List of works - Morten Salling Olesen

Genetic Misdiagnoses and the Potential for Health Disparities

scientific article

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

scientific article

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

scientific article

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

scientific article published on 14 August 2014

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

scientific article

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

scientific article

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

scientific article published on 8 June 2012

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

scientific article

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

scientific article

Multi-ethnic genome-wide association study for atrial fibrillation

article

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

scientific article published on 17 February 2015

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

scientific article published on 11 February 2013

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

scientific article

Familial Aggregation of Lone Atrial Fibrillation in Young Persons

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

scientific article

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

scientific article

Atrial fibrillation: the role of common and rare genetic variants

scientific article published on 10 July 2013

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

scientific article

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

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

article published in 2012

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

scientific article

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

scientific article

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

scientific article published on 23 April 2015

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

scientific article published on 22 July 2014

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 2 October 2012

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

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

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

scientific article published on 18 October 2013

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

scientific article

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

scientific article published on 17 September 2016

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

scientific article published on 9 May 2011

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

scientific journal article

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

scientific article published on 6 October 2016

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

scientific article published on 18 December 2015

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

scientific journal article

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

scientific article published on 19 December 2012

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

scientific article published on 21 February 2014

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

scientific article

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

scientific article published on 07 December 2010

Abnormal atrial activation in young patients with lone atrial fibrillation

scientific article published on 23 September 2010

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

scientific article (publication date: 2014)

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

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

scientific article

Brugada syndrome risk loci seem protective against atrial fibrillation

scientific article

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

scientific article published on 06 June 2017

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

scientific article published on 16 January 2014

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

scientific article published on January 2015

List of works by Morten Salling Olesen

Genetic Misdiagnoses and the Potential for Health Disparities

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

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

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

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

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

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

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

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

Multi-ethnic genome-wide association study for atrial fibrillation

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

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

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

Familial Aggregation of Lone Atrial Fibrillation in Young Persons

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

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

Atrial fibrillation: the role of common and rare genetic variants

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Abnormal atrial activation in young patients with lone atrial fibrillation

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

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

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

Brugada syndrome risk loci seem protective against atrial fibrillation

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

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

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