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
31 - 40 of 79
- Unrestrained poly-ADP-ribosylation provides insights into chromatin regulation and human disease(2021)
Authors: Evgeniia Prokhorova, Thomas Agnew, Anne R. Wondisford, Michael Tellier, Nicole Kaminski, Danique Beijer, James Holder, Josephine Groslambert, Marcin J. Suskiewicz, Kang Zhu, et al.
Pages: 2640 - 2655.e8 - Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness(2020)
Authors: Ana Töpf, Katherine Johnson, Adam Bates, Lauren Phillips, Katherine R. Chao, Eleina M. England, Kristen M. Laricchia, Thomas Mullen, Elise Valkanas, Liwen Xu, et al.
Pages: 1478 - 1488 - Reply: A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia; and Novel GDAP2 pathogenic variants cause autosomal recessive spinocerebellar ataxia-27 (SCAR27) in a Chinese family(2020)
Authors: Ilse Eidhof, Jonathan Baets, Erik-Jan Kamsteeg, Annette Schenck, Bart P. van de Warrenburg
- Genetic diagnosis in hereditary motor neuropathies(2020)
Authors: Danique Beijer, Jonathan Baets, Peter De Jonghe
Number of pages: 205 - Tempering our metrics Finding new ways to refine tried and true instruments(2020)
Authors: Victoria H. Lawson, Jonathan Baets
Pages: 373 - 374 - Pathogenic variants in the myosin chaperone UNC-45B cause progressive myopathy with eccentric cores(2020)
Authors: Sandra Donkervoort, Carl E. Kutzner, Ying Hu, Xaviere Lornage, John Rendu, Tanya Stojkovic, Jonathan Baets, Sarah B. Neuhaus, Jantima Tanboon, Reza Maroofian, et al.
Pages: 1078 - 1095 - The expanding genetic landscape of hereditary motor neuropathies(2020)
Authors: Danique Beijer, Jonathan Baets
Pages: 3540 - 3563 - Myostatin(2020)
Authors: Catherine Koch, Suzie Buono, Alexia Menuet, Anne Robé, Sarah Djeddi, Christine Kretz, Raquel Gomez-Oca, Marion Depla, Arnaud Monseur, Leen Thielemans, et al.
Pages: 1178 - 1189 - Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia(2020)
Authors: Darius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, Miriam Wimmer, Angelica D'Amore, Kathrin Eberhardt, Barbara Brechmann, Marvin Ziegler, Dana M. Jensen, Premsai Nagabhyrava, et al.
Pages: 2929 - 2944 - Clinico-genetic, imaging and molecular delineation of COQ8A-ataxia(2020)
Authors: Andreas Traschuetz, Tommaso Schirinzi, Lucia Laugwitz, Nathan H. Murray, Craig A. Bingman, Selina Reich, Jan Kern, Anna Heinzmann, Gessica Vasco, Enrico Bertini, et al.
Pages: 1 - 13