Researcher
Bart Dermaut
- Disciplines:Medical transcriptomics, Medical genomics, Clinical genetics and molecular diagnostics, Neurological and neuromuscular diseases, Genetics
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 2012 → 30 Sep 2018
Projects
1 - 6 of 6
- Expanding the TDP-43 proteinopathy spectrum from the neuron to the muscle: a clinical, genetic, pathological and multi-omics study paving the way for new therapeutic strategiesFrom16 Sep 2023 → TodayFunding: BOF - doctoral mandates
- Fund Walter Pyleman & Fund Cremers-Opdebeeck: "Expanding the TDP-43 proteinopathy spectrum from the neuron to the muscle: a clinical, genetic, pathological and multi-omics study paving the way for new therapeutic strategies"From1 Sep 2023 → TodayFunding: Foundations, funds and other with scientific goal
- Microelectrode arrays (MEAs): generally used equipment to measure the functional activity of electrogenic cells.From1 Dec 2020 → 30 Nov 2022Funding: BOF - scientific equipment program
- Precision genomics in neurodegenerative brain disease: from patients to small model organisms and single cellsFrom15 Apr 2019 → TodayFunding: BOF - projects
- BOF-ZAP professorship in neurogeneticsFrom1 Oct 2018 → TodayFunding: BOF - ZAP BOF mandates
- Precision genomics in neurodegenerative brain disease: from patients to small model organisms and single cellsFrom1 Oct 2018 → TodayFunding: FWO Odysseus
Publications
21 - 30 of 53
- Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion(2018)
Authors: Jelle van den Ameele, Ivana Jedlickova, Anna Pristoupilova, Anne Sieben, Sara Van Mossevelde, Chantal Ceuterick-de Groote, Helena Hulková, Radoslav Matej, Alfred Meurs, Christine Van Broeckhoven, et al.
Pages: e658 - e663 - Developmental expression of 4-repeat-Tau induces neuronal aneuploidy in Drosophila tauopathy models(2017)
Authors: Nicolas Malmanche, Pierre Dourlen, Marc Gistelinck, Florie Demiautte, Nichole Link, Cloé Dupont, Lies Vanden Broeck, Elisabeth Werkmeister, Philippe Amouyel, Antonino Bongiovanni, et al.
- Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology(2017)
Authors: P Dourlen, FJ Fernandez-Gomez, C Dupont, B Grenier-Boley, C Bellenguez, H Obriot, R Caillierez, Y Sottejeau, J Chapuis, A Bretteville, et al.
Pages: 874 - 883 - TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis(2017)
Authors: Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jonathan Baets, Ellen Gelpi, et al.
Pages: 297 - 309 - ADAM30 downregulates APP-linked defects through cathepsin D activation in Alzheimer's disease(2016)
Authors: Florent Letronne, Geoffroy Laumet, Anne-Marie Ayral, Julien Chapuis, Florie Demiautte, Mathias Laga, Michel E Vandenberghe, Nicolas Malmanche, Florence Leroux, Fanny Eysert, et al.
Pages: 278 - 292 - The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter(2016)
Authors: I Gijselinck, S Van Mossevelde, J van der Zee, Anne Sieben, S Engelborghs, A Ivanoiu, O Deryck, D Edbauer, M Zhang, B Heeman, et al.
Pages: 1112 - 1124 - A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease(2016)
Authors: Jan Verheijen, Tobi Van den Bossche, Julie van der Zee, Sebastiaan Engelborghs, Raquel Sanchez-Valle, Albert Llado, Caroline Graff, Hakan Thonberg, Pau Pastor, Sara Ortega-Cubero, et al.
Pages: 213 - 224 - Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia(2016)
Authors: Sarah Weckhuysen, Elise Marsan, Virginie Lambrecq, Cécile Marchal, Mélanie Morin-Brureau, Isabelle An-Gourfinkel, Michel Baulac, Martine Fohlen, Christine Kallay Zetchi, Margitta Seeck, et al.
Pages: 994 - 1003 - Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort(2016)
Authors: Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Anne Sieben, Jan De Bleecker, Jonathan Baets, Mathieu Vandenbulcke, Koen Van Laere, Sarah Ceyssens, et al.
Pages: 452 - 467 - Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation(2016)
Authors: Tobi Van den Bossche, Kristel Sleegers, Elise Cuyvers, Sebastiaan Engelborghs, Anne Sieben, Arne De Roeck, Caroline Van Cauwenberghe, Steven Vermeulen, Marleen Van den Broeck, Annelies Laureys, et al.
Pages: 2126 - 2133