Citation Impact
Citing Papers
2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death
2018
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
2014 Standout
2016 ESC Position Paper on cancer treatments and cardiovascular toxicity developed under the auspices of the ESC Committee for Practice Guidelines
2016 Standout
Guidelines for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack
2014 Standout
TREM-1 Mediates Inflammatory Injury and Cardiac Remodeling Following Myocardial Infarction
2015
Exonic mutations in SCN9A (Na V 1.7) are found in a minority of patients with erythromelalgia
2014
Features, Evaluation and Treatment Coronavirus (COVID-19)
2020 Standout
Electrical Storm in the Brain and in the Heart: Epilepsy and Brugada Syndrome
2013
Benchmarking the stability of human detergent-solubilised voltage-gated sodium channels for structural studies using eel as a reference
2015 StandoutNobel
Novel Insight Into the Natural History of Short QT Syndrome
2013
Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe
2018 StandoutNobel
Long COVID: major findings, mechanisms and recommendations
2023 Standout
The Clinical Significance of Pregnancy in Brugada Syndrome
2013
Structures of the calcium-activated, non-selective cation channel TRPM4
2017 Nature
Na+ Channel ? Subunits: Overachievers of the Ion Channel Family
2011
Ryanodine receptors and ventricular arrhythmias: Emerging trends in mutations, mechanisms and therapies
2006
Sudden death in patients without structural heart disease
2004
A human ether-á-go-go-related (hERG) ion channel atomistic model generated by long supercomputer molecular dynamics simulations and its use in predicting drug cardiotoxicity
2014 StandoutNobel
Recommendations for Noninvasive Evaluation of Native Valvular Regurgitation
2017 Standout
Voltage-Gated Sodium Channels: Mutations, Channelopathies and Targets
2011
Sudden infant death syndrome–associated mutations in the sodium channel beta subunits
2010
Risk Stratification of Individuals with the Brugada Electrocardiogram: A Meta‐Analysis
2006
J-Point Elevation in Survivors of Primary Ventricular Fibrillation and Matched Control Subjects
2008
hERG potassium channels and cardiac arrhythmia
2006 Nature
Molecular mechanisms of epithelial–mesenchymal transition
2014 Standout
Early cardiac hypertrophy in mice with impaired calmodulin regulation of cardiac muscle Ca2+ release channel
2007 StandoutNobel
Sudden cardiac death with normal heart:
2010
Regulation of the cardiac voltage‐gated Na+ channel (H1) by the ubiquitin‐protein ligase Nedd4
2000
Prognosis research strategy (PROGRESS) 1: A framework for researching clinical outcomes
2013
Genetics of Human Cardiovascular Disease
2012
Exercise Standards for Testing and Training
2013 Standout
A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y
2006
Ventricular Arrhythmias in the Absence of Structural Heart Disease
2012
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)
2003
Network medicine: a network-based approach to human disease
2010 Standout
The genetic basis of long QT and short QT syndromes: A mutation update
2009
ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities
2008 Standout
Mitral regurgitation
2009
Modeling the human Na<sub>v</sub>1.5 sodium channel: structural and mechanistic insights of ion permeation and drug blockade
2017 StandoutNobel
Mouse models of SCN5A-related cardiac arrhythmias
2008
Influência da gestação na evolução clínica materno-fetal de portadoras de cardiomiopatia hipertrófica
2007
A structure-based computational workflow to predict liability and binding modes of small molecules to hERG
2020 StandoutNobel
Serum biochemistry profile, inflammatory cytokines, adipokines and cardiovascular findings in obese dogs
2016
Cardiovascular diseases burden in COVID-19: Systematic review and meta-analysis
2020
Evaluation of genes associated with human myxomatous mitral valve disease in dogs with familial myxomatous mitral valve degeneration
2017
TGFβ and BMP signaling in cardiac cushion formation: Lessons from mice and chicken
2012
A mechanism for sudden infant death syndrome (SIDS): Stress-induced leak via ryanodine receptors
2007
Myocarditis
2011 Standout
Four potassium channel mutations account for 73% of the genetic spectrum underlying long‐QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland
2004
System survival of nontransvenous implantable cardioverter-defibrillators compared to transvenous implantable cardioverter-defibrillators in pediatric and congenital heart disease patients
