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Circulation. Cardiovascular Interventions|September 1, 2025
Technical Advances and Outcomes of Fetal Atrial Septal Intervention for Restrictive or Intact Atrial SeptumBetul Yilmaz Furtun, Mira K Trivedi, Patrick Day, et al.
Nature|July 25, 2006
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17Matt Baker, Ian R Mackenzie, Stuart M Pickering-Brown, et al.
Neuroscience Letters|March 18, 2004
Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's diseaseLynnette J Cook, Luk W Ho, Alison E Taylor, et al.
Acta Neuropathologica|January 18, 2020
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregatesHelen Ling, Ellen Gelpi, Karen Davey, et al.
Ebiomedicine|June 23, 2016
ADAM30 Downregulates APP-Linked Defects Through Cathepsin D Activation in Alzheimer's DiseaseFlorent Letronne, Geoffroy Laumet, Anne-Marie Ayral, et al.
Neuromolecular Medicine|April 13, 2004
Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's diseaseVictoria Busby, Steven Goossens, Petra Nowotny, et al.
Human Molecular Genetics|June 29, 2014
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesJose Bras, Rita Guerreiro, Lee Darwent, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
No evidence that extended tracts of homozygosity are associated with Alzheimer's diseaseRebecca Sims, Sarah Dwyer, Denise Harold, et al.
Neurobiology of Aging|December 9, 2015
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseasesRita Guerreiro, Valentina Escott-Price, Lee Darwent, et al.
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.
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