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M. Renard · SciRah

Researcher profile · Semantic Scholar

M. Renard

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M. Renard — researcher profile on SciRah

h-index: 24
Works: 59
Citations: 2,430

Most-cited papers

FBN1: The Disease-Causing Gene for Marfan Syndrome and Other Genetic Disorders
L. Sakai, D. Keene, M. Renard, J. De Backer
2016Gene318 citations Open access
Semantic Scholar
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection
M. Renard, C. Francis, R. Ghosh, Alan F. Scott +18 more
2018Journal of the American College of Cardiology267 citations Open access
Semantic Scholar
Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.
M. Renard, B. Callewaert, M. Baetens, L. Campens +12 more
2013International Journal of Cardiology172 citations Open access
Semantic Scholar
Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome
J. Oller, N. Méndez-Barbero, E. J. Ruiz, Silvia Villahoz +14 more
2017Nature Medicine167 citations Open access
Semantic Scholar
Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency
M. Renard, T. Holm, R. Veith, B. Callewaert +13 more
2010European Journal of Human Genetics161 citations Open access
Semantic Scholar
The Loeys–Dietz syndrome: an update for the clinician
Christine Van Hemelrijk, M. Renard, B. Loeys
2010Current Opinion in Cardiology145 citations
Semantic Scholar
New insights into the pathogenesis of autosomal dominant cutis laxa with report of five ELN mutations
B. Callewaert, M. Renard, V. Hucthagowder, B. Albrecht +11 more
2011Human Mutation128 citations Open access
Semantic Scholar
In-frame mutations in exon 1 of SKI cause dominant Shprintzen-Goldberg syndrome.
V. Carmignac, J. Thevenon, L. Adès, B. Callewaert +34 more
2012American Journal of Human Genetics114 citations Open access
Semantic Scholar
Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys‐Dietz syndromes
M. Baetens, L. Van Laer, K. De Leeneer, J. Hellemans +11 more
2011Human Mutation91 citations Open access
Semantic Scholar
Gene panel sequencing in heritable thoracic aortic disorders and related entities – results of comprehensive testing in a cohort of 264 patients
L. Campens, B. Callewaert, Laura Muiño Mosquera, M. Renard +4 more
2015Orphanet Journal of Rare Diseases83 citations Open access
Semantic Scholar
The Ghent Marfan Trial--a randomized, double-blind placebo controlled trial with losartan in Marfan patients treated with β-blockers.
Katarina Möberg, S. De Nobele, D. Devos, E. Goetghebeur +8 more
2012International Journal of Cardiology67 citations Open access
Semantic Scholar
Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2.
M. Renard, B. Callewaert, F. Malfait, L. Campens +7 more
2013International Journal of Cardiology62 citations
Semantic Scholar
Identification of binding partners interacting with the α1-N-propeptide of type V collagen.
S. Symoens, M. Renard, C. Bonod-Bidaud, D. Syx +8 more
2011Biochemical Journal58 citations Open access
Semantic Scholar
COL5A1 signal peptide mutations interfere with protein secretion and cause classic Ehlers‐Danlos syndrome
S. Symoens, F. Malfait, M. Renard, J. André +4 more
2009Human Mutation58 citations Open access
Semantic Scholar
An Integrated Framework to Quantitatively Link Mouse-Specific Hemodynamics to Aneurysm Formation in Angiotensin II-infused ApoE −/− mice
B. Trachet, M. Renard, G. De Santis, S. Staelens +4 more
2011Annals of Biomedical Engineering54 citations
Semantic Scholar
Sex, pregnancy and aortic disease in Marfan syndrome
M. Renard, L. Muiño-Mosquera, Elise C. Manalo, S. Tufa +4 more
2017PLoS ONE52 citations Open access
Semantic Scholar
Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical determinant of human vascular elastogenesis
M. Kappanayil, S. Nampoothiri, R. Kannan, M. Renard +8 more
2012Orphanet Journal of Rare Diseases51 citations Open access
Semantic Scholar
Intrinsic cardiomyopathy in Marfan syndrome: results from in-vivo and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans
L. Campens, M. Renard, B. Trachet, P. Segers +5 more
2015Pediatric Research48 citations
Semantic Scholar
Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm
S. Elbitar, M. Renard, P. Arnaud, N. Hanna +31 more
2020Genetics in Medicine43 citations Open access
Semantic Scholar
Replacing Vascular Corrosion Casting by In Vivo Micro-CT Imaging for Building 3D Cardiovascular Models in Mice
B. Vandeghinste, B. Trachet, M. Renard, C. Casteleyn +4 more
2011Molecular Imaging and Biology41 citations Open access
Semantic Scholar
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
L. Muiño-Mosquera, Felke Steijns, Tjorven Audenaert, Ilse Meerschaut +7 more
2018Circulation Genomic and Precision Medicine34 citations Open access
Semantic Scholar
Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity
S. Hadj-Rabia, B. Callewaert, E. Bourrat, M. Kempers +10 more
2013Orphanet Journal of Rare Diseases34 citations Open access
Semantic Scholar
Multiple aneurysms in a patient with aneurysms-osteoarthritis syndrome.
Thomas Martens, I. van Herzeele, F. De Ryck, M. Renard +4 more
2013Annals of Thoracic Surgery26 citations Open access
