Researcher
Jonathan Baets
- Research Expertise:Neurogenetics, molecular genetics, neuropathology, clinical neurology, clinical neurophysiology
- Keywords:NEUROPATHOLOGY, NEURO MUSCULAR DISEASES, PATHOMECHANISM, HEREDITARY NEUROPATHIES, GENETIC DISEASE, Medicine
- Disciplines:Neurosciences, Genetics, Clinical genetics and molecular diagnostics, Neurological and neuromuscular diseases, Neurophysiology, Histology
- Research techniques:molecular genetics, histopathology, clinical neurophysiology
- Users of research expertise:neurologists, neuroscientists, geneticists
Affiliations
- Translational Neurosciences (TNW) (Research group)
Member
From1 Jan 2019 → Today - Neurogenetics Group (Research group)
Member
From1 Jan 2015 → 31 Dec 2018 - Neurogenetics Group (Research group)
Member
From1 Oct 2003 → 31 Dec 2014
Projects
1 - 10 of 13
- Study of SPTAN1 pathomechanisms: the spectrin complex as a central hub in rare neurological and neuromuscular diseases.From1 Jan 2023 → TodayFunding: FWO research project
- KDM5A drives ageing signatures and disturbed muscle regeneration in sporadic Inclusion Body Myositis:
from the deep proteome towards disease models and novel therapies;From1 Oct 2021 → TodayFunding: BOF - doctoral mandates
- Validation and characterization of SPTAN1 mutations as a novel cause for hereditary cerebellar ataxia.From1 Apr 2021 → 31 Mar 2022Funding: BOF - projects
- Unraveling neuromuscular spectrinopathies through SPTAN1 genotype-phenotype correlationsFrom2 Feb 2021 → 31 Dec 2021Funding: Foundations, funds and other with scientific goal
- IMARK. Network for image-based biomarker discovery and evaluationFrom1 Jan 2021 → TodayFunding: IOF - mandates
- Neuro-spectrinopathies: approaching the phenotypical heterogeneity issueFrom1 Nov 2020 → TodayFunding: FWO fellowships
- Neuromuscular disorders: from the omics-age towards novel therapies.From1 Oct 2020 → TodayFunding: FWO fundamental clinical research fellowship
- Multidimensional analysis of the nervous system in health and disease (µNeuro).From1 Jan 2020 → TodayFunding: BOF - research organisations, Fund Recuperation Fiscal Exemption
- Primary muscle degeneration in sporadic Inclusion-Body Myositis: combining deep-proteome data in patient muscle tissue with novel cellular models to pinpoint key mechanisms driving inflammation and aberrant protein expression.From1 Jan 2019 → 31 Dec 2021Funding: FWO research grant KAN
- La myosite à inclusions, une maladie inflammatoire dégénératif : une approche protéomique afin d'identifier les mécanismes perturbant l'homéostasie protéinique.From1 Jan 2018 → 31 Dec 2018Funding: Foundations, funds and other with scientific goal
Publications
1 - 10 of 145
- Distinct features in adult polyglucosan body disease(2023)
Authors: Jonathan De Winter, Gert Cypers, Edwin Jacobs, Tine Deconinck, Willem De Ridder, Sven Dekeyzer, Jonathan Baets
Pages: 148 - 152 - C-terminal frameshift variant of TDP-₄₃ with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD(2023)
Authors: Pedro Ervilha Pereira, Nika Schuermans, Antoon Meylemans, Pontus LeBlanc, Lauren Versluys, Katie E.E. Copley, Jack D.D. Rubien, Christopher Altheimer, Myra Peetermans, Elke Debackere, et al.
Pages: 793 - 814 - HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathies(2023)
Authors: Barbara Tedesco, Leen Vendredy, Elias Adriaenssens, Marta Cozzi, Bob Asselbergh, Valeria Crippa, Riccardo Cristofani, Paola Rusmini, Veronica Ferrari, Elena Casarotto, et al.
Pages: 1 - 23 - A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium(2023)
Authors: Jan L. De Bleecker, Kristl G. Claeys, Stephanie Delstanche, Vinciane Van Parys, Jonathan Baets, Sebastien Tilleux, Gauthier Remiche
Pages: 1 - 9 - A recurrent KPNA3 missense variant causing infantile pure spastic paraplegia(2022)
Authors: Jonathan De Winter, Liedewei Van de Vondel, Stephan Zuchner, Els Ortibus, Jonathan Baets
Pages: 298 - 299 - Genetic pain loss disorders(2022)
Authors: Annette Lischka, Petra Lassuthova, Arman Çakar, Christopher J. Record, Jonas Van lent, Jonathan Baets, Maike F. Dohrn, Jan Senderek, Angelika Lampert, David L. Bennett, et al.
Pages: 1 - 23 - De novo and dominantly inherited SPTAN1 mutations cause spastic paraplegia and cerebellar ataxia(2022)
Authors: Liedewei Van de Vondel, Jonathan De Winter, Danique Beijer, Giulia Coarelli, Melanie Wayand, Robin Palvadeau, Martje G. Pauly, Katrin Klein, Maren Rautenberg, Léna Guillot‐Noël, et al.
Pages: 1175 - 1186 - Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1A(2022)
Authors: Jonas Van lent, Leen Vendredy, Elias Adriaenssens, Bob Asselbergh, Mark Kaji, Sarah Weckhuysen, Ludo Van Den Bosch, Jonathan Baets, Vincent Timmerman
Pages: 1 - 28 - Commentary(2022)
Authors: Liedewei Van de Vondel, Jonathan De Winter, Jonathan Baets
Pages: 1 - 3 - RFC1 repeat expansions(2022)
Authors: Danique Beijer, Maike F. Dohrn, Jonathan De Winter, Sarah Fazal, Andrea Cortese, Tanya Stojkovic, Gorka Fernández-Eulate, Gauthier Remiche, Mattia Gentile, Rudy Van Coster, et al.
Pages: 2156 - 2161
Patents
1 - 2 of 2