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List of works by Philippe Charron

'Ten Commandments' of 2015 ESC Guidelines for diagnosis and management of pericardial diseases

2013 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy: the Task Force on cardiac pacing and resynchronization therapy of the European Society of Cardiology (ESC). Developed in collaboration with the European Heart Rhythm Associ

scientific article published on 24 June 2013

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).

scientific article published on 29 August 2014

2015 ESC Guidelines for the Diagnosis and Management of Pericardial Diseases

2015 ESC Guidelines for the diagnosis and management of pericardial diseases: The Task Force for the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology (ESC)Endorsed by: The European Association for Cardio-Thoraci

scientific article published on 29 August 2015

A familial form of conduction defect related to a mutation in the PRKAG2 gene

article

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy

scientific article published on 12 July 2013

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

scientific article

A new approach for the identification of modifier genes in heart failure

article

A new scoring system for the triage of cardiac tamponade

A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity

scientific article published on 14 November 2012

A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy

scientific article

Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population

scientific article published on 01 July 2003

Acquis et perspective de la génétique des myocardiopathies

scientific article published on 01 February 2001

Advising a cardiac disease gene positive yet phenotype negative or borderline abnormal athlete: is sporting disqualification really necessary?

scientific article

Aspects génétiques de la fibrillation auriculaire

scientific article published on 01 August 2003

Assessment of atrial function by myocardial deformation techniques in hypertrophic cardiomyopathy

scientific article published on 31 December 2020

Atlas of the clinical genetics of human dilated cardiomyopathy

scientific article (publication date: 7 May 2015)

Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy

scientific journal article

Brugada ECG pattern: a physiopathological prospective study based on clinical, electrophysiological, angiographic, and genetic findings

scientific article published on 27 December 2012

Brugada syndrome in pure black Africans

scientific article published on 12 December 2007

Cardiac device implantation in Fabry disease: A retrospective monocentric study

scientific article published on October 2016

CardioPulse ArticlesThe 2015 ESC Guidelines on the diagnosis and management of pericardial diseases‘Ten Commandments’ of 2015 ESC Guidelines for diagnosis and management of pericardial diseasesThe Russian National Congress of Cardiology 2015Germa

article

Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy

article

Charcot-Marie-Tooth features and maculopathy in a patient with Danon disease

scientific article published on 01 October 2004

Clinical Features and Prognostic Implications of Familial Hypertrophic Cardiomyopathy Related to the Cardiac Myosin-Binding Protein C Gene ⬇️

scientific article published on June 9, 1998

Clinical genetics in cardiology

scientific article published on August 2006

Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches

scientific article published on 28 October 2015

Contraction delay of the RV outflow tract in patients with Brugada syndrome is dependent on the spontaneous ST-segment elevation pattern

scientific article published on 26 July 2011

Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia

scientific article

Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.

scientific article published on 03 July 2013

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey.

scientific article published in October 2004

Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts

scientific article published in 2013

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice

scientific article

Diagnosis and management of myocardial involvement in systemic immune-mediated diseases: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Disease

scientific article published on 26 June 2017

Diagnostic Value of Electrocardiography and Echocardiography for Familial Hypertrophic Cardiomyopathy in a Genotyped Adult Population ⬇️

scientific article published on July 1, 1997

Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy

Diagnostic value of a two-dimensional echocardiographic score for left ventricular hypertrophy validated by the Imatron CT scan in familial hypertrophic cardiomyopathy

scientific article published in October 2006

Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped children

scientific article published on 01 September 1998

Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases

scientific article published on 4 December 2012

Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry

scientific article published on 11 November 2020

Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

scientific article

Early identification of mutation carriers in familial hypertrophic cardiomyopathy by combined echocardiography and tissue Doppler imaging

scientific article

Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathy.

scientific article published in November 2000

Epidemiology of walker-related injuries and deaths in the United States

scientific article published on 01 May 1995

European Cardiomyopathy Pilot Registry: EURObservational Research Programme of the European Society of Cardiology

scientific article

European Guidelines on Pericardial Diseases: a Focused Review of Novel Aspects

scientific article published on May 2016

Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy

scientific article published on 20 April 2012

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

scientific article

Expanding the phenotype associated with a desmoplakin dominant mutation: Carvajal/Naxos syndrome associated with leukonychia and oligodontia

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

scientific article

FHL2 expression and variants in hypertrophic cardiomyopathy

scientific article

Familial dilated cardiomyopathy: clinical features in French families.

scientific article published on December 1999

Functional characterization of the cAMP-binding proteins Epac in cardiac myocytes

scientific article published on January 2009

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.

scientific article

Genes and their polymorphisms in mono- and multifactorial cardiomyopathies: towards pharmacogenomics in heart failure

scientific article

Genetic advances in sarcomeric cardiomyopathies: state of the art.

scientific article

Genetic analysis for predictive screening in hypertrophic cardiomyopathy ⬇️

scientific article published on February 24, 2012

Genetic aspects of heart failure.

