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Nature Communications|April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencingCyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics|March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusionsWouter De Coster, Marleen Van den Broeck, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome SequencingCyril Pottier, Fahri Küçükali, Matt Baker, et al.
Medrxiv : the Preprint Server for Health Sciences|May 10, 2023
Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's diseaseRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Nature Genetics|April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseAdam C Naj, Gyungah Jun, Gary W Beecham, et al.
JAMA Neurology|September 10, 2014
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association studyAdam C Naj, Gyungah Jun, Christiane Reitz, et al.
JAMA Neurology|December 23, 2014
Rarity of the Alzheimer disease-protective APP A673T variant in the United StatesLi-San Wang, Adam C Naj, Robert R Graham, et al.
Neurology|June 23, 2012
Novel late-onset Alzheimer disease loci variants associate with brain gene expressionMariet Allen, Fanggeng Zou, High Seng Chai, et al.
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