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Lista de obras de Elijah R Behr

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation

artículo científico publicado en 2013

A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes

artículo científico publicado en 2011

A rare connection: fasciculoventricular pathway in PRKAG2 disease.

artículo científico publicado en 2009

Academic output from EU-funded health research projects

artículo científico publicado en 2012

Accuracy of the 2017 international recommendations for clinicians who interpret adolescent athletes' ECGs: a cohort study of 11 168 British white and black soccer players

scientific article published on 05 July 2019

Acquired long QT syndrome: as risky as congenital long QT syndrome?

artículo científico publicado en 2011

Advances in the management of atrial fibrillation.

artículo científico publicado en 2012

Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients

artículo científico publicado en 2017

An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

scientific article published on 16 January 2020

Antipsychotics and torsadogenic risk: signals emerging from the US FDA Adverse Event Reporting System database.

artículo científico publicado en 2013

Arrhythmias: Opening Pandora's Box -- incidental genetic findings

artículo científico publicado en 2016

Author's reply: To PMID 24585884

artículo científico publicado en 2015

Benign or malignant, early or delayed: the changing face of early repolarization ⬇️

artículo científico publicado el 19 de octubre de 2011

Bipolar leads obtained from the unipolar precordial leads for noise filtering

artículo científico publicado en 2010

Brugada Syndrome: an Update ⬇️

artículo científico publicado el 1 de marzo de 2013

Brugada syndrome and atrial fibrillation: pathophysiology and genetics

artículo científico publicado en 2011

Brugada-like changes in the peripheral leads during diagnostic ajmaline test in patients with suspected Brugada syndrome.

artículo científico publicado en 2009

Burden of sudden cardiac death in persons aged 1 to 49 years: nationwide study in Denmark

artículo científico publicado en 2014

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

scientific article published on 01 September 2019

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome

scientific article published on 01 March 2018

Cardiac arrhythmia management using a noncontact mapping multielectrode array.

artículo científico publicado en 2010

Cardiac evaluation of pediatric relatives in sudden arrhythmic death syndrome: a 2-center experience.

artículo científico

Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome

scientific article published on 01 November 2003

Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome

scientific article published on 01 April 2019

Characterization of early repolarization during ajmaline provocation and exercise tolerance testing ⬇️

artículo científico publicado el 23 de octubre de 2012

Clinical Differentiation Between Physiological Remodeling and Arrhythmogenic Right Ventricular Cardiomyopathy in Athletes With Marked Electrocardiographic Repolarization Anomalies

artículo científico publicado en 2015

Clinical characteristics and circumstances of death in the sudden arrhythmic death syndrome.

artículo científico publicado en 2014

Clinical significance of electrocardiographic right ventricular hypertrophy in athletes: comparison with arrhythmogenic right ventricular cardiomyopathy and pulmonary hypertension.

artículo científico publicado en 2013

Clinical utility of computed electrocardiographic leads

artículo científico publicado en 2014

Common Genetic Variant Risk Score Is Associated With Drug-Induced QT Prolongation and Torsade de Pointes Risk: A Pilot Study.

artículo científico

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

artículo científico publicado en 2013

Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia

artículo científico publicado en 2012

Comparison of Ajmaline and Procainamide Provocation Tests in the Diagnosis of Brugada Syndrome

artículo científico publicado en 2019

Comparison of hypertrophic cardiomyopathy in Afro-Caribbean versus white patients in the UK.

artículo científico publicado en 2016

Computed bipolar precordial leads for improved P wave detection.

artículo científico publicado en 2014

Computed quadripolar electrocardiographic leads for prediction of ventricular tachycardia.

artículo científico publicado en 2013

Diagnostic Yield of Genetic Testing in Young Athletes With T-Wave Inversion

artículo científico publicado en 2018

Drug-associated arrhythmia in the military patient.

artículo científico

Drug-induced Brugada syndrome.

