Stephane Zaffran (Stéphane Zaffran)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 38

Top Venues

International journal of molecular sciences

Nature communications

Development (Cambridge, England)

Molecular genetics & genomic medicine

INSERM Délégation régionale Provence Alpes Cote d'Azur et Corse

Aix-Marseille Université (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

INSERM Délégation régionale Provence Alpes Cote d'Azur et Corse Dec 01 2009

France

Directeur de Recherche :: GMGF

CNRS Délégation Provence et Corse Jan 01 2008 - Nov 30 2009

France

Chargé de recherche :: GMGF

CNRS Délégation Provence et Corse Feb 01 2006 - Dec 31 2008

France

Chargé de recherce :: IBDM

CNRS Délégation Paris B Oct 01 2002 - Jan 31 2006

France

Chargé de recherche :: Institut Pasteur

Education History

Aix-Marseille Université Oct 01 1993 - Feb 06 1997

France

PHD

Publications

Camille E Dumas, Célia Rousset, Christopher De Bono, Claudio Cortés, Estelle Jullian, Fabienne Lescroart, Stephane Zaffran, Noritaka Adachi, Robert G Kelly
Retinoic acid signalling regulates branchiomeric neck muscle development at the head/trunk interface. Development (Cambridge, England) 151 (16) (2024)
Lilia Kraoua, Assaad Louati, Sarra Ben Ahmed, Nesrine Abida, Monia Khemiri, Khaled Menif, Ridha Mrad, Stephane Zaffran, Hager Jaouadi
Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy. Molecular genetics & genomic medicine 12 (6) (2024)
Camille E Dumas, Célia Rousset, Christopher De Bono, Claudio Cortés, Estelle Jullian, Fabienne Lescroart, Stephane Zaffran, Noritaka Adachi, Robert G Kelly
Retinoic acid signalling regulates branchiomeric neck muscle development at the head/trunk interface. Development (Cambridge, England) 151 (16) (2024)
Agatha Ribeiro da Silva, Felix Gunawan, Giulia L M Boezio, Emilie Faure, Alexis Theron, Jean-François Avierinos, SoEun Lim, Shivam Govind Jha, Radhan Ramadass, Stefan Günther, Mario Looso, Stephane Zaffran, Thomas Juan, Didier Y R Stainier
egr3 is a mechanosensitive transcription factor gene required for cardiac valve morphogenesis. Science advances 10 (20) (2024)
Lilia Kraoua, Assaad Louati, Sarra Ben Ahmed, Nesrine Abida, Monia Khemiri, Khaled Menif, Ridha Mrad, Stephane Zaffran, Hager Jaouadi
Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy. Molecular genetics & genomic medicine 12 (6) (2024)
Lilia Kraoua, Assaad Louati, Sarra Ben Ahmed, Nesrine Abida, Monia Khemiri, Khaled Menif, Ridha Mrad, Stephane Zaffran, Hager Jaouadi
Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy. Molecular genetics & genomic medicine 12 (6) (2024)
Agatha Ribeiro da Silva, Felix Gunawan, Giulia L M Boezio, Emilie Faure, Alexis Theron, Jean-François Avierinos, SoEun Lim, Shivam Govind Jha, Radhan Ramadass, Stefan Günther, Mario Looso, Stephane Zaffran, Thomas Juan, Didier Y R Stainier
egr3 is a mechanosensitive transcription factor gene required for cardiac valve morphogenesis. Science advances 10 (20) (2024)
Camille E Dumas, Célia Rousset, Christopher De Bono, Claudio Cortés, Estelle Jullian, Fabienne Lescroart, Stephane Zaffran, Noritaka Adachi, Robert G Kelly
Retinoic acid signalling regulates branchiomeric neck muscle development at the head trunk interface. Development (Cambridge, England) (2024)
Agatha Ribeiro da Silva, Felix Gunawan, Giulia L M Boezio, Emilie Faure, Alexis Theron, Jean-François Avierinos, SoEun Lim, Shivam Govind Jha, Radhan Ramadass, Stefan Günther, Mario Looso, Stephane Zaffran, Thomas Juan, Didier Y R Stainier
egr3 is a mechanosensitive transcription factor gene required for cardiac valve morphogenesis. Science advances 10 (20) (2024)
Hager Jaouadi, Chris Jopling, Fanny Bajolle, Alexis Théron, Adèle Faucherre, Hilla Gerard, Sarab Al Dybiat, Caroline Ovaert, Damien Bonnet, Jean-François Avierinos, Stephane Zaffran
Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD. Journal of translational medicine 21 (1) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Hager Jaouadi, Chris Jopling, Fanny Bajolle, Alexis Théron, Adèle Faucherre, Hilla Gerard, Sarab Al Dybiat, Caroline Ovaert, Damien Bonnet, Jean-François Avierinos, Stephane Zaffran
Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD. Journal of translational medicine 21 (1) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Hager Jaouadi, Chris Jopling, Fanny Bajolle, Alexis Théron, Adèle Faucherre, Hilla Gerard, Sarab Al Dybiat, Caroline Ovaert, Damien Bonnet, Jean-François Avierinos, Stephane Zaffran
Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD. Journal of translational medicine 21 (1) (2023)
Gaëlle Odelin, Adèle Faucherre, Damien Marchese, Amélie Pinard, Hager Jaouadi, Solena Le Scouarnec, null null, Raphaël Chiarelli, Younes Achouri, Emilie Faure, Marine Herbane, Alexis Theron, Jean-François Avierinos, Chris Jopling, Gwenaëlle Collod-Béroud, René Rezsohazy, Stephane Zaffran
Variations in the poly-histidine repeat motif of HOXA1 contribute to bicuspid aortic valve in mouse and zebrafish. Nature communications 14 (1) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Stephane Zaffran, Lilia Kraoua, Hager Jaouadi
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy. International journal of molecular sciences 24 (4) (2023)
Gaëlle Odelin, Adèle Faucherre, Damien Marchese, Amélie Pinard, Hager Jaouadi, Solena Le Scouarnec, null null, Raphaël Chiarelli, Younes Achouri, Emilie Faure, Marine Herbane, Alexis Theron, Jean-François Avierinos, Chris Jopling, Gwenaëlle Collod-Béroud, René Rezsohazy, Stephane Zaffran
Variations in the poly-histidine repeat motif of HOXA1 contribute to bicuspid aortic valve in mouse and zebrafish. Nature communications 14 (1) (2023)
Hager Jaouadi, Chris Jopling, Fanny Bajolle, Alexis Théron, Adèle Faucherre, Hilla Gerard, Sarab Al Dybiat, Caroline Ovaert, Damien Bonnet, Jean-François Avierinos, Stephane Zaffran
Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD. Journal of translational medicine 21 (1) (2023)
Gaëlle Odelin, Adèle Faucherre, Damien Marchese, Amélie Pinard, Hager Jaouadi, Solena Le Scouarnec, null null, Raphaël Chiarelli, Younes Achouri, Emilie Faure, Marine Herbane, Alexis Theron, Jean-François Avierinos, Chris Jopling, Gwenaëlle Collod-Béroud, René Rezsohazy, Stephane Zaffran
Variations in the poly-histidine repeat motif of HOXA1 contribute to bicuspid aortic valve in mouse and zebrafish. Nature communications 14 (1) (2023)
Hager Jaouadi, Caroline Ovaert, Chloé Wanert, Aline Cano, Caroline Ovaert, Stephane Zaffran
Dilated-Left Ventricular Non-Compaction Cardiomyopathy in a Pediatric Case with SPEG Compound Heterozygous Variants. International journal of molecular sciences 23 (9) (2022)
Xionghui Lin, Benjamin Swedlund, Mai-Linh Nu Ton, Shila Ghazanfar, Carolina Guibentif, Catherine Paulissen, Elodie Baudelet, Elise Plaindoux, Younes Achouri, Emilie Calonne, Christine Dubois, William Mansfield, Stephane Zaffran, John C Marioni, Francois Fuks, Berthold Göttgens, Fabienne Lescroart, Cédric Blanpain
Mesp1 controls the chromatin and enhancer landscapes essential for spatiotemporal patterning of early cardiovascular progenitors. Nature cell biology 24 (7) (2022)
Hager Jaouadi, Sonia Chabrak, Saida Lahbib, Sonia Abdelhak, Stephane Zaffran
Identification of two variants in AGRN and RPL3L genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance. Clinical case reports 10 (2) (2022)
Hager Jaouadi, Hilla Gérard, Alexis Theron, Gwenaëlle Collod-Béroud, Frédéric Collart, Jean-François Avierinos, Stephane Zaffran
Identification of non-synonymous variations in ROBO1 and GATA5 genes in a family with bicuspid aortic valve disease. Journal of human genetics 67 (9) (2022)
Lilia Kraoua, Hager Jaouadi, Mohamed Allouche, Ahlem Achour, Hakim Kaouther, Habib Ben Ahmed, Lilia Chaker, Faouzi Maazoul, Fatma Ouarda, Stephane Zaffran, Ridha M'rad
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. Molecular genetics & genomic medicine 10 (7) (2022)
