Papers - UENO SHINJI
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Longitudinal change in anterior chamber depth and its determinants: a median 4.9-year follow-up of 2,247 Japanese adults
Inooka, T; Tomita, R; Kominami, T; Fujikawa, S; Kojima, T; Ueno, S; Ito, Y; Nishiguchi, KM; Yuki, K
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY 2026.3
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Deletion involving exon 18 of RPGRIP1 is a major cause of achromatopsia.
Inooka T, Mizobuchi K, Hayashi T, Suga A, Tsunoda K, Kuniyoshi K, Kondo H, Ota J, Kominami T, Yoshitake K, Minematsu N, Iwata T, Kondo M, Nishiguchi KM, Ueno S
Retina (Philadelphia, Pa.) 2026.3
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Association of High-Density Lipoprotein Cholesterol with Macular Structure in Nonglaucomatous Individuals
Inooka, T; Tomita, R; Suzumura, A; Fujikawa, S; Kimura, Y; Kominami, T; Kojima, T; Ueno, S; Ito, Y; Nishiguchi, KM; Yuki, K
OPHTHALMOLOGY SCIENCE 6 ( 3 ) 101073 2026.3
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Electroretinography (ERG) alterations following positional changes in gas-filled eyes after a vitrectomy
Ichinohe, H; Yamabe, Y; Fujibayashi, S; Imura, E; Odagiri, Y; Narumi, T; Okado, S; Ueno, S
DOCUMENTA OPHTHALMOLOGICA 2026.2
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Risk Factors for Adult Axial Length Elongation: A 5-Year Population-Based Cohort Study
Inooka, T; Kimura, Y; Fujikawa, S; Yasuda, S; Kominami, T; Kojima, T; Ueno, S; Ito, Y; Nishiguchi, KM; Yuki, K
OPHTHALMOLOGY SCIENCE 6 ( 2 ) 101011 2026.2
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Clinical and genetic characterization of <i>REEP6</i>-associated retinopathy in a Japanese cohort
Tsuboi, T; Mizobuchi, K; Yoshitake, K; Kuniyoshi, K; Kominami, T; Ueno, S; Nishiguchi, KM; Kusaka, S; Iwata, T; Hayashi, T; Nakano, T
JAPANESE JOURNAL OF OPHTHALMOLOGY 2026.1
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Macular retinal function after autologous retinal transplantation in patients with refractory macular holes
Arasaki, R; Inoue, T; Terasaki, H; Ueno, S; Tsunoda, K; Takeuchi, J; Kitahata, S; Yanagi, Y; Maruyama-Inoue, M; Kadonosono, K
DOCUMENTA OPHTHALMOLOGICA 151 ( 3 ) 229 - 237 2025.12
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特集 遺伝性網膜疾患の最新情報 ２ 遺伝性網膜疾患の診断の進歩
上野 真治
眼科 67 ( 11 ) 1139 - 1144 2025.10
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Classification of fundus autofluorescence images based on macular function in retinitis pigmentosa using convolutional neural networks
Kominami, T; Ueno, S; Ota, J; Inooka, T; Oda, M; Mori, K; Nishiguchi, KM
JAPANESE JOURNAL OF OPHTHALMOLOGY 69 ( 2 ) 236 - 244 2025.3
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EVALUATION OF RETINAL ARTERIOLES IN RETINITIS PIGMENTOSA
Ota, J; Inooka, T; Tomita, R; Kominami, T; Koyanagi, Y; Ito, Y; Terasaki, H; Nishiguchi, KM; Ueno, S
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES 45 ( 3 ) 532 - 540 2025.3
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Assessment of factors affecting anterior chamber depth from data obtained from health checkup participants in Japan
Inooka, T; Kominami, T; Tomita, R; Suzumura, A; Matsuno, T; Ota, J; Koyanagi, Y; Takeyama, H; Ueno, S; Ito, Y; Nishiguchi, KM; Yuki, K
SCIENTIFIC REPORTS 14 ( 1 ) 30342 2024.12
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臨床報告 外傷性毛様体解離に伴う低眼圧黄斑症に対して毛様体扁平部冷凍凝固およびガス・タンポナーデで治療した1例
野月 徳実, 鈴木 幸彦, 小堀 宏理, 古川 智美, 丹藤 利夫, 上野 真治, 片岡 英樹, 山上 美情子
臨床眼科 78 ( 12 ) 1399 - 1405 2024.11
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GENETIC ETIOLOGY AND CLINICAL FEATURES OF ACHROMATOPSIA IN JAPAN
Inooka, T; Hayashi, T; Tsunoda, K; Kuniyoshi, K; Kondo, H; Mizobuchi, K; Suga, A; Iwata, T; Yoshitake, K; Kondo, M; Goto, K; Ota, J; Kominami, T; Nishiguchi, KM; Ueno, S
