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Brain : a Journal of Neurology|October 8, 2025
Large-scale genetic characterization of Parkinson's disease in the African and African admixed populationsFulya Akçimen, Kimberly Paquette, Peter Wild Crea, et al.American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, 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|February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architectureRuth Chia, Marya S Sabir, Sara Bandres-Ciga, et al.The New England Journal of Medicine|November 10, 2021
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report, Damian Smedley, Katherine R Smith, et al.Science (New York, N.Y.)|June 23, 2018
Analysis of shared heritability in common disorders of the brain, Verneri Anttila, Brendan Bulik-Sullivan, et al.Pageof 247