Researcher
Bart Loeys
- Keywords:Medicine
- Disciplines:Cardiac and vascular medicine, Diagnostics, Molecular and cell biology, Physiology, Other clinical sciences, Other medical and health sciences, Developmental genetics, Genetics, Clinical genetics and molecular diagnostics
Affiliations
- Medical Genetics (MEDGEN) (Research group)
Responsible
From1 Oct 2022 → Today - Medical Genetics (MEDGEN) (Research group)
Responsible
From1 Jan 2022 → 30 Sep 2022 - Medical Genetics (MEDGEN) (Research group)
Member
From1 Dec 2010 → 31 Dec 2021
Projects
21 - 30 of 64
- Infrastructure for zebrafish modeling of human diseaseFrom1 Dec 2020 → 30 Nov 2021Funding: Fund Recuperation Fiscal Exemption
- In search of genetic modifiers for aortopathy in Loeys-Dietz families with a SMAD3 mutation.From1 Nov 2020 → TodayFunding: FWO fellowships
- Elucidating the pathogenicity of genetic variants of uncertain significance in Brugada syndrome patients by functional modelling in hiPSC-derived cardiomyocytes and zebrafish.From1 Nov 2020 → TodayFunding: FWO fellowships
- Cardiogenomics.From1 Oct 2020 → TodayFunding: BOF - ZAP BOF mandates
- Optical mapping of in vivo cardiac mechanics in zebrafish: exploring the pathogenesis and mode of inheritance in catecholaminergic polymorphic ventricular tachycardia.From1 Oct 2020 → 30 Sep 2022Funding: FWO fellowships
- Multi-well microelectrode array (MEA): a bridge to highthroughput electrophysiology.From1 May 2020 → TodayFunding: FWO Medium Size Research Infrastructure
- Subsidy for Center Medical Genetics.From1 Jan 2020 → 31 Dec 2021Funding: Other Flemish public, semi-private and pararegional institutions not mentioned elsewhere
- Pathomechanistic study of biglycan mutations in aortopathy and skeletal dysplasia.From1 Jan 2020 → 31 Dec 2023Funding: FWO research project (including WEAVE projects)
- BMP signalling in vascular biology and disease signallingFrom1 Jan 2020 → TodayFunding: FWO scientific research network
- Discovering the role of titin (TTN) in anthracycline-induced cardiac dysfunction in breast cancer.From1 Nov 2019 → 31 Oct 2021Funding: FWO fellowships
Publications
1 - 10 of 253
- Flemish network on rare connective tissue diseases (CTD)(2024)
Authors: Y. Piette, F. van den Bossche, J. Aerts, N. Aerts, S. Ajeganova, V. Badot, N. Berghen, D. Blockmans, G. Brusselle, N. Caeyers, et al.
Pages: 26 - 33 - Homozygous SMAD6 variants in two unrelated patients with craniosynostosis and radioulnar synostosis(2024)
Authors: Ilse Luyckx, Isaac Scott Walton, Nele Boeckx, Kristof Van Schil, Chingyiu Pang, Helen Lord, Christopher Mark Watson, David T. Bonthron, Lut Van Laer, Andrew O.M. Wilkie, et al.
Pages: 363 - 368 - Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome(2024)
Authors: Josephina Meester, Anne Hebert, Maaike Bastiaansen, Laura Rabaut, Jarl Bastianen, Nele Boeckx, Kathryn Ashcroft, Paldeep S. Atwal, Antoine Benichou, Clarisse Billon, et al.
Pages: 1 - 9 - Decoding the genetic puzzle of inherited cardiac arrhythmias(2024)
Authors: Eline Simons, Maaike Alaerts, Bart Loeys, Dorien Schepers
Number of pages: 201 - 2023 ESC Guidelines for the management of cardiomyopathies Developed by the task force on the management of cardiomyopathies of the European Society of Cardiology (ESC)(2023)
Authors: Elena Arbelo, Alexandros Protonotarios, Juan R. Gimeno, Eloisa Arbustini, Roberto Barriales-Villa, Cristina Basso, Connie R. Bezzina, Elena Biagini, Nico A. Blom, Rudolf A. de Boer, et al.
Pages: 3503 - 3626 - Structural genomic variants in thoracic aortic disease(2023)
Authors: Josephina Meester, Anne Hebert, Bart Loeys
Pages: 157 - 161 - Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier(2023)
Authors: Melanie Perik, Emmanuela Govaerts, Steven Laga, Inge Goovaerts, Johan Saenen, Emeline Van Craenenbroeck, Josephina Meester, Ilse Luyckx, Inez Rodrigus, Aline Verstraeten, et al.
Pages: 1 - 7 - Growth charts for Marfan syndrome in the Netherlands and analysis of genotype-phenotype relationships(2023)
Authors: Peter Lauffer, Gerard Pals, Aeilko H. Zwinderman, Floor A.M. Postema, Marieke J.H. Baars, Eelco Dulfer, Yvonne Hilhorst-Hofstee, Arjan C. Houweling, Marlies Kempers, Ingrid P.C. Krapels, et al.
Pages: 479 - 489 - Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseases(2023)
Authors: Sofia Papadimitriou, Barbara Gravel, Charlotte Nachtegael, Elfride De Baere, Bart Loeys, Miikka Vikkula, Guillaume Smits, Tom Lenaerts
Pages: 1 - 11 - Genetic association analysis of 77,539 genomes reveals rare disease etiologies(2023)
Authors: Daniel Greene, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P.J. Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, et al.
Pages: 679 - 688