Show
Sort by
-
- Journal Article
- A1
- open access
No association of CpG SNP rs9357140 with onset age in Belgian C9orf72 repeat expansion carriers
-
- 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
Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability
-
- Journal Article
- A1
- open access
An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease
-
- 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
-
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
-
- Journal Article
- A1
- open access
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation
-
- Journal Article
- A1
- open access
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease
-
STXBP1 encephalopathy : a neurodevelopmental disorder including epilepsy
-
- 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
-
Genome-wide association interaction analysis for Alzheimer's disease
-
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia