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Cerebellum (London, England)|October 3, 2022
Clinical Trial-Ready Patient Cohorts for Multiple System Atrophy: Coupling Biospecimen and iPSC Banking to Longitudinal Deep-PhenotypingAlain Ndayisaba, Ariana T Pitaro, Andrew S Willett, et al.
Cell|July 23, 2019
An Integrative Model of Cellular States, Plasticity, and Genetics for GlioblastomaCyril Neftel, Julie Laffy, Mariella G Filbin, 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.
Archives of Neurology|April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationAlice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System AtrophyFranziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Human Molecular Genetics|May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesGiovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Acta Neuropathologica|November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathyKurt Farrell, SoongHo Kim, Natalia Han, et al.
Nature Genetics|February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsVivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Medrxiv : the Preprint Server for Health Sciences|May 10, 2023
Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's diseaseRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
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