Hiroyuki Kondo

ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 15

Top Venues

Ophthalmic genetics

Japanese journal of ophthalmology

Scientific reports

Human genome variation

This page only lists publications with an associated author ORCID identifier.

Publications

Shuqian Dong, Tongdan Zou, Fangyuan Zhen, Ting Wang, Yongwei Zhou, Jiahui Wu, Tatsuo Nagata, Itsuka Matsushita, Bo Gong, Hiroyuki Kondo, Qiuming Li, Houbin Zhang
Association of variants in GJA8 with familial acorea-microphthalmia-cataract syndrome. European journal of human genetics : EJHG (2023)
Itsuka Matsushita, Hiroto Izumi, Shinji Ueno, Takaaki Hayashi, Kaoru Fujinami, Kazushige Tsunoda, Takeshi Iwata, Yoshiaki Kiuchi, Hiroyuki Kondo
Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal Hypoplasia. Genes 14 (7) (2023)
Hirofumi Morita, Itsuka Matsushita, Yoshihisa Fujino, Akira Obana, Hiroyuki Kondo
Measuring macular pigment optical density using reflective images of confocal scanning laser system. Japanese journal of ophthalmology (2023)
Mamika Asano, Katsuhiko Yokoyama, Kazuma Oku, Itsuka Matsushita, Kenichi Kimoto, Toshiaki Kubota, Hiroyuki Kondo
Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in COL2A1 gene. Ophthalmic genetics 43 (4) (2022)
Kei Mizobuchi, Takaaki Hayashi, Noriko Oishi, Daiki Kubota, Shuhei Kameya, Koichiro Higasa, Takuma Futami, Hiroyuki Kondo, Katsuhiro Hosono, Kentaro Kurata, Yoshihiro Hotta, Kazutoshi Yoshitake, Takeshi Iwata, Tomokazu Matsuura, Tadashi Nakano
Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN. Journal of clinical medicine 10 (11) (2021)
Toshiaki Asano, Kazuma Oku, Hiroyuki Kondo
Familial exudative vitreoretinopathy with TGFBR2 mutation without signs of Loeys-Dietz syndrome. Ophthalmic genetics 42 (5) (2021)
Kazuma Oku, Kei Tokutsu, Shinya Matsuda, Hiroyuki Kondo
Epidemiologic study of rhegmatogenous retinal detachment in Japan from the Diagnosis Procedure Combination database over a 2-year period (2014-2015). Japanese journal of ophthalmology 65 (6) (2021)
Itsuka Matsushita, Hirofumi Morita, Hiroyuki Kondo
Autosomal dominant foveal hypoplasia without visible macular abnormalities and PAX6 mutations. Japanese journal of ophthalmology 64 (6) (2020)
Hiroyuki Kondo, Kazushi Fujimoto, Mamika Imagawa, Kazuma Oku, Itsuka Matsushita, Takaaki Hayashi, Tatsuo Nagata
Electroretinograms of eyes with Stickler syndrome. Documenta ophthalmologica. Advances in ophthalmology 140 (3) (2019)
Hiroyuki Kondo, Kazuma Oku, Satoshi Katagiri, Takaaki Hayashi, Tadashi Nakano, Akiko Iwata, Kazuki Kuniyoshi, Shunji Kusaka, Atsushi Hiyoshi, Eiichi Uchio, Mineo Kondo, Noriko Oishi, Shuhei Kameya, Atsushi Mizota, Nobuhisa Naoi, Shinji Ueno, Hiroko Terasaki, Takeshi Morimoto, Masayoshi Iwaki, Kazutoshi Yoshitake, Daisuke Iejima, Kaoru Fujinami, Kazushige Tsunoda, Kei Shinoda, Takeshi Iwata
Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis. Human genome variation 6 (2019)
Satoshi Katagiri, Maki Iwasa, Takaaki Hayashi, Katsuhiro Hosono, Takahiro Yamashita, Kazuki Kuniyoshi, Shinji Ueno, Mineo Kondo, Hisao Ueyama, Hisakazu Ogita, Yoshinori Shichida, Hidehito Inagaki, Hiroki Kurahashi, Hiroyuki Kondo, Masahito Ohji, Yoshihiro Hotta, Tadashi Nakano
Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy. Scientific reports 8 (1) (2018)
Katsuhiro Hosono, Sachiko Nishina, Tadashi Yokoi, Satoshi Katagiri, Hirotomo Saitsu, Kentaro Kurata, Daisuke Miyamichi, Akiko Hikoya, Kei Mizobuchi, Tadashi Nakano, Shinsei Minoshima, Maki Fukami, Hiroyuki Kondo, Miho Sato, Takaaki Hayashi, Noriyuki Azuma, Yoshihiro Hotta
Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing. Scientific reports 8 (1) (2018)
Hiroyuki Kondo, Eiichi Uchio, Shunji Kusaka, Koichiro Higasa
Risk allele of the FZD4 gene for familial exudative vitreoretinopathy. Ophthalmic genetics 39 (3) (2017)
Yusuke Sano, Yusuke Matsukane, Akihisa Watanabe, Ko-Hei Sonoda, Hiroyuki Kondo
Lack of FOXE3 coding mutation in a case of congenital aphakia. Ophthalmic genetics 39 (1) (2017)
Hiroyuki Kondo, Itsuka Matsushita, Tatsuo Nagata, Takaaki Hayashi, Masashi Kakinoki, Eiichi Uchio, Mineo Kondo, Masahito Ohji, Shunji Kusaka
Novel mutations in the COL2A1 gene in Japanese patients with Stickler syndrome. Human genome variation 3 (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Hiroyuki Kondo