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
41 - 50 of 63
- Inherited cardiac arrhythmias: identification of novel genes and development of a new diagnostic tool for translating genetic diagnosis into precision medicine.From1 Jan 2017 → 31 Dec 2020Funding: BOF - Concerted Research Project from 1994
- Towards a better understanding of the molecular mechanisms underlying thoracic aortic aneurysms and dissections.From1 Jan 2017 → 31 Dec 2020Funding: FWO research project (including WEAVE projects)
- Genomics and innovative induced pluripotent stem cell (iPSC) modeling to improve understanding of pathomechanisms underlying Brugada syndrome (BrS).From1 Jan 2017 → 31 Dec 2020Funding: FWO Strategic Basic Research Grant
- Disentangling the role of the X-chromosome in the pathogenesis of thoracic aortic aneurysms and dissections.From1 Oct 2016 → 30 Sep 2019Funding: FWO fellowships
- Improving care for cohenisopathies: from heart phenotypes to novel therapies (CoHEART).From1 May 2016 → 30 Apr 2019Funding: FWO research project (including WEAVE projects)
- Exploration of the genetic basis of thoracic aortic aneurysm with focus on bicuspid aortic valve related aortopathy.From1 Oct 2015 → 30 Sep 2020Funding: FWO fundamental clinical research fellowship
- GENOMED - Genomics in Medicine.From1 Jan 2015 → 31 Dec 2019Funding: BOF - Other initiatives, Fund Recuperation Fiscal Exemption
- Identification and characterisation of genes involved in bicuspid aortic valve associated aortopathy.From1 Jan 2015 → 31 Dec 2018Funding: IWT personal funding - strategic basic research grants
- High-Frequency Ultrasound Imaging System Vevo 2100.From19 May 2014 → 31 Dec 2018Funding: Hercules - Small and Medium size research infrastructure
- The (patho)genetic study of bicuspid aortic valve and associated aortic aneurysmFrom1 Oct 2013 → 30 Sep 2016Funding: BOF - Doctoral projects
Publications
1 - 10 of 252
- 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: 1 - 6 - 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 - Decoding the genetic puzzle of inherited cardiac arrhythmias(2024)
Authors: Eline Simons, Maaike Alaerts, Bart Loeys, Dorien Schepers
Number of pages: 201 - Structural genomic variants in thoracic aortic disease(2023)
Authors: Josephina Meester, Anne Hebert, Bart Loeys
Pages: 157 - 161 - 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 - Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population(2023)
Authors: Ewa Sieliwonczyk, Maaike Alaerts, Eline Simons, Dirk Snyders, Aleksandra Nijak, Bert Vandendriessche, Dorien Schepers, Dogan Akdeniz, Emeline Van Craenenbroeck, Katleen Knaepen, et al.
Pages: 1 - 12 - IPSC reprogramming of two patients with spondyloepimetaphyseal dysplasia (SEMD, biglycan type)(2023)
Authors: Pauline De Kinderen, Silke Peeters, Laura Rabaut, Geert Mortier, Peter Ponsaerts, Bart Loeys, Aline Verstraeten, Josephina Meester
Pages: 1 - 5 - 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 - A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation(2023)
Authors: Lotte Van Den Heuvel, Josephina Meester, Melanie Perik, Paul Coucke, Bart Loeys
Pages: 1 - 4 - Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation(2023)
Authors: Ilse Van Gucht, Lucia Buccioli, Laura Rabaut, Ivanna Fedoryshchenko, Josephina Meester, Lut Van Laer, Bart Loeys, Aline Verstraeten
Pages: 1 - 5