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 → TodayFunding: 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
1 - 10 of 75
- Myelin protein zero mutation-related hereditary neuropathies(2024)
Authors: Juliane Bremer, Axel Meinhardt, Istvan Katona, Jan Senderek, Elke K. Kaemmerer-Gassler, Andreas Roos, Andreas Ferbert, J. Michael Schroeder, Stefan Nikolin, Kay Nolte, et al.
Pages: 1 - 20 - Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients(2024)
Authors: Laura Krumm, Tatyana Pozner, Naime Zagha, Roland Coras, Philipp Arnold, Thanos Tsaktanis, Kathryn Scherpelz, Marie Y. Davis, Johanna Kaindl, Iris Stolzer, et al.
Pages: 1 - 25 - Responsiveness of the scale for the assessment and rating of ataxia and natural history in 884 recessive and early onset ataxia patients(2023)
Authors: Andreas D. Traschuetz, Astrid Adarmes-Gomez, Mathieu Anheim, Jonathan Baets, Bernard Brais, Cynthia Gagnon, Janina Gburek-Augustat, Sarah Doss, Hasmet A. Hanagasi, Christoph Kamm, et al.
Pages: 470 - 485 - 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 - 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 - A homozygous loss of function variant in POPDC3(2023)
Authors: Willem De Ridder, Geert de Vries, Kristof Van Schil, Tine Deconinck, Vincent Mouly, Volker Straub, Jonathan Baets
Pages: 432 - 439 - A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing(2023)
Authors: Anne-Sophie Denomme-Pichon, Leslie Matalonga, Elke de Boer, Adam Jackson, Elisa Benetti, Siddharth Banka, Ange-Line Bruel, Andrea Ciolfi, Jill Clayton-Smith, Bruno Dallapiccola, et al.
Pages: 1 - 15 - Twist exome capture allows for lower average sequence coverage in clinical exome sequencing(2023)
Authors: Burcu Yaldiz, Erdi Kucuk, Juliet Hampstead, Tom Hofste, Rolph Pfundt, Jordi Corominas Galbany, Tuula Rinne, Helger G. Yntema, Alexander Hoischen, Marcel Nelen, et al.
Pages: 1 - 9 - Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14(2023)
Authors: Adam Jackson, Sheng-Jia Lin, Elizabeth A. Jones, Kate E. Chandler, David Orr, Celia Moss, Zahra Haider, Gavin Ryan, Simon Holden, Mike Harrison, et al.
Pages: 1 - 19 - Autosomal recessive cerebellar ataxias in Europe(2023)
Authors: Andreas Traschuetz, Astrid D. Adarmes-Gomez, Mathieu Anheim, Jonathan Baets, Bjoern H. Falkenburger, Janina Gburek-Augustat, Sarah Doss, Christoph Kamm, Peter Klivenyi, Marcus Grobe-Einsler, et al.
Pages: 1109 - 1112