Lista de obras - Stig Haunsø - Dominio Público Uruguay

A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction

artículo científico publicado en 2017

A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease

artículo científico publicado en 2009

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation

artículo científico publicado en 2013

A novel nonsense variant in Nav1.5 cofactor MOG1 eliminates its sodium current increasing effect and may increase the risk of arrhythmias

artículo científico publicado en 2011

Abnormal atrial activation in young patients with lone atrial fibrillation

scientific article published on 23 September 2010

Abnormal atrial activation is common in patients with arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2010

An angiotensin II type 1 receptor activation switch patch revealed through evolutionary trace analysis

artículo científico publicado en 2010

Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy

artículo científico publicado en 2016

Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease

artículo científico publicado en 2017

Association Between Heart Rate at Rest and Incident Atrial Fibrillation (from the Copenhagen Electrocardiographic Study).

artículo científico publicado en 2016

Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction.

artículo científico publicado en 2017

Associations between common ECG abnormalities and out-of-hospital cardiac arrest.

artículo científico publicado en 2019

Atrial fibrillation: the role of common and rare genetic variants

artículo científico publicado en 2013

Biased Signaling of the Angiotensin II Type 1 Receptor Can Be Mediated through Distinct Mechanisms ⬇️

artículo científico publicado el 30 de noviembre de 2010

Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest

Brugada syndrome risk loci seem protective against atrial fibrillation

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Calcimimetic, AMG 073, induces relaxation on isolated rat aorta

artículo científico publicado en 2007

Calcium receptor is functionally expressed in rat neonatal ventricular cardiomyocytes

artículo científico publicado en 2005

Cardiac symptoms before sudden cardiac death caused by coronary artery disease: a nationwide study among young Danish people

artículo científico publicado en 2013

Cardiac symptoms before sudden cardiac death caused by hypertrophic cardiomyopathy: a nationwide study among the young in Denmark

artículo científico publicado en 2016

Characterizations of a loss-of-function mutation in the Kir3.4 channel subunit.

artículo científico publicado en 2007

Clinical implications of electrocardiographic bundle branch block in primary care

artículo científico publicado en 2019

Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation

article published in 2015

Common and rare variants in SCN10A modulate the risk of atrial fibrillation

artículo científico publicado en 2015

Common genetic variants and risk of ischemic heart failure: an evaluation of a negative genetic study

artículo científico publicado en 2015

Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians.

artículo científico publicado en 2011

Cyclin D2 induces proliferation of cardiac myocytes and represses hypertrophy.

artículo científico publicado en 2004

Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.

artículo científico publicado en 2017

Differences in autonomic balance in patients with cardioinhibitory and vasodepressor type of reflex syncope during head-up tilt test and active standing

artículo científico publicado en 2012

Differences in clinical characteristics in patients with first ST-segment elevation myocardial infarction and ventricular fibrillation according to sex.

artículo científico publicado en 2017

Differences in investigations of sudden unexpected deaths in young people in a nationwide setting

artículo científico publicado en 2011

Different regulation of p27 and Akt during cardiomyocyte proliferation and hypertrophy

scientific article published on 01 April 2007

Downregulation of aquaporin-1 in alveolar microvessels in lungs adapted to chronic heart failure

scientific article published on 04 January 2011

Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis

artículo científico publicado en 2020

Editorial: Sudden cardiac death – the challenge to cardiology ⬇️

artículo científico publicado el 1 de octubre de 2010

Effect of intermittent versus continuous parathyroid hormone in the cardiovascular system of rats

artículo científico publicado en 2010

Effects of pharmacological modulation of the ATP-sensitive potassium channels on the development of warm-up angina pectoris

artículo científico publicado en 2005

Electrocardiographic PR Interval Duration and Cardiovascular Risk: Results From the Copenhagen ECG Study

artículo científico publicado en 2017

Electrocardiographic Preexcitation and Risk of Cardiovascular Morbidity and Mortality: Results From the Copenhagen ECG Study

artículo científico publicado en 2017

Electrocardiographic Tpeak-Tend interval and risk of cardiovascular morbidity and mortality: Results from the Copenhagen ECG study

artículo científico publicado en 2015

Electrocardiographic precordial ST-segment deviations and the risk of cardiovascular death: results from the Copenhagen ECG Study

artículo científico publicado en 2014

Epilepsy and risk of death and sudden unexpected death in the young: a nationwide study.