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES 44 ( 10 ) 1836 - 1844 2024.10
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Genetic and Clinical Features of<i> ABCA4</i>-Associated Retinopathy in a Japanese Nationwide Cohort
Mizobuchi, K; Hayashi, T; Tanaka, K; Kuniyoshi, K; Murakami, Y; Nakamura, N; Torii, K; Mizota, A; Sakai, D; Maeda, A; Kominami, T; Ueno, S; Kusaka, S; Nishiguchi, KM; Ikeda, Y; Kondo, M; Tsunoda, K; Hotta, Y; Nakano, T
AMERICAN JOURNAL OF OPHTHALMOLOGY 264 36 - 43 2024.8
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Disease-specific variant interpretation highlighted the genetic findings in 2325 Japanese patients with retinitis pigmentosa and allied diseases
Goto, K; Koyanagi, Y; Akiyama, M; Murakami, Y; Fukushima, M; Fujiwara, K; Iijima, H; Yamaguchi, M; Endo, M; Hashimoto, K; Ishizu, M; Hirakata, T; Mizobuchi, K; Takayama, M; Ota, J; Sajiki, A; Kominami, T; Ushida, H; Fujita, K; Kaneko, H; Ueno, S; Hayashi, T; Terao, C; Hotta, Y; Murakami, A; Kuniyoshi, K; Kusaka, S; Wada, Y; Abe, T; Nakazawa, T; Ikeda, Y; Momozawa, Y; Sonoda, KH; Nishiguchi, KM
JOURNAL OF MEDICAL GENETICS 61 ( 7 ) 613 - 620 2024.7
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Nationwide epidemiologic survey on incidence of macular dystrophy in Japan
Ueno, S; Hayashi, T; Tsunoda, K; Aoki, T; Kondo, M
JAPANESE JOURNAL OF OPHTHALMOLOGY 68 ( 3 ) 167 - 173 2024.5
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Case report: A case of unilateral combined central retinal vein occlusion, incomplete central retinal artery occlusion, and papillitis following a third dose of COVID-19 vaccination
Furukawa, A; Suzuki, Y; Nozuki, N; Kurosaka, N; Kogawa, S; Hara, S; Ueno, S
FRONTIERS IN OPHTHALMOLOGY 4 1352962 2024.2
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Silencing of ocular transthyretin, a gene responsible for hereditary transthyretin amyloidosis, by intravitreal injection of an siRNA conjugate into rabbit eyes
Watanabe, T; Takihara, Y; Jono, H; Fujimoto, T; Tasaki, M; Isoguchi, A; Urahashi, Y; Shimoda, T; Takahashi, E; Ando, Y; Ueno, S; Ueda, M; Inoue, T
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 694 149397 2024.1
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A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD.
Suga A, Mizobuchi K, Inooka T, Yoshitake K, Minematsu N, Tsunoda K, Kuniyoshi K, Kawai Y, Omae Y, Tokunaga K, NCBN Controls WGS Consortium, Hayashi T, Ueno S, Iwata T
Genetics in medicine open 2 101843 2024
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Bilateral simultaneous endophthalmitis after immediately sequential bilateral cataract surgery.
Kogawa S, Suzuki Y, Furukawa A, Kurosaka N, Nozuki N, Ueno S
American journal of ophthalmology case reports 32 101886 2023.12
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One-Year Outcomes of Oral Treatment With Alga Capsules Containing Low Levels of 9-<i> cis</i>-fi-Carotene in RDH5-Related Fundus Albipunctatus
Mizobuchi Kei, Hayashi Takaaki, Ueno Shinji, Kondo Mineo, Terasaki Hiroko, Aoki Takuya, Nakano Tadashi
AMERICAN JOURNAL OF OPHTHALMOLOGY 254 193 - 202 2023.10
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Pathogenic variants of <i>MFRP</i> and <i>PRSS56</i> genes are major causes of nanophthalmos in Japanese patients
Ota Junya, Inooka Taiga, Okado Satoshi, Maeda Natsuki, Koyanagi Yoshito, Kominami Taro, Nishiguchi Koji M., Ueno Shinji
OPHTHALMIC GENETICS 44 ( 5 ) 423 - 429 2023.9
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NOTCH2NLC GGC repeat expansion causes retinal pathology of NIID patients
Sone J., Ueno S., Akagi A., Miyahara H., Tamai C., Riku Y., Yabata H., Koizumi R., Hashizume Y., Sobue G., Yoshida M., Iwasaki Y.
