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Movement Disorders : Official Journal of the Movement Disorder Society|June 25, 2019
SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's DiseaseRubén Fernández-Santiago, Núria Martín-Flores, Francesca Antonelli, et al.Nature Neuroscience|September 1, 2014
Genetic variability in the regulation of gene expression in ten regions of the human brainAdaikalavan Ramasamy, Daniah Trabzuni, Sebastian Guelfi, et al.American Journal of Human Genetics|August 20, 2025
Tackling a disease on a global scale, the Global Parkinson's Genetics Program, GP2: A new generation of opportunitiesCornelis Blauwendraat, Alastair J Noyce, Ignacio F Mata, et al.Journal of Neuropathology and Experimental Neurology|October 2, 2015
A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick DiseasePawel Tacik, Michael DeTure, Kelly M Hinkle, et al.Acta Neuropathologica|June 6, 2014
Differential clinicopathologic and genetic features of late-onset amnestic dementiasMelissa E Murray, Ashley Cannon, Neill R Graff-Radford, et al.Acta Neuropathologica|September 13, 2012
Neuropathologically defined subtypes of Alzheimer's disease differ significantly from neurofibrillary tangle-predominant dementiaNicholas J Janocko, Kevin A Brodersen, Alexandra I Soto-Ortolaza, et al.Acta Neuropathologica|May 12, 2026
Molecular profiling of alpha-synuclein pathology and seeding activity in Parkinson's diseaseZeynep Bengisu Kaya, Danilyn Amerna, Ananya Susarla, et al.Journal of the Neurological Sciences|February 7, 2018
Comparison of clinical features among Parkinson's disease subtypes: A large retrospective study in a single centerTakuya Konno, Angela Deutschländer, Michael G Heckman, et al.Mechanisms of Ageing and Development|May 29, 2007
Familial genes in sporadic disease: common variants of alpha-synuclein gene associate with Parkinson's diseaseOwen A Ross, David Gosal, Jeremy T Stone, et al.Acta Neuropathologica|May 13, 2015
Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synucleinNaoya Aoki, Philip J Boyer, Cheryl Lund, et al.Pageof 77