Gustavo Egea unpaid guest prof. Publications Gustavo Egea Sex-and age-dependent neurovascular abnormalities linked to neuroinflammation lead to exacerbated post-ischemic brain injury in Marfan syndrome mice Source Redox Biology - ISSN 2213-2317-83 (2025) p. 1-23 Author(s) Gemma Manich, Belen Perez, …

Silke Peeters unpaid staff Publications Silke Peeters An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Source Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Author(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J. Coucke, Bart Loeys …

Silke Peeters onbezoldigd medewerker Publicaties Silke Peeters An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Bron Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Auteur(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J. Coucke, Bart…

Gustavo Egea onbezoldigd gastprofessor Publicaties Gustavo Egea Sex-and age-dependent neurovascular abnormalities linked to neuroinflammation lead to exacerbated post-ischemic brain injury in Marfan syndrome mice Bron Redox Biology - ISSN 2213-2317-83 (2025) p. 1-23 Auteur(s) Gemma Manich, Belen Per…

Lotte Van Den Heuvel unpaid staff Publications Lotte Van Den Heuvel An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Source Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Author(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J. Couck…

Josephina Meester assistant professor - postdoc researcher FWO Publications Josephina Meester Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Source Genome medicine -…

Josephina Meester docent - postdoc mandaat FWO Publicaties Josephina Meester Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Bron Genome medicine - ISSN 1756-994X-16:…

Lotte Van Den Heuvel onbezoldigd medewerker Publicaties Lotte Van Den Heuvel An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Bron Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Auteur(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J…

Lotte Van Den Heuvel unpaid staff Research Lotte Van Den Heuvel Research team Medical Genetics (MEDGEN) Discovery of genetic modifiers of the phenotypical cardiovascular variability in Marfan syndrome to pave the road to individualized treatment protocols. 01/11/2019 - 31/10/2024 Abstract Marfan syn…

Reihaneh Asadi doctoraatsbursaal Onderzoek Reihaneh Asadi Onderzoeksgroep Medische Genetica (MEDGEN) CRISPR-screening in iPSC-model voor Marfan: een routekaart naar mechanismen en behandeling van aneurysma's. 01/11/2025 - 31/10/2026 Abstract Thoracaal aorta-aneurysma en dissectie (TAAD), waaronder h…

Lotte Van Den Heuvel onbezoldigd medewerker Onderzoek Lotte Van Den Heuvel Onderzoeksgroep Medische Genetica (MEDGEN) Ontdekking van genetische modifiers die de fenotypische cardiovasculaire variabiliteit in Marfan syndroom verklaren voor meer geïndividualiseerde behandelingen. 01/11/2019 - 31/10/2…

Silke Peeters unpaid staff Research Silke Peeters Research team Medical Genetics (MEDGEN) Expertise Our research is focused on the elucidation of the genetic mechanisms causing congenital anomalies and heritable connective tissue disorders with focus on cardiovascular -and growth disorders IPSC-chon…

Silke Peeters onbezoldigd medewerker Onderzoek Silke Peeters Onderzoeksgroep Medische Genetica (MEDGEN) Expertise Ons onderzoek is gericht op de opheldering van de genetische mechanismen die genetische afwijkingen en erfelijke bindweefselaandoeningen veroorzaken, met de nadruk op cardiovasculaire- e…

Wouter Steyaert senior onderzoeker Onderzoek Wouter Steyaert Onderzoeksgroep Medische Genetica (MEDGEN) Expertise Mijn onderzoek richt zich op het vinden van geneesmiddelen voor zeldzame aortapathologieën zoals Marfan syndroom, Loeys-Dietz syndroom en niet-syndromale thoracale aorta aneurysma's. Hi…

Eline Vanaken onbezoldigd medewerker Publicaties Eline Vanaken Six at Sixty : the revised Ghent nosology for Marfan syndrome turns 15-what we have gained, what we have missed Bron Journal of medical genetics - ISSN 0022-2593-62:11 (2025) p. 739-740 Auteur(s) Bart Loeys, Reihaneh Asadi, Eline Vanaken…

Reihaneh Asadi doctoraatsbursaal Publicaties Reihaneh Asadi Six at Sixty : the revised Ghent nosology for Marfan syndrome turns 15-what we have gained, what we have missed Bron Journal of medical genetics - ISSN 0022-2593-62:11 (2025) p. 739-740 Auteur(s) Bart Loeys, Reihaneh Asadi, Eline Vanaken, H…

Lucia Buccioli predoc researcher FWO Publications Lucia Buccioli Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Source International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 Author(s) Ir…

Irene Valdivia Callejon predoc researcher FWO Publications Irene Valdivia Callejon Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Source International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p.…

Wendy Dewals unpaid staff Publications Wendy Dewals Arterial aneurysm and dissection : toward the evolving phenotype of Tatton-Brown-Rahman syndrome Source Journal of medical genetics - ISSN 0022-2593-61:9 (2024) p. 870-877 Author(s) Vicken Totten, Gisela Teixido-Tura, Fermina Lopez-Grondona, Paula …

Lucia Buccioli predoc mandaat FWO Publicaties Lucia Buccioli Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Bron International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 Auteur(s) Irene Va…

Irene Valdivia Callejon predoc mandaat FWO Publicaties Irene Valdivia Callejon Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Bron International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 …

Wendy Dewals onbezoldigd medewerker Publicaties Wendy Dewals Arterial aneurysm and dissection : toward the evolving phenotype of Tatton-Brown-Rahman syndrome Bron Journal of medical genetics - ISSN 0022-2593-61:9 (2024) p. 870-877 Auteur(s) Vicken Totten, Gisela Teixido-Tura, Fermina Lopez-Grondona,…

Bart Loeys gewoon hoogleraar Publicaties Bart Loeys Hooked on translation : leveraging next-generation models to advance interpretation of cardiac variants of uncertain significance, a Brugada syndrome perspective Bron Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2026,223…

Aline Verstraeten associate research professor Publications Aline Verstraeten The complex heritability in thoracic aortic aneurysm and dissection : from clinical insights to stem cell disease modelling Source Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2025,233 p. Author…

Ilse Luyckx senior researcher Publications Ilse Luyckx Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals Source Journal of medical genetics - ISSN 0022-2593-62:3 (2025) p. 199-205 Author(s) Julie Richer, Joe Davis Velchev, Sharan Goobie, Christie A. Boswell-Patterson, Ingrid M.B.H…