Shin-Ichi Usami

ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 31

Top Venues

Institute of Mountain Science, Shinshu University

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Institute of Mountain Science, Shinshu University Apr 1o 2020

Japan

Dr.

Publications

Jun Shinagawa, Hidekane Yoshimura, Shin-Ya Nishio, Yutaka Takumi, Shin-Ichi Usami
The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantation. Acta oto-laryngologica (2023)
Jun Shinagawa, Hidekane Yoshimura, Shin-Ya Nishio, Yutaka Takumi, Shin-Ichi Usami
The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantation. Acta oto-laryngologica (2023)
Masayuki Kawakita, Satoshi Iwasaki, Hideaki Moteki, Shin-Ya Nishio, Tomoki Kosho, Shin-Ichi Usami
Otological Features of Patients with Musculocontractural Ehlers-Danlos Syndrome Caused by Pathogenic Variants in CHST14 (mcEDS- CHST14 ). Genes 14 (7) (2023)
Jun Shinagawa, Hidekane Yoshimura, Shin-Ya Nishio, Yutaka Takumi, Shin-Ichi Usami
The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantation. Acta oto-laryngologica (2023)
Vedat Topsakal, Sumit Agrawal, Marcus Atlas, Wolf-Dieter Baumgartner, Kevin Brown, Iain A Bruce, Stefan Dazert, Rudolf Hagen, Luis Lassaletta, Robert Mlynski, Christopher H Raine, Gunesh P Rajan, Joachim Schmutzhard, Georg Mathias Sprinzl, Hinrich Staecker, Shin-Ichi Usami, Vincent van Rompaey, Mario E Zernotti, Paul van de Heyning
Minimally Traumatic Cochlear Implant Surgery: Expert Opinion in 2010 and 2020. Journal of personalized medicine 12 (10) (2022)
Shin-Ichi Usami, Yuichi Isaka, Maiko Miyagawa, Shin-Ya Nishio
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) (2022)
Hidekane Yoshimura, Masahiro Takahashi, Satoshi Iwasaki, Jun Shinagawa, Ikkei Takashimizu, Fumio Nagai, Takatoshi Yotsuyanagi, Shin-Ichi Usami
Vibrant soundbridge implantation prior to auricular reconstruction with unilateral microtia-atresia. Clinical case reports 9 (8) (2021)
Natsumi Uehara, Takeshi Fujita, Daisuke Yamashita, Jun Yokoi, Sayaka Katsunuma, Akinobu Kakigi, Shin-Ya Nishio, Ken-Ichi Nibu, Shin-Ichi Usami
Genetic background in late-onset sensorineural hearing loss patients. Journal of human genetics (2021)
Yoh-Ichiro Iwasa, Shin-Ya Nishio, Hidekane Yoshimura, Akiko Sugaya, Yuko Kataoka, Yukihide Maeda, Yukihiko Kanda, Kyoko Nagai, Yasushi Naito, Hiroshi Yamazaki, Tetsuo Ikezono, Han Matsuda, Masako Nakai, Risa Tona, Yuika Sakurai, Remi Motegi, Hidehiko Takeda, Marina Kobayashi, Chiharu Kihara, Takashi Ishino, Shin-Ya Morita, Satoshi Iwasaki, Masahiro Takahashi, Sakiko Furutate, Shin-Ichiro Oka, Toshinori Kubota, Yasuhiro Arai, Yumiko Kobayashi, Daisuke Kikuchi, Tomoko Shintani, Noriko Ogasawara, Yohei Honkura, Shuji Izumi, Misako Hyogo, Yuzuru Ninoyu, Mayumi Suematsu, Jun Nakayama, Nana Tsuchihashi, Mayuri Okami, Hideaki Sakata, Hiroshi Yoshihashi, Taisuke Kobayashi, Kozo Kumakawa, Tadao Yoshida, Tomoko Esaki, Shin-Ichi Usami
Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan. Human genetics (2021)
Hidekane Yoshimura, Shin-Ya Nishio, Shin-Ichi Usami
Milestones toward cochlear gene therapy for patients with hereditary hearing loss. Laryngoscope investigative otolaryngology 6 (5) (2021)
Shin-Ichi Usami, Shin-Ya Nishio
The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients. Human genetics (2021)
Ken Hiramatsu, Shin-Ya Nishio, Shin-Ichiro Kitajiri, Tomohiro Kitano, Hideaki Moteki, Shin-Ichi Usami, null On Behalf Of The Deafness Gene Study Consortium
Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants. Genes 12 (10) (2021)
Shin-Ya Nishio, Shin-Ichi Usami
Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss. Human genetics (2021)
Yoh-Ichiro Iwasa, Shin-Ya Nishio, Hidekane Yoshimura, Akiko Sugaya, Yuko Kataoka, Yukihide Maeda, Yukihiko Kanda, Kyoko Nagai, Yasushi Naito, Hiroshi Yamazaki, Tetsuo Ikezono, Han Matsuda, Masako Nakai, Risa Tona, Yuika Sakurai, Remi Motegi, Hidehiko Takeda, Marina Kobayashi, Chiharu Kihara, Takashi Ishino, Shin-Ya Morita, Satoshi Iwasaki, Masahiro Takahashi, Sakiko Furutate, Shin-Ichiro Oka, Toshinori Kubota, Yasuhiro Arai, Yumiko Kobayashi, Daisuke Kikuchi, Tomoko Shintani, Noriko Ogasawara, Yohei Honkura, Shuji Izumi, Misako Hyogo, Yuzuru Ninoyu, Mayumi Suematsu, Jun Nakayama, Nana Tsuchihashi, Mayuri Okami, Hideaki Sakata, Hiroshi Yoshihashi, Taisuke Kobayashi, Kozo Kumakawa, Tadao Yoshida, Tomoko Esaki, Shin-Ichi Usami
Correction to: Detailed clinical features and genotype-phenotype correlation in an OTOF-related hearing loss cohort in Japan. Human genetics (2021)
Yasunori Maeda, Akira Sasaki, Shuya Kasai, Shinichi Goto, Shin-Ya Nishio, Kaori Sawada, Itoyo Tokuda, Ken Itoh, Shin-Ichi Usami, Atsushi Matsubara
Correction to: Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan. Human genome variation 7 (2020)
Shin-Ichi Usami, Shin-Ya Nishio, Hideaki Moteki, Maiko Miyagawa, Hidekane Yoshimura
Cochlear Implantation From the Perspective of Genetic Background. Anatomical record (Hoboken, N.J. : 2007) 303 (3) (2020)
Keitaro Miyake, Kyoko Shirai, Nobuhiro Nishiyama, Sachie Kawaguchi, Yoko Ohta, Atsushi Kawano, Shin-Ichi Usami, Tomohiro Kitano, Kiyoaki Tsukahara
Cochlear implantation in a patient with a POU4F3 mutation. Clinical case reports 9 (1) (2020)
Hiroki Miyajima, Hideaki Moteki, Timothy Day, Shin-Ya Nishio, Takaaki Murata, Tetsuo Ikezono, Hidehiko Takeda, Satoko Abe, Satoshi Iwasaki, Masahiro Takahashi, Yasushi Naito, Hiroshi Yamazaki, Yukihiko Kanda, Shin-Ichiro Kitajiri, Shin-Ichi Usami
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss. Scientific reports 10 (1) (2020)
Yasunori Maeda, Akira Sasaki, Shuya Kasai, Shinichi Goto, Shin-Ya Nishio, Kaori Sawada, Itoyo Tokuda, Ken Itoh, Shin-Ichi Usami, Atsushi Matsubara
Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan. Human genome variation 7 (2020)
Jun Shinagawa, Hideaki Moteki, Shin-Ya Nishio, Kenji Ohyama, Koshi Otsuki, Satoshi Iwasaki, Shin Masuda, Chie Oshikawa, Yumi Ohta, Yasuhiro Arai, Masahiro Takahashi, Naoko Sakuma, Satoko Abe, Yuika Sakurai, Hirofumi Sakaguchi, Takashi Ishino, Natsumi Uehara, Shin-Ichi Usami
Prevalence and clinical features of hearing loss caused by EYA4 variants. Scientific reports 10 (1) (2020)
Karuna Maekawa, Shin-Ya Nishio, Satoko Abe, Shin-Ichi Goto, Yohei Honkura, Satoshi Iwasaki, Yukihiko Kanda, Yumiko Kobayashi, Shin-Ichiro Oka, Mayuri Okami, Chie Oshikawa, Naoko Sakuma, Hajime Sano, Masayuki Shirakura, Natsumi Uehara, Shin-Ichi Usami
Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort. Genes 10 (10) (2019)
Yoh Yokota, Hideaki Moteki, Shin-Ya Nishio, Tomomi Yamaguchi, Keiko Wakui, Yumiko Kobayashi, Kenji Ohyama, Hiromitsu Miyazaki, Rina Matsuoka, Satoko Abe, Kozo Kumakawa, Masahiro Takahashi, Hirofumi Sakaguchi, Natsumi Uehara, Takashi Ishino, Tomoki Kosho, Yoshimitsu Fukushima, Shin-Ichi Usami
