scispace - formally typeset
F

Fahri Küçükali

Researcher at University of Antwerp

Publications -  18
Citations -  669

Fahri Küçükali is an academic researcher from University of Antwerp. The author has contributed to research in topics: Biology & Medicine. The author has an hindex of 2, co-authored 6 publications receiving 56 citations.

Papers
More filters
Journal ArticleDOI

New insights into the genetic etiology of Alzheimer’s disease and related dementias

Céline Bellenguez, +401 more
- 01 Apr 2022 - 
TL;DR: This paper performed a two-stage genome-wide association study with 111,326 clinically diagnosed/proxy AD cases and 677,663 controls and found 75 risk loci, of which 42 were new at the time of analysis.
Journal ArticleDOI

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

Itziar de Rojas, +359 more
TL;DR: In this article, a large genetic association study was performed by merging all available case-control datasets and by-proxy study results (discovery n = 409,435 and validation size n = 58,190).
Posted ContentDOI

New insights on the genetic etiology of Alzheimer’s and related dementia

Céline Bellenguez, +262 more
- 04 Oct 2020 - 
TL;DR: A genome-wide significant association of 31 new loci with the risk of AD is reported, with the involvement of gene sets related to amyloid and Tau, but also microglia, in which increased gene expression corresponds to more significant AD risk.
Journal ArticleDOI

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

Iris E. Jansen, +145 more
TL;DR: The largest collaborative effort on genetics underlying CSF biomarkers was established by the European Alzheimer & Dementia Biobank (EADB), including 31 cohorts with a total of 13,116 individuals (discovery n = 8074; replication n = 5042 individuals) as discussed by the authors .
Journal ArticleDOI

Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease.

Yann Le Guen, +108 more
- 31 May 2022 - 
TL;DR: The large risk reductions reported here suggest that protein chemistry and functional assays of these variants should be pursued, as they have the potential to guide drug development targeting APOE.