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
- Impact of α-spectrin mutations on the cytoskeleton and organelle organization in neurodegeneration (SpecDroHuman).From1 Sep 2023 → TodayFunding: HORIZON.1.2 - Marie Skłodowska-Curie-actions (MSCA)
- Dissecting the role of the KDM5A overactivity in the pathophysiology of sporadic Inclusion Body myositis : from the deep proteome towards disease models and novel therapies.From27 Apr 2023 → 26 Apr 2024Funding: Foundations, funds and other with scientific goal
- Study of SPTAN1 pathomechanisms: the spectrin complex as a central hub in rare neurological and neuromuscular diseases.From1 Jan 2023 → TodayFunding: FWO research project
- Agreement Born-Bunge Institute and University of Antwerp, 2023-2027.From1 Jan 2023 → TodayFunding: Fund Recuperation Fiscal Exemption
- 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
- 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
21 - 30 of 79
- Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia(2021)
Authors: Manuela Wiessner, Reza Maroofian, Meng-Yuan Ni, Andrea Pedroni, Juliane S. Muller, Rolf Stucka, Christian Beetz, Stephanie Efthymiou, Filippo M. Santorelli, Ahmed A. Alfares, et al.
Pages: 1422 - 1434 - High prevalence of sporadic late-onset nemaline myopathy in a cohort of whole-exome sequencing negative myopathy patients(2021)
Authors: Willem De Ridder, Peter De Jonghe, Volker Straub, Jonathan Baets
Pages: 1154 - 1160 - Efficacy and safety of bimagrumab in sporadic inclusion body myositis(2021)
Authors: Anthony A. Amato, Michael G. Hanna, Pedro M. Machado, Umesh A. Badrising, Hector Chinoy, Olivier Benveniste, Ananda Krishna Karanam, Min Wu, László B. Tankó, Agnes Annette Schubert-Tennigkeit, et al.
Pages: e1595 - e1607 - Assessment of sacsin turnover in patients with ARSACS implications for molecular diagnosis and pathogenesis(2021)
Authors: Fabiana Longo, Daniele De Ritis, Annarita Miluzio, Davide Fraticelli, Jonathan Baets, Marina Scarlato, Filippo M. Santorelli, Stefano Biffo, Francesca Maltecca
Pages: E2315 - E2327 - Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT)(2021)
Authors: James F. Howard, Vera Bril, Tuan Vu, Chafic Karam, Stojan Peric, Temur Margania, Hiroyuki Murai, Malgorzata Bilinska, Roman Shakarishvili, Marek Smilowski, et al.
Pages: 526 - 536 - The ARCA registry(2021)
Authors: Andreas Traschuetz, Selina Reich, Astrid D. Adarmes, Mathieu Anheim, Mahmoud Reza Ashrafi, Jonathan Baets, A. Nazli Basak, Enrico Bertini, Bernard Brais, Cynthia Gagnon, et al.
- Cerebellar ataxia in progressive supranuclear palsy(2021)
Authors: David Crosiers, Anne Sieben, Sarah Ceyssens, Paul Parizel, Jonathan Baets
Pages: 599 - 602 - Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis(2021)
Authors: Julie van der Zee, Lubina Dillen, Yalda Baradaran Heravi, Helena Gossye, Cemile Kocoglu, Ivy Cuijt, Bart Dermaut, Anne Sieben, Jonathan Baets, Peter De Jonghe, et al.
- Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation(2021)
Authors: Danique Beijer, Hong Joo Kim, Lin Guo, Kevin O’Donovan, Inès Mademan, Tine Deconinck, Kristof Van Schil, Charlotte M. Fare, Lauren E. Drake, Alice F. Ford, et al.
- PCYT2 mutations disrupting etherlipid biosynthesis(2021)
Authors: Jonathan De Winter, Willem De Ridder, Matthis Synofzik, Stephan L. Zuchner, Philip Van Damme, Werner Spileers, Jonathan Baets, Jonathan de Winter, Danique Beijer, Matthis Synofzik, et al.