BRAIN PATHOLOGY 33 2023.9
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Functional Characteristics of Diverse <i>PAX6</i> Mutations Associated with Isolated Foveal Hypoplasia
Matsushita Itsuka, Izumi Hiroto, Ueno Shinji, Hayashi Takaaki, Fujinami Kaoru, Tsunoda Kazushige, Iwata Takeshi, Kiuchi Yoshiaki, Kondo Hiroyuki
GENES 14 ( 7 ) 2023.7
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Genetic characteristics of retinitis pigmentosa and allied diseases in 2063 Japanese patients
Nishiguchi Koji, Koyanagi Yoshito, Akiyama Masato, Murakami Yusuke, Iijima Hanae, Endo Mikiko, Ueno Shinji, Hayashi Takaaki, Hotta Yoshihiro, Murakami Akira, Wada Yuko, Abe Toshiaki, Nakazawa Toru, Ikeda Yasuhiro, Sonoda Koh-Hei, Goto Kensuke
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 64 ( 8 ) 2023.6
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A light-gated cation channel with high reactivity to weak light
Hososhima Shoko, Ueno Shinji, Okado Satoshi, Inoue Ken-ichi, Konno Masae, Yamauchi Yumeka, Inoue Keiichi, Terasaki Hiroko, Kandori Hideki, Tsunoda Satoshi P.
SCIENTIFIC REPORTS 13 ( 1 ) 7625 2023.5
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NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment
Sone Jun, Ueno Shinji, Akagi Akio, Miyahara Hiroaki, Tamai Chisato, Riku Yuichi, Yabata Hiroyuki, Koizumi Ryuichi, Hattori Tomohiro, Hirose Hiroshi, Koyanagi Yoshito, Kobayashi Rei, Okada Hisashi, Kishimoto Yoshiyuki, Hashizume Yoshio, Sobue Gen, Yoshida Mari, Iwasaki Yasushi
ACTA NEUROPATHOLOGICA COMMUNICATIONS 11 ( 1 ) 71 2023.5
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Assessment of factors affecting flicker ERGs recorded with RETeval from data obtained from health checkup screening
Inooka Taiga, Kominami Taro, Yasuda Shunsuke, Koyanagi Yoshito, Ota Junya, Okado Satoshi, Tomita Ryo, Ito Yasuki, Iwase Takeshi, Terasaki Hiroko, Nishiguchi Koji M., Ueno Shinji
PLOS ONE 18 ( 4 ) e0284686 2023.4
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Phase 1b study on the repurposing of meclizine hydrochloride for children with achondroplasia.
Matsushita M, Kitoh H, Mishima K, Kamiya Y, Kato D, Takemoto G, Sawamura K, Ueno S, Yasuhiro N, Nishida K, Imagama S
PloS one 18 ( 7 ) e0283425 2023
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A Japanese boy with Bardet-Biedl syndrome caused by a novel homozygous variant in the ARL6 gene who was initially diagnosed with retinitis punctata albescens: A case report.
Mizumoto K, Kato K, Fujinami K, Sugita T, Sugita I, Hattori A, Saitoh S, Ueno S, Tsunoda K, Iwata T, Kondo M
Medicine 101 ( 50 ) e32161 2022.12
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A case of herpes zoster ophthalmicus with optic neuritis of the total length of the optic nerve in the orbital space and ischemic optic neuropathy.
