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authFullName_s : Philippe Charron

Multicenter Experience With Catheter Ablation for Ventricular Tachycardia in Lamin A/C Cardiomyopathy

Saurabh Kumar , Alexander F.A. Androulakis , Jean-Marc Sellal , Philippe Maury , Estelle Gandjbakhch , et al.
Circulation. Arrhythmia and electrophysiology, 2016, 9 (8), pp.e004357. ⟨10.1161/CIRCEP.116.004357⟩
Journal articles hal-03233139v1
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FHL2 expression and variants in hypertrophic cardiomyopathy

Felix W. Friedrich , Silke Reischmann , Aileen Schwalm , Andrea Unger , Deepak Ramanujam , et al.
Basic Research in Cardiology, 2014, 109, pp.451. ⟨10.1007/s00395-014-0451-8⟩
Journal articles hal-01110561v1

High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutations

Julien Thevenon , Gabriel Laurent , Flavie Ader , Pascal Laforêt , Didier Klug , et al.
EP-Europace, 2017, 19 (4), pp.651-659. ⟨10.1093/europace/euw067⟩
Journal articles hal-01444277v1
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Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methods

Pascal Amedro , Oscar Werner , Hamouda Abassi , Aymeric Boisson , Luc Souilla , et al.
Health and Quality of Life Outcomes, 2021, 19 (1), pp.187. ⟨10.1186/s12955-021-01825-6⟩
Journal articles hal-03310460v2

Prognosis of Adults With Isolated Left Ventricular Non-Compaction: Results of a Prospective Multicentric Study

Hilla Gerard , Nicolas Iline , Hélène Martel , Karine Nguyen , Pascale Richard , et al.
Frontiers in Cardiovascular Medicine, 2022, 9, ⟨10.3389/fcvm.2022.856160⟩
Journal articles hal-03999097v1

Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure

Mohammed Majid Akhtar , Massimiliano Lorenzini , Menelaos Pavlou , Juan Pablo Ochoa , Constantinos O’mahony , et al.
JAMA Cardiology, 2021, ⟨10.1001/jamacardio.2021.1106⟩
Journal articles hal-03280888v1
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FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations

Flavie Ader , Pascal de Groote , Patricia Réant , Caroline Rooryck-Thambo , Delphine Dupin-Deguine , et al.
Clinical Genetics, 2019, 96 (4), pp.317-329. ⟨10.1111/cge.13594⟩
Journal articles hal-02268422v1
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Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity

Pascale Richard , Flavie Ader , Maguelonne Roux , Erwan Donal , Jean-Christophe Eicher , et al.
Clinical Genetics, 2019, 95 (3), pp.356-367. ⟨10.1111/cge.13484⟩
Journal articles hal-02055778v1
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Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia

Joel Fedida , Veronique Fressart , Philippe Charron , Elodie Surget , Tiphaine Hery , et al.
PLoS ONE, 2017, 12 (8), pp.e0181840. ⟨10.1371/journal.pone.0181840⟩
Journal articles hal-01579640v1
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Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathy

Isabelle Marey , Véronique Fressart , Caroline Rambaud , Paul Fornès , Laurent Martin , et al.
SAGE Open Medicine, 2020, 15 (1), pp.435-446. ⟨10.1515/med-2020-0150⟩
Journal articles hal-02898070v1
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Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: results of a systematic screening.

Nathalie Roux-Buisson , Estelle Gandjbakhch , Erwan Donal , Vincent Probst , Jean-Claude Deharo , et al.
Heart Rhythm, 2014, pp.1999-2009
Journal articles inserm-01120324v1
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Psychosocial Impact of Predictive Genetic Testing in Hereditary Heart Diseases: The PREDICT Study

Celine Bordet , Sandrine Brice , Carole Maupain , Estelle Gandjbakhch , Bertrand Isidor , et al.
Journal of Clinical Medicine, 2020, 9 (5), pp.1365. ⟨10.3390/jcm9051365⟩
Journal articles hal-02882035v1
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Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction

Marie Cambon-Viala , Hilla Gerard , Karine Nguyen , Pascale Richard , Flavie Ader , et al.
Journal of Cardiac Failure, 2021, 27 (6), pp.677-681. ⟨10.1016/j.cardfail.2021.01.007⟩
Journal articles hal-04073195v1
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Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

Ulrike Esslinger , Sophie Garnier , Agathe Korniat , Carole Proust , Georgios Kararigas , et al.
PLoS ONE, 2020, 15 (2), pp.e0229472. ⟨10.1371/journal.pone.0229472⟩
Journal articles hal-02949402v1

Inherited Cardiomyopathies Revealed by Clinically Suspected Myocarditis

Flavie Ader , Elodie Surget , Philippe Charron , Alban Redheuil , Amir Zouaghi , et al.
Circulation: Genomic and Precision Medicine, 2020, 13 (4), pp.e002744. ⟨10.1161/CIRCGEN.119.002744⟩
Journal articles inserm-03996719v1
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Genotype-phenotype correlations of pathogenic variants in the FLNC gene

Flavie Ader , Eric Villard , Céline Ledeuil , Philippe Charron , Pascale Richard
Médecine/Sciences, 2018, 34, pp.39-41. ⟨10.1051/medsci/201834s211⟩
Journal articles inserm-03996754v1
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Natural history of Barth syndrome: a national cohort study of 22 patients.

