Loss-of-function variants in ABCA7 confer risk of Alzheimer's diseaseDemGene, Andrés Ingason, Hannes Helgason et al.|Nature Genetics|2015Cited by 332
Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?Mikko Hiltunen, Hilkka Soininen|European Journal of Human Genetics|2000Cited by 52
Cerebrospinal fluid proteome profiling across the Alzheimer’s disease continuum: a step towards solving the equation for ‘X’Sophia Weiner, Johan Gobom, Mathias Sauer et al.|Molecular Neurodegeneration|2025Cited by 4