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
1 - 10 of 63
- Fibrillinopathies in mice and humans: from single cell to therapeutic targeting.From1 Jan 2024 → TodayFunding: FWO research project (including WEAVE projects)
- Using human iPSC-derived models to investigate the divergent pathomechanisms underlying biglycan-related Meester-Loeys syndrome and X-linked spondyloepimetaphyseal dysplasia.From1 Nov 2023 → TodayFunding: FWO fellowships
- Towards patient-specific aorta-on-a-chip models for thoracic aortic aneurysm and dissection.From1 Nov 2023 → TodayFunding: FWO fellowships
- Pushing boundaries in Loeys-Dietz syndrome research through aorta-on-a-chip development.From1 Oct 2023 → TodayFunding: BOF - doctoral mandates
- Identification of disease-associated bicuspid aortic valve-related aortopathy genes by using single cell exploration of a smad6 mouse model for outflow tract abnormalities (Grant Award voor Ilse Luyckx).From4 Apr 2023 → TodayFunding: Foundations, funds and other with scientific goal
- Application of new genomics technology on the road to personalized medicine.From1 Nov 2022 → TodayFunding: Fund Recuperation Fiscal Exemption
- Investigating thoracic aortic aneurysm pathogenesis at single-cell resolution.From1 Nov 2022 → TodayFunding: FWO fellowships
- Identification of novel treatment targets through improved pathomechanistic insight in IPO8 deficient aortopathy.From1 Nov 2022 → TodayFunding: FWO fellowships
- Support BOF EU Horizon Europe project (Horizon Europe - EIC pathfinder Challenge: Cardiogenomics.From4 Oct 2022 → 3 Oct 2023Funding: BOF - projects
- Interrogation of the contribution of endothelial cells to aortic aneurysmal disease: unraveling the TGF-ß paradox and the role of nitric oxide.From1 Oct 2022 → TodayFunding: FWO senior postdoctoral fellowship
Publications
221 - 230 of 252
- New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish(2010)
Authors: Deborah J. Morris-Rosendahl, Reeval Segel, A. Peter Born, Christoph Conrad, Bart Loeys, Susan Sklower Brooks, Laura Mueller, Christine Zeschnigk, Christina Botti, Ron Rabinowitz, et al.
Pages: 1100 - 1106 - Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome(2010)
Authors: Bart Loeys, E. E. Gerber, D. Riegert-Johnson, S. Iqbal, P. Whiteman, V. McConnell, C. R. Chillakuri, D. Macaya, P. J. Coucke, A. De Paepe, et al.
- Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features(2010)
Authors: Elke Verstraeten, Sofie Symoens, Marjolijn Renard, Bert Callewaert, Kristof Vandekerckhove, Julie De Backer, Fransiska Malfait, Paul Coucke, Anne De Paepe, Bart Loeys
Pages: 119 - 122 - Clinical utility gene card for: Marfan syndrome type 1 and related phenotypes [FBN1](2010)
Authors: Mine Arslan-Kirchner, Eloisa Arbustini, Catherine Boileau, Anne Child, Gwenaelle Collod-Beroud, Anne De Paepe, Joerg Epplen, Guillaume Jondeau, Bart Loeys, Laurence Faivre
- Het Marfansyndroom(2010)
Authors: J. de Backer, M. Renard, P. Coucke, Lut Van Laer, A. de Paepe, Bart Loeys
Pages: 1024 - 1028 - Renal insufficiency, a frequent complication with age in oral-facial-digital syndrome type I(2010)
Authors: S. Saal, L. Faivre, Bernard Aral, N. Gigot, A. Toutain, L. Van Maldergem, A. Destree, I. Maystadt, J-P Cosyns, P-S Jouk, et al.
Pages: 258 - 265 - Musculoskeletal Findings of Loeys-Dietz Syndrome(2010)
Authors: Gurkan Erkula, Paul D. Sponseller, Laura C. Paulsen, Gretchen L. Oswald, Bart Loeys, Harry C. Dietz
Pages: 1876 - 1883 - Neuroradiologic Manifestations of Loeys-Dietz Syndrome Type 1(2009)
Authors: V. J. Rodrigues, S. Elsayed, Bart Loeys, H. C. Dietz, D. M. Yousem
Pages: 1614 - 1619 - Challenges for CNV interpretation in clinical molecular karyotyping(2009)
Authors: Karen Buysse, Barbara Della Chiaie, Rudy Van Coster, Bart Loeys, Anne De Paepe, Frank Speleman, Björn Menten
Pages: 398 - 403 - Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutation(2009)
Authors: L. Faivre, G. Collod-Beroud, B. Callewaert, A. Child, C. Binquet, E. Gautier, Bart Loeys, E. Arbustini, K. Mayer, M. Arslan-Kirchner, et al.
Pages: 491 - 501