Marjolijn Renard

Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection

Marjolijn Renard, Catherine Francis, Rajarshi Ghosh et al. · Journal of the American College of Cardiology · 2018 · 289 citations · Full text

Clinical Validity, Aortic Diseases, Genetics +7

Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome

Jorge Oller, Nerea Méndez‐Barbero, Erly J. Ruiz et al. · Nature Medicine · 2017 · 172 citations

Inflammation, Metalloprotease Adamts1, Marfan Syndrome +12

Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD

Marjolijn Renard, Bert Callewaert, Machteld Baetens et al. · International Journal of Cardiology · 2011 · 166 citations · Full text

Acta2 Mutations, Molecular Physiology, Signal Transduction +9

Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency

Marjolijn Renard, Tammy M. Holm, Regan Veith et al. · European Journal of Human Genetics · 2010 · 150 citations · Full text

Inflammation, Fibrosis, Cardiovascular Manifestations +9

New insights into the pathogenesis of autosomal‐dominant cutis laxa with report of five<i>ELN</i>mutations

Bert Callewaert, Marjolijn Renard, Vishwanathan Hucthagowder et al. · Human Mutation · 2011 · 133 citations · Full text