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Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Suga A, Yoshitake K, Minematsu N, Tsunoda K, Fujinami K, Miyake Y, Kuniyoshi K, Hayashi T, Mizobuchi K, Ueno S, Terasaki H, Kominami T, Nao-I N, Mawatari G, Mizota A, Shinoda K, Kondo M, Kato K, Sekiryu T, Nakamura M, Kusuhara S, Yamamoto H, Yamamoto S, Mochizuki K, Kondo H, Matsushita I, Kameya S, Fukuchi T, Hatase T, Horiguchi M, Shimada Y, Tanikawa A, Yamamoto S, Miura G, Ito N, Murakami A, Fujimaki T, Hotta Y, Tanaka K, Iwata T. Suga A, et al. Among authors: nao i n. Hum Mutat. 2022 Dec;43(12):2251-2264. doi: 10.1002/humu.24492. Epub 2022 Nov 7. Hum Mutat. 2022. PMID: 36284460
Comparison of combination therapy of prednisolone and cyclosporine with corticosteroid pulse therapy in Vogt-Koyanagi-Harada disease.
Ono T, Goto H, Sakai T, Nitta F, Mizuki N, Takase H, Kaneko Y, Hori J, Nakano S, Nao-I N, Ohguro N, Miyata K, Tomita M, Mochizuki M; Japan VKH Disease Treatment Study Group. Ono T, et al. Among authors: nao i n. Jpn J Ophthalmol. 2022 Mar;66(2):119-129. doi: 10.1007/s10384-021-00878-w. Epub 2021 Oct 24. Jpn J Ophthalmol. 2022. PMID: 34689288 Clinical Trial.
CLEC3B is a novel causative gene for macular-retinal dystrophy.
Zhou R, Mawatari G, Cai XB, Shen RJ, Wang YH, Wang YT, Guo YM, Guo FY, Yuan J, Pan D, Nao-I N, Jin ZB. Zhou R, et al. Among authors: nao i n. Genet Med. 2022 Jun;24(6):1249-1260. doi: 10.1016/j.gim.2022.02.012. Epub 2022 Mar 22. Genet Med. 2022. PMID: 35331648 Free article.
Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants.
Mawatari G, Fujinami K, Liu X, Yang L, Fujinami-Yokokawa Y, Komori S, Ueno S, Terasaki H, Katagiri S, Hayashi T, Kuniyoshi K, Miyake Y, Tsunoda K, Yoshitake K, Iwata T, Nao-I N; JEGC study group. Mawatari G, et al. Among authors: nao i n. Hum Genome Var. 2020 Feb 10;7:3. doi: 10.1038/s41439-019-0086-2. eCollection 2020. Hum Genome Var. 2020. PMID: 32047640 Free PMC article.
Clinical and genetic characteristics of 14 patients from 13 Japanese families with RPGR-associated retinal disorder: report of eight novel variants.
Mawatari G, Fujinami K, Liu X, Yang L, Yokokawa YF, Komori S, Ueno S, Terasaki H, Katagiri S, Hayashi T, Kuniyoshi K, Miyake Y, Tsunoda K, Yoshitake K, Iwata T, Nao-I N; JEGC study group. Mawatari G, et al. Among authors: nao i n. Hum Genome Var. 2019 Aug 2;6:34. doi: 10.1038/s41439-019-0065-7. eCollection 2019. Hum Genome Var. 2019. PMID: 31645972 Free PMC article.
69 results