artículo científico publicado en 2009

Drug-induced arrhythmia: pharmacogenomic prescribing?

artículo científico publicado en 2012

Drugs and life-threatening ventricular arrhythmia risk: results from the DARE study cohort.

artículo científico publicado en 2017

Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study

artículo científico publicado en 2018

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

ESC guidance for the diagnosis and management of cardiovascular disease during the COVID-19 pandemic: part 2—care pathways, treatment, and follow-up

artículo científico publicado en 2021

Early repolarisation: controversies and clinical implications ⬇️

artículo científico publicado el 22 de marzo de 2012

Electrocardiographic differentiation between 'benign T-wave inversion' and arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2019

Electrocardiographic methods for diagnosis and risk stratification in the Brugada syndrome

artículo científico publicado en 2014

Elite athletes with recurrent ERS

artículo científico publicado en 2003

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

artículo científico publicado en 2020

Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

scholarly article published in Nature Genetics

Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome

artículo científico publicado en 2019

Etiology of Sudden Death in Sports: Insights From a United Kingdom Regional Registry.

artículo científico publicado en 2016

Evaluation After Sudden Death in the Young: A Global Approach

scientific article published on 19 August 2019

Evaluation of the Achieve Mapping Catheter in cryoablation for atrial fibrillation: a prospective randomized trial.

artículo científico publicado en 2015

Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes

artículo científico publicado en 2013

Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome

artículo científico publicado en 2018

Familial cardiological evaluation in sudden arrhythmic death syndrome: essential but challenging

scientific article published on 20 March 2013

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype

artículo científico publicado en 2015

Fever vs drug: Battling with the Brugada syndrome substrate.

artículo científico publicado en 2017

Fever-Related Arrhythmic Events in the Multicenter Survey on Arrhythmic Events in Brugada Syndrome (SABRUS).

artículo científico publicado en 2018

Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome.

artículo científico publicado en 2015

Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome

artículo científico publicado en 2005

Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients

artículo científico publicado en 2018

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic biomarkers in Brugada syndrome.

artículo científico

Genetic risk for acquired arrhythmia

scientific article published on 01 September 2003

Genetic susceptibility and the Brugada syndrome

scientific article published on 01 October 2019

Genetic testing for inherited cardiac disease ⬇️

artículo científico publicado el 30 de julio de 2013

Genetic testing in idiopathic ventricular fibrillation: Searching for a needle in a haystack?

artículo científico publicado en 2017

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

artículo científico publicado en 2013

Genotype-phenotype association in patients with SCN4A mutation - Authors' reply

scientific article published on 06 June 2019

Getting to the heart of the matter: investigating the idiopathic sudden cardiac death of a previous well soldier

scientific article published on 17 March 2019

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.

artículo científico publicado en 2013

Heart Rhythm UK position statement on clinical indications for implantable cardioverter defibrillators in adult patients with familial sudden cardiac death syndromes

scientific article published on 01 August 2010

High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia.

artículo científico publicado en 2006

Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair.

artículo científico publicado en 2008

Impact of clinical and genetic findings on the management of young patients with Brugada syndrome

artículo científico publicado en 2016

Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest

scientific article published on 1 September 2019

Inherited cardiomyopathies

artículo científico publicado en 2011

Inherited cardiomyopathies

scientific article published on 02 May 2019

Integration of genetic testing into diagnostic pathways for cardiomyopathies: a clinical consensus statement by the ESC Council on Cardiovascular Genomics

artículo científico publicado en 2024

Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics

artículo científico publicado en 2022

Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants

scientific article published on 11 May 2018

Late gadolinium enhancement in Brugada syndrome: A marker for subtle underlying cardiomyopathy?

artículo científico

Letter by Bastiaenen and Behr Regarding Article, “Early Repolarization: Electrocardiographic Phenotypes Associated With Favorable Long-Term Outcome” ⬇️

artículo científico publicado el 13 de diciembre de 2011

Long-QT syndrome and torsades de pointes in a patient with Takotsubo cardiomyopathy: an unusual case

artículo científico publicado en 2008

Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?

