Flavie Ader

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 19

Top Venues

Circulation. Genomic and precision medicine

Clinical genetics

Cells

Biology open

Université Paris-Sud (MSC)

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

Education History

Université Paris-Sud Sep 01 2013 - Sep 01 2014

France

MSC :: Chimie

Publications

Youssef Ed Demri, Clarisse Billon, Mohamed El Hachmi, Mohamed Dembélé, Albert A Hagège, Pascale Richard, Flavie Ader, Diala Kraiche, Damien Bonnet, Xavier Jeunemaitre, Karim Wahbi
Prediction of Positive Genetic Testing for Arrhythmogenic Left Ventricular Cardiomyopathy. Circulation. Genomic and precision medicine (2024)
Alexis Hermida, Flavie Ader, Guillaume Jedraszak, Guillaume Viboud, Véronique Fressart, Anne-Claire Bréhin, Marion Gérard, Diala Kraiche, Asurélien Palmyre, Olivier Paziaud, Elena Popescu, Julie Proukhnitzky, Mikael Laredo, Pascale Richard, Géraldine Vedrenne, Agathe Vernier, Philippe Charron, Estelle Gandjbakhch
Prevalence and Significance of Rare Genetic Variants in AKAP9 in Inherited Cardiac Diseases. Circulation. Genomic and precision medicine 17 (1) (2024)
Flavie Ader, Guillaume Jedraszak, Alexandre Janin, Clarisse Billon, Nathalie Roux Buisson, Adrien Bloch, Meriem Bensalah, Anachiara De Sandre-Giovannoli, Adeline Goudal, Luisa Marsili, Cécile Cazeneuve, Philippe Charron, Gilles Millat, Pascale Richard, null null
Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical genetics 105 (6) (2024)
Flavie Ader, Guillaume Jedraszak, Alexandre Janin, Clarisse Billon, Nathalie Roux Buisson, Adrien Bloch, Meriem Bensalah, Anachiara De Sandre-Giovannoli, Adeline Goudal, Luisa Marsili, Cécile Cazeneuve, Philippe Charron, Gilles Millat, Pascale Richard, null null
Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical genetics (2024)
Alexis Hermida, Flavie Ader, Guillaume Jedraszak, Guillaume Viboud, Véronique Fressart, Anne-Claire Bréhin, Marion Gérard, Diala Kraiche, Asurélien Palmyre, Olivier Paziaud, Elena Popescu, Julie Proukhnitzky, Mikael Laredo, Pascale Richard, Géraldine Vedrenne, Agathe Vernier, Philippe Charron, Estelle Gandjbakhch
Prevalence and Significance of Rare Genetic Variants in AKAP9 in Inherited Cardiac Diseases. Circulation. Genomic and precision medicine 17 (1) (2024)
Alexis Hermida, Flavie Ader, Guillaume Jedraszak, Guillaume Viboud, Véronique Fressart, Anne Claire Bréhin, Marion Gérard, Diala Kraiche, Asurélien Palmyre, Olivier Paziaud, Elena Popescu, Julie Proukhnitzky, Mikael Laredo, Pascale Richard, Geraldine Vedrenne, Agathe Vernier, Philippe Charron, Estelle Gandjbakhch
Prevalence and Significance of Rare Genetic Variants in AKAP9 in Inherited Cardiac Diseases. Circulation. Genomic and precision medicine (2024)
Flavie Ader, Guillaume Jedraszak, Alexandre Janin, Clarisse Billon, Nathalie Roux Buisson, Adrien Bloch, Meriem Bensalah, Anachiara De Sandre-Giovannoli, Adeline Goudal, Luisa Marsili, Cécile Cazeneuve, Philippe Charron, Gilles Millat, Pascale Richard, null null
Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical genetics 105 (6) (2024)
Youssef Ed Demri, Clarisse Billon, Mohamed El Hachmi, Mohamed Dembélé, Albert A Hagège, Pascale Richard, Flavie Ader, Diala Kraiche, Damien Bonnet, Xavier Jeunemaitre, Karim Wahbi
Prediction of Positive Genetic Testing for Arrhythmogenic Left Ventricular Cardiomyopathy. Circulation. Genomic and precision medicine 17 (4) (2024)
Alexis Hermida, Flavie Ader, Gilles Millat, Guillaume Jedraszak, Philippe Maury, Romain Cador, Pierre Antoine Catalan, Gaël Clerici, Nicolas Combes, Pascal De Groote, Delphine Dupin-Deguine, Romain Eschalier, Laurence Olivier-Faivre, Patricia Garcia, Benoit Guillon, Alexandre Janin, Beatrice Kugener, Marylin Lackmy, Mikael Laredo, Xavier Maximin Le Guillou Horn, François Lesaffre, Hugues Lucron, Antoine Milhem, Gwenaël Nadeau, Karine Nguyen, Asurélien Palmyre, Elodie Perdreau, François Picard, Nicolas Rebotier, Pascale Richard, Caroline Rooryck, Julien Seitz, Alain Verloes, Agathe Vernier, Pierre Winum, Grace-A-Dieu Yabeta, Océane Bouchot, Philippe Chevalier, Philippe Charron, Estelle Gandjbakhch
NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis. Circulation. Genomic and precision medicine (2023)