scientific article

Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy

scientific article

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

scientific article published on 07 September 2010

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience

scientific article

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

scientific article published on 15 January 2021

Genotype-phenotype analysis in four families with mutations in β-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy

article

Genotype–phenotype correlations in familial hypertrophic cardiomyopathy A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes

article

Génétique des cardiomyopathies hypertrophiques

scientific article published on 01 May 2003

Génétique des cardiomyopathies héréditaires

Heritable Disease and Sperm Donation

scientific article published in The Journal of the American Medical Association

High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study

scientific article

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

scientific article published in April 2017

Homozygotes for a R869G Mutation in the β -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy

article

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

scientific article (publication date: 6 May 2003)

Hypertrophic obstructive cardiomyopathy

scientific article published on 29 November 2016

Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene

article

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

scientific article

Involvement of BAG3 and HSPB7 loci in various etiologies of systolic heart failure: Results of a European collaboration assembling more than 2000 patients

scientific article published in April 2015

Isolated left ventricular non-compaction in adults: clinical and echocardiographic features in 105 patients. Results from a French registry

article

Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers.

scientific article published on November 2016

Malignant response to ajmaline challenge in SCN5A mutation carriers: Experience from a large familial study

article

Molecular genetics in hypertrophic cardiomyopathy: towards individualized management of the disease

scientific article

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

scientific article published in August 2016

Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy

scientific article

Multimodality imaging in restrictive cardiomyopathies: an EACVI expert consensus document: In collaboration with the 'Working Group on myocardial and pericardial diseases' of the European Society of Cardiology Endorsed by the Indian Academy of Echoc

scientific article published on 16 May 2017

Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene

article

Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy

scientific article (publication date: July 2003)

Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.

scientific article published on 11 April 2016

Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

scientific article

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy

scientific article

Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy.

scientific article published on 14 September 2017

Natural history of Barth syndrome: a national cohort study of 22 patients

scientific article

New Insight into the Variable Expression of Arrhythmogenic Right Ventricular Cardiomyopathy Provided by the Analysis of a Plakophilin-2 Splice Mutation

Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease

scientific article published in March 2006

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations Prediction of clinical status—is molecular genetics a new tool for the management of hypertrophic cardiomyopathy in

article

Penetrance of familial hypertrophic cardiomyopathy

scientific article published on January 1, 1997

Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy.

scientific article

Pregnancy in women with a cardiomyopathy: Outcomes and predictors from a retrospective cohort

scientific article

Prenatal molecular diagnosis in RASA1-related disease

scientific article published on 12 October 2017

Prenatal molecular diagnosis in hypertrophic cardiomyopathy: report of the first case

article by Philippe Charron et al published September 2004 in Prenatal Diagnosis

Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Results of a systematic screening

article

Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases

scientific article published on 19 January 2016

Quantitative Expression of the Mutated Lamin A/C Gene in Patients With Cardiolaminopathy

article

Recommendations for the diagnosis and management of hypertrophic cardiomyopathy in 2014

Recurrent Pericarditis: Modern Approach in 2016.

scientific article published on June 2016

Recurrent suspected myocarditis combined with infrahisian conduction disturbances revealing a desminopathy

scientific article published on 9 June 2015

Relation between QT duration and maximal wall thickness in familial hypertrophic cardiomyopathy

scientific article published on August 2002

Reversible Severe Eosinophilic Endomyocardial Fibrosis During Pregnancy: A Case Report

scientific article

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

scientific article published on 01 January 2012

Risk stratification of sudden death in hypertrophic cardiomyopathy in 2016

scientific article published on 24 May 2016

Role of Genetic Testing in Inherited Cardiovascular Disease: A Review.

scientific article published on 9 August 2017

Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasia

scientific article published on 14 July 2013

Screening patients with hypertrophic cardiomyopathy for Fabry disease using a filter-paper test: the FOCUS study

scientific article published on 9 November 2010

Significance of deep T-wave inversions in asymptomatic athletes with normal cardiovascular examinations: practical solutions for managing the diagnostic conundrum

scientific article

Sporadic arrhythmogenic right ventricular cardiomyopathy/dysplasia due to a de novo mutation

scientific article published on 16 January 2009

Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathies

scientific article

The Public Health Burden of Cardiomyopathies: Insights from a Nationwide Inpatient Study

scientific article published on 27 March 2020

The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the

scientific article published on 05 April 2015

The heart of genomics

Triage strategy for urgent management of cardiac tamponade: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

scientific article published on 7 July 2014

What Should the Cardiologist know about Lamin Disease?

scientific article published on September 2012

What's new in 2015 ESC guidelines on pericardial diseases?

scientific article

Wytyczne ESC dotyczące rozpoznawania i leczenia chorób osierdzia w 2015 roku

article published in 2015

Wytyczne ESC dotyczące rozpoznawania i postępowania w kardiomiopatii przerostowej w 2014 roku

scientific article published on 01 January 2014

[2015 ESC Guidelines for the diagnosis and management of pericardial diseases. Task Force for the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology (ESC)]

scientific article published on 01 December 2015

[A familial form of conduction defects associated with a PRKAG2 gene mutation]

scientific article published on 01 September 2007

[Classification of the cardiomyopathies]

scientific article published on 01 May 2008

[Diagnosis of hypertrophic cardiomyopathy. Validation of criteria using genetics]

scientific article published on 01 December 1998

[Genetic counseling in cardiology]

scientific article published on 01 November 2003

[Hypertrophic cardiomyopathies]

scientific article published on 01 November 2003

[Idiopathic cardiomyopathies]

scientific article published on 01 October 2002

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