Published in Brain Pathol on October 05, 2016
Roles of tau protein in health and disease. Acta Neuropathol (2017) 0.80
An integrated map of genetic variation from 1,092 human genomes. Nature (2012) 59.82
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. Nature (1998) 15.24
Ensembl 2015. Nucleic Acids Res (2014) 8.30
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc Natl Acad Sci U S A (1998) 6.13
Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol (1998) 5.42
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. Science (1998) 4.07
Tau pathology and neurodegeneration. Lancet Neurol (2013) 2.66
Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly. FEBS Lett (1998) 2.26
Autosomal dominant dementia with widespread neurofibrillary tangles. Ann Neurol (1997) 1.98
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. Neurology (1994) 1.97
Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging. Neuropathol Appl Neurobiol (2015) 1.86
Accelerated filament formation from tau protein with specific FTDP-17 missense mutations. FEBS Lett (1999) 1.57
Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments. FEBS Lett (1999) 1.53
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration. Neurology (1999) 1.52
Invited review: Neuropathology of tauopathies: principles and practice. Neuropathol Appl Neurobiol (2015) 1.50
Phenotypic variation in hereditary frontotemporal dementia with tau mutations. Ann Neurol (1999) 1.39
An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies. Acta Neuropathol (2006) 1.24
Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe. Hum Mutat (2003) 1.20
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits. J Neuropathol Exp Neurol (1999) 1.12
Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation. Eur J Neurol (2008) 1.11
Pick's disease is associated with mutations in the tau gene. Ann Neurol (2000) 1.10
Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation. Brain (2004) 1.09
Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration. Acta Neuropathol (2014) 0.98
A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease. Neurology (2005) 0.97
Early-onset, rapidly progressive familial tauopathy with R406W mutation. Neurology (2002) 0.92
Mutational analysis in early-onset familial dementia in the Japanese population. The role of PSEN1 and MAPT R406W mutations. Dement Geriatr Cogn Disord (2008) 0.92
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome. Mov Disord (2008) 0.90
A novel tau mutation, p.K317N, causes globular glial tauopathy. Acta Neuropathol (2015) 0.84
Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation. Neuropathol Appl Neurobiol (2007) 0.83
Juvenile frontotemporal dementia with parkinsonism associated with tau mutation G389R. J Alzheimers Dis (2013) 0.82
Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome. Ann N Y Acad Sci (2000) 0.81
A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease. J Neuropathol Exp Neurol (2015) 0.79
Familial frontotemporal dementia associated with the novel MAPT mutation T427M. J Neurol (2005) 0.77
Slowly progressive behavioural presentation in two UK cases with the R406W MAPT mutation. Neuropathol Appl Neurobiol (2015) 0.75
Association of Mild Cognitive Impairment With Exposure to General Anesthesia for Surgical and Nonsurgical Procedures: A Population-Based Study. Mayo Clin Proc (2016) 1.56
Whole-exome sequencing as a diagnostic tool in a family with episodic ataxia type 1. Mayo Clin Proc (2015) 0.77
AV-1451 Tau and β-Amyloid PET Imaging in Dementia with Lewy Bodies. Ann Neurol (2016) 0.76
An MRI-Based Atlas for Correlation of Imaging and Pathologic Findings in Alzheimer's Disease. J Neuroimaging (2016) 0.75
Alzheimer Disease: Scientific Breakthroughs and Translational Challenges. Mayo Clin Proc (2017) 0.75