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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 5
2004 7
2005 4
2006 5
2007 3
2008 2
2009 1
2010 7
2011 4
2012 4
2013 6
2014 16
2015 10
2016 16
2017 13
2018 13
2019 18
2020 18
2021 9
2022 12
2023 5
2024 3

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164 results

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Page 1
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: iwata t. Hum Mutat. 2022 Dec;43(12):2251-2264. doi: 10.1002/humu.24492. Epub 2022 Nov 7. Hum Mutat. 2022. PMID: 36284460
METTL23 mutation alters histone H3R17 methylation in normal-tension glaucoma.
Pan Y, Suga A, Kimura I, Kimura C, Minegishi Y, Nakayama M, Yoshitake K, Iejima D, Minematsu N, Yamamoto M, Mabuchi F, Takamoto M, Shiga Y, Araie M, Kashiwagi K, Aihara M, Nakazawa T, Iwata T. Pan Y, et al. Among authors: iwata t. J Clin Invest. 2022 Nov 1;132(21):e153589. doi: 10.1172/JCI153589. J Clin Invest. 2022. PMID: 36099048 Free PMC article.
Biological Magnetic Resonance Data Bank.
Hoch JC, Baskaran K, Burr H, Chin J, Eghbalnia HR, Fujiwara T, Gryk MR, Iwata T, Kojima C, Kurisu G, Maziuk D, Miyanoiri Y, Wedell JR, Wilburn C, Yao H, Yokochi M. Hoch JC, et al. Among authors: iwata t. Nucleic Acids Res. 2023 Jan 6;51(D1):D368-D376. doi: 10.1093/nar/gkac1050. Nucleic Acids Res. 2023. PMID: 36478084 Free PMC article.
Exploring the Genetic Landscape of Childhood Glaucoma.
Pan Y, Iwata T. Pan Y, et al. Among authors: iwata t. Children (Basel). 2024 Apr 9;11(4):454. doi: 10.3390/children11040454. Children (Basel). 2024. PMID: 38671671 Free PMC article. Review.
Significance of optineurin mutations in glaucoma and other diseases.
Minegishi Y, Nakayama M, Iejima D, Kawase K, Iwata T. Minegishi Y, et al. Among authors: iwata t. Prog Retin Eye Res. 2016 Nov;55:149-181. doi: 10.1016/j.preteyeres.2016.08.002. Epub 2016 Sep 29. Prog Retin Eye Res. 2016. PMID: 27693724 Review.
Molecular genetics of inherited normal tension glaucoma.
Pan Y, Iwata T. Pan Y, et al. Among authors: iwata t. Indian J Ophthalmol. 2024 May 1;72(Suppl 3):S335-S344. doi: 10.4103/IJO.IJO_3204_23. Epub 2024 Feb 23. Indian J Ophthalmol. 2024. PMID: 38389252 Free article.
Three cases of acute-onset bilateral photophobia.
Ueno S, Inooka D, Meinert M, Ito Y, Tsunoda K, Fujinami K, Iwata T, Ohde H, Terasaki H. Ueno S, et al. Among authors: iwata t. Jpn J Ophthalmol. 2019 Mar;63(2):172-180. doi: 10.1007/s10384-018-00649-0. Epub 2019 Jan 2. Jpn J Ophthalmol. 2019. PMID: 30604114
164 results