2009
Electrical Storm in Brugada Syndrome during Pregnancy
2010
De Novo Mutation in the SCN5A Gene Associated with Brugada Syndrome
2015
Inherited disorders of voltage-gated sodium channels
2005
In vitro pharmacologic testing using human induced pluripotent stem cell-derived cardiomyocytes
2009 StandoutNobel
Genetics and cardiac channelopathies
2010
Long-term follow-up of primary prophylactic implantable cardioverter-defibrillator therapy in Brugada syndrome
2007
Risk Stratification in Brugada Syndrome
2011
Functional Genomic Analysis of C. elegans Molting
2005 StandoutNobel
Epidemiology of valvular heart disease in the adult
2011
Long-term efficacy of low doses of quinidine on malignant arrhythmias in Brugada syndrome with an implantable cardioverter-defibrillator: A case series and literature review
2012
Clinical spectrum of patients with a Brugada ECG
2008
Assessing the proarrhythmic potential of drugs: Current status of models and surrogate parameters of torsades de pointes arrhythmias
2006
Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects
2013
Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults
2008
NAFLD: A multisystem disease
2015 Standout
Ranolazine inhibition of hERG potassium channels: Drug–pore interactions and reduced potency against inactivation mutants
2014
The usual suspects in sudden cardiac death of the young: a focus on inherited arrhythmogenic diseases
2014
Calcific aortic stenosis
2016
Therapy for the Brugada Syndrome
2006
Myocarditis
2009 Standout
ACVIM consensus guidelines for the diagnosis and treatment of myxomatous mitral valve disease in dogs
2019 Standout
ACVIM consensus statement: Guidelines for the identification, evaluation, and management of systemic hypertension in dogs and cats
2018 Standout
Trascendencia clínica del embarazo en el síndrome de Brugada
2013
Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a
2002
The Fibroblast Growth Factor signaling pathway
2015 Standout
Fibrosis, not cell size, delineates β-myosin heavy chain reexpression during cardiac hypertrophy and normal aging in vivo
2006 StandoutNobel
The kinase Grk2 regulates Nedd4/Nedd4-2-dependent control of epithelial Na + channels
2004 StandoutNobel
The face of postural tachycardia syndrome – insights from a large cross‐sectional online community‐based survey
2019
Increased Risk of Arrhythmic Events in Long-QT Syndrome With Mutations in the Pore Region of the Human Ether-a-go-go–Related Gene Potassium Channel
2002
Magnesium in Man: Implications for Health and Disease
2014 Standout
Transparent Reporting of a multivariable prediction model for Individual Prognosis Or Diagnosis (TRIPOD): Explanation and Elaboration
2015 Standout
SIDS and Other Sleep-Related Infant Deaths: Expansion of Recommendations for a Safe Infant Sleeping Environment
2011 Standout
Crystallographic insights into sodium-channel modulation by the β4 subunit
2013
Cardiovascular effects of Danshen
2007 Standout
Cardiac Sodium Channel Gene Variants and Sudden Cardiac Death in Women
2007
Fine-Scale Genetic Structure in Finland
2017
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death
2006
Cardiac Ion Channels
2009
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)
2003
Next Generation of Fluorine-Containing Pharmaceuticals, Compounds Currently in Phase II–III Clinical Trials of Major Pharmaceutical Companies: New Structural Trends and Therapeutic Areas
2016 Standout
Management of Acute Myocarditis and Chronic Inflammatory Cardiomyopathy
2020 Standout
Brugada Syndrome: Report of the Second Consensus Conference
2005 Standout
2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death
2015 Standout
Recent Stem Cell Advances: Induced Pluripotent Stem Cells for Disease Modeling and Stem Cell–Based Regeneration
2010 StandoutNobel
Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture
2011 StandoutNobel
Neuropathic Pain: From Mechanisms to Treatment
2020 Standout
Fibroblast Growth Factor Homologous Factor 13 Regulates Na + Channels and Conduction Velocity in Murine Hearts
2011
Contemporary Definitions and Classification of the Cardiomyopathies
2006 Standout
Quantitative Serum Nuclear Magnetic Resonance Metabolomics in Cardiovascular Epidemiology and Genetics
2015 Standout
Aortic-Valve Stenosis — From Patients at Risk to Severe Valve Obstruction
2014
ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities
2008 Standout
The Biological Basis for Cardiac Repair After Myocardial Infarction
2016 Standout
2020 ACC/AHA Guideline for the Management of Patients With Valvular Heart Disease: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines
2020 Standout
Pharmacology of the Na v 1.1 domain IV voltage sensor reveals coupling between inactivation gating processes
2017 StandoutNobel
Andersen–Tawil syndrome: Clinical and molecular aspects
2013
Síndrome de Brugada y embarazo: indagando en el papel de las hormonas sexuales en las canalopatías iónicas
2014
Genetic Characteristics of Children and Adolescents With Long-QT Syndrome Diagnosed by School-Based Electrocardiographic Screening Programs
2013
2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death
2015
Sudden Death Associated With Short-QT Syndrome Linked to Mutations in HERG
2003
GENETIC FIBRILLINOPATHIES : NEW INSIGHTS IN MOLECULAR DIAGNOSIS AND CLINICAL MANAGEMENT
2003
Cardiac Ion Channels
2002
Part 14: Pediatric Advanced Life Support
2010 Standout
Structural insights into TRPM8 inhibition and desensitization
2019 StandoutScienceNobel
AHA/ACCF/HRS Recommendations for the Standardization and Interpretation of the Electrocardiogram
2009 Standout
Hypermorphic mutation of the voltage-gated sodium channel encoding gene Scn10a causes a dramatic stimulus-dependent neurobehavioral phenotype
2011 StandoutNobel
Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia
2001
Mouse Model of SCN5A -Linked Hereditary Lenegre’s Disease
2005
2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death
2017
ATP-sensitive potassium channel (K ATP )–dependent regulation of cardiotropic viral infections
2011 StandoutNobel
Works of Vincent Probst being referenced
Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome
2010
MOG1
2011
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease
2008
SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome
2009
TRPM4 non-selective cation channel variants in long QT syndrome
2017
2018 ESC Guidelines for the diagnosis and management of syncope
2018
Filamin-A-Related Myxomatous Mitral Valve Dystrophy: Genetic, Echocardiographic and Functional Aspects
2011
Usefulness of Fetuin-A and C-Reactive Protein Concentrations for Prediction of Outcome in Acute Coronary Syndromes (from the French Registry of Acute ST-Elevation Non-ST-Elevation Myocardial Infarction [FAST-MI])
2012
Electropharmacological characterization of cardiac repolarization in German shepherd dogs with an inherited syndrome of sudden death: abnormal response to potassium channel blockers
2000
Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation
2005
Drugs and Brugada syndrome patients: Review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)
2009
Response to intravenous ajmaline: a retrospective analysis of 677 ajmaline challenges
2009
Monomorphic Ventricular Tachycardia Due to Brugada Syndrome Successfully Treated by Hydroquinidine Therapy in a 3‐Year‐Old Child
2005
SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes
2020
Cardiac conduction defects associate with mutations in SCN5A
1999
Ventricular Fibrillation with Prominent Early Repolarization Associated with a Rare Variant of KCNJ8/KATP Channel
2008
Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel
2013
Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease
2003
Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome
2010
Fine-scale human genetic structure in Western France
2014
Long-Term Follow-Up of Patients With Short QT Syndrome
2011
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
2008
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients
2002
Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation
2013
Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28
2000
Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies
2008
Novel Brugada SCN5A Mutation Leading to ST Segment Elevation in the Inferior or the Right Precordial Leads
2003
[Familial hypertrophic cardiomyopathy. French study of the duration and outcome of pregnancy].
2002
Familial Aggregation of Calcific Aortic Valve Stenosis in the Western Part of France
2006
Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy
2006
Clinical Aspects and Prognosis of Brugada Syndrome in Children
2007
NovelSCN5AMutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family
2001
Long-Term Prognosis of Individuals With Right Precordial ST-Segment–Elevation Brugada Syndrome
2005
P6-62
2006