vestibular Preservation After Cochlear Implantation Using the Round Window Approach by Keita Tsukada, Shin-ichi Usami, Shin-ichi Usami

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Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study. by Maiko Miyagawa, Shin-ya Nishio, Shin-ichi Usami

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Milestones toward cochlear gene therapy for patients with hereditary hearing loss by Hidekane Yoshimura, Shin‐Ya Nishio, Shin‐Ichi Usami

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Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients. by Yoh-Ichiro Iwasa, Shin-Ya Nishio, Shin-Ichi Usami

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Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants by Keita Tsukada, Shin-ya Nishio, Yutaka Takumi, Shin-ichi Usami

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The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B by Kizuki Watanabe, Shin-ya Nishio, Shin-ichi Usami, the Deafness Gene Study Consortium

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Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS. by Maiko Miyagawa, Shin-ya Nishio, Takuo Ikeda, Kunihiro Fukushima, Shin-ichi Usami

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Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients. by Maiko Miyagawa, Takehiko Naito, Shin-ya Nishio, Naoyuki Kamatani, Shin-ichi Usami

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Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients. by Kentaro Mori, Hideaki Moteki, Maiko Miyagawa, Shin-Ya Nishio, Shin-Ichi Usami

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Compound heterozygous dominant and recessive GJB2 mutations cause deafness with palmoplantar keratoderma by Yasuhiro Arai, Masahiro Takahashi, Naoko Sakuma, Shin-Ya Nisio, Nobuhiko Oridate, Shin-Ichi Usami

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A novel case of concurrent occurrence of demyelinating-polyneuropathy-causing PMP22 duplication and SOX10 gene mutation producing severe hypertrophic neuropathy by Nozomu Matsuda, Koushi Ootsuki, Shunsuke Kobayashi, Ayaka Nemoto, Hitoshi Kubo, Shin-ichi Usami, Kazuaki Kanani

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Deafness gene expression patterns in the mouse cochlea found by microarray analysis. by Hidekane Yoshimura, Yutaka Takumi, Shin-ya Nishio, Nobuyoshi Suzuki, Yoh-ichiro Iwasa, Shin-ichi Usami

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Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study. by Shin-ichi Usami, Shin-ya Nishio, Makoto Nagano, Satoko Abe, Toshikazu Yamaguchi, Deafness Gene Study Consortium

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Vibrant soundbridge implantation prior to auricular reconstruction with unilateral microtia‐atresia by Hidekane Yoshimura, Masahiro Takahashi, Satoshi Iwasaki, Jun Shinagawa, Ikkei Takashimizu, Fumio Nagai, Takatoshi Yotsuyanagi, Shin‐ichi Usami

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Cochlear implantation in a patient with a POU4F3 mutation by Keitaro Miyake, Kyoko Shirai, Nobuhiro Nishiyama, Sachie Kawaguchi, Yoko Ohta, Atsushi Kawano, Shin‐ichi Usami, Tomohiro Kitano, Kiyoaki Tsukahara

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Gene expression pattern after insertion of dexamethasone-eluting electrode into the guinea pig cochlea. by Yutaka Takumi, Shin-ya Nishio, Kenneth Mugridge, Tomohiro Oguchi, Shigenari Hashimoto, Nobuyoshi Suzuki, Satoshi Iwasaki, Claude Jolly, Shin-ichi Usami

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Congenital Membranous Stapes Footplate Producing Episodic Pressure-Induced Perilymphatic Fistula Symptoms by Han Matsuda, Yasuhiko Tanzawa, Tatsuro Sekine, Tomohiro Matsumura, Shiho Saito, Susumu Shindo, Shin-ichi Usami, Yasuhiro Kase, Akinori Itoh, Tetsuo Ikezono

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Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A by Takao Ukaji, Mikako Takahashi-Shibata, Daisuke Arai, Harumi Tsutsumi, Shori Tajima, Wado Akamatsu, Fumihiko Matsumoto, Katsuhisa Ikeda, Shin-ichi Usami, Kazusaku Kamiya

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Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation. by Takehiko Naito, Shin-ya Nishio, Yoh-ichiro Iwasa, Takuya Yano, Kozo Kumakawa, Satoko Abe, Kotaro Ishikawa, Hiromi Kojima, Atsushi Namba, Chie Oshikawa, Shin-ichi Usami

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Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23 by Daisuke Arai, Mikako Takahashi-Shibata, Takao Ukaji, Harumi Tsutsumi, Shori Tajima, Shin-ya Nishio, Kei-ichi Ishikawa, Wado Akamatsu, Fumihiko Matsumoto, Katsuhisa Ikeda, Shin-ichi Usami, Kazusaku Kamiya

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