Lista de obras - Morten Salling Olesen - Dominio Público Uruguay

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

A polymorphism associated with increased levels of YKL-40 and the risk of early onset of lone atrial fibrillation

artículo científico publicado en 2013

Abnormal atrial activation in young patients with lone atrial fibrillation

scientific article published on 23 September 2010

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Association of rs2200733 at 4q25 with early onset of lone atrial fibrillation in young patients

Atrial fibrillation: the role of common and rare genetic variants

artículo científico publicado en 2013

Brugada syndrome risk loci seem protective against atrial fibrillation

artículo científico publicado en 2014

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

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

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

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

Distinguishing pathogenic mutations from background genetic noise in cardiology: the use of large genome databases for genetic interpretation.

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

Familial Aggregation of Lone Atrial Fibrillation in Young Persons

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

artículo científico publicado en 2012

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

artículo científico publicado en 2014

Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation

artículo científico publicado en 2017

Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p.M200V mutation

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 Misdiagnoses and the Potential for Health Disparities

artículo científico publicado en 2016

Genetic aspects of lone atrial fibrillation: what do we know?

artículo científico

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

artículo científico publicado en 2013

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

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 Brugada syndrome in new exome data.

artículo científico publicado en 2013

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

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

artículo científico publicado en 2010

Inflammatory single nucleotide polymorphisms and the risk of atrial fibrillation: a case control study

Insights into the genome-wide association studies of the electrocardiographic early repolarization pattern

artículo científico publicado en 2012

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

artículo científico publicado en 2014

Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants.

artículo científico publicado en 2016

Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant.

artículo científico publicado en 2014

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

artículo científico publicado en 2013

KCNE1 G38S polymorphism is not the cause of long QT syndrome

artículo científico publicado en 2015

Letter by Olesen et al Regarding Article, “MOG1: A New Susceptibility Gene for Brugada Syndrome” ⬇️

artículo científico publicado el 1 de octubre de 2011

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

Multi-ethnic genome-wide association study for atrial fibrillation

article

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 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

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

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

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

artículo científico publicado en 2015

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 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

Reevaluation of genetic variants previously associated with arrhythmogenic right ventricular cardiomyopathy integrating population-based cohorts and proteomics data

artículo científico publicado en 2019

Risk Prediction of Atrial Fibrillation Based on Electrocardiographic Interatrial Block.

artículo científico publicado en 2018

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

artículo científico publicado en 2013

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

SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation

artículo científico publicado en 2014

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

Short QT syndrome as an inherited condition ⬇️

artículo científico publicado en 2011

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

artículo científico publicado en 2010

The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases

article by BO GREGERS WINKEL et al published 6 August 2012 in Journal of Cardiovascular Electrophysiology

The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death

scientific journal article

The role of common genetic variants in atrial fibrillation

artículo científico publicado en 2016

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

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

artículo científico publicado en 2011

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

artículo científico publicado en 2010

Lista de obras de Morten Salling Olesen

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

A polymorphism associated with increased levels of YKL-40 and the risk of early onset of lone atrial fibrillation

Abnormal atrial activation in young patients with lone atrial fibrillation

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

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

Association of rs2200733 at 4q25 with early onset of lone atrial fibrillation in young patients

Atrial fibrillation: the role of common and rare genetic variants

Brugada syndrome risk loci seem protective against atrial fibrillation

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

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

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

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

Distinguishing pathogenic mutations from background genetic noise in cardiology: the use of large genome databases for genetic interpretation.

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

Familial Aggregation of Lone Atrial Fibrillation in Young Persons

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

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

Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation

Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p.M200V mutation

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

Genetic Misdiagnoses and the Potential for Health Disparities

Genetic aspects of lone atrial fibrillation: what do we know?

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

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

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

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

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

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

Inflammatory single nucleotide polymorphisms and the risk of atrial fibrillation: a case control study

Insights into the genome-wide association studies of the electrocardiographic early repolarization pattern

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants.

Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant.

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

KCNE1 G38S polymorphism is not the cause of long QT syndrome

Letter by Olesen et al Regarding Article, “MOG1: A New Susceptibility Gene for Brugada Syndrome” ⬇️

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

Multi-ethnic genome-wide association study for atrial fibrillation

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

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

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

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

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

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

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

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

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

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

Reevaluation of genetic variants previously associated with arrhythmogenic right ventricular cardiomyopathy integrating population-based cohorts and proteomics data

Risk Prediction of Atrial Fibrillation Based on Electrocardiographic Interatrial Block.

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

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

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

SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation

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

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

Short QT syndrome as an inherited condition ⬇️

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

The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases

The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death

The role of common genetic variants in atrial fibrillation

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

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

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