Satoshi Katagiri

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2014-2021
Publications (10 Years): 16

Top Venues

Scientific reports

Documenta ophthalmologica. Advances in ophthalmology

Journal of ophthalmology

International journal of molecular sciences

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

Publications

Yuka Saito, Hiroshi Horiguchi, Kei Mizobuchi, Satoshi Katagiri, Hisato Gunji, Tadashi Nakano
Effectiveness of the Heads-Up Surgery System for Retinal Surgery in a Patient with Severe Photophobia. International medical case reports journal 14 (2021)
Takaaki Hayashi, Katsuhiro Hosono, Akiko Kubo, Kentaro Kurata, Satoshi Katagiri, Kei Mizobuchi, Minehiro Kurai, Norihito Mamiya, Mineo Kondo, Toshiaki Tachibana, Hirotomo Saitsu, Tsutomu Ogata, Tadashi Nakano, Yoshihiro Hotta
Long-term observation of a Japanese mucolipidosis IV patient with a novel homozygous p.F313del variant of MCOLN1. American journal of medical genetics. Part A 182 (6) (2020)
Lizhu Yang, Kaoru Fujinami, Shinji Ueno, Kazuki Kuniyoshi, Takaaki Hayashi, Mineo Kondo, Atsushi Mizota, Nobuhisa Naoi, Kei Shinoda, Shuhei Kameya, Yu Fujinami-Yokokawa, Xiao Liu, Gavin Arno, Nikolas Pontikos, Taro Kominami, Hiroko Terasaki, Hiroyuki Sakuramoto, Satoshi Katagiri, Kei Mizobuchi, Natsuko Nakamura, Go Mawatari, Toshihide Kurihara, Masayuki Ohta, Yozo Miyake, Kazutoshi Yoshitake, Takeshi Iwata, Kazushige Tsunoda, null null
Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency. Scientific reports 10 (1) (2020)
Wakana Ninomiya, Kei Mizobuchi, Takaaki Hayashi, Sachiyo Okude, Satoshi Katagiri, Akiko Kubo, Nami Masuhara, Tadashi Nakano
Electroretinographic abnormalities associated with pregabalin: a case report. Documenta ophthalmologica. Advances in ophthalmology 140 (3) (2020)
Satoshi Katagiri, Katsuhiro Hosono, Takaaki Hayashi, Noriyuki Murai, Eiichi Wake, Ichiro Miyata, Kei Mizobuchi, Kentaro Kurata, Tomokazu Matsuura, Tadashi Nakano, Yoshihiro Hotta
Novel biallelic splice-site BBS1 variants in Bardet-Biedle syndrome: a case report of the first Japanese patient. Documenta ophthalmologica. Advances in ophthalmology 141 (1) (2020)
Kazuki Kuniyoshi, Takaaki Hayashi, Shuhei Kameya, Satoshi Katagiri, Kei Mizobuchi, Toshiaki Tachibana, Daiki Kubota, Hiroyuki Sakuramoto, Kazushige Tsunoda, Kaoru Fujinami, Kazutoshi Yoshitake, Takeshi Iwata, Tadashi Nakano, Shunji Kusaka
Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy. International journal of molecular sciences 21 (4) (2020)
Yu Fujinami-Yokokawa, Kaoru Fujinami, Kazuki Kuniyoshi, Takaaki Hayashi, Shinji Ueno, Atsushi Mizota, Kei Shinoda, Gavin Arno, Nikolas Pontikos, Lizhu Yang, Xiao Liu, Hiroyuki Sakuramoto, Satoshi Katagiri, Kei Mizobuchi, Taro Kominami, Hiroko Terasaki, Natsuko Nakamura, Shuhei Kameya, Kazutoshi Yoshitake, Yozo Miyake, Toshihide Kurihara, Masayuki Ohta, Hiroaki Miyata, Takeshi Iwata, Kazushige Tsunoda, null null
Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association. Scientific reports 10 (1) (2020)
Takaaki Hayashi, Katsuhiro Hosono, Kentaro Kurata, Satoshi Katagiri, Kei Mizobuchi, Shinji Ueno, Mineo Kondo, Tadashi Nakano, Yoshihiro Hotta
Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy. Documenta ophthalmologica. Advances in ophthalmology 140 (2) (2019)
Tomoko Kutsuma, Satoshi Katagiri, Takaaki Hayashi, Kazutoshi Yoshitake, Daisuke Iejima, Tamaki Gekka, Kenichi Kohzaki, Kei Mizobuchi, Yukari Baba, Ryo Terauchi, Tomokazu Matsuura, Shinji Ueno, Takeshi Iwata, Tadashi Nakano
Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses. Documenta ophthalmologica. Advances in ophthalmology 138 (3) (2019)
Kentaro Kurata, Katsuhiro Hosono, Takaaki Hayashi, Kei Mizobuchi, Satoshi Katagiri, Daisuke Miyamichi, Sachiko Nishina, Miho Sato, Noriyuki Azuma, Tadashi Nakano, Yoshihiro Hotta
X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers. International journal of molecular sciences 20 (6) (2019)
Kei Mizobuchi, Takaaki Hayashi, Satoshi Katagiri, Kazutoshi Yoshitake, Kaoru Fujinami, Lizhu Yang, Kazuki Kuniyoshi, Kei Shinoda, Shigeki Machida, Mineo Kondo, Shinji Ueno, Hiroko Terasaki, Tomokazu Matsuura, Kazushige Tsunoda, Takeshi Iwata, Tadashi Nakano
Characterization of GUCA1A-associated dominant cone/cone-rod dystrophy: low prevalence among Japanese patients with inherited retinal dystrophies. Scientific reports 9 (1) (2019)
Satoshi Katagiri, Takaaki Hayashi, Kazutoshi Yoshitake, Noriyuki Murai, Zenichi Matsui, Hiroyuki Kubo, Hiroyuki Satoh, Senya Matsufuji, Tsuyoshi Takamura, Takashi Yokoo, Yoshihiro Omori, Takahisa Furukawa, Takeshi Iwata, Tadashi Nakano
Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome. Scientific reports 8 (1) (2018)
Masaki Nakamura, Koji Komatsu, Satoshi Katagiri, Takaaki Hayashi, Tadashi Nakano
Reconstruction of Photoreceptor Outer Layers after Steroid Therapy in Solar Retinopathy. Case reports in ophthalmological medicine 2018 (2018)
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)
Satoshi Katagiri, Yuya Negishi, Kei Mizobuchi, Mitsuyoshi Urashima, Tadashi Nakano, Takaaki Hayashi
ABCC6 Gene Analysis in 20 Japanese Patients with Angioid Streaks Revealing Four Frequent and Two Novel Variants and Pseudodominant Inheritance. Journal of ophthalmology 2017 (2017)
Satoshi Katagiri, Takaaki Hayashi, Masakazu Akahori, Takeshi Itabashi, Jo Nishino, Kazutoshi Yoshitake, Masaaki Furuno, Kazuho Ikeo, Tetsuji Okada, Hiroshi Tsuneoka, Takeshi Iwata
RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa. Journal of ophthalmology 2014 (2014)

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Publication Activity (10 Years)

Top Topics

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Satoshi Katagiri