Semantic Scholar
Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort
J. Meester, Silke Peeters, Lotte J. F. Van Den Heuvel, G. Vandeweyer +23 more
2022Genetics in Medicine24 citations Open access
Semantic Scholar
Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections.
J. De Backer, M. Renard, L. Campens, L. M. Mosquera +4 more
2015Current pharmaceutical design16 citations
Semantic Scholar
A heart for fibrillin: spatial arrangement in adult wild-type murine myocardial tissue
Felke Steijns, J. van Hengel, P. Sips, J. De Backer +1 more
2018Histochemistry and Cell Biology14 citations
Semantic Scholar
Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome
S. L. Van Driest, L. Sleeper, B. Gelb, S. Morris +20 more
2020Jornal de Pediatria13 citations Open access
Semantic Scholar
Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice
M. Renard, Suzanne Vanhauwaert, M. Vanhomwegen, A. Rihani +11 more
2018Scientific Reports13 citations Open access
Semantic Scholar
Absence of Cardiovascular Manifestations in a Haploinsufficient Tgfbr1 Mouse Model
M. Renard, B. Trachet, C. Casteleyn, L. Campens +14 more
2014PLoS ONE11 citations Open access
Semantic Scholar
Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects.
A. Boel, J. Burger, M. Vanhomwegen, A. Beyens +11 more
2020Human Molecular Genetics10 citations Open access
Semantic Scholar
Unraveling the Role of TGFβ Signaling in Thoracic Aortic Aneurysm and Dissection Using Fbn1 Mutant Mouse Models.
V. Deleeuw, Eric J. Carlson, M. Renard, K. Zientek +13 more
2023Matrix Biology9 citations Open access
Semantic Scholar
Longitudinal follow-up of ascending versus abdominal aortic aneurysm formation in angiotensin II-infused ApoE mice
B. Trachet, M. Renard, C. Van der Donckt, S. Deleye +5 more
2014Artery Research8 citations Open access
Semantic Scholar
Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious Mice
Felke Steijns, Máté I. Tóth, A. Demolder, L. E. Larsen +6 more
2020Italian National Conference on Sensors7 citations Open access
Semantic Scholar
New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections.
L. Campens, M. Renard, B. Callewaert, P. Coucke +2 more
2013Polskie Archiwum Medycyny Wewnetrznej7 citations Open access
Semantic Scholar
MEK1/2 Inhibition in Murine Heart and Aorta After Oral Administration of Refametinib Supplemented Drinking Water
Felke Steijns, N. Bracke, M. Renard, J. De Backer +6 more
2020Frontiers in Pharmacology5 citations Open access
Semantic Scholar
Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome
Felke Steijns, M. Renard, M. Vanhomwegen, P. Vermassen +6 more
2020International Journal of Molecular Sciences5 citations Open access
Semantic Scholar
Genes in Thoracic Aortic Aneurysms and Dissections – Do they Matter?
J. De Backer, M. Renard, L. Campens, K. François +3 more
2013Aorta5 citations Open access
Semantic Scholar
Correction: Sex, pregnancy and aortic disease in Marfan syndrome
M. Renard, L. Muiño-Mosquera, Elise C. Manalo, S. Tufa +4 more
2018PLoS ONE4 citations Open access
Semantic Scholar
SmgGDS, a new piece in the thoracic aortic aneurysm and dissection puzzle.
M. Renard
2018Journal of Thoracic Disease2 citations Open access
Semantic Scholar
SLC2A knockout mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects
A. Boel, J. Burger, M. Vanhomwegen, A. Beyens +11 more
2019bioRxiv1 citations Open access
Semantic Scholar
Reply: More Genes for Thoracic Aortic Aneurysms and Dissections.
M. Renard, D. Milewicz, J. De Backer
2019Journal of the American College of Cardiology1 citations Open access
Semantic Scholar
Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndrome
Elke Verstraeten, S. Symoens, M. Renard, B. Callewaert +7 more
2010Clinical Dysmorphology1 citations
Semantic Scholar
Intercalated discs : specialized cytoskeletal anchors in cardiac muscle
J. van Hengel, M. D. De Smet, A. Kremer, S. Lippens +3 more
20190 citations
Semantic Scholar
TGFβ and aortic disease severity in MFS
M. Renard, Elise C. Manalo, S. Tufa, D. Keene +2 more
20180 citations
Semantic Scholar
Study of the molecular pathogenesis of thoracic aortic aneurysms
M. Renard
20130 citations
Semantic Scholar
Marfan related cardiomyopathy: an in vivo and in vitro study of the fbn1C1039G/+ mouse model
L. Campens, M. Renard, B. Trachet, P. Segers +2 more
20130 citations
Semantic Scholar
Hemodynamics in Ascending and Abdominal Aorta Aneurysm Formation in the ApoE−/− Angiotensin II Mouse Model
B. Trachet, M. Renard, J. Bols, S. Staelens +2 more
20120 citations
Semantic Scholar
Development of a novel COL3A1 transgenic mouse model for vascular Ehlers Danlos Syndrome
Yike Kang, S. Symoens, F. Malfait, P. Coucke +12 more
20120 citations
Semantic Scholar
Is there a role for hemodynamics in AAA formation? A longitudinal in-vivo study in ApoE -/- mice
B. Trachet, M. Renard, G. De Santis, S. Staelens +3 more
20110 citations
Semantic Scholar
A longitudinal study in ApoE mice comparing baseline hemodynamics to endstage aneurysm location in a mouse-specific way
B. Trachet, M. Renard, G. De Santis, S. Staelens +4 more
20110 citations
Semantic Scholar

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