Kudo T, Yamauchi K, Suzuki Y, Nakazawa M, Ueno S
American journal of ophthalmology case reports 28 101756 2022.12
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Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing
Suga Akiko, Yoshitake Kazutoshi, Minematsu Naoko, Tsunoda Kazushige, Fujinami Kaoru, Miyake Yozo, Kuniyoshi Kazuki, Hayashi Takaaki, Mizobuchi Kei, Ueno Shinji, Terasaki Hiroko, Kominami Taro, Nao-I Nobuhisa, Mawatari Go, Mizota Atsushi, Shinoda Kei, Kondo Mineo, Kato Kumiko, Sekiryu Tetsuju, Nakamura Makoto, Kusuhara Sentaro, Yamamoto Hiroyuki, Yamamoto Shuji, Mochizuki Kiyofumi, Kondo Hiroyuki, Matsushita Itsuka, Kameya Shuhei, Fukuchi Takeo, Hatase Tetsuhisa, Horiguchi Masayuki, Shimada Yoshiaki, Tanikawa Atsuhiro, Yamamoto Shuichi, Miura Gen, Ito Nana, Murakami Akira, Fujimaki Takuro, Hotta Yoshihiro, Tanaka Koji, Iwata Takeshi
HUMAN MUTATION 43 ( 12 ) 2251 - 2264 2022.11
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Automatic Screening of the Eyes in a Deep-Learning-Based Ensemble Model Using Actual Eye Checkup Optical Coherence Tomography Images
Hirota Masakazu, Ueno Shinji, Inooka Taiga, Ito Yasuki, Takeyama Hideo, Inoue Yuji, Watanabe Emiko, Mizota Atsushi
APPLIED SCIENCES-BASEL 12 ( 14 ) 2022.7
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Ablation of Ctrp9, Ligand of AdipoR1, and Lower Number of Cone Photoreceptors in Mouse Retina.
Inooka D, Omori Y, Ouchi N, Ohashi K, Kawakami Y, Koyanagi Y, Koike C, Terasaki H, Nishiguchi KM, Ueno S
Investigative ophthalmology & visual science 63 ( 5 ) 14 2022.5
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Clinical findings in eyes with BEST1-related retinopathy complicated by choroidal neovascularization.
Miyagi M, Takeuchi J, Koyanagi Y, Mizobuchi K, Hayashi T, Ito Y, Terasaki H, Nishiguchi KM, Ueno S
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 260 ( 4 ) 1125 - 1137 2022.4
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Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients.
Murakami Y, Koyanagi Y, Fukushima M, Yoshimura M, Fujiwara K, Akiyama M, Momozawa Y, Ueno S, Terasaki H, Oishi A, Miyata M, Ikeda H, Tsujikawa A, Mizobuchi K, Hayashi T, Fujinami K, Tsunoda K, Park JY, Han J, Kim M, Lee CS, Kim SJ, Park TK, Joo K, Woo SJ, Ikeda Y, Sonoda KH
Ophthalmology. Retina 5 ( 12 ) 1269 - 1279 2021.12
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Regional differences in genes and variants causing retinitis pigmentosa in Japan.
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
Japanese journal of ophthalmology 65 ( 3 ) 338 - 343 2021.5
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Erratum to Association Between Retinal Layer Thickness and Perfusion Status in Extramacular Areas in Diabetic Retinopathy. Am J Ophthalmol 2020; 215:25-36.
Ito H, Ito Y, Kataoka K, Ueno S, Takeuchi J, Nakano Y, Fujita A, Horiguchi E, Kaneko H, Iwase T, Terasaki H
American journal of ophthalmology 2021.4
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Clinical characteristics and high resolution retinal imaging of retinitis pigmentosa caused by RP1 gene variants.
Ueno S, Koyanagi Y, Kominami T, Ito Y, Kawano K, Nishiguchi KM, Rivolta C, Nakazawa T, Sonoda KH, Terasaki H
Japanese journal of ophthalmology 64 ( 5 ) 485 - 496 2020.9
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RP2-associated retinal disorder in a Japanese cohort: Report of novel variants and a literature review, identifying a genotype-phenotype association.
Fujinami K, Liu X, Ueno S, Mizota A, Shinoda K, Kuniyoshi K, Fujinami-Yokokawa Y, Yang L, Arno G, Pontikos N, Kameya S, Kominami T, Terasaki H, Sakuramoto H, Nakamura N, Kurihara T, Tsubota K, Miyake Y, Yoshiake K, Iwata T, Tsunoda K, Japan Eye Genetics Consortium Study Group.
American journal of medical genetics. Part C, Seminars in medical genetics 184 ( 3 ) 675 - 693 2020.9
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Longitudinal Changes of Macular Curvature in Patients with Retinitis Pigmentosa.
Meinert M, Ueno S, Komori S, Koyanagi Y, Sayo A, Andreasson S, Kominami T, Ito Y, Terasaki H
Translational vision science & technology 9 ( 10 ) 11 2020.9
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Relationship Between Macular Curvature and Common Causative Genes of Retinitis Pigmentosa in Japanese Patients.
