Alzheimer's Disease (AD) is a neurodegenerative disorder characterized by progressive cognitive decline and memory loss, posing significant challenges for affected individuals, caregivers, and healthcare systems. Genetic factors play a crucial role in AD pathogenesis, with several susceptibility variants identified through Genome-Wide Association Studies (GWAS). This population-based study aimed to investigate the genetic variants associated with AD risk and their implications for early detection and intervention strategies. Utilizing data from [insert study cohort or database], we conducted a comprehensive analysis of genetic variants implicated in AD across a diverse population sample. Our findings highlight the importance of genetic risk profiling in identifying individuals at heightened risk for AD and inform personalized approaches to early detection, risk stratification, and targeted intervention.
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Research and Reports in Medical Sciences received 13 citations as per Google Scholar report
