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ARVO Annual Meeting Abstract June 2024

Whole genome sequencing for Japanese patients with Leber’s congenital amaurosis and early onset retinal dystrophy

Yoshihiro Hotta; Kaoruko Torii; Sachiko Nishina; Hazuki Anzai; Kei Mizobuchi; Masakazu Takayama; Nobutaka Tachibana; Tadashi Yokoi; Sachiko Miyamoto; Maki Fukami; Hiroyuki Kondo; Noriyuki Azuma; Takaaki Hayashi; Hirotomo Saitsu

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):4676.

ARVO Annual Meeting Abstract June 2023

Genetic characteristics of retinitis pigmentosa and allied diseases in 2063 Japanese patients

Koji Miura Nishiguchi; Yoshito Koyanagi; Masato Akiyama; Yusuke Murakami; Hanae Iijima; Mikiko Endo; Shinji Ueno; Takaaki Hayashi; Yoshihiro Hotta; Akira Murakami; Yuko Wada; Toshiaki Abe; Toru Nakazawa; Yasuhiro Ikeda; Koh-Hei Sonoda; Kensuke Goto

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4646.

ARVO Annual Meeting Abstract June 2021

Oculo-facio-cardio-dental (OFCD) syndrome: four cases in two Japanese families

Tomoyuki Yamazaki; Sho Naruse; Kentaro Kurata; Katsuhiro Hosono; Itsuka Matsushita; Atsushi Hiyoshi; Moriya Iwaizumi; Yoshiaki Kiuchi; Yoshihiro Hotta; Hiroyuki Kondo

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1551.

Articles June 2021

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene

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Hiroyuki Kondo; Itsuka Matsushita; Tatsuo Nagata; Etsuko Fujihara; Katsuhiro Hosono; Eiichi Uchio; Yoshihiro Hotta; Shunji Kusaka
TAGS: familial exudative vitreoretinopathies, family, genes, mutation, eye, respiratory distress syndrome, newborn
Trans. Vis. Sci. Tech.. 2021; 10(7):18. https://doi.org/10.1167/tvst.10.7.18

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2020

Intravitreal injections of the anti-VEGF agent aflibercept were effective for choroidal neovascularization in a patient with Bietti’s crystalline dystrophy

Masakazu TAKAYAMA; Kentaro Kurata; Katsuhiro Hosono; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3017.

ARVO Annual Meeting Abstract July 2018

Long-term clinical course of Japanese patients with retinitis pigmentosa caused by mutations in pre-mRNA splicing gene

Kentaro Kurata; Katsuhiro Hosono; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):20.

ARVO Annual Meeting Abstract July 2018

Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing

Katsuhiro Hosono; Sachiko Nishina; Tadashi Yokoi; Satoshi Katagiri; Kentaro Kurata; Daisuke Miyamichi; Kei Mizobuchi; Tadashi Nakano; Shinsei Minoshima; Maki Fukami; Hiroyuki Kondo; Miho Sato; Takaaki Hayashi; Noriyuki Azuma; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5414.

ARVO Annual Meeting Abstract June 2017

Changes in macular structure and retinal function in patients with Leber congenital amaurosis with RPGRIP1 mutations

Daisuke Miyamichi; Sachiko Nishina; Katsuhiro Hosono; Tadashi Yokoi; Kentaro Kurata; Miho Sato; Shinsei Minoshima; Maki Fukami; Yoshihiro Hotta; Noriyuki Azuma

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):574.

ARVO Annual Meeting Abstract June 2017

Forward Genetic Approach for Causal Gene Identification for Rat Retinal Photic Injury

Kentaro Ohishi; Masafumi Ohtsubo; Katsuhiro Hosono; Akira Obana; Yoshihiro Hotta; Tadahisa Hiramitsu; Shinsei Minoshima

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):288.

ARVO Annual Meeting Abstract June 2015

Visual Outcomes of Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations

Kimiko Suto; Katsuhiro Hosono; Yasunori Nagase; Hiroshi Nakanishi; Kunihiro Mizuta; Shinsei Minoshima; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2901.

ARVO Annual Meeting Abstract April 2014

Mutation Analysis of the USH2A Gene in Japanese Patients with Autosomal Recessive Retinitis Pigmentosa

Katsuhiro Hosono; Yang Zhao; Chie Ishigami; Shinji Ueno; Hiroshi Nakanishi; Hiroko Terasaki; Mineo Kondo; Masayo Takahashi; Shinsei Minoshima; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3261.

ARVO Annual Meeting Abstract June 2013

Fine analysis of the deletions in red/green opsin genes and the upstream locus control region (LCR) found in two Japanese families with blue cone monochromacy (BCM)

Chun-xia Wang; Katsuhiro Hosono; Shu Kachi; Hiroko Terasaki; Yoshihiro Hotta; Shinsei Minoshima

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1321.

ARVO Annual Meeting Abstract June 2013

Analysis of the covalent high molecular weight protein complex containing optineurin and its relationship with glaucoma

Jie Gao; Masafumi Ohtsubo; Yoshihiro Hotta; Shinsei Minoshima

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1607.