artículo científico

Expression profiling reveals differences in metabolic gene expression between exercise-induced cardiac effects and maladaptive cardiac hypertrophy

artículo científico publicado en 2005

Extracellular calcium sensing in rat aortic vascular smooth muscle cells

artículo científico publicado en 2006

Extracellular signal-regulated kinases control expression of G protein-coupled receptor kinase 2 (GRK2)

artículo científico publicado en 2002

Factors Associated With and Outcomes After Ventricular Fibrillation Before and During Primary Angioplasty in Patients With ST-Segment Elevation Myocardial Infarction.

artículo científico publicado en 2015

Familial atrial fibrillation predicts increased risk of mortality: a study in Danish twins

artículo científico publicado en 2012

Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation

scientific article published on 31 January 2018

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

artículo científico publicado en 2008

Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation

artículo científico publicado en 2014

Gender differences in sudden cardiac death in the young-a nationwide study

artículo científico publicado en 2017

Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years

Genetic modifier of the QTc interval associated with early-onset atrial fibrillation

artículo científico publicado en 2013

Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation

artículo científico publicado en 2019

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

artículo científico publicado en 2013

Genetic variation in the inwardly rectifying K channel subunits KCNJ3 (GIRK1) and KCNJ5 (GIRK4) in patients with sinus node dysfunction

artículo científico publicado en 2010

Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis

artículo científico publicado en 2013

Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse

artículo científico publicado en 2020

High prevalence of genetic variants previously associated with LQT syndrome in new exome data

artículo científico publicado en 2012

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation

artículo científico publicado en 2012

IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation

scientific journal article

Identification of a core set of genes that signifies pathways underlying cardiac hypertrophy

artículo científico publicado en 2004

Incidence and etiology of sports-related sudden cardiac death in Denmark--implications for preparticipation screening

artículo científico publicado en 2010

Incidence and risk factors of ventricular fibrillation before primary angioplasty in patients with first ST-elevation myocardial infarction: a nationwide study in Denmark

artículo científico publicado en 2015

Incomplete right bundle branch block: a novel electrocardiographic marker for lone atrial fibrillation

artículo científico publicado en 2010

Increased natriuretic peptide receptor A and C gene expression in rats with pressure-overload cardiac hypertrophy

artículo científico publicado en 2005

Involvement of cyclin D activity in left ventricle hypertrophy in vivo and in vitro

artículo científico publicado en 2002

J-shaped association between QTc interval duration and the risk of atrial fibrillation: results from the Copenhagen ECG study

artículo científico publicado en 2013

Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation

artículo científico publicado en 2020

Loss-of-function polymorphic variants of the human angiotensin II type 1 receptor

artículo científico publicado en 2004

Low disease prevalence and inappropriate implantable cardioverter defibrillator shock rate in Brugada syndrome: a nationwide study

artículo científico publicado en 2012

MAP kinase protects G protein-coupled receptor kinase 2 from proteasomal degradation

artículo científico publicado en 2005

Missense Variants in Plakophilin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy Patients – Disease-Causing or Innocent Bystanders?

