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
11 - 20 of 53
- A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene(2022)
Authors: Maria del Rocio Pérez Baca, Eva Jacobs, Lies Vantomme, Pontus LeBlanc, Elke Bogaert, Annelies Dheedene, Laurenz De Cock, Bart Dermaut, Aidin Foroutan, Jennifer Kerkhof, et al.
Number of pages: 1 - Proteome profiling of RNF213 depleted cells reveals nitric oxide regulator DDAH1 antilisterial activity(2021)
Authors: Lia Martina, Caroline Asselman, Fabien Henri Thery, Katie Boucher, Louis Delhaye, Teresa Maia, Bart Dermaut, Sven Eyckerman, Francis Impens
- Ring finger protein 213 assembles into a sensor for ISGylated proteins with antimicrobial activity(2021)
Authors: Fabien Henri Thery, Lia Martina, Caroline Asselman, Heidi Repo, Y Zhang, Koen Sedeyn, Georgios Moschonas, C Bredow, QW Teo, J Zhang, et al.
- Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation(2021)
Authors: Antoon Meylemans, Katrien Hertegonne, Bart Dermaut, Dimitri Hemelsoet
Pages: 23 - 35 - Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations(2020)
Authors: Federica Perrone, Maria Bjerke, Elisabeth Hens, Anne Sieben, Maarten Timmers, Arne De Roeck, Rik Vandenberghe, Kristel Sleegers, Jean-Jacques Martin, Peter P. De Deyn, et al.
- Biotinidase deficiency: A treatable cause of opticospinal syndrome in young adults(2019)
Authors: Vincent Van Iseghem, Mathieu Sprengers, Julie De Zaeytijd, Sindic CJM, B Willekens, Bart Dermaut, Dimitri Hemelsoet, Guy Laureys
Pages: 64 - 65 - Future perspectives of genome-scale sequencing(2018)
Authors: Wouter Steyaert, Bart Dermaut, Dimitri Hemelsoet, Wim Terryn, Bruce Poppe
Pages: 7 - 10 - IRF2BPL is associated with neurological phenotypes(2018)
Authors: Paul C Marcogliese, Vandana Shashi, Rebecca C Spillmann, Nicholas Stong, Jill A Rosenfeld, Mary Kay Koenig, Julian A Martínez-Agosto, Matthew Herzog, Agnes H Chen, Patricia I Dickson, et al.
Pages: 245 - 260 - Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease(2018)
Authors: Elena S Gusareva, Jean-Claude Twizere, Kristel Sleegers, Pierre Dourlen, Jose F Abisambra, Shelby Meier, Ryan Cloyd, Blaine Weiss, Bart Dermaut, Kyrylo Bessonov, et al.
- Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort(2018)
Authors: Jan Verheijen, Julie van der Zee, Ilse Gijselinck, Tobi Van den Bossche, Lubina Dillen, Bavo Heeman, Estrella Gómez-Tortosa, Albert Lladó, Raquel Sanchez-Valle, Caroline Graff, et al.
Pages: 245.e1 - 245.e7