Researcher
Marjolijn Renard
- Disciplines:Epigenetics, Clinical genetics and molecular diagnostics, Immunogenetics, Genetics
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → 1 Nov 2019 - Department of Civil engineering (Department)
Member
From1 Oct 2010 → 28 Feb 2013 - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 2006 → 30 Sep 2018
Projects
1 - 1 of 1
- Study of the genetic basis and molecular pathogenesis of cardiovascular manifestations in heritable thoracic aortic aneurysmsFrom1 Oct 2014 → 1 Nov 2019Funding: FWO fellowships, BOF - Other initiatives
Publications
1 - 10 of 55
- Unraveling the role of TGFβ signaling in thoracic aortic aneurysm and dissection using Fbn1 mutant mouse models(2023)
Authors: Violette Deleeuw, Eric Carlson, Marjolijn Renard, Keith D. Zientek, Phillip A. Wilmarth, Ashok P. Reddy, Elise C. Manalo, Sara F. Tufa, Douglas R. Keene, Margie Olbinado, et al.
Pages: 17 - 33 - Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm(2021)
Authors: Sandy Elbitar, Marjolijn Renard, Pauline Arnaud, Nadine Hanna, Marie-Paule Jacob, Dong-Chuan Guo, Ko Tsutsui, Marie-Sylvie Gross, Ketty Kessler, Laurent Tosolini, et al.
Pages: 111 - 122 - Ambulatory electrocardiographic monitoring and ectopic beat detection in conscious mice(2020)
Authors: Felke Steijns, Máté István Tóth, Anthony Demolder, Lars Emil Larsen, Jana Desloovere, Marjolijn Renard, Robrecht Raedt, Patrick Segers, Julie De Backer, Patrick Sips
- MEK1/2 inhibition in murine heart and aorta after oral administration of refametinib supplemented drinking water(2020)
Authors: Felke Steijns, Nathalie Bracke, Marjolijn Renard, Julie De Backer, Patrick Sips, Nathan Debunne, Evelien Wynendaele, Frederick Verbeke, Bart De Spiegeleer, Laurence Campens
- Spontaneous right ventricular pseudoaneurysms and increased arrhythmogenicity in a mouse model of Marfan syndrome(2020)
Authors: Felke Steijns, Marjolijn Renard, Marine Vanhomwegen, Petra Vermassen, Jana Desloovere, Robrecht Raedt, Lars Emil Larsen, Máté István Tóth, Julie De Backer, Patrick Sips
- Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects(2020)
Authors: Annekatrien Boel, Joyce Burger, Marine Vanhomwegen, Aude Beyens, Marjolijn Renard, Sander Barnhoorn, Christophe Casteleyn, Dieter Reinhardt, Benedicte Descamps, Christian Vanhove, et al.
Pages: 1476 - 1488 - Reply: More genes for thoracic aortic aneurysms and dissections(2019)
Authors: Marjolijn Renard, Dianna M Milewicz, Julie De Backer
Pages: 529 - 530 - A heart for fibrillin : spatial arrangement in adult wild-type murine myocardial tissue(2018)
Authors: Felke Steijns, Jolanda van Hengel, Patrick Sips, Julie De Backer, Marjolijn Renard
Pages: 271 - 280 - Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice(2018)
Authors: Marjolijn Renard, Suzanne Vanhauwaert, Marine Vanhomwegen, Ali Rihani, Niels Vandamme, Steven Goossens, Geert Berx, Pieter Van Vlierberghe, Jody J Haigh, Bieke Decaesteker, et al.
- Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology guidelines for the interpretation of sequenced variants in the FBN1 gene for Marfan syndrome : proposal for a disease- and gene-specific guideline(2018)
Authors: Laura Muiño Mosquera, Felke Steijns, Tjorven Audenaert, Ilse Meerschaut, Anne De Paepe, Wouter Steyaert, Sofie Symoens, Paul Coucke, Bert Callewaert, Marjolijn Renard, et al.