Bart Dermaut
6PUBLICATIONS
27CO-AUTHORS
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Publications (6)
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|Apr 10, 2026
Genetic Landscape of Monogenic Parkinson's Disease in the African Population-A Systematic Review.Zelalem Banjaw, Zerihun Assefa, Elke Bogaert
|Mar 04, 2025
Myopathic aggregation-prone variants in the TDP-43 prion-like domain: genetics paving the way.Pedro Ervilha Pereira, Jan L De Bleecker, Elke Bogaert
|Nov 03, 2023
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.Nika Schuermans, Salima El Chehadeh, Dimitri Hemelsoet
|May 08, 2023
Exome Sequencing and Multigene Panel Testing in 1,411 Patients With Adult-Onset Neurologic Disorders.Nika Schuermans, Hannah Verdin, Jody Ghijsels
|Mar 31, 2023
C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD.Pedro Ervilha Pereira, Nika Schuermans, Antoon Meylemans
|Oct 02, 2021
Ring finger protein 213 assembles into a sensor for ISGylated proteins with antimicrobial activity.Fabien Thery, Lia Martina, Caroline Asselman
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Frequent Collaborators
2 joint publications
Dimitri Hemelsoet
1 joint publications
Caroline Asselman
1 joint publications
Yifeng Zhang
1 joint publications
Koen Sedeyn
1 joint publications
George D Moschonas
1 joint publications
Clara Bredow
1 joint publications
Denzel Eggermont
1 joint publications
Nico Callewaert
1 joint publications
Xavier Saelens
1 joint publications
Klaus-Peter Knobeloch
