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Acta Neuropathologica|October 29, 2014
Primary age-related tauopathy (PART): a common pathology associated with human agingJohn F Crary, John Q Trojanowski, Julie A Schneider, et al.
Acta Neuropathologica|August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-USara Alidadiani, Júlia Faura, Sarah Wynants, et al.
Molecular Neurodegeneration|July 6, 2025
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypesCristina T Vicente, Tejasvi Niranjan, Elise Coopman, et al.
Acta Neuropathologica|December 13, 2022
LATE-NC staging in routine neuropathologic diagnosis: an updatePeter T Nelson, Edward B Lee, Matthew D Cykowski, et al.
Acta Neuropathologica|May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degenerationHazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.
Journal of Neuropathology and Experimental Neurology|December 28, 2020
Early Selective Vulnerability of the CA2 Hippocampal Subfield in Primary Age-Related TauopathyJamie M Walker, Timothy E Richardson, Kurt Farrell, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear PalsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.
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