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2024年

原著論文

1. Inooka T, Hayashi T, Tsunoda K, Kuniyoshi K, Kondo H, Mizobuchi K, Suga A, Iwata T, Yoshitake K, Kondo M, Goto K, Ota J, Kominami T, Nishiguchi KM, Ueno S.
   GENETIC ETIOLOGY AND CLINICAL FEATURES OF ACHROMATOPSIA IN JAPAN
   Retina. 2024 Oct 1;44(10):1836-1844.
2. Taiga Inooka , Taro Kominami , Ryo Tomita , Ayana Suzumura , Tsuyoshi Matsuno , Junya Ota , Yoshito Koyanagi , Hideo Takeyama , Shinji Ueno , Yasuki Ito , Koji M Nishiguchi , Kenya Yuki .
   Assessment of factors affecting anterior chamber depth from data obtained from health checkup participants in Japan
   Sci Rep. 2024 Dec 5;14(1):30342.
3. Akiko Suga , Kei Mizobuchi , Taiga Inooka , Kazutoshi Yoshitake , Naoko Minematsu , Kazushige Tsunoda , Kazuki Kuniyoshi , Yosuke Kawai , Yosuke Omae , Katsushi Tokunaga ; NCBN Controls WGS Consortium; Takaaki Hayashi , Shinji Ueno , Takeshi Iwata.
   A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD
   Genet Med Open.2024 Mar 26:2:101843.
4. Ueno S, Hayashi T, Tsunoda K, Aoki T, Kondo M.
   Nationwide epidemiologic survey on incidence of macular dystrophy in Japan
   Jpn J Ophthalmol. 2024 May;68(3):167-173.
5. Furukawa A, Suzuki Y, Nozuki N, Kurosaka N, Kogawa S, Hara S, Ueno S.
   Case report: A case of unilateral combined central retinal vein occlusion, incomplete central retinal artery occlusion, and papillitis following a third dose of COVID-19 vaccination
   Front Ophthalmol (Lausanne). 2024 Feb 23:4:1352962.
6. Goto K, Koyanagi Y, Akiyama M, Murakami Y, Fukushima M, Fujiwara K, Iijima H, Yamaguchi M, Endo M, Hashimoto K, Ishizu M, Hirakata T, Mizobuchi K, Takayama M, Ota J, Sajiki AF, Kominami T, Ushida H, Fujita K, Kaneko H, Ueno S, Hayashi T, Terao C, Hotta Y, Murakami A, Kuniyoshi K, Kusaka S, Wada Y, Abe T, Nakazawa T, Ikeda Y, Momozawa Y, Sonoda KH, Nishiguchi KM.
   Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
   J Med Genet. 2024 Mar 18:jmg-2023-109750.
7. Mizobuchi K, Hayashi T, Tanaka K, Kuniyoshi K, Murakami Y, Nakamura N, Torii K, Mizota A, Sakai D, Maeda A, Kominami T, Ueno S, Kusaka S, Nishiguchi KM, Ikeda Y, Kondo M, Tsunoda K, Hotta Y, Nakano T.
   Genetic and clinical features of ABCA4-associated retinopathy in a Japanese nationwide cohort
   Am J Ophthalmol. 2024 Mar 16:S0002-9394(24)00110-7.
8. Watanabe T, Takihara Y, Jono H, Fujimoto T, Tasaki M, Isoguchi A, Urahashi Y, Shimoda T, Takahashi E, Ando Y, Ueno S, Ueda M, Inoue T.
   Silencing of ocular transthyretin, a gene responsible for hereditary transthyretin amyloidosis, by intravitreal injection of an siRNA conjugate into rabbit eyes.
   Biochem Biophys Res Commun. 2024 Jan 29;694:149397.