Hayashi Takaaki

ハヤシタカアキ | Hayashi Takaaki

Affiliation and department：
Job title： Professor

Research field (1)： Ophthalmology

Research keywords (5)： Inherited Retinal Dystrophy , Genetic Testing , Retinitis Pigmentosa , Macular Dystrophy , Hereditary Optic Neuropathy

Research theme for competitive and other funds (11)：

2024 - 2027 黄斑ジストロフィの遺伝子型に基づく病態解明とデータベース構築に向けた基盤研究
2022 - 2025 遺伝性網膜・視神経ジストロフィの症例収拾および疾患別頻度の検討
2021 - 2024 進行性遺伝性網膜疾患の治療に向けた全エクソーム解析と疾患表現型の同定
2017 - 2020 Clinical and genetic characterization of inherited cone dysfunction syndrome
2017 - 2020 Clinical and genetic research for the treatment of retinal detachment in Stickler syndrome

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Papers (266)：

篠原大輔, 林孝彰, 伊藤晴康, 金月勇, 井上雄, 中野匡. HLA-B27関連ぶどう膜炎を伴う強直性脊椎炎にアダリムマブを導入した2例. 眼科臨床紀要. 2024. 17. 4. 343-349
Shinji Ueno, Takaaki Hayashi, Kazushige Tsunoda, Takuya Aoki, Mineo Kondo. Nationwide epidemiologic survey on incidence of macular dystrophy in Japan. Japanese Journal of Ophthalmology. 2024
Naoko Fukunaga, Takaaki Hayashi, Yuki Yamada, Kei Mizobuchi, Arihito Ohta, Tadashi Nakano. A novel stop-gain NF1 variant in neurofibromatosis type 1 and bilateral optic atrophy without optic gliomas. Ophthalmic Genetics. 2024. 45. 2. 186-192
Akiko Suga, Kei Mizobuchi, Taiga Inooka, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kazuki Kuniyoshi, Yosuke Kawai, Yosuke Omae, Katsushi Tokunaga, et al. A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD. Genetics in Medicine Open. 2024. 101843-101843
Kensuke Goto, Yoshito Koyanagi, Masato Akiyama, Yusuke Murakami, Masatoshi Fukushima, Kohta Fujiwara, Hanae Iijima, Mitsuyo Yamaguchi, Mikiko Endo, Kazuki Hashimoto, et al. Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases. Journal of Medical Genetics. 2024

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MISC (247)：

福田有紀, 大平亮, 五十嵐若菜, 奥出祥代, 溝渕圭, 林孝彰, 中野匡. S錐体のコントラスト感度低下を認めた顕性遺伝性視神経萎縮の1例. 日本視能訓練士協会誌. 2024. 53. 167-167
近藤峰生, 齋藤航, 石田晋, 國吉一樹, 上野真治, 林孝彰, 中野匡, 早川卓浩, 角田和繁, 慶野博, et al. 多発消失性白点症候群(MEWDS)の初診時視力に影響を与える因子. 眼科臨床紀要. 2023. 16. 10. 741-742
國吉一樹, 角田和繁, 林孝彰, 永江由季, 藤波芳, 須賀晶子, 岩田岳, 日下俊次. 眼底所見が正常な錐体ジストロフィ. 眼科臨床紀要. 2023. 16. 9. 680-680
佐藤朋子, 國吉一樹, 林孝彰, 溝渕圭, 西脇弘一, 初川嘉一, 中野匡, 日下俊次. KCNV2網膜症同胞例の長期経過. 眼科臨床紀要. 2023. 16. 6. 456-457
林孝彰, 溝渕圭, 亀谷修平, 吉田正樹, 中野匡. 確定診断に時間を要したOPA1変異関連視神経萎縮の1例. 眼科臨床紀要. 2023. 16. 6. 459-460

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Lectures and oral presentations (3)：

Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance.
(Investigative ophthalmology & visual science 2019)
High-Resolution Retinal Imaging Reveals Preserved Cone Photoreceptor Density and Choroidal Thickness in Female Carriers of Choroideremia.
(Ophthalmic surgery, lasers & imaging retina 2019)
Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort.
(Molecular vision 2019)

Works (4)：

Education (2)：

Professional career (1)：

Work history (5)：

Awards (4)：

2023/04 - The JOS Best Paper Award Clinical and Genetic Characteristics of Japanese Patients with Enhanced S-cone Syndrome
2019 - 日本網膜色素変性症協会(JRPS) 研究助成第23回受賞
2006 - 慈恵医師会研究奨励賞
1999 - 上原記念生命科学財団海外留学助成ポストドクトラルフェローシップ

Association Membership(s) (5)：

日本網膜硝子体学会 , 日本眼科学会 , 日本小児眼科学会 , 日本臨床視覚電気生理学会 , 日本眼循環学会

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