Kurata K, Hosono K, Takayama M, Katsuno M, Saitsu H, Ogata T, Hotta Y: Retinitis pigmentosa with optic neuropathy and COQ2 mutations: A case report. Am J Ophthalmol Case Rep. 2022 Jan 20;25:101298. doi: 10.1016/j.ajoc.2022.101298. eCollection 2022 Mar. [0.426]
Takahashi Y, Date H, Oi H, Adachi T, Imanishi N, Kimura E, Takizawa H, Kosugi S, Matsumoto N, Kosaki K, Matsubara Y; IRUD Consortium; Mizusawa H. Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures. J Hum Genet. 2022 Sep;67(9):505-513. doi: 10.1038/s10038-022-01025-0. Epub 2022 Mar 23. [3.767]
Sano Y, Koyanagi Y, Wong JH, Murakami Y, Fujiwara K, Endo M, Aoi T, Hashimoto K, Nakazawa T, Wada Y, Ueno S, Gao D, Murakami A, Hotta Y, Ikeda Y, Nishiguchi KM, Momozawa Y, Sonoda KH, Akiyama M, Fujimoto A: Likely pathogenic structural variants in genetically unsolved patients with retinitis pigmentosa revealed by long-read sequencing. J Med Genet. 2022 Nov;59(11):1133-1138. doi: 10.1136/jmedgenet-2022-108428. Epub 2022 Jun 15. PMID: 35710107 [5.945]
Hikoya A, Hosono KOno K, Arai S, Tachibana N, Kurata K, Torii K, Sato M, Saitsu H, Ogata T, Hotta Y: A case of siblings with juvenile retinitis pigmentosa associated with NEK1 gene variants. Ophthalmic Genet. 2022 Nov 7:1-6. doi: 10.1080/13816810.2022.2141788. Online ahead of print. PMID: 36341712 [1.274]
Arai S, Suzuki H, Hayashi S, Inagaki R, Haseoka T, Hikoya A, Komori M, Shimizu T, Muhammad NH, Hotta Y, Sato M: Intraocular pressure at different gaze positions in patients with highly myopic strabismus. Jpn J Ophthalmol. 2022 Nov;66(6):572-578. doi: 10.1007/s10384-022-00939-8. Epub 2022 Sep 9. PMID: 36083359 [2.211]
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Itai T, Wang Z, Nishimura G, Ohashi H, Guo L, Wakano Y, Sugiura T, Hayakawa H, Okada M, Saisu T, Kitta A, Doi H, Kurosawa K, Hotta Y, Hosono K, Sato M, Shimizu K, Takikawa K, Watanabe S, Ikeda N, Suzuki M, Fujita A, Uchiyama Y, Tsuchida N, Miyatake S, Miyake N, Matsumoto N, Ikegawa S: De novo heterozygous variants in KIF5B cause kyphomelic dysplasia. Clin Genet. 2022 Jul;102(1):3-11. doi: 10.1111/cge.14133. Epub 2022 Apr 5. PMID: 35342932 [4.296]
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. 2022 Jan;66(1):87-93. doi: 10.1007/s10384-021-00879-9. Epub 2021 Oct 16. PMID: 34655005 [2.211]
Mamun MA, Nabi MM, Sato T, Aramaki S, Takanashi Y, Sakamoto T, Hizume K, Mori C, Yasue M, Ozaki M, Islam A, Kahyo T, Horikawa M, Takahashi Y, Okazaki S, Ohishi K, Nagashima Y, Seno K, Hotta Y, Setou M: Coenzyme Q10 in the eye isomerizes by sunlight irradiation. Sci Rep. 2022 Jul 15;12(1):12104. doi: 10.1038/s41598-022-16343-8. [4.997]
Takeda Y, Suzuki H, Hosono K, Hikoya A, Komori M, Inagaki R, Haseoka T, Arai S, Takagi Y, Hotta Y, Sato M: Exophthalmos associated with chronic progressive external ophthalmoplegia. Jpn J Ophthalmol. 2022 May;66(3):314-319. doi: 10.1007/s10384-022-00920-5. Epub 2022 Apr 19. PMID: 35438395 [2.211]
Kfir J, Wygnanski-Jaffe T, Farzavandi S, Wei Z, Yam JC, de Faber JT, Orge FH, Aznauryan I, Tsai CB, de Liano RG, Natarajan S, Dadeya SC, Agrawal S, Sato M, Shemesh R, Mezer E; CPMTPPO Study Group: The impact of the first peak of the COVID-19 pandemic on childhood myopia control practice patterns among ophthalmologists-an international pediatric ophthalmology and strabismus council global perspective. Graefes Arch Clin Exp Ophthalmol. 2023 Jan;261(1):233-240. doi: 10.1007/s00417-022-05864-7. [3.535]
Morikawa H, Nishina S, Torii K, Hosono K, Yokoi T, Shigeyasu C, Yamada M, Kosuga M, Fukami M, Saitsu H, Azuma N, Hori Y, Hotta Y. A pediatric case of congenital stromal corneal dystrophy caused by the novel variant c.953del of the DCN gene. Hum Genome Var. 2023 Mar 24;10(1):9. doi: 10.1038/s41439-023-00239-8. [0.586]
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