Multiprotein bridging factor 1 cooperates with c-Jun and is necessary for cardiac hypertrophy in vitro

artículo científico publicado en 2003

Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2012

Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data

artículo científico publicado en 2013

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

artículo científico publicado en 2011

Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients

artículo científico publicado en 2007

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

artículo científico publicado en 2012

Nationwide (Denmark) study of symptoms preceding sudden death due to arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2014

Nationwide study of sudden cardiac death in persons aged 1-35 years

artículo científico publicado en 2010

New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2013

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

artículo científico publicado en 2013

New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome

artículo científico publicado en 2014

Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes

artículo científico publicado en 2018

Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality

artículo científico publicado en 2016

Oligomerization of wild type and nonfunctional mutant angiotensin II type I receptors inhibits galphaq protein signaling but not ERK activation

artículo científico publicado en 2004

P-wave duration and the risk of atrial fibrillation: Results from the Copenhagen ECG Study

artículo científico publicado en 2015

Pacemaker implantation in a patient with brugada and sick sinus syndrome

artículo científico publicado en 2013

Potassium dynamics are attenuated in hyperkalemia and a determinant of QT adaptation in exercising hemodialysis patients

scientific article published on 30 May 2013

Prevalence of family history in patients with reflex syncope

artículo científico publicado en 2013

Prior myocardial infarction in the young: predisposes to a high relative risk but low absolute risk of a sudden cardiac death

artículo científico

Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval

artículo científico publicado en 2015

Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation

artículo científico publicado en 2018

Rare variants in GJA5 are associated with early-onset lone atrial fibrillation

artículo científico publicado en 2012

Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts

artículo científico publicado en 2019

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

artículo científico publicado en 2005

Revascularization compared to medical treatment in patients with silent vs. symptomatic residual ischemia after thrombolyzed myocardial infarction--the DANAMI study

artículo científico publicado en 2006

Risk Prediction of Atrial Fibrillation Based on Electrocardiographic Interatrial Block.

artículo científico publicado en 2018

Risk factors and causes of sudden noncardiac death: A nationwide cohort study in Denmark

artículo científico publicado en 2015

Risk of atrial fibrillation as a function of the electrocardiographic PR interval: results from the Copenhagen ECG Study

artículo científico publicado en 2013

Risk of cardiovascular disease in family members of young sudden cardiac death victims

artículo científico publicado en 2012

Risk prediction of cardiovascular death based on the QTc interval: evaluating age and gender differences in a large primary care population

artículo científico publicado en 2014

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

artículo científico publicado en 2015

S-petasin and butterbur lactones dilate vessels through blockage of voltage gated calcium channels and block DNA synthesis

artículo científico publicado en 2008

SCN1Bb R214Q found in 3 patients: 1 with Brugada syndrome and 2 with lone atrial fibrillation

article published in 2012

Screening of KCNN3 in patients with early-onset lone atrial fibrillation

Screening of the ito regulatory subunit klf15 in patients with early-onset lone atrial fibrillation

artículo científico publicado en 2013

Screening of three novel candidate genes in arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2011

Sick Sinus Syndrome, Progressive Cardiac Conduction Disease, Atrial Flutter and Ventricular Tachycardia Caused by a Novel SCN5A Mutation

article published in 2010

Single nucleotide polymorphisms in inflammatory genes and the risk of early onset of lone atrial fibrillation

artículo científico publicado en 2010

Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics

artículo científico publicado en 2012

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

artículo científico publicado en 2012

Sports-related sudden cardiac death in a competitive and a noncompetitive athlete population aged 12 to 49 years: data from an unselected nationwide study in Denmark

artículo científico publicado en 2014

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

scientific article published on 29 March 2017

Sudden cardiac death and coronary disease in the young: A nationwide cohort study in Denmark

artículo científico publicado en 2017

Sudden cardiac death in children (1-18 years): symptoms and causes of death in a nationwide setting

artículo científico publicado en 2013

Sudden cardiac death in young adults with previous hospital-based psychiatric inpatient and outpatient treatment: a nationwide cohort study from Denmark

artículo científico publicado en 2015

Sudden death in young persons with uncontrolled asthma--a nationwide cohort study in Denmark

