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Journal of Neurology, Neurosurgery, and Psychiatry|April 5, 2022
Development of a sensitive trial-ready poly(GP) CSF biomarker assay for C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosisKatherine M Wilson, Eszter Katona, Idoia Glaria, et al.Neuroimage. Clinical|April 25, 2021
Differential early subcortical involvement in genetic FTD within the GENFI cohortMartina Bocchetta, Emily G Todd, Georgia Peakman, et al.Neurobiology of Aging|March 21, 2018
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementiaStéphanie Philtjens, Sara Van Mossevelde, Julie van der Zee, et al.Human Brain Mapping|March 10, 2023
Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementiaAurélie Bussy, Jake P Levy, Tristin Best, et al.Neuroimage. Clinical|December 15, 2019
White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI studyCarole H Sudre, Martina Bocchetta, Carolin Heller, et al.Brain : a Journal of Neurology|November 24, 2025
Cellular signatures underlying functional resilience in presymptomatic frontotemporal dementiaKamen A Tsvetanov, Maura Malpetti, P Simon Jones, et al.Science Translational Medicine|February 5, 2025
Proteomic analysis reveals distinct cerebrospinal fluid signatures across genetic frontotemporal dementia subtypesAitana Sogorb-Esteve, Sophia Weiner, Joel Simrén, et al.Neurobiology of Aging|March 23, 2015
Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium studyElise Cuyvers, Julie van der Zee, Karolien Bettens, et al.Human Mutation|September 29, 2015
Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium CohortRita Cacace, Tobi Van den Bossche, Sebastiaan Engelborghs, et al.Pageof 21