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ADER Flavie
ADER Flavie
Sorbonne Université- Hôpital Pitié Salpatrière
Verified email at aphp.fr
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Cited by
Year
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
R Tadros, C Francis, X Xu, AMC Vermeer, AR Harper, R Huurman, ...
Nature genetics 53 (2), 128-134, 2021
1712021
Postartesunate delayed hemolysis is a predictable event related to the lifesaving effect of artemisinins
S Jauréguiberry, PA Ndour, C Roussel, F Ader, I Safeukui, M Nguyen, ...
Blood, The Journal of the American Society of Hematology 124 (2), 167-175, 2014
1532014
Targeted panel sequencing in adult patients with left ventricular non‐compaction reveals a large genetic heterogeneity
P Richard, F Ader, M Roux, E Donal, JC Eicher, N Aoutil, O Huttin, ...
Clinical Genetics 95 (3), 356-367, 2019
802019
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations
F Ader, P De Groote, P Réant, C Rooryck‐Thambo, D Dupin‐Deguine, ...
Clinical Genetics 96 (4), 317-329, 2019
792019
Delayed-onset hemolytic anemia in patients with travel-associated severe malaria treated with artesunate, France, 2011–2013
S Jauréguiberry, M Thellier, PA Ndour, F Ader, C Roussel, R Sonneville, ...
Emerging infectious diseases 21 (5), 804, 2015
592015
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25. 1 and 22q11. 23
S Garnier, M Harakalova, S Weiss, M Mokry, V Regitz-Zagrosek, ...
European heart journal 42 (20), 2000-2011, 2021
552021
High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutations
J Thevenon, G Laurent, F Ader, P Laforêt, D Klug, A Duva Pentiah, ...
Europace 19 (4), 651-659, 2017
492017
Association of left ventricular systolic dysfunction among carriers of truncating variants in filamin C with frequent ventricular arrhythmia and end-stage heart failure
MM Akhtar, M Lorenzini, M Pavlou, JP Ochoa, C O’mahony, ...
JAMA cardiology 6 (8), 891-901, 2021
452021
Routine application of Raman spectroscopy in the quality control of hospital compounded ganciclovir
A Amin, P Bourget, F Vidal, F Ader
International Journal of Pharmaceutics 474 (1-2), 193-201, 2014
292014
Potential selection of genetically balanced spermatozoa based on the hypo-osmotic swelling test in chromosomal rearrangement carriers
A Rouen, L Carlier, S Heide, M Egloff, P Marzin, F Ader, M Schwartz, ...
Reproductive BioMedicine Online 35 (4), 372-378, 2017
252017
Inherited cardiomyopathies revealed by clinically suspected myocarditis: highlights from genetic testing
F Ader, E Surget, P Charron, A Redheuil, A Zouaghi, A Maltret, E Marijon, ...
Circulation: Genomic and Precision Medicine 13 (4), e002744, 2020
242020
A novel gain‐of‐function mutation in SCN5A responsible for multifocal ectopic Purkinje‐related premature contractions
N Doisne, V Waldmann, A Redheuil, X Waintraub, V Fressart, F Ader, ...
Human Mutation 41 (4), 850-859, 2020
222020
Phenotype/genotype relationship in left ventricular noncompaction: ion channel gene mutations are associated with preserved left ventricular systolic function and biventricular …
M Cambon-Viala, H Gerard, K Nguyen, P Richard, F Ader, JF Pruny, ...
Journal of Cardiac Failure 27 (6), 677-681, 2021
152021
Psychosocial impact of predictive genetic testing in hereditary heart diseases: the PREDICT study
C Bordet, S Brice, C Maupain, E Gandjbakhch, B Isidor, A Palmyre, ...
Journal of clinical medicine 9 (5), 1365, 2020
152020
External validation of risk factors for malignant ventricular arrhythmias in lamin A/C mutation carriers.
M Thuillot, C Maupain, E Gandjbakhch, X Waintraub, F Hidden-Lucet, ...
European Journal of Heart Failure 21 (2), 253-254, 2019
152019
Contribution and limits of a non‐intrusive Raman spectroscopic method compared with HPLC for routine application to pre‐delivery analytical control of two major camptothecin …
A Amin, P Bourget, F Ader, F Vidal, C Neuzillet, A Baillet‐Guffroy
Journal of Raman Spectroscopy 46 (12), 1283-1290, 2015
82015
Prognosis of adults with isolated left ventricular non-compaction: Results of a prospective multicentric study
H Gerard, N Iline, H Martel, K Nguyen, P Richard, E Donal, JC Eicher, ...
Frontiers in Cardiovascular Medicine 9, 856160, 2022
72022
A 14q distal chromoanagenesis elucidated by whole genome sequencing
F Ader, S Heide, P Marzin, A Afenjar, F Diguet, SC Bastaraud, ...
European Journal of Medical Genetics 63 (4), 103776, 2020
62020
The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms
N Chatron, G Giannuzzi, PA Rollat-Farnier, F Diguet, E Porcu, T Yammine, ...
bioRxiv, 2020.07. 17.206771, 2020
42020
Drosophila CRISPR/Cas9 mutants as tools to analyse cardiac filamin function and pathogenicity of human FLNC variants
F Ader, M Russi, L Tixier-Cardoso, E Jullian, E Martin, P Richard, E Villard, ...
Biology Open 11 (9), bio059376, 2022
32022
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