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
11 - 20 of 253
- 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 - 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 - 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 - 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 - 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 - Novel association of the NOTCH pathway regulator MIB1 gene with the development of bicuspid aortic valve(2023)
Authors: Idit Tessler, Juliette Albuisson, Rebeca Pineiro-Sabaris, Aline Verstraeten, Hatem Elif Kamber Kaya, Marcos Siguero-Alvarez, Guillaume Goudot, Donal MacGrogan, Ilse Luyckx, Shoshana Shpitzen, et al.
Pages: 721 - 731 - Marfan Syndrome(2023)
Authors: Annemiek Snoeckx, Bart Loeys
Pages: 1 - 10 - Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping(2023)
Authors: Ewa Sieliwonczyk, Bert Vandendriessche, Charlotte Claes, Evy Mayeur, Maaike Alaerts, Philip Holmgren, Tycho Canter Cremers, Dirk Snyders, Bart Loeys, Dorien Schepers
Pages: 1 - 13 - HTAD patient pathway(2023)
Authors: Maryanne Caruana, Marieke J. Baars, Evy Bashiardes, Kalman Benke, Erik Bjorck, Andrei Codreanu, Elena de Moya Rubio, Julia Dumfarth, Arturo Evangelista, Maarten Groenink, et al.
Pages: 1 - 9