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Flavie Ader

Observed names: Ader F, Ader, F, Ader, F., Ader, Flavie, F A Ader, F Ader, F. Ader
Observed institutions: Hôpital Necker-Enfants Malades, Inserm, University of Groningen, Université Paris Cité, Sorbonne Université, Institut Necker Enfants Malades, Hôpital Armand-Trousseau, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Unité de recherche sur les maladies cardiovasculaires et métaboliques, Fondation pour l’innovation en Cadiométabolisme et Nutrition, Université Paris Descartes, Maladies génétiques d’expression pédiatrique, Université Pierre-et-Marie-Curie
ORCID: 0000-0001-7891-3385
Observed ORCID: 0000-0001-7891-3385
OpenAlex ID: A5017743797
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
2021 · Rafik Tadros, Catherine Francis, et al. · Nature Genetics · 284
Postartesunate delayed hemolysis is a predictable event related to the lifesaving effect of artemisinins
2014 · Stéphane Jauréguiberry, Papa A. Ndour, et al. · Blood · 151
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations
2019 · Flavie Ader, Pascal De Groote, et al. · Clinical Genetics · 115
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
2021 · Sophie Garnier, Magdalena Harakalova, et al. · European Heart Journal · 94
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Clinical features and outcomes in carriers of pathogenic desmoplakin variants
2024 · Alessio Gasperetti, Richard T Carrick, et al. · European Heart Journal · 85
Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure
2021 · Mohammed Majid Akhtar, Massimiliano Lorenzini, et al. · JAMA Cardiology · 77
Targeted panel sequencing in adult patients with left ventricular non‐compaction reveals a large genetic heterogeneity
2018 · Pascale Richard, Flavie Ader, et al. · Clinical Genetics · 77
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A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers
2024 · Richard T Carrick, Alessio Gasperetti, et al. · European Heart Journal · 70
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Delayed-Onset Hemolytic Anemia in Patients with Travel-Associated Severe Malaria Treated with Artesunate, France, 2011–2013
2015 · Stéphane Jauréguiberry, Marc Thellier, et al. · Emerging infectious diseases · 66
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PFMG2025–integrating genomic medicine into the national healthcare system in France
2025 · Caroline Abadie, Aldja Abderrahmane, et al. · The Lancet Regional Health - Europe · 57
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Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular Cardiomyopathy
2024 · Alessio Gasperetti, Richard Carrick, et al. · JACC Advances · 48
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Inherited Cardiomyopathies Revealed by Clinically Suspected Myocarditis
2020 · Flavie Ader, Elodie Surget, et al. · Circulation Genomic and Precision Medicine · 45
Routine application of Raman spectroscopy in the quality control of hospital compounded ganciclovir
2014 · Alexandre Amin, Philippe Bourget, et al. · International Journal of Pharmaceutics · 45
High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due toPRKAG2mutations
2016 · Julien Thevenon, Gabriel Laurent, et al. · EP Europace · 43
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Prognostic Role of Myocarditis-Like Episodes and Their Treatment in Patients With Pathogenic Desmoplakin Variants
2025 · Alessio Gasperetti, Steven A. Muller, et al. · Circulation · 36
A novel gain‐of‐function mutation in SCN5A responsible for multifocal ectopic Purkinje‐related premature contractions
2020 · Nicolas Doisne, Victor Waldmann, et al. · Human Mutation · 31
Psychosocial Impact of Predictive Genetic Testing in Hereditary Heart Diseases: The PREDICT Study
2020 · Céline Bordet, Sandrine Brice, et al. · Journal of Clinical Medicine · 26
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External Validation of Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers
2019 · Marine Thuillot, Carole Maupain, et al. · European Journal of Heart Failure · 23
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Titin-related familial dilated cardiomyopathy: factors associated with disease onset
2025 · Renee Johnson, Robert A Fletcher, et al. · European Heart Journal · 20
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Potential selection of genetically balanced spermatozoa based on the hypo-osmotic swelling test in chromosomal rearrangement carriers
2017 · Alexandre Rouen, Léa Carlier, et al. · Reproductive BioMedicine Online · 20
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Systematic analysis of SCN5A variants associated with inherited cardiac diseases
2024 · Alexis Hermida, Guillaume Jedraszak, et al. · Heart Rhythm · 16
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction
2021 · Marie Cambon-Viala, Hilla Gerard, et al. · Journal of Cardiac Failure · 15
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The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms
2020 · Nicolas Chatron, Giuliana Giannuzzi, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 14
Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy
2024 · Flavie Ader, Guillaume Jedraszak, et al. · Clinical Genetics · 10
NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis
2023 · Alexis Hermida, Flavie Ader, et al. · Circulation Genomic and Precision Medicine · 10
Works count: 100
Citation count: 1,605
H-index: 20
I10-index: 25
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