Validation of genome-wide association study (GWAS)-identified disease risk alleles with patient-specific stem cell lines.
Ontology highlight
ABSTRACT: While the past decade has seen great progress in mapping loci for common diseases, studying how these risk alleles lead to pathology remains a challenge. Age-related macular degeneration (AMD) affects 9 million older Americans, and is characterized by the loss of the retinal pigment epithelium (RPE). Although the closely linked genome-wide association studies ARMS2/HTRA1 genes, located at the chromosome 10q26 locus, are strongly associated with the risk of AMD, their downstream targets are unknown. Low population frequencies of risk alleles in tissue banks make it impractical to study their function in cells derived from autopsied tissue. Moreover, autopsy eyes from end-stage AMD patients, where age-related RPE atrophy and fibrosis are already present, cannot be used to determine how abnor
SUBMITTER: Yang J
PROVIDER: S-EPMC4049304 | biostudies-literature | 2014 Jul
REPOSITORIES: biostudies-literature
ACCESS DATA