Publications by authors named "Go Mawatari"

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Baseline Relationships between Visual Function and Inflammatory Markers in the Registry of Moderated-Stage Retinitis Pigmentosa.
Takahiro Hisai, Sakurako Shimokawa, Masatoshi Fukushima, Kohta Fujiwara, Yoshito Koyanagi, Go Mawatari

Ophthalmol Sci· January 2026

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Clinical characteristics of EYS-associated retinal dystrophy in 291 Japanese patients.
Yoshito Koyanagi, Yusuke Murakami, Taro Kominami, Masatoshi Fukushima, Kensuke Goto, Go Mawatari

NPJ Genom Med· December 2025

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Study protocol for a prospective natural history registry investigating the relationships between inflammatory markers and disease progression in retinitis pigmentosa: the RP-PRIMARY study.
Yusuke Murakami, Takahiro Hisai, Sakurako Shimokawa, Masatoshi Fukushima, Kohta Fujiwara, Go Mawatari

Jpn J Ophthalmol· May 2025

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Efficacy of a wearable night-vision aid in patients with concentric peripheral visual field loss: a randomized, crossover trial.
Go Mawatari, Shogo Hiwatashi, Tsubasa Motani, Saori Nagatomo, Eri Ando

Jpn J Ophthalmol· July 2024

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Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Akiko Suga, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kaoru Fujinami, Go Mawatari

Hum Mutat· December 2022

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CLEC3B is a novel causative gene for macular-retinal dystrophy.
Rong Zhou, Go Mawatari, Xue-Bi Cai, Ren-Juan Shen, Ya-Han Wang

Genet Med· June 2022

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Genetic and Phenotypic Landscape of -Associated Retinal Dystrophy in Japan.
Akio Oishi, Kaoru Fujinami, Go Mawatari, Nobuhisa Naoi, Yasuhiro Ikeda

Genes (Basel)· November 2021

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Base Curve of Progressive Addition Lenses Influences Clear Vision and Stereopsis Area.
Go Mawatari, Saeko Uchida, Nobuhisa Nao-I

Clin Optom (Auckl)· December 2020

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Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency.
Lizhu Yang, Kaoru Fujinami, Shinji Ueno, Kazuki Kuniyoshi, Takaaki Hayashi, Go Mawatari

Sci Rep· March 2020

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Correction to: Clinical and genetic characteristics of 14 patients from 13 Japanese families with -associated retinal disorder: report of eight novel variants.
Go Mawatari, Kaoru Fujinami, Xiao Liu, Lizhu Yang, Yu Fujinami-Yokokawa

Hum Genome Var· February 2020

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Clinical and genetic characteristics of 14 patients from 13 Japanese families with -associated retinal disorder: report of eight novel variants.
Go Mawatari, Kaoru Fujinami, Xiao Liu, Lizhu Yang, Yu-Fujinami Yokokawa

Hum Genome Var· August 2019

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Modified muscle transposition procedure for a case of inferior rectus muscle aplasia.
Shinji Makino, Kozue Hozawa, Reiko Kondo, Mika Kanai, Haruko Suto, Go Mawatari

Case Rep Ophthalmol· April 2015

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