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Human Molecular Genetics|May 26, 2011
Ataxin-2 repeat-length variation and neurodegenerationOwen A Ross, Nicola J Rutherford, Matt Baker, et al.JAMA Neurology|November 18, 2014
Clinical correlations with Lewy body pathology in LRRK2-related Parkinson diseaseLorraine V Kalia, Anthony E Lang, Lili-Naz Hazrati, et al.Nature Neuroscience|November 1, 2025
TDP-43-dependent mis-splicing of KCNQ2 triggers intrinsic neuronal hyperexcitability in ALS/FTDBrian J Joseph, Kelly A Marshall, Peter Harley, et al.Nature Medicine|April 15, 2020
Large-scale proteomic analysis of Alzheimer's disease brain and cerebrospinal fluid reveals early changes in energy metabolism associated with microglia and astrocyte activationErik C B Johnson, Eric B Dammer, Duc M Duong, et al.JAMA Neurology|January 13, 2025
Longitudinal FDG-PET Metabolic Change Along the Lewy Body ContinuumDaniel Ferreira, Scott A Przybelski, Timothy G Lesnick, et al.Annals of Neurology|November 7, 2025
Association between Human Leukocyte Antigen Alleles and Neuropathological Outcomes in Lewy Body DiseaseMarios Gavrielatos, Michael G Heckman, Alexandra I Soto-Beasley, et al.Neurobiology of Aging|May 29, 2014
Ataxin-2 as potential disease modifier in C9ORF72 expansion carriersMarka van Blitterswijk, Bianca Mullen, Michael G Heckman, et al.Science Translational Medicine|January 17, 2024
TMEM106B core deposition associates with TDP-43 pathology and is increased in risk SNP carriers for frontotemporal dementiaJordan D Marks, Virginia Estades Ayuso, Yari Carlomagno, et al.Nature Communications|June 20, 2024
Gliovascular transcriptional perturbations in Alzheimer's disease reveal molecular mechanisms of blood brain barrier dysfunctionÖzkan İş, Xue Wang, Joseph S Reddy, et al.Nature Genetics|December 27, 2011
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRosa Rademakers, Matt Baker, Alexandra M Nicholson, et al.Pageof 152