Stéphane Zaffran

Biochemistry, Genetics and Molecular Biology · Life Sciences

42h-index8.8kcitations182works3.62yr avg
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Research Topics

Congenital heart defects research(99), Congenital Heart Disease Studies(48), Cardiac Valve Diseases and Treatments(34), Developmental Biology and Gene Regulation(28), Cardiomyopathy and Myosin Studies(14)

Publications182 total

Genome and Transcriptome-Wide Analyses Identify Multiple Candidate Genes and a Significant Polygenic Contribution in Bicuspid Aortic Valve
Circulation·2026
Fostamatinib and the risk of acute aortic dissection in immune thrombocytopenia
British Journal of Clinical Pharmacology·2025Open Access
Loss of primary cilia triggers leaflet remodelling and bicuspid aortic valve formation
Cardiovascular Research·2025Open Access
Corrigendum: Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysis
Frontiers in Medicine·2025Open Access
EGFR-Mediated Mechanotransduction in Aortic Valve Cells: A Key Pathway in Response to Wall Shear Stress
2025Open Access
Multi-modal refinement of the human heart atlas during the first gestational trimester
Development·2025· 7 citedOpen Access
How to Study Gene Expression and Gain of Function of Hoxb1 in Mouse Heart Development
Methods in molecular biology·2025Open Access
Contributors
Elsevier eBooks·2024Open Access
Establishment of a double blood circulation in the developing mouse heart
Elsevier eBooks·2024
Gastruloids are competent to specify both cardiac and skeletal muscle lineages
Nature Communications·2024· 13 citedOpen Access
Multi-modal refinement of the human heart atlas during the first gestational trimester
2024Open Access
Beyond genomic studies of congenital heart defects through systematic modelling and phenotyping
Disease Models & Mechanisms·2024· 3 citedOpen Access
Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysis
Frontiers in Medicine·2024Open Access
Retinoic acid signalling regulates branchiomeric neck muscle development at the head/trunk interface
Development·2024· 3 citedOpen Access
Homozygous <i>TNNI3</i> frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy
Molecular Genetics & Genomic Medicine·2024· 3 citedOpen Access
Degenerative mitral regurgitation due to flail leaflet: sex-related differences in presentation, management, and outcomes
European Heart Journal·2024· 19 citedOpen Access
<i>egr3</i> is a mechanosensitive transcription factor gene required for cardiac valve morphogenesis
Science Advances·2024· 13 citedOpen Access
Identification of Greb1l as a genetic determinant of crisscross heart in mice showing torsion of the heart tube by shortage of progenitor cells
Developmental Cell·2023· 11 citedOpen Access
Identification of Greb1l as a genetic determinant of criss-cross heart in mice showing torsion of the heart tube by shortage of progenitor cells
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Identification of Greb1l as a genetic determinant of criss-cross heart in mice showing torsion of the heart tube by shortage of progenitor cells
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
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Frequent Co-authors

Robert G. Kelly(11), Margaret Buckingham(8), Sonia Stefanovic(7), Fanny Bajolle(5), Manfred Frasch(5), Lucile Ryckebüsch(5), Karen Niederreither(5), M. Roux(5), Martine Astier(5), Michel Sémériva(5), Nicolas Bertrand(4), Heather Etchevers(4), Nicolas Bertrand(4), Brigitte Laforest(4), Emilie Faure(4), Sigolène M. Meilhac(3), Richard P. Harvey(3), Nigel A. Brown(3), Magali Théveniau‐Ruissy(3), Christopher De Bono(3)