Show
Sort by
-
- Journal Article
- A1
- open access
Subclinical epileptiform activity in the Alzheimer continuum : association with disease, cognition and detection method
-
- Journal Article
- A1
- open access
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers
-
Hippocampal sclerosis in frontotemporal dementia : when vascular pathology meets neurodegeneration
-
- Journal Article
- A1
- open access
Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations
-
- Journal Article
- A1
- open access
Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export
-
- Journal Article
- A1
- open access
Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability
-
Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion
-
- Journal Article
- A1
- open access
An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease
-
- Journal Article
- A1
- open access
Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family
-
- Journal Article
- A1
- open access
Clinical variability and onset age modifiers in an extended Belgian GRN founder family
-
Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease
-
- Journal Article
- A1
- open access
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
-
- Journal Article
- A1
- open access
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
-
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients
-
Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion
-
- Journal Article
- A1
- open access
TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
-
PSP and small vessel disease : more than occasional co-occurence?
-
- Journal Article
- A2
- open access
Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD
-
- Journal Article
- A1
- open access
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation
-
- Journal Article
- A1
- open access
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
-
- Journal Article
- A1
- open access
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease
-
Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanism.
-
- Journal Article
- A1
- open access
A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42
-
- Journal Article
- A1
- open access
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
-
- Journal Article
- A1
- open access
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
-
Genome-wide association interaction analysis for Alzheimer's disease
-
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
-
- Journal Article
- A1
- open access
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
-
- Journal Article
- A1
- open access
TDP-43 loss-of-function causes neuronal loss due to defective steroid receptor-mediated gene program switching in Drosophila
-
Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients
-
Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort
-
A pan-European study of the C9orf72 repeat associated with FTLD : geographic prevalence, genomic instability, and intermediate repeats
-
- Journal Article
- A1
- open access
The genetics and neuropathology of frontotemporal lobar degeneration
-
Identification of novel causal genes for frontotemporal lobar degeneration using whole genome sequencing
-
Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts
-
Distinct clinical characteristics of C9orf72 expansion carriers compared to GRN, MAPT and non-mutation carries in a Flanders-Belgian FTLD cohort
-
A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum : a gene identification study
-
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
-
Belgian Fabry study: prevalence of Fabry disease in a cohort of 1000 young patients with cerebrovascular disease
-
Arginine vasopressin receptor gene-based single-nucleotide polymorphism analysis in attention deficit hyperactivity disorder
-
Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models
-
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
-
- Conference Paper
- C3
- open access
Gene expression profiling to identify microvascular changes in Alzheimer's disease mouse models
-
- Journal Article
- A1
- open access
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro
-
Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response
-
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
-
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia
-
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
-
The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 years
-
Mean age-of-onset of familial Alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
-
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family
-
Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementia
-
- Journal Article
- A1
- open access
Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum
-
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region
-
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample
-
Genetic testing has no place as a routine diagnostic test in sporadic and familial cases of Alzheimer's disease
-
Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease
-
Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementia patients
-
A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaques
-
Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan: reply
-
Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family
-
Digenic progressive external ophthalmoplegiain a sporadic patient: recessive mutationsin POLG and C10orf2/Twinkle
-
Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy
-
PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease
-
Early cognitive decline is associated with prion protein codon 129 polymorphism
-
The gene encoding nicastrin, a major γ-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample
-
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
-
Amyloid β secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease
-
Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob disease phenotype
-
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia
-
Identification of the tumor metastasis suppressor Nm23-H1/Nm23-R1 as a constituent of the centrosome
-
The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease
-
Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia
-
Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion
-
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression
-
Mutation screening of the tau gene in patients with early-onset Alzheimer's disease
-
The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease
-
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Aβ42 secretion
-
Presenilins and Alzheimer's disease: identification of proteins that interact with presenilin I using the yeast two-hybrid system
-
Primary and secondary structure of the 18S ribosomal RNA of the bird spider Eurypelma californica and evolutionary relationships among eukaryotic phyla