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 64
- 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
- Unlocking the missing heritability of thoracic aortic aneurysms.From1 Nov 2023 → TodayFunding: FWO senior postdoctoral fellowship
- 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
Publications
31 - 40 of 253
- The genetics and typical traits of thoracic aortic aneurysm and dissection(2022)
Authors: Jotte Rodrigues Bento, Josephina Meester, Ilse Luyckx, Silke Peeters, Aline Verstraeten, Bart Loeys
Pages: 223 - 253 - Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes(2022)
Authors: Aleksandra Nijak, Eline Simons, Bert Vandendriessche, Dieter Van de Sande, Erik Fransen, Ewa Sieliwonczyk, Ilse Van Gucht, Emeline Van Craenenbroeck, Johan Saenen, Hein Heidbuchel, et al.
- Indications and utility of cardiac genetic testing in athletes(2022)
Authors: Silvia Castelletti, Belinda Gray, Cristina Basso, Elijah R. Behr, Lia Crotti, Perry M. Elliott, Cecilia M. Gonzalez Corcia, Flavio D'Ascenzi, Jodie Ingles, Bart Loeys, et al.
Pages: 1582 - 1591 - Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia(2022)
Authors: Alexandre Persu, Piotr Dobrowolski, Heather L. Gornik, Jeffrey W. Olin, David Adlam, Michel Azizi, Pierre Boutouyrie, Rosa Maria Bruno, Marion Boulanger, Jean-Baptiste Demoulin, et al.
Pages: 65 - 83 - Genomics and innovative induced pluripotent stem cell (iPSC) modeling to improve understanding of pathomechanisms underlying Brugada syndrome (BrS)(2022)
Authors: Aleksandra Nijak, Bart Loeys, Maaike Alaerts, Alain Labro
Number of pages: 234 - Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort(2022)
Authors: Josephina Meester, Silke Peeters, Lotte Van Den Heuvel, Geert Vandeweyer, Erik Fransen, Elizabeth Cappella, Harry C. Dietz, Geoffrey Forbus, Bruce D. Gelb, Elizabeth Goldmuntz, et al.
Pages: 1045 - 1053 - The role of biglycan in the healthy and thoracic aneurysmal aorta(2022)
Authors: Josephina Meester, Pauline De Kinderen, Aline Verstraeten, Bart Loeys
Pages: C1214 - C1222 - Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutation(2022)
Authors: Eline Simons, Aleksandra Nijak, Bart Loeys, Maaike Alaerts
Pages: 1 - 4 - Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder(2022)
Authors: Marije Meuwissen, Aline Verstraeten, Emmanuelle Ranza, Justyna Iwaszkiewicz, Maaike Bastiaansen, Ligia Monica Mateiu, Merlijn Nemegeer, Josephina Meester, Alexandra Afenjar, Michelle Amaral, et al.
Pages: 1583 - 1591 - Generation and validation of an iPSC line (BBANTWi008-A) from a Loeys-Dietz Syndrome type 3 patient(2022)
Authors: Joe Davis Velchev, Aline Verstraeten, Josephina Meester, Peter Ponsaerts, Julie Richer, Maaike Alaerts, Bart Loeys
Pages: 1 - 4