Clinical implications of recent advances in primary open-angle glaucoma genetics.
Ontology highlight
ABSTRACT: Over the last decade, genetic studies, including genome-wide association studies (GWAS), have accelerated the discovery of genes and genomic regions contributing to primary open-angle glaucoma (POAG), a leading cause of irreversible vision loss. Here, we review the findings of genetic studies of POAG published in English prior to September 2019. In total, 74 genomic regions have been associated at a genome-wide level of significance with POAG susceptibility. Recent POAG GWAS provide not only insight into global and ethnic-specific genetic risk factors for POAG susceptibility across populations of diverse ancestry, but also important functional insights underlying biological mechanisms of glaucoma pathogenesis. In this review, we also summarize the genetic overlap between POAG, glaucoma end
SUBMITTER: Choquet H
PROVIDER: S-EPMC7002426 | biostudies-literature | 2020 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA