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Heart (British Cardiac Society)|January 11, 2025
Modern clinical genetics in cardiologyPhilippe Charron, Julie Proukhnitzky
JACC. Case Reports|July 28, 2021
Saw-Tooth Cardiomyopathy: Clinical Presentation and Genetic AnalysisJulie Proukhnitzky, Jérôme Garot, Céline Bordet, et al.
ESC Heart Failure|February 16, 2024
Pregnancy and cardiac maternal outcomes in women with inherited cardiomyopathy: interest of the CARPREG II risk scoreThomas Wallet, Lise Legrand, Richard Isnard, et al.
Archives of Cardiovascular Diseases|April 26, 2024
Molecular genetic screening after non-ischaemic sudden cardiac arrest and no overt cardiomyopathy in real life: A major tool for the aetiological diagnostic work-upOrianne Weizman, Estelle Gandjbakhch, Isabelle Magnin-Poull, et al.
European Journal of Preventive Cardiology|February 14, 2025
A family-based strategy to identify and prevent premature cardiovascular disease: a feasibility pilot-studyPierre Charleux, Niki Procopi, Ghilas Rahoual, et al.
Circulation Research|March 17, 2020
Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial CardiomyopathyNadine Suffee, Thomas Moore-Morris, Bernd Jagla, et al.
Heart Rhythm|May 16, 2026
Sudden cardiac death and major arrhythmic events in patients with Fabry disease: risk stratification in the FHFc multicenter studyYassine Temmar, Julie Proukhnitzky, Nicolas Lamblin, et al.
Clinical Genetics|January 23, 2025
Exploring the Familial Phenotypic Variability Associated With TTN Truncating Variants in Cardiomyopathies: Variant Spectrum, Genotype-Phenotype Correlation and Consequences in Genetic CounselingMarie Massier, Pascal de Groote, Erwan Donal, et al.
Orphanet Journal of Rare Diseases|June 10, 2025
Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosisAurélien Palmyre, Fairouz Koraichi, Flavie Ader, et al.
International Journal of Cardiology|November 16, 2024
Clinical impact of genetic testing in a large cohort of pediatric cardiomyopathiesFlavie Ader, Neil Derridj, Anne Claire Brehin, et al.
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