原著論文
1.Structural Changes in Optical Coherence Tomography Underlying Spots of Increased Autofluorescence in the Perilesional Zone of Geographic Atrophy.
Oishi M, Oishi A, Lindner M, Pfau M, Schmitz-Valckenberg S, Holz FG, Fleckenstein M.
Invest Ophthalmol Vis Sci. 2017 Jun 1;58(7):3303-3310. doi: 10.1167/iovs.17-21498.
2.Next-generation sequencing-based comprehensive molecular analysis of 43 Japanese patients with cone and cone-rod dystrophies.
Oishi M, Oishi A, Gotoh N, Ogino K, Higasa K, Iida K, Makiyama Y, Morooka S, Matsuda F, Yoshimura N.
Mol Vis. 2016 Feb 20;22:150-60. eCollection 2016.
3.Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing.
Oishi M, Oishi A, Gotoh N, Ogino K, Higasa K, Iida K, Makiyama Y, Morooka S, Matsuda F, Yoshimura N.
Invest Ophthalmol Vis Sci. 2014 Oct 16;55(11):7369-75. doi: 10.1167/iovs.14-15458.
4.Wide-field fundus autofluorescence abnormalities and visual function in patients with cone and cone-rod dystrophies.
Oishi M, Oishi A, Ogino K, Makiyama Y, Gotoh N, Kurimoto M, Yoshimura N.
Invest Ophthalmol Vis Sci. 2014 May 20;55(6):3572-7. doi: 10.1167/iovs.14-13912.
5.Association between ZIC2, RASGRF1, and SHISA6 genes and high myopia in Japanese subjects.
Oishi M, Yamashiro K, Miyake M, Akagi-Kurashige Y, Kumagai K, Nakata I, Nakanishi H, Yoshikawa M, Oishi A, Gotoh N, Tsujikawa A; Nagahama Study Group; Yamada R, Matsuda F, Yoshimura N.
Invest Ophthalmol Vis Sci. 2013 Nov 13;54(12):7492-7. doi: 10.1167/iovs.13-12825.
6.Contrast visual acuity in patients with retinitis pigmentosa assessed by a contrast sensitivity tester.
Oishi M, Nakamura H, Hangai M, Oishi A, Otani A, Yoshimura N.
Indian J Ophthalmol. 2012 Nov-Dec;60(6):545-9. doi: 10.4103/0301-4738.103793.
7.Detection Sensitivity of Retinitis Pigmentosa Progression Using Static Perimetry and Optical Coherence Tomography.
Hasegawa T, Oishi A, Ikeda HO, Numa S, Miyata M, Otsuka Y, Oishi M, Tsujikawa A.
Transl Vis Sci Technol. 2021 Jul 1;10(8):31. doi: 10.1167/tvst.10.8.31.
8.Evaluation of outer nuclear layer overshadowed by retinal vessels in retinitis pigmentosa.
Otsuka Y, Oishi A, Miyata M, Uji A, Oishi M, Hasegawa T, Numa S, Ikeda HO, Tsujikawa A.
Eye (Lond). 2022 May;36(5):1042-1049. doi: 10.1038/s41433-021-01578-y. Epub 2021 May 11.
9.Clinical Characteristics, Differential Diagnosis and Genetic Analysis of Concentric Retinitis Pigmentosa.
Nakahara M, Oishi A, Miyata M, Ikeda HO, Hasegawa T, Numa S, Otsuka Y, Oishi M, Matsuda F, Tsujikawa A.
Life (Basel). 2021 Mar 22;11(3):260. doi: 10.3390/life11030260.
10.EYS is a major gene involved in retinitis pigmentosa in Japan: genetic landscapes revealed by stepwise genetic screening.
Numa S, Oishi A, Higasa K, Oishi M, Miyata M, Hasegawa T, Ikeda HO, Otsuka Y, Matsuda F, Tsujikawa A.
Sci Rep. 2020 Nov 27;10(1):20770. doi: 10.1038/s41598-020-77558-1.
11.Wavelength of light and photophobia in inherited retinal dystrophy.
Otsuka Y, Oishi A, Miyata M, Oishi M, Hasegawa T, Numa S, Ikeda HO, Tsujikawa A.
Sci Rep. 2020 Sep 9;10(1):14798. doi: 10.1038/s41598-020-71707-2.
12.Wide-field fundus autofluorescence imaging in patients with hereditary retinal degeneration: a literature review.
Oishi A, Miyata M, Numa S, Otsuka Y, Oishi M, Tsujikawa A.
Int J Retina Vitreous. 2019 Dec 12;5(Suppl 1):23. doi: 10.1186/s40942-019-0173-z. eCollection 2019.
