Rchr
J-GLOBAL ID:200901057809126706
Update date: Sep. 11, 2024
Hotta Yoshihiro
ホッタ ヨシヒロ | Hotta Yoshihiro
Affiliation and department:
Job title:
Professor
Research field (3):
Ophthalmology
, Molecular biology
, Genetics
Research keywords (3):
遺伝学
, 眼科学
, Ophthalmology
Research theme for competitive and other funds (31):
- 2020 - 2024 わが国の難治性未診断眼疾患に対する新しい疾患概念の確立と診断法の開発に関する研究
- 2018 - 2021 Functional analysis of PANK4 and elucidation of an onset mechanism in age-related macular degeneration
- 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
- 2014 - 2017 Development of genetic diagnosis for Japanese Retinitis Pigmentosa patients using next generation sequencer
- 2013 - 2017 Investigation of a new mechanism of age-related macular degeneration using a rat model of retinal photic injury: targeted exome analysis for a responsible genomic region
- 2013 - 2015 The development and clinical application of EYS gene mutation diagnosis in Japanese Retinitis pigmentosa patients
- 2011 - 2013 Investigation for the genetic factor of glaucoma in another viewpoint: an analysis of possible involvement of copy number variation (CNV) in genome
- 2011 - 2013 Genetic Diagnosis System for Retinitis Pigmentosa Patients: Large-scale collection and mutation analyses of Japanese RP patients
- 2011 - 2012 Genotype-phenotype analysis and prevalence study of disease-causing mutations in the EYS gene among Japanese patients with retinitis pigmentosa
- 2010 - 2012 Identification of candidate genes responsible for an increased susceptibility of age-related macular degeneration using an animal model and its application to gene diagnosis.
- 2005 - 2009 Exploration of disease-causative and -associated genes and prospect of novel molecular/cellular phenomenon
- 2005 - 2007 Establishment of immortalized culture-cells derived from cone and rod photoreceptors and construction of in vitro model system of retinal diseases
- 2002 - 2003 Study of pathophysiology and treatment of superior oblique palsy.
- 2002 - 2003 Analysis of pathology in usher syndrome by method of molecular biology.
- 2000 - 2001 Molecular genetic analysis of hereditary retinal diseases
- 1998 - 2000 A study concerning the association between genotype and phenotype in the inherited ocular diseases
- 1996 - 1998 Analysis of gene mutations in retinal dystrophies
- 1995 - 1996 Molecular biological study of corneal dystrophy
- 1993 - 1995 Candidate gene approach of retinitis pigmentosa
- 1993 - 1994 Candidate gene approach in corneal degenerations
- 1989 - 1990 DNA Diagnosis of X-linked Chorioretinal Degenerations
- 眼科領域の遺伝学
- 眼科領域の難病に対する新しい治療法
- 網膜変性の候補遺伝子アプロ-チ
- 角膜変性症の候補遺伝子アプロ-チ
- New therapy for the ocular incurable diseases
- Candidate gene approach for retinal degenerations
- Candidate gene approach for corneal dystrophies
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Papers (286):
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小澤 由季, 彦谷 明子, 立花 信貴, 古森 美和, 高木 啓伍, 福田 冬季子, 石垣 英俊, 平出 拓也, 伊藤 祐介, 堀田 喜裕, et al. ビタミンA欠乏症から眼球乾燥症をきたした自閉スペクトラム症児の2例. 眼科臨床紀要. 2024. 17. 4. 357-357
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高木 啓伍, 西村 香澄, 土屋 陽子, 瀧 伶, 武田 優, 高地 貴行, 堀田 喜裕, 佐藤 美保. シクロスポリンによって発症したと思われる無症状の薬剤性頭蓋内圧亢進症. 眼科臨床紀要. 2024. 17. 4. 357-358
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Kei Mizobuchi, Takaaki Hayashi, Koji Tanaka, Kazuki Kuniyoshi, Yusuke Murakami, Natsuko Nakamura, Kaoruko Torii, Atsushi Mizota, Daiki Sakai, Akiko Maeda, et al. Genetic and clinical features of ABCA4-associated retinopathy in a Japanese nationwide cohort. American journal of ophthalmology. 2024
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清水 瑞己, 彦谷 明子, 古森 美和, 立花 信貴, 江内田 寛, 堀田 喜裕, 佐藤 美保. 内斜視術後に巨大なmuscle cystを生じた1例. 眼科臨床紀要. 2024. 17. 3. 275-275
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荒川 あかり, 鳥居 薫子, 高山 理和, 長谷岡 宗, 溝渕 圭, 林 孝彰, 佐藤 美保, 堀田 喜裕. 37年間経過観察したABCA4関連網膜ジストロフィの1例. 日本眼科学会雑誌. 2024. 128. 臨増. 296-296
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MISC (159):
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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
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林 孝彰, 溝渕 圭, 榎本 暢子, 細野 克博, 堀田 喜裕, 松浦 知和, 中野 匡. 日本人家族性ドルーゼンの4家系におけるEFEMP1変異のハプロタイプ解析. 日本眼科学会雑誌. 2022. 126. 臨増. 203-203
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佐藤 美保, 加藤 光広, 田島 敏広, 川村 孝, 仁科 幸子, 根岸 貴志, 柿原 寛子, 初川 嘉一, 松村 望, 三木 淳司, et al. 中隔視神経異形成症の眼科診療に関する研究. 眼科臨床紀要. 2018. 11. 5. 395-400
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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
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Two cases of neuroretinitis as manifestation of cat scratch disease. 2017. 71. 9. 1345-1351
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Books (18):
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眼科領域の分子遺伝学
眼科診療プラクティス 1999
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Mutation spectrum in the REP-1 gene of Japanese choroideremia patients
Plenum Publishers, New York 1999
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眼科診療便利手帖
診断と治療社 1998
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眼科臨床医のためのやさしい分子生物学
診断と治療社 1998
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ノックアウトマウス・データブック
中山書店 1997
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Professional career (1):
Committee career (2):
Awards (3):
- 2022/04 - 日本眼科学会 日本眼科学会賞
- 2000 - ROHTO賞
- 2000 - 日本眼科学会学術奨励賞
Association Membership(s) (3):
日本先天異常学会
, 日本人類遺伝学会
, 日本眼科学会
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