artículo científico publicado en 2015

Sudden unexpected death caused by stroke: A nationwide study among children and young adults in Denmark

artículo científico publicado en 2017

Sudden unexpected death in infancy in Denmark

artículo científico publicado en 2010

Symptoms Before Sudden Arrhythmic Death Syndrome: A Nationwide Study Among the Young in Denmark

artículo científico publicado en 2015

The angiotensin II type 1 receptor antagonist Losartan binds and activates bradykinin B2 receptor signaling

artículo científico publicado en 2010

The human angiotensin AT(1) receptor supports G protein-independent extracellular signal-regulated kinase 1/2 activation and cellular proliferation

artículo científico publicado en 2008

The pathogenicity of genetic variants previously associated with left ventricular non-compaction

artículo científico publicado en 2015

The prevalence and relevance of the Brugada-type electrocardiogram in the Danish general population: data from the Copenhagen City Heart Study

artículo científico publicado en 2010

The role of the sodium current complex in a nonreferred nationwide cohort of sudden infant death syndrome

Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation

artículo científico publicado en 2013

Visit-to-Visit Variability of Hemoglobin A in People Without Diabetes and Risk of Major Adverse Cardiovascular Events and All-Cause Mortality

article

Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis

artículo científico publicado en 2011

[Cardiac syncope--unexpected sudden cardiac death]

scientific article published on 01 June 2006

[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease].

artículo científico publicado en 2010

[Dynamic ECG changes as a result of Brugada syndrome, an overlooked diagnosis?]

artículo científico publicado en 2005

[Evident decline in mortality from ischaemic heart disease in Denmark from 1970 to 2015] ⬇️

scientific article published on 01 September 2020

[G receptor kinases. A family of "natural" receptor blockers]

scientific article published on 01 November 2004

[Less endocarditis prophylaxis]

scientific article published on 01 February 2010

[Molecular-biological methods of diagnosing colon-related Streptococcus bovis endocarditis]

artículo científico publicado en 2007

[New European randomized placebo-controlled study casts doubt on the use of nicotinic acid in the treatment of familial hypercholesterolemia]

[Sudden unexpected cardiac death in an 18-year-old female with familial hypercholesterolaemia]

[Treatment and prognosis after acute coronary syndrome]

artículo científico publicado en 2007

Lista de obras de Stig Haunsø

A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction

A Novel SCN5A Mutation in a Patient with Coexistence of Brugada Syndrome Traits and Ischaemic Heart Disease

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation

A novel nonsense variant in Nav1.5 cofactor MOG1 eliminates its sodium current increasing effect and may increase the risk of arrhythmias

Abnormal atrial activation in young patients with lone atrial fibrillation

Abnormal atrial activation is common in patients with arrhythmogenic right ventricular cardiomyopathy

An angiotensin II type 1 receptor activation switch patch revealed through evolutionary trace analysis

Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy

Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease

Association Between Heart Rate at Rest and Incident Atrial Fibrillation (from the Copenhagen Electrocardiographic Study).

Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction.

Associations between common ECG abnormalities and out-of-hospital cardiac arrest.

Atrial fibrillation: the role of common and rare genetic variants

Biased Signaling of the Angiotensin II Type 1 Receptor Can Be Mediated through Distinct Mechanisms ⬇️

Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest

Brugada syndrome risk loci seem protective against atrial fibrillation

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

Calcimimetic, AMG 073, induces relaxation on isolated rat aorta

Calcium receptor is functionally expressed in rat neonatal ventricular cardiomyocytes

Cardiac symptoms before sudden cardiac death caused by coronary artery disease: a nationwide study among young Danish people

Cardiac symptoms before sudden cardiac death caused by hypertrophic cardiomyopathy: a nationwide study among the young in Denmark

Characterizations of a loss-of-function mutation in the Kir3.4 channel subunit.