13.Multimodal Imaging for Differential Diagnosis of Bietti Crystalline Dystrophy.
Oishi A, Oishi M, Miyata M, Hirashima T, Hasegawa T, Numa S, Tsujikawa A.
Ophthalmol Retina. 2018 Oct;2(10):1071-1077. doi: 10.1016/j.oret.2018.02.012. Epub 2018 Apr 4.
14.Concentric Choriocapillaris Flow Deficits in Retinitis Pigmentosa Detected Using Wide-Angle Swept-Source Optical Coherence Tomography Angiography.
Miyata M, Oishi A, Hasegawa T, Oishi M, Numa S, Otsuka Y, Uji A, Kadomoto S, Hata M, Ikeda HO, Tsujikawa A.
Invest Ophthalmol Vis Sci. 2019 Mar 1;60(4):1044-1049. doi: 10.1167/iovs.18-26176.
15.Diabetic Nonperfused Areas in Macular and Extramacular Regions on Wide-Field Optical Coherence Tomography Angiography.
Yasukura S, Murakami T, Suzuma K, Yoshitake T, Nakanishi H, Fujimoto M, Oishi M, Tsujikawa A.
Invest Ophthalmol Vis Sci. 2018 Dec 3;59(15):5893-5903. doi: 10.1167/iovs.18-25108.
16.Relationship between Ocular Deviation and Visual Function in Retinitis Pigmentosa.
Miyata M, Oishi A, Ogino K, Oishi M, Hasegawa T, Nagasaku Y, Ikeda HO, Ohtsuki H, Tsujikawa A.
Sci Rep. 2018 Oct 5;8(1):14880. doi: 10.1038/s41598-018-33211-6.
17.Long-term efficacy and safety of anti-VEGF therapy in retinitis pigmentosa: a case report.
Miyata M, Oishi A, Oishi M, Hasegawa T, Ikeda HO, Tsujikawa A.
BMC Ophthalmol. 2018 Sep 14;18(1):248. doi: 10.1186/s12886-018-0914-z.
18.Decorrelation Signal of Diabetic Hyperreflective Foci on Optical Coherence Tomography Angiography.
Murakami T, Suzuma K, Dodo Y, Yoshitake T, Yasukura S, Nakanishi H, Fujimoto M, Oishi M, Tsujikawa A.
Sci Rep. 2018 Jun 11;8(1):8798. doi: 10.1038/s41598-018-27192-9.
19.Choriocapillaris flow deficit in Bietti crystalline dystrophy detected using optical coherence tomography angiography.
Miyata M, Oishi A, Hasegawa T, Ishihara K, Oishi M, Ogino K, Sugahara M, Hirashima T, Hata M, Yoshikawa M, Tsujikawa A.
Br J Ophthalmol. 2018 Sep;102(9):1208-1212. doi: 10.1136/bjophthalmol-2017-311313. Epub 2017 Dec 2.
20.A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration.
Kawashima-Kumagai K, Yamashiro K, Yoshikawa M, Miyake M, Ming GCC, Fan Q, Koh JY, Saito M, Sugahara-Kuroda M, Oishi M, Akagi-Kurashige Y, Nakata I, Nakanishi H, Gotoh N, Oishi A, Tamura H, Ooto S, Tsujikawa A, Kurimoto Y, Sekiryu T, Matsuda F, Khor CC, Cheng CY, Wong TY, Yoshimura N.
Sci Rep. 2017 Aug 3;7(1):7173. doi: 10.1038/s41598-017-07526-9.
21.Prevalence, Natural Course, and Prognostic Role of Refractile Drusen in Age-Related Macular Degeneration.
Oishi A, Thiele S, Nadal J, Oishi M, Fleckenstein M, Schmid M, Holz FG, Schmitz-Valckenberg S.
Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2198-2206. doi: 10.1167/iovs.16-20781.
22.Screening for SLC7A14 gene mutations in patients with autosomal recessive or sporadic retinitis pigmentosa.
Sugahara M, Oishi M, Oishi A, Ogino K, Morooka S, Gotoh N, Kang I, Yoshimura N.
Ophthalmic Genet. 2017 Jan-Feb;38(1):70-73. doi: 10.3109/13816810.2015.1136336. Epub 2016 Mar 30.
23.Efficacy of Column Scatter Plots for Presenting Retinitis Pigmentosa Phenotypes in a Japanese Cohort.
Ogino K, Oishi A, Oishi M, Gotoh N, Morooka S, Sugahara M, Hasegawa T, Miyata M, Yoshimura N.
