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Nature Aging|April 28, 2023
RNA sequencing of whole blood reveals early alterations in immune cells and gene expression in Parkinson's diseaseDavid W Craig, Elizabeth Hutchins, Ivo Violich, et al.
Neurobiology of Disease|February 25, 2019
Assessment of APOE in atypical parkinsonism syndromesMarya S Sabir, Cornelis Blauwendraat, Sarah Ahmed, et al.
American Journal of Human Genetics|November 20, 2010
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasmaMinerva M Carrasquillo, Alexandra M Nicholson, NiCole Finch, et al.
Plos One|July 30, 2011
Pathogenic LRRK2 mutations do not alter gene expression in cell model systems or human brain tissueMichael J Devine, Alice Kaganovich, Mina Ryten, et al.
Research Square|October 27, 2023
An ANXA11 P93S variant dysregulates TDP-43 and causes corticobasal syndromeAllison Snyder, Veronica H Ryan, James Hawrot, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 3, 2016
Caspase-1 causes truncation and aggregation of the Parkinson's disease-associated protein α-synucleinWei Wang, Linh T T Nguyen, Christopher Burlak, et al.
Molecular Neurodegeneration|January 24, 2018
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylationJesús Madero-Pérez, Elena Fdez, Belén Fernández, et al.
Brain : a Journal of Neurology|December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseRina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
Genomics, Proteomics & Bioinformatics|November 22, 2024
ProtPipe: A Multifunctional Data Analysis Pipeline for Proteomics and PeptidomicsZiyi Li, Cory A Weller, Syed Shah, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|June 26, 2024
An ANXA11 P93S variant dysregulates TDP-43 and causes corticobasal syndromeAllison Snyder, Veronica H Ryan, James Hawrot, et al.
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