Citations (30)
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Read on this site (5)
Hidekane Yoshimura, Hideaki Moteki, Shin-ya Nishio & Shin-ichi Usami. (2020) Electric-acoustic stimulation with longer electrodes for potential deterioration in low-frequency hearing. Acta Oto-Laryngologica 140:8, pages 624-630.
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Hideaki Moteki, Shin-Ya Nishio, Maiko Miyagawa, Keita Tsukada, Yoshihiro Noguchi & Shin-Ichi Usami. (2018) Feasibility of hearing preservation for residual hearing with longer cochlear implant electrodes. Acta Oto-Laryngologica 138:12, pages 1080-1085.
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Shin-ya Nishio & Shin-ichi Usami. (2017) Outcomes of cochlear implantation for the patients with specific genetic etiologies: a systematic literature review. Acta Oto-Laryngologica 137:7, pages 730-742.
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Hideaki Moteki, Shin-ya Nishio, Maiko Miyagawa, Keita Tsukada, Satoshi Iwasaki & Shin-ichi Usami. (2017) Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearing. Acta Oto-Laryngologica 137:5, pages 516-521.
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Shin-Ichi Usami, Hideaki Moteki, Keita Tsukada, Maiko Miyagawa, Shin-Ya Nishio, Yutaka Takumi, Satoshi Iwasaki, Kozo Kumakawa, Yasushi Naito, Haruo Takahashi, Yukihiko Kanda & Tetsuya Tono. (2014) Hearing preservation and clinical outcome of 32 consecutive electric acoustic stimulation (EAS) surgeries. Acta Oto-Laryngologica 134:7, pages 717-727.
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Articles from other publishers (25)
Anke Tropitzsch, Thore Schade-Mann, Philipp Gamerdinger, Saskia Dofek, Björn Schulte, Martin Schulze, Sarah Fehr, Saskia Biskup, Tobias B. Haack, Petra Stöbe, Andreas Heyd, Jennifer Harre, Anke Lesinski-Schiedat, Andreas Büchner, Thomas Lenarz, Athanasia Warnecke, Marcus Müller, Barbara Vona, Ernst Dahlhoff, Hubert Löwenheim & Martin Holderried. (2023) Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing Loss. Ear & Hearing 44:6, pages 1464-1484.
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Shin-ichiro Oka, Masahiro Takahashi, Sakiko Furutate, Shogo Oyamada, Shin-ya Nishio, Shin-ichi Usami & Satoshi Iwasaki. (2023) A Study on Genetic Background in Cochlear Implant Patients人工内耳患者における遺伝的背景に関する検討. Practica Oto-Rhino-Laryngologica 116:11, pages 1065-1070.
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Chee-Yee Lee, Pei-Hsuan Lin, Cheng-Yu Tsai, Yu-Ting Chiang, Hong-Ping Chiou, Ko-Yin Chiang, Pei-Lung Chen, Jacob Shu-Jui Hsu, Tien-Chen Liu, Hung-Pin Wu, Chen-Chi Wu & Chuan-Jen Hsu. (2022) Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical Implications. Biomedicines 10:8, pages 1846.
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Pey-Yu Chen, Cheng-Yu Tsai, Jiunn-Liang Wu, Yi-Lu Li, Che-Ming Wu, Kuang-Chao Chen, Chung-Feng Hwang, Hung-Pin Wu, Hung-Ching Lin, Yen-Fu Cheng, Ming-Yu Lo, Tien-Chen Liu, Ting-Hua Yang, Pei-Lung Chen, Chuan-Jen Hsu & Chen-Chi Wu. (2021) Hearing Features and Cochlear Implantation Outcomes in Patients With PathogenicMYO15AVariants: a Multicenter Observational Study. Ear & Hearing 43:4, pages 1198-1207.
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Natsumi Uehara, Takeshi Fujita, Daisuke Yamashita, Jun Yokoi, Sayaka Katsunuma, Akinobu Kakigi, Shin-ya Nishio, Ken-ichi Nibu & Shin-ichi Usami. (2021) Genetic background in late-onset sensorineural hearing loss patients. Journal of Human Genetics 67:4, pages 223-230.
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Shin-ichi Usami, Yuichi Isaka, Maiko Miyagawa & Shin-ya Nishio. (2022) Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss. Human Genetics 141:3-4, pages 903-914.
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Shin-ichi Usami & Shin-ya Nishio. (2021) The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients. Human Genetics 141:3-4, pages 665-681.
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Tong Zhao, Peng Ma, Fangfang Zhao, Tihua Zheng, Bin Yan, Qiang Zhang, Jing Yuan, Bing Hu, Ying Yang, Juan Hu, Ruishuang Geng, Bo Hua Hu, Tengyang Sun, Qing Yin Zheng & Bo Li. (2021)
Phenotypic differences in the inner ears of CBA/CaJ and C57BL/6J mice carrying missense and single base pair deletion mutations in the
Cdh23
gene
. Journal of Neuroscience Research 99:10, pages 2743-2758.