Koyanagi Y, Ueno S, Ito Y, Kominami T, Komori S, Akiyama M, Murakami Y, Ikeda Y, Sonoda KH, Terasaki H
Investigative ophthalmology & visual science 61 ( 10 ) 6 2020.8
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Changes in intraocular pressure and aqueous flare in eyes with multiple evanescent white dot syndrome.
Ito Y, Ito M, Ueno S, Kataoka K, Takeuchi J, Kominami T, Takayama K, Terasaki H
Japanese journal of ophthalmology 64 ( 4 ) 378 - 384 2020.7
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Association Between Retinal Layer Thickness and Perfusion Status in Extramacular Areas in Diabetic Retinopathy.
Ito H, Ito Y, Kataoka K, Ueno S, Takeuchi J, Nakano Y, Fujita A, Horiguchi E, Kaneko H, Iwase T, Terasaki H
American journal of ophthalmology 215 25 - 36 2020.7
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Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association.
Fujinami-Yokokawa Y, Fujinami K, Kuniyoshi K, Hayashi T, Ueno S, Mizota A, Shinoda K, Arno G, Pontikos N, Yang L, Liu X, Sakuramoto H, Katagiri S, Mizobuchi K, Kominami T, Terasaki H, Nakamura N, Kameya S, Yoshitake K, Miyake Y, Kurihara T, Tsubota K, Miyata H, Iwata T, Tsunoda K, Japan Eye Genetics Consortium.
Scientific reports 10 ( 1 ) 9531 2020.6
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Clinical and Genetic Characteristics of 15 Affected Patients From 12 Japanese Families with <i>GUCY2D</i>-Associated Retinal Disorder.
Liu X, Fujinami K, Kuniyoshi K, Kondo M, Ueno S, Hayashi T, Mochizuki K, Kameya S, Yang L, Fujinami-Yokokawa Y, Arno G, Pontikos N, Sakuramoto H, Kominami T, Terasaki H, Katagiri S, Mizobuchi K, Nakamura N, Yoshitake K, Miyake Y, Li S, Kurihara T, Tsubota K, Iwata T, Tsunoda K, Japan Eye Genetics Consortium.
Translational vision science & technology 9 ( 6 ) 2 2020.5
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Japan-Retinal Detachment Registry Report I: preoperative findings in eyes with primary retinal detachment
Sakamoto Taiji, Kawano Sumihiro, Kawasaki Ryo, Hirakata Akito, Yamashita Hidetoshi, Yamamoto Shuichi, Ishibashi Tatsuro, Yamamoto Shuichi, Baba Takayuki, Sato Eiju, Kitahashi Masayasu, Tatsumi Tomoaki, Miura Gen, Niizawa Tomohiro, Sakamoto Taiji, Yamakiri Keita, Yamashita Toshifumi, Otsuka Hiroki, Sameshima Seiji, Yoshinaga Narimasa, Sonoda Shozo, Hirakata Akito, Koto Takashi, Inoue Makoto, Hirota Kazunari, Itoh Yuji, Orihara Tadashi, Emoto Yoshinobu, Sano Masahiko, Takahashi Hiroyuki, Tokizawa Ryo, Yamashita Hidetoshi, Nishitsuka Koichi, Kaneko Yutaka, Nishi Katsuhiro, Yoshida Akitoshi, Ono Shinji, Hirokawa Hiroyuki, Sogawa Kenji, Omae Tsuneaki, Ishibazawa Akihiro, Kishi Shoji, Akiyama Hideo, Matsumoto Hidetaka, Mukai Ryo, Morimoto Masahiro, Nakazawa Mitsuru, Suzuki Yukihiko, Kudo Takashi, Adachi Kobu, Ishida Susumu, Noda Kousuke, Kase Satoru, Mori Syouhei, Ando Ryo, Saito Michiyuki, Suzuki Tomohiro, Takahashi Kanji, Nagai Yoshimi, Nakauchi Tadashi, Yamada Haruiko, Kusaka Shuji, Tsujioka Daishi, Tsujikawa Akitaka, Suzuma Kiyoshi, Ishibashi Tatsuro, Sonoda Koh-Hei, Ikeda Yasuhiro, Kohno Riichiro, Ishikawa Keijiro, Kondo Mineo, Kozawa Maki, Kitaoka Takashi, Tsuiki Eiko, Ogura Yuichiro, Yoshida Munenori, Morita Hiroshi, Kato Aki, Hirano Yoshio, Sugitani Kazuhiko, Terasaki Hiroko, Iwase Takeshi, Ito Yasuki, Ueno Shinji, Kaneko Hiroki, Nonobe Norie, Kominami Taro, Azuma Noriyuki, Yokoi Tadashi, Shimada Hiroyuki, Nakashizuka Hiroyuki, Hattori Takayuki, Shinojima Ari, Kutagawa Yorihisa, Shiraga Fumio, Morizane Yuki, Kimura Shuhei, Ikeda Tsunehiko, Kida Teruyo, Sato Takaki, Fukumoto Masanori, Emi Kazuyuki, Nakashima Hiroshi, Ohji Masahito, Kakinoki Masashi, Sawada Osamu, Takeuchi Shinobu, Tanaka Sumiyoshi, Iida Tomohiro, Koizumi Hideki, Maruko Ichiro, Hasegawa Taiji, Kogure Akiko, Iijima Hiroyuki, Oshiro Tomohiro, Tateno Yasushi, Kikushima Wataru, Sugiyama Atsushi, Yoneyama Seigo, Kadonosono Kazuaki, Sato Shimpei, Yamane Shin
JAPANESE JOURNAL OF OPHTHALMOLOGY 64 ( 1 ) 1 - 12 2020.1
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Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-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.