Charlotte Rigaud , Anne-Sophie Lebre , Renaud Touraine , Blandine Beaupain , Chris Ottolenghi , et al.
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.70. ⟨10.1186/1750-1172-8-70⟩
Journal articles inserm-00823569v1

External validation of risk factors for malignant ventricular arrhythmias in lamin A/C mutation carriers

Marine Thuillot , Carole Maupain , Estelle Gandjbakhch , Xavier Waintraub , Françoise Hidden-Lucet , et al.
European Journal of Heart Failure, 2019, 21 (2), pp.253-254. ⟨10.1002/ejhf.1384⟩
Journal articles hal-02153574v1
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Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.

Veronique Fressart , Guillaume Duthoit , Erwan Donal , Vincent Probst , Jean-Claude Deharo , et al.
EP-Europace, 2010, 12 (6), pp.861-8. ⟨10.1093/europace/euq104⟩
Journal articles inserm-00588266v1
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The Public Health Burden of Cardiomyopathies: Insights from a Nationwide Inpatient Study

Simon Lannou , Nicolas Mansencal , Cécile Couchoud , Mathilde Lassalle , Olivier Dubourg , et al.
Journal of Clinical Medicine, 2020, 9 (4), pp.920. ⟨10.3390/jcm9040920⟩
Journal articles hal-02883447v1
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Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients

Sophie Garnier , Christian Hengstenberg , Nicolas Lamblin , Olivier Dubourg , Pascal de Groote , et al.
International Journal of Cardiology, 2015, 189, pp.105-107. ⟨10.1016/j.ijcard.2015.04.003⟩
Journal articles hal-01143379v1
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Global and regional echocardiographic strain to assess the early phase of hypertrophic cardiomyopathy due to sarcomeric mutations

Guillaume Baudry , Nicolas Mansencal , Amélie Reynaud , Pascale Richard , Olivier Dubourg , et al.
European Heart Journal - Cardiovascular Imaging, 2019, 21 (3), pp.291-298. ⟨10.1093/ehjci/jez084⟩
Journal articles hal-02883415v1
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Saw-Tooth Cardiomyopathy: Clinical Presentation and Genetic Analysis

Julie Proukhnitzky , Jérôme Garot , Céline Bordet , Lise Legrand , Flavie Ader , et al.
JACC: Case Reports, 2020, 2 (8), pp.1205-1209. ⟨10.1016/j.jaccas.2020.05.072⟩
Journal articles inserm-03996698v1
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The value of electrocardiography and echocardiography in distinguishing Fabry disease from sarcomeric hypertrophic cardiomyopathy

Nicolas Junqua , Damien Legallois , Sophie Segard , Olivier Lairez , Patricia Réant , et al.
Archives of cardiovascular diseases, 2020, 113 (8-9), pp.542-550. ⟨10.1016/j.acvd.2020.04.008⟩
Journal articles hal-02945476v1

Prevalence of familial hypercholesterolaemia in patients presenting with premature acute coronary syndrome

Marie Hauguel-Moreau , Vincent Aïdan , Hélène Hergault , Alain Beauchet , Marion Pépin , et al.
Archives of cardiovascular diseases, 2022, 115 (2), pp.87-95. ⟨10.1016/j.acvd.2021.11.005⟩
Journal articles hal-04006296v1
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Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition

Marie Gizon , Laëtitia Duboscq-Bidot , Lina El Kassar , Pierre Bobin , Flavie Ader , et al.
Stem Cell Research, 2022, 60, pp.102680. ⟨10.1016/j.scr.2022.102680⟩
Journal articles hal-03549731v1
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Multifocal Ectopic Purkinje-Related Premature Contractions: A New SCN5A-Related Cardiac Channelopathy.

Gabriel Laurent , Samuel Saal , Mohamed Yassine Amarouch , Delphine M. Béziau , Roos F. J. Marsman , et al.
Journal of the American College of Cardiology, 2012, 60 (2), pp.144-56. ⟨10.1016/j.jacc.2012.02.052⟩
Journal articles inserm-00719034v1
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Whole Exome Sequencing Reveals a Large Genetic Heterogeneity and Revisits the Causes of Hypertrophic Cardiomyopathy

Karine Nguyen , Stéphane Roche , Erwan Donal , Sylvie Odent , Jean-Christophe Eicher , et al.
Circulation: Genomic and Precision Medicine, 2019, 12 (5), pp.e002500. ⟨10.1161/CIRCGEN.119.002500⟩
Journal articles hal-02140150v1
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Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches

Mine Arslan-Kirchner , Eloisa Arbustini , Catherine Boileau , Philippe Charron , Anne Child , et al.
European Journal of Human Genetics, 2015, 24 (1), pp.146 - 150. ⟨10.1038/ejhg.2015.225⟩
Journal articles hal-01670149v1

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

Ulrike Esslinger , Sophie Garnier , Agathe Korniat , Carole Proust , Georgios Kararigas , et al.
PLoS ONE, 2017, 12 (3), pp.e0172995. ⟨10.1371/journal.pone.0172995⟩
Journal articles hal-03571195v1