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The Lancet. Neurology|November 9, 2019
Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort studyEmma L van der Ende, Lieke H Meeter, Jackie M Poos, et al.
Brain : a Journal of Neurology|February 21, 2018
Left frontal hub connectivity delays cognitive impairment in autosomal-dominant and sporadic Alzheimer's diseaseNicolai Franzmeier, Emrah Düzel, Frank Jessen, et al.
Molecular Psychiatry|March 23, 2019
The BDNFVal66Met SNP modulates the association between beta-amyloid and hippocampal disconnection in Alzheimer's diseaseNicolai Franzmeier, Jinyi Ren, Alexander Damm, et al.
Human Mutation|December 24, 2016
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral SclerosisJulie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, et al.
Neurology|April 8, 2021
Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar DegenerationJulio C Rojas, Ping Wang, Adam M Staffaroni, et al.
The Lancet. Neurology|December 8, 2019
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort studyKatrina M Moore, Jennifer Nicholas, Murray Grossman, et al.
Nature Medicine|September 22, 2022
Temporal order of clinical and biomarker changes in familial frontotemporal dementiaAdam M Staffaroni, Melanie Quintana, Barbara Wendelberger, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
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