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Nature Genetics|November 21, 2022
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's diseaseHenne Holstege, Marc Hulsman, Camille Charbonnier, et al.Acta Neuropathologica|May 28, 2019
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevitySven J van der Lee, Olivia J Conway, Iris Jansen, et al.JAMA Psychiatry|December 1, 2017
Association of Cerebral Amyloid-β Aggregation With Cognitive Functioning in Persons Without DementiaWillemijn J Jansen, Rik Ossenkoppele, Betty M Tijms, et al.JAMA Psychiatry|January 22, 2025
Depressive Symptoms and Amyloid PathologyWietse A Wiels, Julie E Oomens, Sebastiaan Engelborghs, et al.Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
APOE stratified genome-wide association studies provide novel insights into the genetic etiology of Alzheimers's diseaseJesper Qvist Thomassen, Leonard Hampton, Brittany Ulms, et al.Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Genomic analyses reveal new insights into Alzheimer's diseaseEmil Uffelmann, Douglas P Wightman, Shahram Bahrami, et al.JAMA|May 20, 2015
Prevalence of cerebral amyloid pathology in persons without dementia: a meta-analysisWillemijn J Jansen, Rik Ossenkoppele, Dirk L Knol, et al.Nature Communications|April 21, 2026
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagyJigyasha Timsina, Chenyang Jiang, Daniel L McCartney, et al.JAMA Neurology|January 31, 2022
Prevalence Estimates of Amyloid Abnormality Across the Alzheimer Disease Clinical SpectrumWillemijn J Jansen, Olin Janssen, Betty M Tijms, et al.Nature Communications|June 8, 2021
Common variants in Alzheimer's disease and risk stratification by polygenic risk scoresItziar de Rojas, Sonia Moreno-Grau, Niccolo Tesi, et al.Pageof 80