Clinical implications of electrocardiographic bundle branch block in primary care

Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation

Common and rare variants in SCN10A modulate the risk of atrial fibrillation

Common genetic variants and risk of ischemic heart failure: an evaluation of a negative genetic study

Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians.

Cyclin D2 induces proliferation of cardiac myocytes and represses hypertrophy.

Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.

Differences in autonomic balance in patients with cardioinhibitory and vasodepressor type of reflex syncope during head-up tilt test and active standing

Differences in clinical characteristics in patients with first ST-segment elevation myocardial infarction and ventricular fibrillation according to sex.

Differences in investigations of sudden unexpected deaths in young people in a nationwide setting

Different regulation of p27 and Akt during cardiomyocyte proliferation and hypertrophy

Downregulation of aquaporin-1 in alveolar microvessels in lungs adapted to chronic heart failure

Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis

Editorial: Sudden cardiac death – the challenge to cardiology ⬇️

Effect of intermittent versus continuous parathyroid hormone in the cardiovascular system of rats

Effects of pharmacological modulation of the ATP-sensitive potassium channels on the development of warm-up angina pectoris

Electrocardiographic PR Interval Duration and Cardiovascular Risk: Results From the Copenhagen ECG Study

Electrocardiographic Preexcitation and Risk of Cardiovascular Morbidity and Mortality: Results From the Copenhagen ECG Study

Electrocardiographic Tpeak-Tend interval and risk of cardiovascular morbidity and mortality: Results from the Copenhagen ECG study

Electrocardiographic precordial ST-segment deviations and the risk of cardiovascular death: results from the Copenhagen ECG Study

Epilepsy and risk of death and sudden unexpected death in the young: a nationwide study.

Expression profiling reveals differences in metabolic gene expression between exercise-induced cardiac effects and maladaptive cardiac hypertrophy

Extracellular calcium sensing in rat aortic vascular smooth muscle cells

Extracellular signal-regulated kinases control expression of G protein-coupled receptor kinase 2 (GRK2)

Factors Associated With and Outcomes After Ventricular Fibrillation Before and During Primary Angioplasty in Patients With ST-Segment Elevation Myocardial Infarction.

Familial atrial fibrillation predicts increased risk of mortality: a study in Danish twins

Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation

Gender differences in sudden cardiac death in the young-a nationwide study

Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years

Genetic modifier of the QTc interval associated with early-onset atrial fibrillation

Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

Genetic variation in the inwardly rectifying K channel subunits KCNJ3 (GIRK1) and KCNJ5 (GIRK4) in patients with sinus node dysfunction

Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis

Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse

High prevalence of genetic variants previously associated with LQT syndrome in new exome data

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation

IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation

Identification of a core set of genes that signifies pathways underlying cardiac hypertrophy

Incidence and etiology of sports-related sudden cardiac death in Denmark--implications for preparticipation screening

Incidence and risk factors of ventricular fibrillation before primary angioplasty in patients with first ST-elevation myocardial infarction: a nationwide study in Denmark

Incomplete right bundle branch block: a novel electrocardiographic marker for lone atrial fibrillation

Increased natriuretic peptide receptor A and C gene expression in rats with pressure-overload cardiac hypertrophy

Involvement of cyclin D activity in left ventricle hypertrophy in vivo and in vitro

J-shaped association between QTc interval duration and the risk of atrial fibrillation: results from the Copenhagen ECG study

Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation

Loss-of-function polymorphic variants of the human angiotensin II type 1 receptor

Low disease prevalence and inappropriate implantable cardioverter defibrillator shock rate in Brugada syndrome: a nationwide study

MAP kinase protects G protein-coupled receptor kinase 2 from proteasomal degradation

Missense Variants in Plakophilin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy Patients – Disease-Causing or Innocent Bystanders?

Multiprotein bridging factor 1 cooperates with c-Jun and is necessary for cardiac hypertrophy in vitro

Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy

Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients