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Hypertrophic obstructive cardiomyopathy

The Lancet (British edition), 2017-03, Vol.389 (10075), p.1253-1267

2017

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High intraspecific genome diversity in the model arbuscular mycorrhizal symbiont Rhizophagus irregularis

The New phytologist, 2018-12, Vol.220 (4), p.1161-1171

2018

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

Journal of the American College of Cardiology, 2016-11, Vol.68 (21), p.2299-2307

2016

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The 2015 ESC Guidelines on the diagnosis and management of pericardial diseases

European heart journal, 2015-11, Vol.36 (42), p.2873-2874

2015

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VariantDetective: an accurate all-in-one pipeline for detecting consensus bacterial SNPs and SVs

Bioinformatics (Oxford, England), 2024-02, Vol.40 (2)

2024

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Extreme diversification of the mating type–high-mobility group (MATA-HMG) gene family in a plant-associated arbuscular mycorrhizal fungus

The New phytologist, 2014-01, Vol.201 (1), p.254-268

2014

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

European journal of heart failure, 2011-02, Vol.13 (2), p.177-185

2011

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Evidence for the sexual origin of heterokaryosis in arbuscular mycorrhizal fungi

Nature microbiology, 2016-03, Vol.1 (6), p.16033

2016

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

European journal of heart failure, 2019-02, Vol.21 (2), p.253-254

2019

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

Orphanet journal of rare diseases, 2013-05, Vol.8 (1), p.70-70

2013

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

Archives of cardiovascular diseases, 2022-02, Vol.115 (2), p.87-95

2022

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Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition

Stem cell research, 2022-04, Vol.60, p.102680-102680, Article 102680

2022

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Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected control

Stem cell research, 2021-04, Vol.52, p.102245-102245, Article 102245

2021

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Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathy

Open medicine (Warsaw, Poland), 2020-01, Vol.15 (1), p.435-446

2020

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Prospective follow-up in various subtypes of cardiomyopathies: insights from the ESC EORP Cardiomyopathy Registry

European heart journal. Quality of care & clinical outcomes, 2021-04, Vol.7 (2), p.134-142

2021

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Influence of genomic variations on glanders serodiagnostic antigens using integrative genomic and transcriptomic approaches

Frontiers in veterinary science, 2023-12, Vol.10, p.1217135-1217135

2023

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

Journal of clinical medicine, 2020-03, Vol.9 (4), p.920

2020

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

European journal of human genetics : EJHG, 2016-01, Vol.24 (1), p.e1-150

2016

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

European heart journal, 2005-04, Vol.26 (8), p.794-803

2005

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

European heart journal, 2009-09, Vol.30 (17), p.2128-2136

2009

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

Cardiovascular research, 2008-01, Vol.77 (1), p.118-125

2008

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

Neuromuscular disorders : NMD, 2012-03, Vol.22 (3), p.211-218

2012

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Hypertrophic obstructive cardiomyopathy

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

High intraspecific genome diversity in the model arbuscular mycorrhizal symbiont Rhizophagus irregularis

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

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

The 2015 ESC Guidelines on the diagnosis and management of pericardial diseases

VariantDetective: an accurate all-in-one pipeline for detecting consensus bacterial SNPs and SVs

Extreme diversification of the mating type–high-mobility group (MATA-HMG) gene family in a plant-associated arbuscular mycorrhizal fungus

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

Evidence for the sexual origin of heterokaryosis in arbuscular mycorrhizal fungi

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

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

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

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

Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition

Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected control

Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathy

Prospective follow-up in various subtypes of cardiomyopathies: insights from the ESC EORP Cardiomyopathy Registry

Influence of genomic variations on glanders serodiagnostic antigens using integrative genomic and transcriptomic approaches

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

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

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

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

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

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

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