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Marijne Vandebergh
Marijne Vandebergh
VIB-UAntwerp Center for Molecular Neurology
Verified email at uantwerpen.vib.be - Homepage
Title
Cited by
Cited by
Year
Genetic architecture of adaptive immune system identifies key immune regulators
V Lagou, JE Garcia-Perez, I Smets, L Van Horebeek, M Vandebergh, ...
Cell reports 25 (3), 798-810. e6, 2018
462018
Machine learning identifies an immunological pattern associated with multiple juvenile idiopathic arthritis subtypes
E Van Nieuwenhove, V Lagou, L Van Eyck, J Dooley, U Bodenhofer, ...
Annals of the rheumatic diseases 78 (5), 617-628, 2019
382019
Genetics of multiple sclerosis: lessons from polygenicity
A Goris, M Vandebergh, JL McCauley, J Saarela, C Cotsapas
The Lancet Neurology 21 (9), 830-842, 2022
372022
Effects of vitamin D and body mass index on disease risk and relapse hazard in multiple sclerosis: a Mendelian randomization study
M Vandebergh, B Dubois, A Goris
Neurology: Neuroimmunology & Neuroinflammation 9 (3), e1165, 2022
322022
CHIT1 at diagnosis reflects long‐term multiple sclerosis disease activity
E Oldoni, I Smets, K Mallants, M Vandebergh, L Van Horebeek, K Poesen, ...
Annals of neurology 87 (4), 633-645, 2020
302020
Locus for severity implicates CNS resilience in progression of multiple sclerosis
IMSGC MultipleMS
Nature 619, 323-331, 2023
292023
Smoking and multiple sclerosis risk: a Mendelian randomization study
M Vandebergh, A Goris
Journal of Neurology 267 (10), 3083-3091, 2020
272020
Environmental risk factors in multiple sclerosis: Bridging Mendelian randomization and observational studies
M Vandebergh, N Degryse, B Dubois, A Goris
Journal of Neurology 269 (8), 4565-4574, 2022
202022
Body mass index, interleukin-6 signaling and multiple sclerosis: a mendelian randomization study
M Vandebergh, S Becelaere, CHARGE Inflammation Working Group, ...
Frontiers in immunology 13, 834644, 2022
182022
Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis
M Vandebergh, TFM Andlauer, Y Zhou, K Mallants, F Held, L Aly, ...
Annals of neurology 89 (5), 884-894, 2021
182021
Genetic basis for relapse rate in multiple sclerosis: association with LRP2 genetic variation
K Hilven, M Vandebergh, I Smets, K Mallants, A Goris, B Dubois
Multiple Sclerosis, 2018
162018
Quantitative MRI phenotypes capture biological heterogeneity in multiple sclerosis patients
I Smets, A Goris, M Vandebergh, J Demeestere, S Sunaert, P Dupont, ...
Scientific Reports 11 (1), 1-11, 2021
52021
Reliability and Validity of Smartphone Cognitive Testing for Frontotemporal Lobar Degeneration
AM Staffaroni, AL Clark, JC Taylor, HW Heuer, M Sanderson-Cimino, ...
JAMA Network Open 7 (4), e244266-e244266, 2024
2024
Large-scale network analysis of the cerebrospinal fluid proteome identifies molecular signatures of frontotemporal lobar degeneration
R Saloner, A Staffaroni, E Dammer, ECB Johnson, E Paolillo, A Wise, ...
2024
Genome-wide association study reveals different T cell distributions in peripheral blood of healthy individuals at high genetic risk of type 1 diabetes and long COVID
CML Laura Deecke, Jan Homann, David Goldeck, Felix Luessi, Marijne ...
MedRxiv, 2024
2024
Gene specific effects on brain volume and cognition of TMEM106B in frontotemporal lobar degeneration
M Vandebergh, EM Ramos, N Corriveau-Lecavalier, VK Ramanan, ...
medRxiv, 2024.04. 05.24305253, 2024
2024
From susceptibility to heterogeneity in multiple sclerosis: insights from genetic epidemiology
M Vandebergh, A Goris, B Dubois
2022
Chr8p23 region implicated in genetic basis for demyelination in multiple sclerosis patients
I Smets, A Goris, M Moisse, M Vandebergh, V Lagou, J Demeestere, ...
Multiple Sclerosis Journal 24, 387-387, 2018
2018
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