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
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: 1 - 6 - 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