Shin-Ya Nishio

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 27

Top Venues

Genes

Scientific reports

International journal of molecular sciences

Acta oto-laryngologica

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

Publications

Ikuyo Miyanohara, Junichiro Ohori, Minako Tabuchi, Shin-Ya Nishio, Masaru Yamashita, Shin-Ichi Usami
Comprehensive Genetic Evaluation in Patients with Special Reference to Late-Onset Sensorineural Hearing Loss. Genes 15 (5) (2024)
Naoko Sakuma, Shin-Ya Nishio, Shin-Ichi Goto, Yohei Honkura, Kiyoshi Oda, Hidehiko Takeda, Marina Kobayashi, Kozo Kumakawa, Satoshi Iwasaki, Masahiro Takahashi, Taku Ito, Yasuhiro Arai, Yasuhiro Isono, Natsuko Obara, Takeshi Matsunobu, Kimihiro Okubo, Shin-Ichi Usami
Detailed Clinical Features of PTPRQ -Associated Hearing Loss Identified in a Large Japanese Hearing Loss Cohort. Genes 15 (4) (2024)
Claudia Steinacher, Dietmar Rieder, Jasmin E Turner, Nita Solanky, Shin-Ya Nishio, Shin-Ichi Usami, Barbara Hausott, Anneliese Schrott-Fischer, Jozsef Dudas
Validation of RNA Extraction Methods and Suitable Reference Genes for Gene Expression Studies in Developing Fetal Human Inner Ear Tissue. International journal of molecular sciences 25 (5) (2024)
Claudia Steinacher, Dietmar Rieder, Jasmin E Turner, Nita Solanky, Shin-Ya Nishio, Shin-Ichi Usami, Barbara Hausott, Anneliese Schrott-Fischer, Jozsef Dudas
Validation of RNA Extraction Methods and Suitable Reference Genes for Gene Expression Studies in Developing Fetal Human Inner Ear Tissue. International journal of molecular sciences 25 (5) (2024)
Claudia Steinacher, Dietmar Rieder, Jasmin E Turner, Nita Solanky, Shin-Ya Nishio, Shin-Ichi Usami, Barbara Hausott, Anneliese Schrott-Fischer, Jozsef Dudas
Validation of RNA Extraction Methods and Suitable Reference Genes for Gene Expression Studies in Developing Fetal Human Inner Ear Tissue. International journal of molecular sciences 25 (5) (2024)
Naoko Sakuma, Shin-Ya Nishio, Shin-Ichi Goto, Yohei Honkura, Kiyoshi Oda, Hidehiko Takeda, Marina Kobayashi, Kozo Kumakawa, Satoshi Iwasaki, Masahiro Takahashi, Taku Ito, Yasuhiro Arai, Yasuhiro Isono, Natsuko Obara, Takeshi Matsunobu, Kimihiro Okubo, Shin-Ichi Usami
Detailed Clinical Features of PTPRQ -Associated Hearing Loss Identified in a Large Japanese Hearing Loss Cohort. Genes 15 (4) (2024)
Ikuyo Miyanohara, Junichiro Ohori, Minako Tabuchi, Shin-Ya Nishio, Masaru Yamashita, Shin-Ichi Usami
Comprehensive Genetic Evaluation in Patients with Special Reference to Late-Onset Sensorineural Hearing Loss. Genes 15 (5) (2024)
Ikuyo Miyanohara, Junichiro Ohori, Minako Tabuchi, Shin-Ya Nishio, Masaru Yamashita, Shin-Ichi Usami
Comprehensive Genetic Evaluation in Patients with Special Reference to Late-Onset Sensorineural Hearing Loss. Genes 15 (5) (2024)
Naoko Sakuma, Shin-Ya Nishio, Shin-Ichi Goto, Yohei Honkura, Kiyoshi Oda, Hidehiko Takeda, Marina Kobayashi, Kozo Kumakawa, Satoshi Iwasaki, Masahiro Takahashi, Taku Ito, Yasuhiro Arai, Yasuhiro Isono, Natsuko Obara, Takeshi Matsunobu, Kimihiro Okubo, Shin-Ichi Usami
Detailed Clinical Features of PTPRQ -Associated Hearing Loss Identified in a Large Japanese Hearing Loss Cohort. Genes 15 (4) (2024)
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)
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)
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)
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)
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)
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)
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)
Shin-Ya Nishio, Isabelle Schrauwen, Hideaki Moteki, Hela Azaiez
Advances in Molecular Genetics and the Molecular Biology of Deafness. BioMed research international 2016 (2016)

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Publication Activity (10 Years)

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Shin-Ya Nishio