Frequency and clinical features of hearing loss caused by STRC deletions. Scientific reports 9 (1) (2019)
Rika Yasukawa, Hideaki Moteki, Shin-Ya Nishio, Kotaro Ishikawa, Satoko Abe, Yohei Honkura, Misako Hyogo, Ryota Mihashi, Tetsuo Ikezono, Tomoko Shintani, Noriko Ogasawara, Kyoko Shirai, Hiroshi Yoshihashi, Takashi Ishino, Koshi Otsuki, Tsukasa Ito, Kazuma Sugahara, Shin-Ichi Usami
The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss. Genes 10 (10) (2019)
Michie Ideura, Shin-Ya Nishio, Hideaki Moteki, Yutaka Takumi, Maiko Miyagawa, Teruyuki Sato, Yumiko Kobayashi, Kenji Ohyama, Kiyoshi Oda, Takamichi Matsui, Tsukasa Ito, Hiroshi Suzumura, Kyoko Nagai, Shuji Izumi, Nobuhiro Nishiyama, Manabu Komori, Kozo Kumakawa, Hidehiko Takeda, Yoko Kishimoto, Satoshi Iwasaki, Sakiko Furutate, Kotaro Ishikawa, Masato Fujioka, Hiroshi Nakanishi, Jun Nakayama, Rie Horie, Yumi Ohta, Yasushi Naito, Mariko Kakudo, Hirofumi Sakaguchi, Yuko Kataoka, Kazuma Sugahara, Naohito Hato, Takashi Nakagawa, Nana Tsuchihashi, Yukihiko Kanda, Chiharu Kihara, Tetsuya Tono, Ikuyo Miyanohara, Akira Ganaha, Shin-Ichi Usami
Comprehensive analysis of syndromic hearing loss patients in Japan. Scientific reports 9 (1) (2019)
Yoh-Ichiro Iwasa, Shin-Ya Nishio, Akiko Sugaya, Yuko Kataoka, Yukihiko Kanda, Mirei Taniguchi, Kyoko Nagai, Yasushi Naito, Tetsuo Ikezono, Rie Horie, Yuika Sakurai, Rina Matsuoka, Hidehiko Takeda, Satoko Abe, Chiharu Kihara, Takashi Ishino, Shin-Ya Morita, Satoshi Iwasaki, Masahiro Takahashi, Tsukasa Ito, Yasuhiro Arai, Shin-Ichi Usami
OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients. PloS one 14 (5) (2019)
Satoko Abe, Hidehiko Takeda, Shin-Ya Nishio, Shin-Ichi Usami
Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation. Human genome variation 5 (2018)
Masafumi Kobayashi, Maiko Miyagawa, Shin-Ya Nishio, Hideaki Moteki, Taro Fujikawa, Kenji Ohyama, Hirofumi Sakaguchi, Ikuyo Miyanohara, Akiko Sugaya, Yasushi Naito, Shin-Ya Morita, Yukihiko Kanda, Masahiro Takahashi, Kotaro Ishikawa, Yuki Nagano, Tetsuya Tono, Chie Oshikawa, Chiharu Kihara, Haruo Takahashi, Yoshihiro Noguchi, Shin-Ichi Usami
WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis. PloS one 13 (3) (2018)
Shin-Ya Nishio, Hideaki Moteki, Shin-Ichi Usami
Simple and efficient germline copy number variant visualization method for the Ion AmpliSeq™ custom panel. Molecular genetics & genomic medicine (2018)
Yoh-Ichiro Iwasa, Keita Tsukada, Masafumi Kobayashi, Tomohiro Kitano, Kentaro Mori, Hidekane Yoshimura, Hisakuni Fukuoka, Shin-Ichi Usami
Bilateral delayed endolymphatic hydrops evaluated by bilateral intratympanic injection of gadodiamide with 3T-MRI. PloS one 13 (12) (2018)
Satoko Abe, Shin-Ya Nishio, Yoh Yokota, Hideaki Moteki, Kozo Kumakawa, Shin-Ichi Usami
Diagnostic pitfalls for GJB2-related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing loss. Clinical case reports 6 (11) (2018)
Tomohiro Kitano, Maiko Miyagawa, Shin-Ya Nishio, Hideaki Moteki, Kiyoshi Oda, Kenji Ohyama, Hiromitsu Miyazaki, Hiroshi Hidaka, Ken-Ichi Nakamura, Takaaki Murata, Rina Matsuoka, Yoko Ohta, Nobuhiro Nishiyama, Kozo Kumakawa, Sakiko Furutate, Satoshi Iwasaki, Takechiyo Yamada, Yumi Ohta, Natsumi Uehara, Yoshihiro Noguchi, Shin-Ichi Usami
POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. PloS one 12 (5) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Shin-Ichi Usami