Nathalie Vadrot, Flavie Ader, Maryline Moulin, Marie Merlant, Françoise Chapon, Estelle Gandjbakhch, Fabien Labombarda, Pascale Maragnes, Patricia Réant, Caroline Rooryck, Vincent Probst, Erwan Donal, Pascale Richard, Ana Ferreiro, Brigitte Buendia
Abnormal Cellular Phenotypes Induced by Three TMPO /LAP2 Variants Identified in Men with Cardiomyopathies. Cells 12 (2) (2023)
Nathalie Vadrot, Flavie Ader, Maryline Moulin, Marie Merlant, Françoise Chapon, Estelle Gandjbakhch, Fabien Labombarda, Pascale Maragnes, Patricia Réant, Caroline Rooryck, Vincent Probst, Erwan Donal, Pascale Richard, Ana Ferreiro, Brigitte Buendia
Abnormal Cellular Phenotypes Induced by Three TMPO /LAP2 Variants Identified in Men with Cardiomyopathies. Cells 12 (2) (2023)
Eva Kohaut, Flavie Ader, Caroline Rooryck, Fanny Pelluard, Maryse Bonnière, Gwenaelle André, Fanny Sauvestre, Philippe Roth, Diala Khraiche, Bettina Bessières, Tania Attie-Bitach, Pascale Richard
Morphological and genetic causes of fetal cardiomyopathies. Clinical genetics (2023)
Claire Perret, Carole Proust, Ulrike Esslinger, Flavie Ader, Jan Haas, Jean-François Pruny, Richard Isnard, Pascale Richard, David-Alexandre Trégouët, Philippe Charron, François Cambien, Eric Villard
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis. Clinical genetics (2023)
Nathalie Vadrot, Flavie Ader, Maryline Moulin, Marie Merlant, Françoise Chapon, Estelle Gandjbakhch, Fabien Labombarda, Pascale Maragnes, Patricia Réant, Caroline Rooryck, Vincent Probst, Erwan Donal, Pascale Richard, Ana Ferreiro, Brigitte Buendia
Abnormal Cellular Phenotypes Induced by Three TMPO /LAP2 Variants Identified in Men with Cardiomyopathies. Cells 12 (2) (2023)
Nathalie Vadrot, Flavie Ader, Maryline Moulin, Marie Merlant, Françoise Chapon, Estelle Gandjbakhch, Fabien Labombarda, Pascale Maragnes, Patricia Réant, Caroline Rooryck, Vincent Probst, Erwan Donal, Pascale Richard, Ana Ferreiro, Brigitte Buendia
Abnormal Cellular Phenotypes Induced by Three TMPO /LAP2 Variants Identified in Men with Cardiomyopathies. Cells 12 (2) (2023)
Flavie Ader, Maria Russi, Laura Tixier-Cardoso, Estelle Jullian, Elodie Martin, Pascale Richard, Eric Villard, Veronique Monnier
Drosophila CRISPR/Cas9 mutants as tools to analyse cardiac filamin function and pathogenicity of human FLNC variants. Biology open 11 (9) (2022)
Rafik Tadros, Catherine Francis, Xiao Xu, Alexa M C Vermeer, Andrew R Harper, Roy Huurman, Ken Kelu Bisabu, Roddy Walsh, Edgar T Hoorntje, Wouter P Te Rijdt, Rachel J Buchan, Hannah G van Velzen, Marjon A van Slegtenhorst, Jentien M Vermeulen, Joost Allard Offerhaus, Wenjia Bai, Antonio de Marvao, Najim Lahrouchi, Leander Beekman, Jacco C Karper, Jan Herman Veldink, Elham Kayvanpour, Antonis Pantazis, A John Baksi, Nicola Whiffin, Francesco Mazzarotto, Geraldine Sloane, Hideaki Suzuki, Deborah Schneider-Luftman, Paul Elliott, Pascale Richard, Flavie Ader, Eric Villard, Peter Lichtner, Thomas Meitinger, Michael W T Tanck, van J Peter Tintelen, Andrew Thain, David McCarty, Robert A Hegele, Jason D Roberts, Julie Amyot, Marie-Pierre Dubé, Julia Cadrin-Tourigny, Geneviève Giraldeau, Philippe L L'Allier, Patrick Garceau, Jean-Claude Tardif, S Matthijs Boekholdt, R Thomas Lumbers, Folkert W. Asselbergs, Paul J R Barton, Stuart A Cook, Sanjay K Prasad, Declan P O'Regan, Jolanda van der Velden, Karin J H Verweij, Mario Talajic, Guillaume Lettre, Yigal M Pinto, Benjamin Meder, Philippe Charron, Rudolf A de Boer, Imke Christiaans, Michelle Michels, Arthur A M Wilde, Hugh C Watkins, Paul M Matthews, James Simon Ware, Connie R Bezzina
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Nature genetics 53 (2) (2021)
Nicolas Doisne, Victor Waldmann, Alban Redheuil, Xavier Waintraub, Véronique Fressart, Flavie Ader, Lucie Fossé, Françoise Hidden-Lucet, Estelle Gandjbakhch, Nathalie Neyroud
A novel gain-of-function mutation in SCN5A responsible for multifocal ectopic Purkinje-related premature contractions. Human mutation 41 (4) (2020)
Flavie Ader, Pascal De Groote, Patricia Réant, Caroline Rooryck-Thambo, Delphine Dupin-Deguine, Caroline Rambaud, Diala Khraiche, Claire Perret, Jean François Pruny, Michèle Mathieu-Dramard, Marion Gérard, Yann Troadec, Laurent Gouya, Xavier Jeunemaitre, Lionel Van Maldergem, Albert Hagège, Eric Villard, Philippe Charron, Pascale Richard
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations. Clinical genetics 96 (4) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Flavie Ader