Human genome variation 7 3 2020
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Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance
Kameya Shuhei, Fujinami Kaoru, Ueno Shinji, Hayashi Takaaki, Kuniyoshi Kazuki, Ideta Ryuichi, Kikuchi Sachiko, Kubota Daiki, Yoshitake Kazutoshi, Katagiri Satoshi, Sakuramoto Hiroyuki, Kominami Taro, Terasaki Hiroko, Yang Lizhu, Fujinami-Yokokawa Yu, Liu Xiao, Arno Gavin, Pontikos Nikolas, Miyake Yozo, Iwata Takeshi, Tsunoda Kazushige, Mizota Atsushi, Shinoda Kei, Nakamura Natsuko, Mizobuchi Kei, Nishimura Toshihide, Hayashizaki Yoshihide, Kondo Mineo, Shimozawa Nobuhiro, Horiguchi Masayuki, Yamamoto Shuichi, Kuze Manami, Naoi Nobuhisa, Machida Shigeki, Shimada Yoshiaki, Nakamura Makoto, Fujikado Takashi, Yoshihiro Hotta, Takahashi Masayo, Mochizuki Kiyofumi, Murakami Akira, Kondo Hiroyuki, Ishida Susumu, Nakazawa Mitsuru, Hatase Tetsuhisa, Matsunaga Tatsuo, Maeda Akiko, Noda Kosuke, Tanikawa Atsuhiro, Yamamoto Syuji, Yamamoto Hiroyuki, Araie Makoto, Aihara Makoto, Nakazawa Toru, Sekiryu Tetsuju, Kashiwagi Kenji, Kosaki Kenjiro, Piero Carninci, Fukuchi Takeo, Hayashi Atsushi, Hosono Katsuhiro, Mori Keisuke, Tanaka Kouji, Furuya Kouiti, Suzuki Keiichirou, Kohata Ryo, Yanagi Yasuo, Minegishi Yuriko, Iejima Daisuke, Suga Akiko, Rossmiller Brian P., Pan Yang, Oshima Tomoko, Nakayama Mao, Yamamoto Megumi, Minematsu Naoko, Mori Daisuke, Kijima Yusuke, Mawatari Go, Kurata Kentaro, Yamada Norihiro, Itoh Masayoshi, Kawaji Hideya, Murakawa Yasuhiro
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 60 ( 10 ) 3432 - 3446 2019.8
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Course of loss of photoreceptor function and progressive Müller cell gliosis in rhodopsin P347L transgenic rabbits.
Ueno S, Kominami T, Okado S, Inooka D, Kondo M, Terasaki H
Experimental eye research 184 192 - 200 2019.7
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Biological Characteristics of Subsilicone Oil Fluid and Differences With Other Ocular Humors.
Shimizu H, Kaneko H, Suzumura A, Takayama K, Namba R, Funahashi Y, Kataoka K, Iwase T, Hwang SJ, Ito S, Yamada K, Ueno S, Ito Y, Terasaki H
Translational vision science & technology 8 ( 1 ) 28 2019.1
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Clinical and genetic characteristics of 14 patients from 13 Japanese families with <i>RPGR</i>-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.
Human genome variation 6 34 2019
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Supernormal Flicker ERGs in Eyes With Central Retinal Vein Occlusion: Clinical Characteristics, Prognosis, and Effects of Anti-VEGF Agent.