artículo científico

Low prevalence of risk markers in cases of sudden death due to Brugada syndrome relevance to risk stratification in Brugada syndrome.

artículo científico publicado en 2011

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndrome

artículo científico publicado en 2014

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice

artículo científico publicado en 2017

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death

artículo científico publicado en 2012

Myocardial Inflammation in Brugada Syndrome

scientific article published on 01 March 2019

New Insights Into the Genetic Basis of Inherited Arrhythmia Syndromes.

artículo científico publicado en 2016

New approaches to predicting the risk of sudden death.

artículo científico publicado en 2016

Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches.

artículo científico publicado en 2012

Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy

scientific article published on 23 July 2019

Noncardiac genetic predisposition in sudden infant death syndrome

scientific article published on 24 August 2018

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

artículo científico publicado en 2014

Novel electrocardiographic criteria for the diagnosis of arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2015

Obesity and sudden cardiac death in the young: Clinical and pathological insights from a large national registry

artículo científico publicado en 2018

Optimum dose of digoxin

artículo científico publicado en 1997

Paediatric evaluation for inherited conditions: how do we investigate?

scientific article published on 03 December 2010

Pharmacological treatment of acquired QT prolongation and torsades de pointes.

artículo científico publicado en 2015

Prevalence and significance of Brugada-type ECG in 12,012 apparently healthy European subjects.

artículo científico publicado en 2007

Prevalence and significance of an isolated long QT interval in elite athletes

artículo científico publicado en 2007

Prevalence of the type 1 Brugada electrocardiogram in Caucasian patients with suspected coronary spasm

artículo científico publicado en 2011

Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

artículo científico publicado en 2018

Proof of concept study of a novel pacemapping algorithm as a basis to guide ablation of ventricular arrhythmias.

artículo científico publicado en 2018

QRS-ST-T triangulation with repolarization shortening as a precursor of sustained ventricular tachycardia during acute myocardial ischemia

artículo científico publicado en 2014

Relationship Between Distance and Change in Surface ECG Morphology During Pacemapping as a Guide to Ablation of Ventricular Arrhythmias: Implications for the Spatial Resolution of Pacemapping.

artículo científico publicado en 2017

Reply: Are T-Inversions in Chest Leads Always Benign?

artículo científico publicado en 2017

Reply: How Often Does Athlete Sudden Cardiac Death Occur Outside the Context of Exertion?

artículo científico publicado en 2016

Reply: Search for Evidence-Based Medicine for Brugada Syndrome: The Complex Network of the Brugada Syndrome

artículo científico publicado en 2016

Reply: Understanding the Mechanism of T-Wave Inversion in Athletes May Be Key to Best Management

artículo científico publicado en 2015

Response by Sheikh et al to Letter Regarding Article, "Diagnostic Yield of Genetic Testing in Young Athletes With T-Wave Inversion"

scientific article published on 01 February 2019

Risk score for the exclusion of arrhythmic events in arrhythmogenic right ventricular cardiomyopathy at first presentation

scientific article published on 01 May 2019

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.

artículo científico publicado en 2015

SARS-CoV-2, COVID-19 and inherited arrhythmia syndromes

scientific article published on 31 March 2020

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families

artículo científico publicado en 2020

SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups

artículo científico publicado en 2018

SEMCARE: Multilingual Semantic Search in Semi-Structured Clinical Data

artículo científico publicado en 2016

Significance of QRS prolongation during diagnostic ajmaline test in patients with suspected Brugada syndrome.

