Search

Your search keyword '"Van Broeckhoven, Christine"' showing total 1,577 results

Search Constraints

Start Over You searched for: Author "Van Broeckhoven, Christine" Remove constraint Author: "Van Broeckhoven, Christine" Language english Remove constraint Language: english
1,577 results on '"Van Broeckhoven, Christine"'

Search Results

2. Subclinical epileptiform activity in the Alzheimer continuum: association with disease, cognition and detection method

4. Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

5. Multivariate GWAS of Alzheimer’s disease CSF biomarker profiles implies GRIN2D in synaptic functioning

6. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

8. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

9. Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

10. Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

12. Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer’s disease CSF profile of neuronal injury and inflammation

15. The SORL1 p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer's disease.

18. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

23. Clinical variability and onset age modifiers in an extended Belgian GRN founder family

24. C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

26. Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability

27. C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

36. Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

39. Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease

43. Whole‐exome rare‐variant analysis of Alzheimer's disease and related biomarker traits

44. Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease

45. Genome-wide association interaction analysis for Alzheimer's disease

46. Frontotemporal dementia and its subtypes: a genome-wide association study

49. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Catalog

Books, media, physical & digital resources