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
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 - 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: Joyce Burger, Aude Beyens, Marjolijn Renard, Sander Barnhoorn, Christophe Casteleyn, Dieter Reinhardt, Benedicte Descamps, Christian Vanhove, Ingrid van der Pluijm, Jeroen Essers, et al.
Pages: 1476 - 1488 - Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice(2018)
Authors: Marjolijn Renard, Suzanne Vanhauwaert, Ali Rihani, Niels Vandamme, Pieter Van Vlierberghe, Jody J Haigh, Bieke Decaesteker, Irina Lambertz
- 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: Felke Steijns, Tjorven Audenaert, Ilse Meerschaut, Wouter Steyaert, Bert Callewaert, Marjolijn Renard
- SmgGDS, a new piece in the thoracic aortic aneurysm and dissection puzzle(2018)
Authors: Marjolijn Renard
Pages: S4133 - S4136 - Intrinsic cardiomyopathy in Marfan syndrome: results from in- and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans(2015)
Authors: Laurence Campens, Marjolijn Renard, Bram Trachet, Laura Muiño Mosquera, Lynn Sakai
Pages: 256 - 263 - Marfan syndrome and related heritable thoracic aortic aneurysms and dissections(2015)
Authors: Marjolijn Renard, Laurence Campens, Laura Muiño Mosquera, Bert Callewaert, Yskert von Kodolitsch
Pages: 4061 - 4075 - Gene panel sequencing in heritable thoracic aortic disorders and related entities: results of comprehensive testing in a cohort of 264 patients(2015)
Authors: Laurence Campens, Bert Callewaert, Laura Muiño Mosquera, Marjolijn Renard