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
31 - 40 of 53
- Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort(2015)
Authors: Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee, Anne Sieben, Stephanie Philtjens, Bavo Heeman, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Greet De Baets, Veerle Baumer, et al.
Pages: 2116 - 2125 - Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains(2015)
Authors: Jonathan Janssens, Stephanie Philtjens, Gernot Kleinberger, Sara Van Mossevelde, Julie van der Zee, Rita Cacace, Sebastiaan Engelborghs, Anne Sieben, Julia Banzhaf-Strathmann, Lubina Dillen, et al.
- Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanism.(2015)
Authors: Lies Vanden Broeck, Gernot Kleinberger, Julien Chapuis, Marc Gistelinck, Philippe Amouyel, Christine Van Broeckhoven, Jean-Charles Lambert, Patrick Callaerts, Bart Dermaut
Pages: 1121 - 1129 - A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42(2015)
Authors: Kristel Sleegers, Karolien Bettens, Arne De Roeck, Caroline Van Cauwenberghe, Elise Cuyvers, Jan Verheijen, Hanne Struyfs, Jasper Van Dongen, Steven Vermeulen, Sebastiaan Engelborghs, et al.
Pages: 1452 - 1460 - RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder(2015)
Authors: Tim Van Damme, Wouter Steyaert, Bernard Sablonnière, Bart Dermaut
Pages: 1760 - 1766 - Tau phosphorylation regulates the interaction between BIN1's SH3 domain and Tau's proline-rich domain(2015)
Authors: Yoann Sottejeau, Alexis Bretteville, François-Xavier Cantrelle, Nicolas Malmanche, Florie Demiaute, Tiago Mendes, Charlotte Delay, Harmony Alves Dos Alves, Amandine Flaig, Peter Davies, et al.
- HDAC6 is a bruchpilot deacetylase that facilitates neurotransmitter release(2014)
Authors: Katarzyna Miskiewicz, Liya E Jose, Wondwossen M Yeshaw, Jorge S Valadas, Jef Swerts, Sebastian Munck, Fabian Feiguin, Bart Dermaut, Patrik Verstreken
Pages: 94 - 102 - Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia(2014)
Authors: Elise Cuyvers, Karolien Bettens, Stéphanie Philtjens, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Jasper Van Dongen, Nathalie Geerts, Githa Maes, et al.
Pages: 726.e11 - 726.e19 - Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration(2014)
Authors: Julie van der Zee, Gabor G Kovacs, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matej, Mathieu Vandenbulcke, Anne Sieben, Bart Dermaut, Katrien Smets, et al.
Pages: 397 - 410 - Erfelijkheid(2014)
Authors: Bart Dermaut, Sandra Janssens, Ariane Van Tongerloo, Anne De Paepe, Annemie Janssens, Marjolein De Vugt
Pages: 87 - 98