Lisbeth N. Pedersen
Palle Juul Jensens Boulevard 99
Aarhus N, Denmark
Aarhus N, Denmark
Last Updated: 09/26/2026
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Found 19 publications
Publisher Correction: Population genomics of post-glacial western Eurasia.
Journal: Nature
Published: January 18, 2024
100 ancient genomes show repeated population turnovers in Neolithic Denmark.
Journal: Nature
Published: April 06, 2023
Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome.
Journal: Heart rhythm
Published: June 02, 2022
Diagnostic Yield of Genetic Testing in Young Patients With Atrioventricular Block of Unknown Cause.
Journal: Journal of the American Heart Association
Published: April 26, 2022
Dilated cardiomyopathy caused by truncating titin variants: long-term outcomes, arrhythmias, response to treatment and sex differences.
Journal: Journal of medical genetics
Published: May 11, 2020
Implantable cardioverter-defibrillator therapy and device-related complications in young patients with inherited cardiomyopathies or channelopathies: a 17-year cohort study.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: January 09, 2018
Outcome of clinical management in relatives of sudden cardiac death victims.
Journal: International journal of cardiology
Published: December 03, 2017
Multifocal atrial and ventricular premature contractions with an increased risk of dilated cardiomyopathy caused by a Nav1.5 gain-of-function mutation (G213D).
Journal: International journal of cardiology
Published: September 24, 2017
Targeted next generation sequencing in a young population with suspected inherited malignant cardiac arrhythmias.
Journal: European journal of human genetics : EJHG
Published: April 24, 2017
Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome.
Journal: Nature communications
Published: March 01, 2017
A 45-SNP genetic risk score is increased in early-onset coronary artery disease but independent of familial disease clustering.
Journal: Atherosclerosis
Published: November 16, 2016
Last Updated: 09/26/2026