Oligodendrocyte dysfunction and heterogeneity are emerging as key contributors to Alzheimer’s disease (AD) pathology, though cellular mechanisms remain unclear. Using single-nucleus RNA sequencing across three cortical regions from the same individuals, we identified region- and disease-specific transcriptomic changes, including increased mitochondrial genes and loss of cell type signatures. These results highlight the importance of biologically-informed quality control and underscore the value of multi-regional analysis for understanding AD pathogenesis and progression.
misc DDH+26
BibTeXKey: DDH+26