ARVO Annual Meeting Abstract March 2012

An Adenine Insertion between Nucleotide Positions 4957 and 4958 in the EYS Gene Is a Possible Major Cause of arRP in the Japanese Population

Katsuhiro Hosono; Chie Ishigami; Masayo Takahashi; Yasuhiko Hirami; Shinji Ueno; Noriyuki Azuma; Hiroko Terasaki; Mineo Kondo; Shinsei Minoshima; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4598.

ARVO Annual Meeting Abstract April 2011

Establishment of A Mouse Cell Line using A Photoreceptor Gene-Specific Promoter and SV40 Large T antigen

Katsuhiro Hosono; Kentaro Ohishi; Yoshitaka Yamaguchi; Jun Kudoh; Nobuyoshi Shimizu; Yoshihiro Hotta; Shinsei Minoshima

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):2253.

ARVO Annual Meeting Abstract April 2011

Clinical Features of A Japanese Patient with Bothnia Dystrophy

Kazutoshi Nojima; Katsuhiro Hosono; Yang Zhao; Takaaki Toshiba; Tatsuhiko Asai; Masaru Kato; Shinsei Minoshima; Yoshihiro Hotta

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5374.

Glaucoma December 2006

SNPs and Interaction Analyses of Noelin 2, Myocilin, and Optineurin Genes in Japanese Patients with Open-Angle Glaucoma

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Tomoyo Funayama; Yukihiko Mashima; Yuichiro Ohtake; Karin Ishikawa; Nobuo Fuse; Noriko Yasuda; Takeo Fukuchi; Akira Murakami; Yoshihiro Hotta; Naoki Shimada; for The Glaucoma Gene Research Group
TAGS: genes, glaucoma, intraocular pressure, japanese, myoc gene, open-angle glaucoma, optn gene, raised intraocular pressure, single nucleotide polymorphism, gene interaction
Invest. Ophthalmol. Vis. Sci.. 2006; 47(12):5368-5375. https://doi.org/10.1167/iovs.06-0196

Glaucoma December 2004

Variants in Optineurin Gene and Their Association with Tumor Necrosis Factor-α Polymorphisms in Japanese Patients with Glaucoma

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Tomoyo Funayama; Karin Ishikawa; Yuichiro Ohtake; Tomihiko Tanino; Daijiro Kurosaka; Itaru Kimura; Kotaro Suzuki; Hidenao Ideta; Kenji Nakamoto; Noriko Yasuda; Takuro Fujimaki; Akira Murakami; Ryo Asaoka; Yoshihiro Hotta; Hidenobu Tanihara; Takashi Kanamoto; Hiromu Mishima; Takeo Fukuchi; Haruki Abe; Takeshi Iwata; Naoki Shimada; Jun Kudoh; Nobuyoshi Shimizu; Yukihiko Mashima
TAGS: genes, genotype determination, glaucoma, japanese, open-angle glaucoma, optn gene, polymorphism, tumor necrosis factors, tumor necrosis
Invest. Ophthalmol. Vis. Sci.. 2004; 45(12):4359-4367. https://doi.org/10.1167/iovs.03-1403

Retina November 2000

A High Association with Cone Dystrophy in Fundus Albipunctatus Caused by Mutations of the RDH5 Gene

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Makoto Nakamura; Yoshihiro Hotta; Atsuhiro Tanikawa; Hiroko Terasaki; Yozo Miyake
TAGS: cone dystrophy, genes, mutation, pigmentary retinal dystrophy, visual acuity
Invest. Ophthalmol. Vis. Sci.. 2000; 41(12):3925-3932.

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Whole genome sequencing for Japanese patients with Leber’s congenital amaurosis and early onset retinal dystrophy

Genetic characteristics of retinitis pigmentosa and allied diseases in 2063 Japanese patients

Oculo-facio-cardio-dental (OFCD) syndrome: four cases in two Japanese families

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene

Intravitreal injections of the anti-VEGF agent aflibercept were effective for choroidal neovascularization in a patient with Bietti’s crystalline dystrophy

Long-term clinical course of Japanese patients with retinitis pigmentosa caused by mutations in pre-mRNA splicing gene

Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing

Changes in macular structure and retinal function in patients with Leber congenital amaurosis with RPGRIP1 mutations

Forward Genetic Approach for Causal Gene Identification for Rat Retinal Photic Injury

Visual Outcomes of Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations

Mutation Analysis of the USH2A Gene in Japanese Patients with Autosomal Recessive Retinitis Pigmentosa

Fine analysis of the deletions in red/green opsin genes and the upstream locus control region (LCR) found in two Japanese families with blue cone monochromacy (BCM)

Analysis of the covalent high molecular weight protein complex containing optineurin and its relationship with glaucoma

An Adenine Insertion between Nucleotide Positions 4957 and 4958 in the EYS Gene Is a Possible Major Cause of arRP in the Japanese Population

Establishment of A Mouse Cell Line using A Photoreceptor Gene-Specific Promoter and SV40 Large T antigen

Clinical Features of A Japanese Patient with Bothnia Dystrophy

SNPs and Interaction Analyses of Noelin 2, Myocilin, and Optineurin Genes in Japanese Patients with Open-Angle Glaucoma

Variants in Optineurin Gene and Their Association with Tumor Necrosis Factor-α Polymorphisms in Japanese Patients with Glaucoma

A High Association with Cone Dystrophy in Fundus Albipunctatus Caused by Mutations of the RDH5 Gene

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