Transl Vis Sci Technol. 2016 Mar 4;5(2):4. doi: 10.1167/tvst.5.2.4. eCollection 2016 Mar.
24.ASYMMETRIC CONE DISTRIBUTION AND ITS CLINICAL APPEARANCE IN RETINITIS PIGMENTOSA.
Nakagawa S, Oishi A, Ogino K, Morooka S, Oishi M, Sugahara M, Yoshimura N.
Retina. 2016 Jul;36(7):1340-4. doi: 10.1097/IAE.0000000000000904.
25.Wide-Field Fundus Autofluorescence for Retinitis Pigmentosa and Cone/Cone-Rod Dystrophy.
Oishi A, Oishi M, Ogino K, Morooka S, Yoshimura N.
Adv Exp Med Biol. 2016;854:307-13. doi: 10.1007/978-3-319-17121-0_41.
26.Intra-familial Similarity of Wide-Field Fundus Autofluorescence in Inherited Retinal Dystrophy.
Furutani Y, Ogino K, Oishi A, Gotoh N, Makiyama Y, Oishi M, Kurimoto M, Yoshimura N.
Adv Exp Med Biol. 2016;854:299-305. doi: 10.1007/978-3-319-17121-0_40.
27.Next-Generation Sequencing-Based Molecular Diagnosis of Choroideremia.
Shimizu K, Oishi A, Oishi M, Ogino K, Morooka S, Sugahara M, Gotoh N, Yoshimura N.
Case Rep Ophthalmol. 2015 Jul 25;6(2):246-50. doi: 10.1159/000437348. eCollection 2015 May-Aug.
28.Radial fundus autofluorescence in the periphery in patients with X-linked retinitis pigmentosa.
Ogino K, Oishi M, Oishi A, Morooka S, Sugahara M, Gotoh N, Kurimoto M, Yoshimura N.
Clin Ophthalmol. 2015 Aug 17;9:1467-74. doi: 10.2147/OPTH.S89371. eCollection 2015.
29.The Contribution of Genetic Architecture to the 10-Year Incidence of Age-Related Macular Degeneration in the Fellow Eye.
Miyake M, Yamashiro K, Tamura H, Kumagai K, Saito M, Sugahara-Kuroda M, Yoshikawa M, Oishi M, Akagi-Kurashige Y, Nakata I, Nakanishi H, Gotoh N, Oishi A, Matsuda F, Yamada R, Khor CC, Kurimoto Y, Sekiryu T, Tsujikawa A, Yoshimura N.
Invest Ophthalmol Vis Sci. 2015 Aug;56(9):5353-61. doi: 10.1167/iovs.14-16020.
30.Central blood pressure relates more strongly to retinal arteriolar narrowing than brachial blood pressure: the Nagahama Study.
Kumagai K, Tabara Y, Yamashiro K, Miyake M, Akagi-Kurashige Y, Oishi M, Yoshikawa M, Kimura Y, Tsujikawa A, Takahashi Y, Setoh K, Kawaguchi T, Terao C, Yamada R, Kosugi S, Sekine A, Nakayama T, Matsuda F, Yoshimura N; Nagahama Study group.
J Hypertens. 2015 Feb;33(2):323-9. doi: 10.1097/HJH.0000000000000391.
31.Comprehensive replication of the relationship between myopia-related genes and refractive errors in a large Japanese cohort.
Yoshikawa M, Yamashiro K, Miyake M, Oishi M, Akagi-Kurashige Y, Kumagai K, Nakata I, Nakanishi H, Oishi A, Gotoh N, Yamada R, Matsuda F, Yoshimura N; Nagahama Study Group.
Invest Ophthalmol Vis Sci. 2014 Oct 21;55(11):7343-54. doi: 10.1167/iovs.14-15105.
32.Tomographic comparison of cone-rod and rod-cone retinal dystrophies.
Inui E, Oishi A, Oishi M, Ogino K, Makiyama Y, Gotoh N, Kurimoto M, Yoshimura N.
Graefes Arch Clin Exp Ophthalmol. 2014 Jul;252(7):1065-9. doi: 10.1007/s00417-014-2570-1. Epub 2014 Jan 18.
33.Evaluation of pigment epithelium-derived factor and complement factor I polymorphisms as a cause of choroidal neovascularization in highly myopic eyes.
Miyake M, Yamashiro K, Nakanishi H, Nakata I, Akagi-Kurashige Y, Kumagai K, Oishi M, Tsujikawa A, Moriyama M, Ohno-Matsui K, Mochizuki M, Yoshimura N.
Invest Ophthalmol Vis Sci. 2013 Jun 19;54(6):4208-12. doi: 10.1167/iovs.13-12280.
