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EJNMMI Research|January 24, 2022
Validation and test-retest repeatability performance of parametric methods for [11C]UCB-J PETHayel Tuncel, Ronald Boellaard, Emma M Coomans, et al.
Acta Neuropathologica|March 31, 2016
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's diseaseJan Verheijen, Tobi Van den Bossche, Julie van der Zee, et al.
Neurobiology of Aging|November 18, 2017
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohortJan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
Acta Neuropathologica|March 16, 2019
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitabilityRita Cacace, Bavo Heeman, Sara Van Mossevelde, et al.
The Lancet. Neurology|December 14, 2011
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification studyIlse Gijselinck, Tim Van Langenhove, Julie van der Zee, et al.
Brain : a Journal of Neurology|July 30, 2015
Alzheimer's disease cerebrospinal fluid biomarker in cognitively normal subjectsJon B Toledo, Henrik Zetterberg, Argonde C van Harten, 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.
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.
Neurobiology of Aging|June 11, 2018
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patientsYalda Baradaran-Heravi, Lubina Dillen, Hung Phuoc Nguyen, et al.
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