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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

Scientific reports, 2020-03, Vol.10 (1), p.5497-5497, Article 5497

2020

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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

Scientific reports, 2020-06, Vol.10 (1), p.9531-9531, Article 9531

2020

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Gene therapy to rescue retinal degeneration caused by mutations in rhodopsin

Methods in molecular biology (Clifton, N.J.), 2015, Vol.1271, p.391

2015

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Systematic review and meta-analysis of the association between complement factor H I62V polymorphism and risk of polypoidal choroidal vasculopathy in Asian populations

PloS one, 2014-02, Vol.9 (2), p.e88324

2014

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Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector

Proceedings of the National Academy of Sciences - PNAS, 2018-09, Vol.115 (36), p.E8547-E8556

2018

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Gene therapy in animal models of autosomal dominant retinitis pigmentosa

Molecular vision, 2012-10, Vol.18, p.2479-2496

2012

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Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic mice

Human gene therapy, 2012-04, Vol.23 (4), p.356-366

2012

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Gene augmentation for adRP mutations in RHO

Cold Spring Harbor perspectives in medicine, 2014-09, Vol.4 (9), p.a017400-a017400

2014

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132. Gene Therapy With Self-Complementary Recombinant Adeno-Associated Virus in Models of Autosomal Dominant Retinitis Pigmentosa Cause by RHO Mutations

Molecular therapy, 2015-05, Vol.23, p.S54-S54

2015

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Prediction of causative genes in inherited retinal disorder from fundus photography and autofluorescence imaging using deep learning techniques

British journal of ophthalmology, 2021-09, Vol.105 (9), p.1272-1279

2021

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Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance

Investigative ophthalmology & visual science, 2019-08, Vol.60 (10), p.3432-3446

2019

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Four‐port bimanual 23‐gauge vitrectomy for diabetic tractional retinal detachment

Acta ophthalmologica (Oxford, England), 2016-06, Vol.94 (4), p.365-372

2016

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Self-complementary recombinant adeno-associated virus mediated gene therapy in models of autosomal dominant retinitis pigmentosa caused by rho mutations

Rossmiller, Brian

2015

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Ag econ angst crisis revisited: [Collection of two articles including a rejoinder.]

The Australian journal of agricultural and resource economics, 2003-06, Vol.47 (2), p.261-274

2003

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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

Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association

Gene therapy to rescue retinal degeneration caused by mutations in rhodopsin

Systematic review and meta-analysis of the association between complement factor H I62V polymorphism and risk of polypoidal choroidal vasculopathy in Asian populations

Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector

Gene therapy in animal models of autosomal dominant retinitis pigmentosa

Long-term rescue of retinal structure and function by rhodopsin RNA replacement with a single adeno-associated viral vector in P23H RHO transgenic mice

Gene augmentation for adRP mutations in RHO

132. Gene Therapy With Self-Complementary Recombinant Adeno-Associated Virus in Models of Autosomal Dominant Retinitis Pigmentosa Cause by RHO Mutations

Prediction of causative genes in inherited retinal disorder from fundus photography and autofluorescence imaging using deep learning techniques

Phenotypical Characteristics of POC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance

Four‐port bimanual 23‐gauge vitrectomy for diabetic tractional retinal detachment

Self-complementary recombinant adeno-associated virus mediated gene therapy in models of autosomal dominant retinitis pigmentosa caused by rho mutations

Ag econ angst crisis revisited: [Collection of two articles including a rejoinder.]

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