Publications by authors named "Stephane Zaffran"

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Fostamatinib and the risk of acute aortic dissection in immune thrombocytopenia.
Paul Dalmas, Alexis Theron, Rita Badaoui, Stéphane Zaffran, Rayid Mchinda

Br J Clin Pharmacol· December 2025

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Loss of primary cilia triggers leaflet remodelling and bicuspid aortic valve formation.
Damien Marchese, Stéphane Zaffran

Cardiovasc Res· September 2025

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Corrigendum: Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysis.
Hager Jaouadi, Victor Morel, Helene Martel, Pierre Lindenbaum, Lorcan Lamy de la Chapelle, Stéphane Zaffran

Front Med (Lausanne)· May 2025

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Multi-modal refinement of the human heart atlas during the first gestational trimester.
Christopher De Bono, Yichi Xu, Samina Kausar, Marine Herbane, Camille Humbert, Stéphane Zaffran

Development· March 2025

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How to Study Gene Expression and Gain of Function of Hoxb1 in Mouse Heart Development.
Christopher De Bono, Fabienne Lescroart, Stéphane Zaffran

Methods Mol Biol· January 2025

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Beyond genomic studies of congenital heart defects through systematic modelling and phenotyping.
Deborah J Henderson, Ahlam Alqahtani, Bill Chaudhry, Andrew Cook, Lorraine Eley, Stephane Zaffran

Dis Model Mech· November 2024

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Gastruloids are competent to specify both cardiac and skeletal muscle lineages.
Laurent Argiro, Céline Chevalier, Caroline Choquet, Nitya Nandkishore, Adeline Ghata, Stéphane Zaffran

Nat Commun· November 2024

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Exome sequencing data reanalysis of 200 hypertrophic cardiomyopathy patients: the HYPERGEN French cohort 5 years after the initial analysis.
Hager Jaouadi, Victor Morel, Helene Martel, Pierre Lindenbaum, Lorcan Lamy de la Chapelle, Stéphane Zaffran

Front Med (Lausanne)· October 2024

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Retinoic acid signalling regulates branchiomeric neck muscle development at the head/trunk interface.
Camille E Dumas, Célia Rousset, Christopher De Bono, Claudio Cortés, Estelle Jullian, Stéphane Zaffran

Development· August 2024

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Degenerative mitral regurgitation due to flail leaflet: sex-related differences in presentation, management, and outcomes.
Jean-Fançois Avierinos, Christophe Tribouilloy, Francesca Bursi, Francesco Grigioni, Jean-Louis Vanoverschelde, Stéphane Zaffran

Eur Heart J· July 2024

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Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy.
Lilia Kraoua, Assaad Louati, Sarra Ben Ahmed, Nesrine Abida, Monia Khemiri, Stéphane Zaffran

Mol Genet Genomic Med· June 2024

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is a mechanosensitive transcription factor gene required for cardiac valve morphogenesis.
Agatha Ribeiro da Silva, Felix Gunawan, Giulia L M Boezio, Emilie Faure, Alexis Théron, Stéphane Zaffran

Sci Adv· May 2024

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Genetic profile and genotype-phenotype correlations in childhood cardiomyopathy.
Chloé Wanert, Fedoua El Louali, Sarab Al Dybiat, Karine Nguyen, Stéphane Zaffran

Arch Cardiovasc Dis· November 2023

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Identification of Greb1l as a genetic determinant of crisscross heart in mice showing torsion of the heart tube by shortage of progenitor cells.
Ségolène Bernheim, Adrien Borgel, Jean-François Le Garrec, Emeline Perthame, Audrey Desgrange, Stéphane Zaffran

Dev Cell· November 2023

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Genetic and phenotypic continuum of HOXA genes: A case with double HOXA9/HOXA13 mutations.
Hager Jaouadi, Alexis Theron, Giulia Norscini, Jean-François Avierinos, Stéphane Zaffran

Mol Med Rep· March 2023

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Variations in the poly-histidine repeat motif of HOXA1 contribute to bicuspid aortic valve in mouse and zebrafish.
Gaëlle Odelin, Adèle Faucherre, Damien Marchese, Amélie Pinard, Hager Jaouadi, Stéphane Zaffran

Nat Commun· March 2023

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Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy.
Stéphane Zaffran, Lilia Kraoua, Hager Jaouadi

Int J Mol Sci· February 2023

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Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD.
Hager Jaouadi, Chris Jopling, Fanny Bajolle, Alexis Théron, Adèle Faucherre, Stéphane Zaffran

J Transl Med· February 2023

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Prognostic value of forward flow indices in primary mitral regurgitation due to mitral valve prolapse.
Elisabeth Petolat, Alexis Theron, Noemie Resseguier, Cyprien Fabre, Giulia Norscini, Stéphane Zaffran

Front Cardiovasc Med· February 2023

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Variants as Genetic Arrhythmias Triggers for Familial Bileaflet Mitral Valve Prolapse.
Hager Jaouadi, Alexis Théron, Jérôme Hourdain, Hélène Martel, Karine Nguyen, Stéphane Zaffran

Int J Mol Sci· November 2022

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Identification of non-synonymous variations in ROBO1 and GATA5 genes in a family with bicuspid aortic valve disease.
Hager Jaouadi, Hilla Gérard, Alexis Théron, Gwenaelle Collod-Béroud, Frédéric Collart, Stéphane Zaffran

J Hum Genet· September 2022

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Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome.
Lilia Kraoua, Hager Jaouadi, Mohamed Allouche, Ahlem Achour, Hakim Kaouther, Stéphane Zaffran

Mol Genet Genomic Med· July 2022

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Mesp1 controls the chromatin and enhancer landscapes essential for spatiotemporal patterning of early cardiovascular progenitors.
Xionghui Lin, Benjamin Swedlund, Mai-Linh N Ton, Shila Ghazanfar, Carolina Guibentif, Stéphane Zaffran

Nat Cell Biol· July 2022

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Single Cell Approaches to Understand the Earliest Steps in Heart Development.
Fabienne Lescroart, Stéphane Zaffran

Curr Cardiol Rep· June 2022

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Dilated-Left Ventricular Non-Compaction Cardiomyopathy in a Pediatric Case with Compound Heterozygous Variants.
Hager Jaouadi, Fedoua El Louali, Chloé Wanert, Aline Cano, Caroline Ovaert, Stéphane Zaffran

Int J Mol Sci· May 2022

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