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
51 - 60 of 63
- The (patho)genetic study of bicuspid aortic valve and associated aortic aneurysmFrom1 Oct 2013 → 30 Sep 2016Funding: BOF - Doctoral projects
- Bicuspid Related Aortopathy, a Vibrant Exploration (BRAVE).From1 May 2013 → 30 Apr 2018Funding: Fund Recuperation Fiscal Exemption, ERC - Ideas, Own budget, for example: patrimony, inscription fees, gifts
- Mechanistic interrogation of Bicuspid Aortic Valve associated aortapathy.From1 Jan 2013 → 31 Dec 2018Funding: Foreign foundations, funds with scientific view
- Investigation of the genetic basis and the pathogenic mechanisms involved in bicuspid aortic valve associated thoracic aortic aneurysm.From1 Oct 2012 → 30 Sep 2016Funding: BOF - Other initiatives
- The (patho)genetic study of bicuspid aortic valve and associated aortic aneurysm.From1 Oct 2012 → 30 Sep 2013Funding: Fund Recuperation Fiscal Exemption
- Sudden cardiac death: translating genetic technology into improved clinical care.From1 Sep 2012 → 31 Aug 2014Funding: IWT - TBM (Applied Biomedical Research)
- Pathogenetic study of the intersection of two frequent monogenic diseases: the Marfan syndrome and autosomal dominant polycystic kidney disease.From1 Jan 2012 → 31 Dec 2015Funding: IWT personal funding - strategic basic research grants
- Clinical and (patho)genetic study of bicuspid aortic valve and associated aortic aneurysm.From1 Jan 2012 → 31 Dec 2015Funding: FWO research project (including WEAVE projects)
- Physiopathological and genetic study of the intersection of two frequent monogenic disorders: the Marfan syndrome and autosomal dominant polycystic kidney disease.From30 Aug 2011 → 29 Aug 2012Funding: Other Flemish scientific institutions
- Gene and microRNA discovery in the pathogenesis of aortic aneurysms.From26 Jul 2011 → 25 Jul 2012Funding: Foundations, funds and other with scientific goal
Publications
1 - 10 of 252
- 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: 1 - 6 - 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 - Neutrophilic dermatoses and aneurysms(2023)
Authors: Sofie Stappers, Inge Swinnen, Vasiliki Siozopoulou, Julie Bastin, Anthony De Smet, Marc Dubois, Bart Loeys, Olivier Aerts
Pages: e1461 - e1464 - IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC)(2023)
Authors: Pauline De Kinderen, Laura Rabaut, Melanie Perik, Peter Ponsaerts, Bart Loeys, Geert Mortier, Josephina Meester, Aline Verstraeten
Pages: 1 - 5 - 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 - 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 - 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