Nishina S, Hosono K, Ishitani S, Kosaki K, Yokoi T, Yoshida T, Tomita K, Fukami M, Saitsu H, Ogata T, Ishitani T, Hotta Y, Azuma N. Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndrome. J Hum Genet. 2021 Oct;66(10):1021-1027. doi: 10.1038/s10038-021-00909-x. Epub 2021 Feb 27. [3.172]
Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Komori S, Gao D, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda KH. Regional differences in genes and variants causing retinitis pigmentosa in Japan. Jpn J Ophthalmol. 2021 May;65(3):338-343. doi: 10.1007/s10384-021-00824-w. Epub 2021 Feb 25. [2.447]
Mizobuchi K, Hayashi T, Oishi N, Kubota D, Kameya S, Higasa K, Futami T, Kondo H, Hosono K, Kurata K, Hotta Y, Yoshitake K, Iwata T, Matsuura T, Nakano T. Genotype-phenotype correlations in RP1-associated retinal dystrophies: A multi-center cohort study in Japan. J Clin Med. 2021 May 24;10(11):2265. doi: 10.3390/jcm10112265. [5.583]
Kondo H, Matsushita I, Nagata T, Fujihara E, Hosono K, Uchio E, Hotta Y, Kusaka S. Retinal features of family members with familial exudative vitreoretinopathy caused by mutations in KIF11 gene. Transl Vis Sci Technol. 2021 Jun 1;10(7):18. doi: 10.1167/tvst.10.7.18. [3.283]
Ohishi K, Hosono K, Obana A, Noda A, Hiramitsu T, Hotta Y, Minoshima S. Identification of susceptibility loci for light-induced visual impairment in rats. Exp Eye Res. 2021 Sep;210:108688. doi: 10.1016/j.exer.2021.108688. Epub 2021 Jul 5. [3.467]
Iimori H, Suzuki H, Komori M, Hikoya A, Hotta Y, Sato M. Clinical findings of acute acquired comitant esotropia in young patients. Jpn J Ophthalmol. 2021 Oct 16. doi: 10.1007/s10384-021-00879-9. [2.447]
Morimoto H, Hayano S, Ozawa N, Ogura Y, Usui H, Usami T, Ohse A, Otsuka M, Miyachi M, Tokura Y. Questionnaire survey of possible association of allergic diseases with adverse reactions to SARS-CoV-2 vaccination. Vaccines (Basel). 2021 Dec 1;9(12):1421. doi: 10.3390/vaccines9121421. [4.127]
Tachibana N, Hosono K, Nomura S, Arai S, Torii K, Kurata K, Sato M, Shimakawa S, Azuma N, Ogata T, Wada Y, Okamoto N, Saitsu H, Nishina S, Hotta Y. Maternal uniparental isodisomy of chromosome 4 and 8 in patients with retinal dystrophy: SRD5A3-congenital disorders of glycosylation and RP1-related retinitis pigmentosa. Genes (Basel). 2022 Feb 16;13(2):359. doi: 10.3390/genes13020359. [3.688]