artículo científico publicado en 2009

Specificity of Elevated Intercostal Space ECG Recording for the Type 1 Brugada ECG Pattern

artículo científico publicado en 2012

Stress cardiomyopathy and the acquired long QT syndrome

artículo científico publicado en 2011

Subcutaneous or Transvenous Defibrillator Therapy

artículo científico publicado en 2020

Sudden Cardiac Death in Pre-Excitation and Wolff-Parkinson-White: Demographic and Clinical Features

artículo científico publicado en 2017

Sudden Cardiac Death: Pharmacotherapy and Proarrhythmic Drugs: A Nationwide Cohort Study in Denmark

scientific article published on 29 March 2017

Sudden Death Can Be the First Manifestation of Hypertrophic Cardiomyopathy: Data From a United Kingdom Pathology Registry

scientific article published on 01 February 2019

Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy

artículo científico publicado en 2019

Sudden Unexplained Death - Treating the Family

artículo científico publicado en 2014

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

artículo científico publicado en 2008

Sudden cardiac arrest in sports - need for uniform registration: A Position Paper from the Sport Cardiology Section of the European Association for Cardiovascular Prevention and Rehabilitation.

artículo científico publicado en 2015

Sudden cardiac death with autopsy findings of uncertain significance: potential for erroneous interpretation

scientific article published on 13 May 2013

Sudden death and cardiac arrest without phenotype: the utility of genetic testing

artículo científico publicado en 2016

Sudden infant death syndrome and inherited cardiac conditions.

artículo científico publicado en 2017

Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention

artículo científico publicado en 2016

Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions

artículo científico publicado en 2014

Surviving Sudden Death: Where Does Next-Generation Sequencing Fit in the Assessment of Sudden Death Victims and Their Families.

artículo científico publicado en 2017

Takotsubo cardiomyopathy and the long-QT syndrome: an insult to repolarization reserve

artículo científico publicado en 2009

The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy

artículo científico publicado en 2018

The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

artículo científico publicado en 2008

The Prevalence and Significance of the Early Repolarization Pattern in Sudden Arrhythmic Death Syndrome Families

artículo científico publicado en 2016

The genetics of pro-arrhythmic adverse drug reactions.

artículo científico publicado en 2014

The importance of specialist cardiac histopathological examination in the investigation of young sudden cardiac deaths.

artículo científico publicado en 2013

The magnitude of sudden cardiac death in the young: a death certificate-based review in England and Wales.

artículo científico publicado en 2009

The negative effect of red tape on research.

artículo científico publicado en 2005

The nonlinear structure of the desmoplakin plakin domain and the effects of cardiomyopathy-linked mutations

artículo científico publicado en 2011

The phenotype standardization project: improving pharmacogenetic studies of serious adverse drug reactions.

artículo científico publicado en 2011

The prevalence and significance of a short QT interval in 18,825 low-risk individuals including athletes.

artículo científico publicado en 2015

The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote

artículo científico publicado en 2013

The role of genetic testing in unexplained sudden death

artículo científico

The variation of the sarcolipin gene (SLN) in atrial fibrillation, long QT syndrome and sudden arrhythmic death syndrome

article

The ventricular ectopic QRS interval (VEQSI): Diagnosis of arrhythmogenic right ventricular cardiomyopathy in patients with incomplete disease expression.

artículo científico publicado en 2016

The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy

artículo científico publicado en 2019

Therapeutic hypothermia and ventricular fibrillation storm in early repolarization syndrome

artículo científico publicado en 2010

Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

scientific article published on 01 May 2019

Type 1 Brugada electrocardiogram pattern during complete left bundle-branch block due to right ventricular pacing ⬇️

artículo científico publicado el 1 de mayo de 2011

Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site

scientific article published on 01 November 2019

Type I Brugada electrocardiogram pattern during the recovery phase of exercise testing

scientific article published on 28 April 2008

Unexplained sudden death, focussing on genetics and family phenotyping.

artículo científico

Use of non-contact mapping in the treatment of right atrial tachycardias in patients with and without congenital heart disease

scientific article published on 01 August 2008

Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome

artículo científico publicado en 2017

VERP in Brugada syndrome - Very effective risk predictor?

artículo científico publicado en 2015

Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease.

artículo científico publicado en 2016

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