Miyata R, Kondo M, Kato K, Sugimoto M, Matsubara H, Ikesugi K, Ueno S, Yasuda S, Terasaki H
Investigative ophthalmology & visual science 59 ( 15 ) 5854 - 5861 2018.12
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Number of Hyperreflective Foci in the Outer Retina Correlates with Inflammation and Photoreceptor Degeneration in Retinitis Pigmentosa.
Nagasaka Y, Ito Y, Ueno S, Terasaki H
Ophthalmology. Retina 2 ( 7 ) 726 - 734 2018.7
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Associations Between Outer Retinal Structures and Focal Macular Electroretinograms in Patients With Retinitis Pigmentosa.
Kominami T, Ueno S, Kominami A, Nakanishi A, Yasuda S, Piao CH, Okado S, Terasaki H
Investigative ophthalmology & visual science 58 ( 12 ) 5122 - 5128 2017.10
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Differences in ocular findings in two siblings: one with complete and other with incomplete achromatopsia.
Ueno S, Nakanishi A, Sayo A, Kominami T, Ito Y, Hayashi T, Tsunoda K, Iwata T, Terasaki H
Documenta ophthalmologica. Advances in ophthalmology 134 ( 2 ) 141 - 147 2017.4
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Contributions of Second- and Third-Order Retinal Neurons to Cone Electroretinograms After Loss of Rod Function in Rhodopsin P347L Transgenic Rabbits.
Kominami T, Ueno S, Okado S, Nakanishi A, Kondo M, Terasaki H
Investigative ophthalmology & visual science 58 ( 3 ) 1417 - 1424 2017.3
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Short-term focal macular electroretinogram of eyes treated by aflibercept & photodynamic therapy for polypoidal choroidal vasculopathy.
Takayama K, Kaneko H, Kataoka K, Ueno S, Chang-Hua P, Ito Y, Terasaki H
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 255 ( 3 ) 449 - 455 2017.3
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Increased Retinal Thinning after Combination of Internal Limiting Membrane Peeling and Silicone Oil Endotamponade in Proliferative Diabetic Retinopathy.
Kaneko H, Matsuura T, Takayama K, Ito Y, Iwase T, Ueno S, Nonobe N, Yasuda S, Kataoka K, Terasaki H
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde 238 ( 4 ) 226 - 235 2017
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Correlation between miR-148 Expression in Vitreous and Severity of Rhegmatogenous Retinal Detachment.
Tsunekawa T, Kaneko H, Takayama K, Hwang SJ, Oishi A, Nagasaka Y, Ye F, Iwase T, Nonobe N, Ueno S, Ito Y, Yasuda S, Matsuura T, Shimizu H, Suzumura A, Kataoka K, Terasaki H
BioMed research international 2017 3427319 2017
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Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy.
Fujinami K, Kameya S, Kikuchi S, Ueno S, Kondo M, Hayashi T, Shinoda K, Machida S, Kuniyoshi K, Kawamura Y, Akahori M, Yoshitake K, Katagiri S, Nakanishi A, Sakuramoto H, Ozawa Y, Tsubota K, Yamaki K, Mizota A, Terasaki H, Miyake Y, Iwata T, Tsunoda K
Investigative ophthalmology & visual science 57 ( 11 ) 4837 - 46 2016.9
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Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy in Japanese Cohort.
Nakanishi A, Ueno S, Hayashi T, Katagiri S, Kominami T, Ito Y, Gekka T, Masuda Y, Tsuneoka H, Shinoda K, Hirakata A, Inoue M, Fujinami K, Tsunoda K, Iwata T, Terasaki H
American journal of ophthalmology 168 86 - 94 2016.8
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Flicker electroretinograms before and after intravitreal ranibizumab injection in eyes with central retinal vein occlusion.
Yasuda S, Kachi S, Ueno S, Piao CH, Terasaki H
Acta ophthalmologica 93 ( 6 ) e465 - 8 2015.9
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Case of paraneoplastic retinopathy with retinal ON-bipolar cell dysfunction and subsequent resolution of ERGs.
Ueno S, Nakanishi A, Nishi K, Suzuki S, Terasaki H
Documenta ophthalmologica. Advances in ophthalmology 130 ( 1 ) 71 - 6 2015.2
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Significant Correlation between Retinal Venous Tortuosity and Aqueous Vascular Endothelial Growth Factor Concentration in Eyes with Central Retinal Vein Occlusion.
