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Author Details

Carel B Hoyng
Radboud University Medical Center
1989
378
71
PMIDPaper TitleJournal TitlePublished Year
37598860Study of Late-Onset Stargardt Type 1 Disease: Characteristics, Genetics, and Progression.Ophthalmology2024
37749859Quality of life in patients with CRB1-associated retinal dystrophies: A longitudinal study.Acta Ophthalmol2024
37934290Clinical classification of Stargardt disease.Graefes Arch Clin Exp Ophthalmol2024
34348923Charles Bonnet syndrome in patients with Stargardt disease: prevalence and risk factors.Br J Ophthalmol2023
37580831Interaction between genetics and the adherence to the Mediterranean diet: the risk for age-related macular degeneration. Coimbra Eye Study Report 8.Eye Vis (Lond)2023
37979432Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>A.Stem Cell Res2023
37410486Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis.JAMA Ophthalmol2023
37441824Generation of iPSC lines from three Stargardt patients carrying bi-allelic ABCA4 variants.Stem Cell Res2023
37036511Fundus autofluorescence abnormalities can predict fluorescein angiography abnormalities in patients with chronic central serous chorioretinopathy.Graefes Arch Clin Exp Ophthalmol2023
37367859Systemic Metabolomics in a Framework of Genetics and Lifestyle in Age-Related Macular Degeneration.Metabolites2023
37334034Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2a.Ophthalmol Sci2023
37294701Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel.Transl Vis Sci Technol2023
36723966Repeatability of Quantitative Autofluorescence Imaging in a Multicenter Study Involving Patients With Recessive Stargardt Disease 1.Transl Vis Sci Technol2023
36785559Whole genome sequencing for <i>USH2A</i>-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction.HGG Adv2023
36764426Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years.Am J Ophthalmol2023
36727801INCREASING EVIDENCE FOR THE SAFETY OF FOVEA-INVOLVING HALF-DOSE PHOTODYNAMIC THERAPY FOR CHRONIC CENTRAL SEROUS CHORIORETINOPATHY.Retina2023
36524988Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease-associated genes.Genet Med2023
36036675Common and rare genetic risk variants in age-related macular degeneration and genetic risk score in the Coimbra eye study.Acta Ophthalmol2023
36202933Long-term follow-up of chronic central serous chorioretinopathy patients after primary treatment of oral eplerenone or half-dose photodynamic therapy and crossover treatment: SPECTRA trial report No. 3.Graefes Arch Clin Exp Ophthalmol2023
36252678Outcome of Cataract Surgery in Patients With Retinitis Pigmentosa.Am J Ophthalmol2023
34320374CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials.Am J Ophthalmol2022
37645124The STArgardt Remofuscin Treatment Trial (STARTT): design and baseline characteristics of enrolled Stargardt patients.Open Res Eur2022
35379979Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial.Nat Med2022
35672333Scrutinizing pathogenicity of the USH2A c.2276â¿¿Gâ¿¿&gt;â¿¿T; p.(Cys759Phe) variant.NPJ Genom Med2022
35608844Identification of a Complex Allele in IMPG2 as a Cause of Adult-Onset Vitelliform Macular Dystrophy.Invest Ophthalmol Vis Sci2022
35499594[Treatment of age-related macular degeneration: new insights and developments].Ned Tijdschr Geneeskd2022
35533974Spontaneous Resolution of Chronic Central Serous Chorioretinopathy: "Fuji Sign".Ophthalmol Retina2022
35526389Generation of an iPSC line (SCTCi015-A) and isogenic control line (SCTCi015-A-1) from an age-related macular degeneration patient carrying the variant c.355G&gt;A in the CFI gene.Stem Cell Res2022
35526386Generation of an iPSC line (SCTCi014-A) and isogenic control line (SCTCi014-A-1) from an age-related macular degeneration patient carrying the variant c.355G&gt;A in the CFI gene.Stem Cell Res2022
37089696Analysis of hemopexin plasma levels in patients with age-related macular degeneration.Mol Vis2022
35925583Phenotypic Expression of CFH Rare Variants in Age-Related Macular Degeneration Patients in the Coimbra Eye Study.Invest Ophthalmol Vis Sci2022
36053979Common and rare variants in patients with early onset drusen maculopathy.Clin Genet2022
33910932<i>BBS1</i> branchpoint variant is associated with non-syndromic retinitis pigmentosa.J Med Genet2022
35314386The Natural History of Leber Congenital Amaurosis and Cone-Rod Dystrophy Associated with Variants in the GUCY2D Gene.Ophthalmol Retina2022
35069568Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome.Front Immunol2022
35063911Generation and characterization of human induced pluripotent stem cells (iPSCs) from three patients with age-related macular degeneration carrying rare variants in the CFH gene.Stem Cell Res2022
35240203The Phenotypic Course of Age-Related Macular Degeneration for ARMS2/HTRA1: The EYE-RISK Consortium.Ophthalmology2022
35142031Imaging diabetic retinal disease: clinical imaging requirements.Acta Ophthalmol2022
35266249Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A study.Hum Mutat2022
35262734Evaluation of Local Rod and Cone Function in Stargardt Disease.Invest Ophthalmol Vis Sci2022
34864802EFFICACY OF HALF-DOSE PHOTODYNAMIC THERAPY VERSUS HIGH-DENSITY SUBTHRESHOLD MICROPULSE LASER FOR TREATING PIGMENT EPITHELIAL DETACHMENTS IN CHRONIC CENTRAL SEROUS CHORIORETINOPATHY.Retina2022
35078129Generation and characterization of human induced pluripotent stem cells (iPSCs) from three individuals without age-related macular degeneration.Stem Cell Res2022
34431609Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry.Acta Ophthalmol2022
34624300X-Linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients.Ophthalmology2022
34508573Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene.Hum Mol Genet2022
34214454Half-Dose Photodynamic Therapy Versus Eplerenone in Chronic Central Serous Chorioretinopathy (SPECTRA): A Randomized Controlled Trial.Am J Ophthalmol2022
30824420Validation of a model for the prediction of retinopathy in persons with type 1 diabetes.Br J Ophthalmol2021
36246952Genetic Risk in Families with Age-Related Macular Degeneration.Ophthalmol Sci2021
33907369Increased pro-MMP9 plasma levels are associated with neovascular age-related macular degeneration and with the risk allele of rs142450006 near <i>MMP9</i>.Mol Vis2021
33849814Commentary on "Evidence of complement dysregulation in outer retina of Stargardt disease donor eyes".Redox Biol2021
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Collaborators

Caroline C W Klaver
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Susanne Roosing
Radboud University Medical Center
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Freekje van Asten
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Frank G Holz
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Eric H Souied
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Christian Gilissen
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Han G Brunner
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Steffen Schmitz-Valckenberg
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Bram van Ginneken
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Tim M Strom
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Michel Michaelides
Institute of Ophthalmology, University College London
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Rando Allikmets
Columbia University Medical Center
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Gabri??lle H S Buitendijk
Erasmus Medical Center
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Andrew R Webster
Institute of Ophthalmology, University College London
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SriniVas R Sadda
Doheny Eye Institute, University of California Los Angeles
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David G Birch
Retina Foundation of the Southwest
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Martin McKibbin
Leeds Teaching Hospitals NHS Trust
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Sobha Sivaprasad
NIHR Moorfields Biomedical Research Centre, Moorfields Eye Hospital
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Samuel G Jacobson
Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
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Katarina Stingl
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Cornelia M van Duijn
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