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Relative frequencies of Alzheimer disease, Lewy body, vascular and frontotemporal dementia, and hippocampal sclerosis in the State of Florida Brain Bank
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS
