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Neurogenetics|February 22, 2008
Structural genomic variation in ischemic strokeMar Matarin, Javier Simon-Sanchez, Hon-Chung Fung, et al.
NPJ Parkinson'S Disease|May 24, 2024
Profiling complex repeat expansions in RFC1 in Parkinson's diseasePilar Alvarez Jerez, Kensuke Daida, Abigail Miano-Burkhardt, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Haplotype-Resolved DNA Methylation at the APOE Locus identifies Allele-Specific Epigenetic Signatures Relevant to Alzheimer's Disease RiskRylee M Genner, Melissa Meredith, Abraham Moller, et al.
Autophagy|October 28, 2020
Sensitive ELISA-based detection method for the mitophagy marker p-S65-Ub in human cells, autopsy brain, and blood samplesJens O Watzlawik, Xu Hou, Dominika Fricova, et al.
Acta Neuropathologica Communications|December 8, 2020
MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical featuresRebecca R Valentino, Shunsuke Koga, Ronald L Walton, et al.
Parkinsonism & Related Disorders|July 8, 2022
PLA2G6-associated neurodegeneration in four different populations-case series and literature reviewRana Hanna Al-Shaikh, Lukasz M Milanowski, Vikram V Holla, et al.
Acta Neuropathologica|October 15, 2013
Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degenerationNaomi Kouri, Yari Carlomagno, Matthew Baker, et al.
Molecular Neurodegeneration|November 7, 2014
Analysis of COQ2 gene in multiple system atrophyKotaro Ogaki, Shinsuke Fujioka, Michael G Heckman, et al.
Neurobiology of Aging|February 6, 2018
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variantsCristina Razquin, Sara Ortega-Cubero, Estefania Rojo-Bustamante, et al.
Molecular Psychiatry|May 17, 2023
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's diseaseJulie Lake, Caroline Warly Solsberg, Jonggeol Jeffrey Kim, et al.
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