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Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donor

Stem cell research, 2024-02, Vol.74, p.103280-103280, Article 103280

2024

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Natural history of retinitis pigmentosa based on genotype, vitamin A/E supplementation, and an electroretinogram biomarker

JCI insight, 2023-08, Vol.8 (15)

2023

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Transient neurites of retinal horizontal cells exhibit columnar tiling via homotypic interactions

Nature neuroscience, 2009-01, Vol.12 (1), p.35-43

2009

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Beyond Sector Retinitis Pigmentosa: Expanding the Phenotype and Natural History of the Rhodopsin Gene Codon 106 Mutation (Gly-to-Arg) in Autosomal Dominant Retinitis Pigmentosa

Genes, 2021-11, Vol.12 (12), p.1853

2021

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RNA-based therapies in inherited retinal diseases

Therapeutic Advances in Ophthalmology, 2022-01, Vol.14, p.25158414221134602-25158414221134602

2022

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Restoration of Vision and Retinal Responses After Adeno-Associated Virus-Mediated Optogenetic Therapy in Blind Dogs

Translational vision science & technology, 2022-05, Vol.11 (5), p.24

2022

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Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD

Npj genomic medicine, 2021-06, Vol.6 (1), p.53-53, Article 53

2021

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Long‐lived autoreactive memory CD4+ T cells mediate the sustained retinopathy in chronic autoimmune uveitis

The FASEB journal, 2023-04, Vol.37 (4), p.e22855-n/a

2023

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Progressive Maculopathy After Discontinuation of Pentosan Polysulfate Sodium

Ophthalmic surgery, lasers & imaging retina, 2019-10, Vol.50 (10), p.656-659

2019

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Predictive value of genetic testing for inherited retinal diseases in patients with suspected atypical autoimmune retinopathy

American journal of ophthalmology case reports, 2019-09, Vol.15, p.100461-100461, Article 100461

2019

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Management of Cystoid Macular Edema in Retinitis Pigmentosa

Seminars in ophthalmology, 2017-01, Vol.32 (1), p.43-51

2017

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Macular dystrophy with associated retinitis pigmentosa-1 like 1 genetic mutation

Clinical and experimental optometry, 2024-08, Vol.107 (6), p.673-675

2024

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Disparities in Inherited Retinal Degenerations

Seminars in ophthalmology, 2023-02, Vol.38 (2), p.201-206

2023

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Retinal Manifestations in Spinocerebellar Ataxia Type 3

Journal of neuro-ophthalmology, 2024-03, Vol.44 (1), p.e3-e5

2024

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Gene therapy for inherited retinal degenerations: initial successes and future challenges

Journal of neural engineering, 2017-10, Vol.14 (5), p.051002-051002

2017

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Sterile subperiosteal fluid collections accompanying orbital wall infarction in sickle-cell disease

Journal of AAPOS, 2014-10, Vol.18 (5), p.485-487

2014

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An Open-Label Phase II Study Assessing the Safety of Bilateral, Sequential Administration of Retinal Gene Therapy in Participants with Choroideremia: The GEMINI Study

Human gene therapy, 2024-08, Vol.35 (15-16), p.564-575

2024

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Efficient transduction and optogenetic stimulation of retinal bipolar cells by a synthetic adeno‐associated virus capsid and promoter

EMBO molecular medicine, 2014-09, Vol.6 (9), p.1175-1190

2014

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RTN4IP1 -associated non-syndromic optic neuropathy and rod-cone dystrophy

Ophthalmic genetics, 2024-06, Vol.45 (3), p.289-293

2024

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Characterization of Clinical and Immune Responses in an Experimental Chronic Autoimmune Uveitis Model

The American journal of pathology, 2021-03, Vol.191 (3), p.425-437

2021

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Adeno-Associated Virus Serotype 2-hCHM Subretinal Delivery to the Macula in Choroideremia: Two-Year Interim Results of an Ongoing Phase I/II Gene Therapy Trial

Ophthalmology (Rochester, Minn.), 2022-10, Vol.129 (10), p.1177-1191

2022

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Variants of Uncertain Significance: Twins With Identical Pathogenic Gene Mutations in Retinitis Punctata Albescens

Ophthalmic surgery, lasers & imaging retina, 2021-08, Vol.52 (8), p.450-453

2021

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Gene editing technology: Towards precision medicine in inherited retinal diseases

Seminars in ophthalmology, 2021-05, Vol.36 (4), p.176-184

2021

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Self-Reported Functional Vision in USH2A-Associated Retinal Degeneration as Measured by the Michigan Retinal Degeneration Questionnaire

Investigative ophthalmology & visual science, 2024-06, Vol.65 (6), p.5

2024

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Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donor

Natural history of retinitis pigmentosa based on genotype, vitamin A/E supplementation, and an electroretinogram biomarker

Transient neurites of retinal horizontal cells exhibit columnar tiling via homotypic interactions

Beyond Sector Retinitis Pigmentosa: Expanding the Phenotype and Natural History of the Rhodopsin Gene Codon 106 Mutation (Gly-to-Arg) in Autosomal Dominant Retinitis Pigmentosa

RNA-based therapies in inherited retinal diseases

Restoration of Vision and Retinal Responses After Adeno-Associated Virus-Mediated Optogenetic Therapy in Blind Dogs

Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD

Long‐lived autoreactive memory CD4+ T cells mediate the sustained retinopathy in chronic autoimmune uveitis

Progressive Maculopathy After Discontinuation of Pentosan Polysulfate Sodium

Predictive value of genetic testing for inherited retinal diseases in patients with suspected atypical autoimmune retinopathy

Management of Cystoid Macular Edema in Retinitis Pigmentosa

Macular dystrophy with associated retinitis pigmentosa-1 like 1 genetic mutation

Disparities in Inherited Retinal Degenerations

Retinal Manifestations in Spinocerebellar Ataxia Type 3

Gene therapy for inherited retinal degenerations: initial successes and future challenges

Sterile subperiosteal fluid collections accompanying orbital wall infarction in sickle-cell disease

An Open-Label Phase II Study Assessing the Safety of Bilateral, Sequential Administration of Retinal Gene Therapy in Participants with Choroideremia: The GEMINI Study

Efficient transduction and optogenetic stimulation of retinal bipolar cells by a synthetic adeno‐associated virus capsid and promoter

RTN4IP1 -associated non-syndromic optic neuropathy and rod-cone dystrophy

Characterization of Clinical and Immune Responses in an Experimental Chronic Autoimmune Uveitis Model

Adeno-Associated Virus Serotype 2-hCHM Subretinal Delivery to the Macula in Choroideremia: Two-Year Interim Results of an Ongoing Phase I/II Gene Therapy Trial

Phase 1/2 AAV5-hRKp.RPGR (Botaretigene Sparoparvovec) Gene Therapy: Safety and Efficacy in RPGR-Associated X-Linked Retinitis Pigmentosa

Variants of Uncertain Significance: Twins With Identical Pathogenic Gene Mutations in Retinitis Punctata Albescens

Gene editing technology: Towards precision medicine in inherited retinal diseases

Self-Reported Functional Vision in USH2A-Associated Retinal Degeneration as Measured by the Michigan Retinal Degeneration Questionnaire

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