Novel Tau Polymorphisms, Tau Haplotypes, and Splicing in Familial and Sporadic Frontotemporal Dementia
Data up to Jan 2025
Total Citations Per Year
Abstract
References (23)
Amyloid Oligomers Exacerbate Tau Pathology in a Mouse Model of Tauopathy
2012 • 10,051 citations
Frontotemporal lobar degeneration
1998 • 4,937 citations
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
1998 • 3,377 citations
Tau is a candidate gene for chromosome 17 frontotemporal dementia
1998 • 1,344 citations
Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups.
1994 • 1,291 citations
Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17
1998 • 954 citations
Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear Palsy
1999 • 775 citations
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
1998 • 464 citations
Genetic evidence for the involvement of τ in progressive supranuclear palsy
1997 • 387 citations
5′ Splice Site Mutations in tau Associated with the Inherited Dementia FTDP-17 Affect a Stem-Loop Structure That Regulates Alternative Splicing of Exon 10
1999 • 294 citations
A study of the Lund‐Manchester research criteria for frontotemporal dementia
1997 • 218 citations
Inheritance of Frontotemporal Dementia
1999 • 208 citations
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
2000 • 198 citations
Frequency of Tau Gene Mutations in Familial and Sporadic Cases of Non-Alzheimer Dementia
2001 • 170 citations
Sporadic Pick's disease: A tauopathy characterized by a spectrum of pathological τ isoforms in gray and white matter
2002 • 147 citations
Frequency oftau mutations in three series of non-Alzheimer's degenerative dementia
1999 • 137 citations
From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation
1999 • 134 citations
Aberrant Splicing of tau Pre-mRNA Caused by Intronic Mutations Associated with the Inherited Dementia Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17
2000 • 131 citations
The apolipoprotein E ε4 allele is not a significant risk factor for frontotemporal dementia
1998 • 97 citations
Tau gene polymorphisms and apolipoprotein E ε4 may interact to increase risk for Alzheimer’s disease
1999 • 62 citations
Possible association of the tau H1/H1 genotype with primary progressive aphasia
2003 • 43 citations
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
2000 • 41 citations
The extended haplotype of the microtubule associated protein tau gene is not associated with Pick's disease
2001 • 34 citations