S. Philtjens

发表

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

C. van Broeckhoven, S. Engelborghs, R. Vandenberghe, 2013, JAMA neurology.

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

B. Bergmans, K. Sleegers, C. van Broeckhoven, 2018, Neurobiology of Aging.

Chemogenetic activation of astrocytes in the hippocampus and cortex changes the transcriptome of microglia and other cell types

Y. Moon, Jungsu Kim, M. Turnbull, 2020 .

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

S. Pereson, C. Broeckhoven, K. Sleegers, 2012, The Lancet Neurology.

Single-cell resolution analysis of the crosstalk between chemogenically activated astrocytes and microglia

Y. Moon, M. Turnbull, Jungsu Kim, 2020, bioRxiv.

Network analysis reveals strain-dependent response to misfolded tau aggregates

B. Lamb, H. S. Wijeratne, C. Lasagna-Reeves, 2023, bioRxiv.

A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

F. Jessen, G. Frisoni, K. Sleegers, 2012, Human mutation.

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

Patrick Santens, Mathieu Vandenbulcke, Adrian Ivanoiu, 2015, Acta neuropathologica communications.

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

P. Deyn, C. Broeckhoven, K. Sleegers, 2014, Neurobiology of Aging.

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

C. van Broeckhoven, S. Engelborghs, R. Vandenberghe, 2015, Neurology.

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

G. Frisoni, C. Broeckhoven, S. Engelborghs, 2018, Neurobiology of Aging.

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

B. Asselbergh, C. van Broeckhoven, S. Engelborghs, 2021, Acta Neuropathologica Communications.

Homozygous and compound heterozygous rare variants in VPS13C contribute to Lewy body diseases

P. Deyn, B. Asselbergh, S. Engelborghs, 2020 .

Identification of genetic variants regulating the abundance of clinically relevant plasma proteins using the Diversity Outbred mouse model

Jungsu Kim, Hyewon Kim, S. Philtjens, 2020, bioRxiv.

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

B. Lamb, H. S. Wijeratne, Jungsu Kim, 2023, The Journal of experimental medicine.

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

C. van Broeckhoven, S. Engelborghs, R. Vandenberghe, 2013, JAMA neurology.