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The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Neurology|September 13, 2013
C9ORF72 repeat expansions in cases with previously identified pathogenic mutationsMarka van Blitterswijk, Matthew C Baker, Mariely DeJesus-Hernandez, et al.
Archives of Neurology|November 14, 2007
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer diseaseHao Li, Sally Wetten, Li Li, et al.
Brain : a Journal of Neurology|August 4, 2011
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementiaKatya Rascovsky, John R Hodges, David Knopman, et al.
The New England Journal of Medicine|September 23, 2014
Ebola virus disease in West Africa--the first 9 months of the epidemic and forward projections, Bruce Aylward, Philippe Barboza, et al.
Human Molecular Genetics|May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesGiovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2012
Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humansTrygve E Bakken, J Cooper Roddey, Srdjan Djurovic, et al.
Geroscience|January 31, 2025
Dynamic proportional loss of functional connectivity revealed change of left superior frontal gyrus in subjective cognitive decline: an explanatory study based on Chinese and Western cohortsLuyao Wang, Wenjing Hu, Fan Dong, et al.
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