The genetic landscape of Alzheimer disease: clinical implications and perspectives
VIB-UAntwerp Center for Molecular Neurology · University of Antwerp
Abstract
The search for the genetic factors contributing to Alzheimer disease (AD) has evolved tremendously throughout the years. It started from the discovery of fully penetrant mutations in Amyloid precursor protein, Presenilin 1, and Presenilin 2 as a cause of autosomal dominant AD, the identification of the ɛ4 allele of Apolipoprotein E as a strong genetic risk factor for both early-onset and late-onset AD, and evolved to the more recent detection of at least 21 additional genetic risk loci for the genetically complex form of AD emerging from genome-wide association studies and massive parallel resequencing efforts. These advances in AD genetics are positioned in light of the current endeavor directing toward…
Citation impact
- FWCI
- 38.31
- Percentile
- 100%
- References
- 79
Authors
3Topics & keywords
- Presenilin
- Disease
- Genetics
- Alzheimer's disease
- Genome-wide association study
- Apolipoprotein E
- Biology
- Genetic architecture
- Good health and well-being