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. (2021) 難聴の個別化医療を目指して : Toward Personalized Medicine of Deafness. Nippon Jibiinkoka Gakkai Kaiho 124:2, pages 135-147.
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Daisuke Kikuchi, Mitsuyoshi Imaizumi, Koshi Otsuki & Shigeyuki Murono. (2021) Usefulness of Genetic Testing in Deciding the Indication for Electric Acoustic Stimulation残存聴力活用型人工内耳の選択における遺伝子検査の有用性. Practica Oto-Rhino-Laryngologica 114:6, pages 415-419.
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Eric Nisenbaum, Sandra Prentiss, Denise Yan, Aida Nourbakhsh, Molly Smeal, Meredith Holcomb, Ivette Cejas, Fred Telischi & Xue Zhong Liu. (2021) Screening Strategies for Deafness Genes and Functional Outcomes in Cochlear Implant Patients. Otology & Neurotology 42:1, pages 180-187.
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Adrien A. Eshraghi, Sai P. Polineni, Camron Davies, David Shahal, Jeenu Mittal, Zaid Al-Zaghal, Rahul Sinha, Urmi Jindal & Rahul Mittal. (2020) Genotype-Phenotype Correlation for Predicting Cochlear Implant Outcome: Current Challenges and Opportunities. Frontiers in Genetics 11.
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Shin‐ichi Usami, Shin‐ya Nishio, Hideaki Moteki, Maiko Miyagawa & Hidekane Yoshimura. (2020) Cochlear Implantation From the Perspective of Genetic Background. The Anatomical Record 303:3, pages 563-593.
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Bo Li, Tihua Zheng, Caifang Yan, Wenjun Wang, Jinjin Zhang, Luping Zhang, Juan Hu, Li Zhang, Yuzhu Wan, Minyan Zhang & Qingyin Zheng. (2019) Chemical chaperone 4-phenylbutyrate prevents hearing loss and cochlear hair cell death in Cdh23 erl/erl mutant mice. NeuroReport 30:3, pages 145-150.
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Tao Yang, Luo Guo, Longhao Wang & Xiaoyu Yu. 2019. Hearing Loss: Mechanisms, Prevention and Cure. Hearing Loss: Mechanisms, Prevention and Cure
73
92
.
Thomas Parzefall, Alexandra Frohne, Martin Koenighofer, Andreas Kirchnawy, Berthold Streubel, Christian Schoefer, Wolfgang Gstoettner, Klemens Frei & Trevor Lucas. (2017) Identification of a rare COCH mutation by whole-exome sequencing. Wiener klinische Wochenschrift 130:9-10, pages 299-306.
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Paridhy Vanniya. S, C.R. Srikumari Srisailapathy & Ramkumar Kunka Mohanram. (2018) The tip link protein Cadherin-23: From Hearing Loss to Cancer. Pharmacological Research 130, pages 25-35.
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Jason R. Rudman, Christine Mei, Sara E. Bressler, Susan H. Blanton & Xue-Zhong Liu. (2018) Precision medicine in hearing loss. Journal of Genetics and Genomics 45:2, pages 99-109.
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Urszula Lechowicz, Agnieszka Pollak, Agnieszka Frączak, Małgorzata Rydzanicz, Piotr Stawiński, Artur Lorens, Piotr Skarżyński, Henryk Skarżyński, Rafał Płoski & Monika Ołdak. (2017) Application of next‑generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss. Molecular Medicine Reports.
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Anna M. H. Korver, Richard J. H. Smith, Guy Van Camp, Mark R. Schleiss, Maria A. K. Bitner-Glindzicz, Lawrence R. Lustig, Shin-ichi Usami & An N. Boudewyns. (2017) Congenital hearing loss. Nature Reviews Disease Primers 3:1.
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Yuko Kataoka, Akiko Sugaya, Yukihide Maeda, Shin Kariya, Ryotaro Omichi, Kunihiro Fukushima & Kazunori Nishizaki. (2017) Genetic Counseling of a Hearing-impaired Patient with Multiple Genetic Mutations. Nippon Jibiinkoka Gakkai Kaiho 120:2, pages 131-136.
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Maiko Miyagawa, Shin-Ya Nishio & Shin-Ichi Usami. (2016) A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic Epidemiology. Otology & Neurotology 37:2, pages e126-e134.
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Maiko Miyagawa, Shin-ya Nishio, Aya Ichinose, Satoshi Iwasaki, Takaaki Murata, Shin-ichiro Kitajiri & Shin-ichi Usami. (2015)
Mutational Spectrum and Clinical Features of Patients With
ACTG1
Mutations Identified by Massively Parallel DNA Sequencing
. Annals of Otology, Rhinology & Laryngology 124:1_suppl, pages 84S-93S.
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Satoko Abe, Makoto Nagano, Shin-ya Nishio, Kozo Kumakawa & Shin-ichi Usami. (2014) High-Frequency Involved Hearing Loss Caused by Novel Mitochondrial DNA Mutation in 16S Ribosomal RNA Gene. Otology & Neurotology 35:6, pages 1087-1090.
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. (2013) . AUDIOLOGY JAPAN 56:5, pages 527-528.
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