List of works - Britt Maria Beckmann

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

scientific article published on 18 November 2011

A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern

scientific article

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

scientific article published on 3 March 2015

Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA).

scientific article

Atrial Arrhythmias in long-QT syndrome under daily life conditions: a nested case control study

scientific article published on 27 October 2008

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

scientific article published on 01 September 2019

Calmodulin mutations associated with recurrent cardiac arrest in infants

scientific article published on 06 February 2013

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

scientific article

Common variants in KCNN3 are associated with lone atrial fibrillation

scientific article

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

scientific article

Genome-wide association study of PR interval

scientific article

Lack of replication in polymorphisms reported to be associated with atrial fibrillation

scientific article

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

scientific article published on 13 January 2009

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

scientific article published on 10 June 2014

Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study

scientific article published on 04 August 2009

The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)

article

List of works by Britt Maria Beckmann

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

A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA).

Atrial Arrhythmias in long-QT syndrome under daily life conditions: a nested case control study

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

Calmodulin mutations associated with recurrent cardiac arrest in infants

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

Common variants in KCNN3 are associated with lone atrial fibrillation

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

Genome-wide association study of PR interval

Lack of replication in polymorphisms reported to be associated with atrial fibrillation

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study

The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)