Fabienne Lescroart, Stephane Zaffran
Single Cell Approaches to Understand the Earliest Steps in Heart Development. Current cardiology reports 24 (6) (2022)
Hager Jaouadi, Alexis Theron, Jérôme Hourdain, Hélène Martel, Karine Nguyen, Raja Habachi, Jean-Claude Deharo, Frederic Collart, Jean-François Avierinos, Stephane Zaffran
SCN5A Variants as Genetic Arrhythmias Triggers for Familial Bileaflet Mitral Valve Prolapse. International journal of molecular sciences 23 (22) (2022)
Alexis Théron, Anissa Touil, Noémie Résseguier, Gwenaelle Collod-Beroud, Giulia Norscini, Anne-Sophie Simoni, Gaëlle Odelin, Gilbert Habib, Frédéric Collart, Stephane Zaffran, Jean-François Avierinos
Clinical insights into a tertiary care center cohort of patients with bicuspid aortic valve. The international journal of cardiovascular imaging (2021)
Sonia Stefanovic, Heather C Etchevers, Stephane Zaffran
Outflow Tract Formation-Embryonic Origins of Conotruncal Congenital Heart Disease. Journal of cardiovascular development and disease 8 (4) (2021)
Sonia Stefanovic, Brigitte Laforest, Jean-Pierre Desvignes, Fabienne Lescroart, Laurent Argiro, Corinne Maurel-Zaffran, David Salgado, Elise Plaindoux, Christopher De Bono, Kristijan Pazur, Magali Théveniau-Ruissy, Christophe Béroud, Michel Pucéat, Anthony Gavalas, Robert G Kelly, Stephane Zaffran
Hox-dependent coordination of mouse cardiac progenitor cell patterning and differentiation. eLife 9 (2020)
Tui Neri, Emilye Hiriart, Patrick P van Vliet, Emilie Faure, Russell A Norris, Batoul Farhat, Bernd Jagla, Julie Lefrancois, Yukiko Sugi, Thomas Moore-Morris, Stephane Zaffran, Randolph S Faustino, Alexander C Zambon, Jean-Pierre Desvignes, David Salgado, Robert A Levine, José Luis de la Pompa, André Terzic, Sylvia M Evans, Roger Markwald, Michel Pucéat
Human pre-valvular endocardial cells derived from pluripotent stem cells recapitulate cardiac pathophysiological valvulogenesis. Nature communications 10 (1) (2019)
Hager Jaouadi, Amel Ben Chehida, Lilia Kraoua, Heather C Etchevers, Laurent Argiro, Nadia Kasdallah, Sonia Blibech, Valérie Delague, Nicolas Lévy, Néji Tebib, Ridha Mrad, Sonia Abdelhak, Rym Benkhalifa, Stephane Zaffran
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. Genetics research 101 (2019)
Hager Jaouadi, Lilia Kraoua, Lilia Chaker, Alexandre Atkinson, Valérie Delague, Nicolas Levy, Rym Benkhalifa, Ridha Mrad, Sonia Abdelhak, Stephane Zaffran
Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features. Journal of human genetics 63 (10) (2018)
Belén Prados, Paula Gómez-Apiñániz, Tania Papoutsi, Guillermo Luxán, Stephane Zaffran, José María Pérez-Pomares, José Luis de la Pompa
Myocardial Bmp2 gain causes ectopic EMT and promotes cardiomyocyte proliferation and immaturity. Cell death & disease 9 (3) (2018)
Heather C Etchevers, Christian Rose, Birgit Kahle, Helmuth Vorbringer, Frédéric Fina, Pauline Heux, Irina Berger, Benjamin Schwarz, Stephane Zaffran, Nicolas Macagno, Sven Krengel
Giant congenital melanocytic nevus with vascular malformation and epidermal cysts associated with a somatic activating mutation in BRAF. Pigment cell & melanoma research 31 (3) (2018)
Amélie Pinard, Nathalie Eudes, Julia Mitchell, Fanny Bajolle, Maude Grelet, Joséphine Okoronkwo, Damien Bonnet, Gwenaelle Collod-Béroud, Stephane Zaffran
Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect. Molecular biology reports 45 (5) (2018)
Gaëlle Odelin, Emilie Faure, Fanny Coulpier, Maria Di Bonito, Fanny Bajolle, Michèle Studer, Jean-François Avierinos, Patrick Charnay, Piotr Topilko, Stephane Zaffran
Krox20 defines a subpopulation of cardiac neural crest cells contributing to arterial valves and bicuspid aortic valve. Development (Cambridge, England) 145 (1) (2018)

Stephane Zaffran.css-eqlu8i{font-size:small;padding-left:4px;} (Stéphane Zaffran)

Publication Activity (10 Years)

Top Topics

Top Venues

Stephane Zaffran (Stéphane Zaffran)