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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
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank
Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions
Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study
Lrrk2 and chronic inflammation are linked to pallido-ponto-nigral degeneration caused by the N279K tau mutation
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
