Brain-region-aware genetic prioritization separates Alzheimer disease risk from APOE-sensitive β-amyloid burden in public genetic and expression quantitative trait locus resources
By integrating public genetic and expression resources, this study demonstrates that Alzheimer's disease risk and β-amyloid burden represent distinct biological processes, identifying BIN1 as a broad risk anchor while showing that the previously implicated ZNF227 signal is primarily driven by APOE-region variants rather than independent amyloid pathology.