Yasuda S, Kachi S, Kondo M, Ueno S, Kaneko H, Terasaki H
PloS one 10 ( 7 ) e0134267 2015
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Electroretinograms and level of aqueous vascular endothelial growth factor in eyes with hemicentral retinal vein occlusion or branch retinal vein occlusion.
Yasuda S, Kachi S, Ueno S, Ushida H, Piao CH, Kondo M, Terasaki H
Japanese journal of ophthalmology 58 ( 3 ) 232 - 6 2014.5
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Choroidal atrophy in a patient with paraneoplastic retinopathy and anti-TRPM1 antibody.
Ueno S, Ito Y, Maruko R, Kondo M, Terasaki H
Clinical ophthalmology (Auckland, N.Z.) 8 369 - 73 2014
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Relationship between retinal layer thickness and focal macular electroretinogram components after epiretinal membrane surgery.
Hibi N, Ueno S, Ito Y, Piao CH, Kondo M, Terasaki H
Investigative ophthalmology & visual science 54 ( 12 ) 7207 - 14 2013.11
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Whole genome sequencing in patients with retinitis pigmentosa reveals pathogenic DNA structural changes and NEK2 as a new disease gene.
Nishiguchi KM, Tearle RG, Liu YP, Oh EC, Miyake N, Benaglio P, Harper S, Koskiniemi-Kuendig H, Venturini G, Sharon D, Koenekoop RK, Nakamura M, Kondo M, Ueno S, Yasuma TR, Beckmann JS, Ikegawa S, Matsumoto N, Terasaki H, Berson EL, Katsanis N, Rivolta C
Proceedings of the National Academy of Sciences of the United States of America 110 ( 40 ) 16139 - 44 2013.10
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Photoreceptor and post-photoreceptoral contributions to photopic ERG a-wave in rhodopsin P347L transgenic rabbits.
Hirota R, Kondo M, Ueno S, Sakai T, Koyasu T, Terasaki H
Investigative ophthalmology & visual science 53 ( 3 ) 1467 - 72 2012.3
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Analyses of ERG in a patient with intraocular lymphoma.
Yasuda C, Ueno S, Kondo M, Kondo N, Piao CH, Terasaki H
Clinical ophthalmology (Auckland, N.Z.) 4 301 - 6 2010.4
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Supernormal ERG oscillatory potentials in transgenic rabbit with rhodopsin P347L mutation and retinal degeneration.
Sakai T, Kondo M, Ueno S, Koyasu T, Komeima K, Terasaki H
Investigative ophthalmology & visual science 50 ( 9 ) 4402 - 9 2009.9
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Comparison of photopic negative responses elicited by red and white xenon flashes in monkeys.
Miyata K, Ueno S, Kondo M, Koyasu T, Terasaki H
Japanese journal of ophthalmology 52 ( 4 ) 327 - 330 2008.7
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Comparison of focal macular cone ERGs in complete-type congenital stationary night blindness and APB-treated monkeys.
Kondo M, Ueno S, Piao CH, Miyake Y, Terasaki H
Vision research 48 ( 2 ) 273 - 80 2008.1
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Reduction of oscillatory potentials and photopic negative response in patients with autosomal dominant optic atrophy with OPA1 mutations.
Miyata K, Nakamura M, Kondo M, Lin J, Ueno S, Miyake Y, Terasaki H
Investigative ophthalmology & visual science 48 ( 2 ) 820 - 4 2007.2
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Selective amplitude reduction of the PhNR after macular hole surgery: ganglion cell damage related to ICG-assisted ILM peeling and gas tamponade.
Ueno S, Kondo M, Piao CH, Ikenoya K, Miyake Y, Terasaki H
Investigative ophthalmology & visual science 47 ( 8 ) 3545 - 9 2006.8
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Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophy.
Nakamura M, Lin J, Ueno S, Asaoka R, Hirai T, Hotta Y, Miyake Y, Terasaki H
Ophthalmology 113 ( 3 ) 483 - 488.e1 2006.3
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Cone and rod dysfunction in fundus albipunctatus with RDH5 mutation: an electrophysiological study.
Niwa Y, Kondo M, Ueno S, Nakamura M, Terasaki H, Miyake Y
Investigative ophthalmology & visual science 46 ( 4 ) 1480 - 5 2005.4
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Changes in focal macular electroretinograms and foveal thickness after vitrectomy for diabetic macular edema.
Terasaki H, Kojima T, Niwa H, Piao CH, Ueno S, Kondo M, Ito Y, Miyake Y
Investigative ophthalmology & visual science 44 ( 10 ) 4465 - 72 2003.10