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The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR GeneClinical characteristics and natural history of rho-associated retinitis pigmentosa.Increased High-Density Lipoprotein Levels Associated with Age-Related Macular DegenerationVisual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis PigmentosaPrevalence of Age-Related Macular Degeneration in Europe: The Past and the FutureGenome-wide association meta-analysis highlights light-induced signaling as a driver for refractive errorEnlargement of Geographic Atrophy From First Diagnosis to End of LifeThe Sleep Quality- and Myopia-Linked PDE11A-Y727C Variant Impacts Neural Physiology by Reducing Catalytic Activity and Altering Subcellular Compartmentalization of the EnzymeMyopia control in Mendelian forms of myopiaThe Role of GJD2(Cx36) in Refractive Error DevelopmentCRB1-associated retinal dystrophiesAssociation of Genetic Variants With Response to Anti-Vascular Endothelial Growth Factor Therapy in Age-Related Macular DegenerationStargardt diseaseX-linked RetinoschisisThe Natural History of Leber Congenital Amaurosis and Cone-Rod Dystrophy Associated with Variants in the GUCY2D GenePredicting Progression to Advanced Age-Related Macular Degeneration from Clinical, Genetic, and Lifestyle Factors Using Machine LearningQuality of life in patients with CRB1-associated retinal dystrophiesLoss of Gap Junction Delta-2 (GJD2) gene orthologs leads to refractive error in zebrafishDevelopment of refractive errors - what can we learn from inherited retinal dystrophies?Defining inclusion criteria and endpoints for clinical trials
author
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Magda A Meester-Smoor
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lastName
Meester-Smoor