Stephanie Philtjens

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

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Found 13 publications

Deletion of miR-33, a regulator of the ABCA1-APOE pathway, ameliorates neuropathological phenotypes in APP/PS1 mice.

Deletion of miR-33, a regulator of the ABCA1-APOE pathway, ameliorates neuropathological phenotypes in APP/PS1 mice.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: April 25, 2024

Effects of SPI1-mediated transcriptome remodeling on Alzheimer's disease-related phenotypes in mouse models of Aβ amyloidosis.

Effects of SPI1-mediated transcriptome remodeling on Alzheimer's disease-related phenotypes in mouse models of Aβ amyloidosis.

Journal: Nature communications
Published: July 05, 2023

Network analysis reveals strain-dependent response to misfolded tau aggregates.

Network analysis reveals strain-dependent response to misfolded tau aggregates.

Journal: bioRxiv : the preprint server for biology
Published: February 13, 2023

Network analysis identifies strain-dependent response to tau and tau seeding-associated genes.

Network analysis identifies strain-dependent response to tau and tau seeding-associated genes.

Journal: The Journal of experimental medicine
Published: January 29, 2023

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.

Journal: Acta neuropathologica communications
Published: October 21, 2020

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

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

Journal: Neurobiology of aging
Published: November 09, 2017

Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.

Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.

Journal: Neurobiology of aging
Published: September 13, 2017

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.

Journal: Acta neuropathologica communications
Published: October 21, 2015

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.

Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.

Journal: Neurology
Published: May 19, 2015

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia.

Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia.

Journal: Neurobiology of aging
Published: May 08, 2013

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.

Journal: JAMA neurology
Published: January 23, 2013

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats.

Journal: Human mutation
Published: June 29, 2012
Showing 1-12 of 13

Last Updated: 09/26/2026