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Does Vitamin D Mediate the Protective Effects of Time Outdoors On Myopia? Findings From a Prospective Birth Cohort

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SLC39A5mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia

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Mutations in LRPAP1 Are Associated with Severe Myopia in Humans

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Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia

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Homozygous loss-of-function mutation of theLEPREL1gene causes severe non-syndromic high myopia with early-onset cataract

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Exome sequencing reveals CCDC111 mutation associated with high myopia

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Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

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A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population

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Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

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Genome-Wide Analysis Points to Roles for Extracellular Matrix Remodeling, the Visual Cycle, and Neuronal Development in Myopia

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A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population

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Genome-Wide Gene-Environment Study Identifies Glutamate Receptor Gene GRIN2A as a Parkinson's Disease Modifier Gene via Interaction with Coffee

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Exome Sequencing Identifies ZNF644 Mutations in High Myopia

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Prevalence of Refractive Error in the United States, 1999-2004

(2008) Susan Vitale   ARCHIVES OF OPHTHALMOLOGY