Hosono Katsuhiro

ホソノカツヒロ | Hosono Katsuhiro

Affiliation and department：

Research field (1)： Ophthalmology

Research keywords (2)：網膜色素変性 , 遺伝性網膜疾患

Research theme for competitive and other funds (10)：

2022 - 2026 小児期に発症する網膜ジストロフィの分子遺伝学的基盤の構築に関する研究
2017 - 2020 Development of the simple diagnostic method for the patients with chronic progressive external ophthalmoplegia and the construction of the database
2017 - 2020 Construction of a comprehensive regional medical system and development of diagnostic method for rare and undiagnosed eye disease patients in Japan
2016 - 2019 Development of diagnosis program and clinical application with congenital visual impairment patients for tailor-made medicine
2015 - 2018 3D-analysis using biometric technology and the database construction for elucidating the pathological mechanism with congenital cataract

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Papers (86)：

Hazuki Morikawa, Sachiko Nishina, Kaoruko Torii, Katsuhiro Hosono, Tadashi Yokoi, Chika Shigeyasu, Masakazu Yamada, Motomichi Kosuga, Maki Fukami, Hirotomo Saitsu, et al. A pediatric case of congenital stromal corneal dystrophy caused by the novel variant c.953del of the DCN gene. Human genome variation. 2023. 10. 1. 9-9
森川葉月, 仁科幸子, 林孝彰, 鳥居薫子, 細野克博, 佐藤美保, 横井匡, 深見真紀, 才津浩智, 東範行, et al. RPGRIP1遺伝子変異によるレーバー先天盲の臨床像. 日本眼科学会雑誌. 2023. 127. 臨増. 232-232
Akiko Hikoya, Katsuhiro Hosono, Kaoru Ono, Shinji Arai, Nobutaka Tachibana, Kentaro Kurata, Kaoruko Torii, Miho Sato, Hirotomo Saitsu, Tsutomu Ogata, et al. A case of siblings with juvenile retinitis pigmentosa associated with NEK1 gene variants. Ophthalmic genetics. 2022. 44. 5. 1-6
山崎智幸, 成瀬翔, 倉田健太郎, 細野克博, 松下五佳, 日吉篤史, 岩泉守哉, 木内良明, 堀田喜裕, 近藤寛之. わが国のOculo-Facio-Cardio-Dental症候群の2家系4症例の臨床像. 眼科臨床紀要. 2022. 15. 6. 416-416
Yu Takeda, Hiroko Suzuki, Katsuhiro Hosono, Akiko Hikoya, Miwa Komori, Risako Inagaki, Takashi Haseoka, Shinji Arai, Yuri Takagi, Yoshihiro Hotta, et al. Exophthalmos associated with chronic progressive external ophthalmoplegia. Japanese journal of ophthalmology. 2022. 66. 3. 314-319

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MISC (7)：

Kentaro Ohishi, Masafumi Ohtsubo, Katsuhiro Hosono, Akira Obana, Yoshihiro Hotta, Tadahisa Hiramitsu, Shinsei Minoshima. Forward genetic analysis revealed a causal gene responsible for susceptibility to rat retinal photic injury. HUMAN GENOMICS. 2018. 12
Kentaro Ohishi, Masafumi Ohtsubo, Katsuhiro Hosono, Akira Obana, Yoshihiro Hotta, Tadahisa Hiramitsu, Shinsei Minoshima. Forward Genetic Approach for Causal Gene Identification for Rat Retinal Photic Injury. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 2017. 58. 8
Genetic testing in retinal dystrophy. 2015. 69. 12. 1590-1595
Kimiko Suto, Katsuhiro Hosono, Yasunori Nagase, Hiroshi Nakanishi, Kunihiro Mizuta, Shinsei Minoshima, Yoshihiro Hotta. Visual Outcomes of Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 2015. 56. 7
細野克博, 堀田喜裕. 網膜色素変性 (特集眼と遺伝). 眼科. 2014. 56. 5. 569-574

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Patents (1)：

EYS遺伝子の変異を検出するためのプライマー、プローブ、マイクロアレイ、及び、これらを備える検出キット、並びに、網膜色素変性症原因遺伝子変異の検査方法、網膜色素変性症への遺伝的感受性の検査方法

Professional career (1)：

Awards (2)：

Association Membership(s) (2)：

THE JAPAN SOCIETY OF HUMAN GENETICS , JAPANESE OPHTHALMOLOGICAL SOCIETY

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