| New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants C Andreasen, JB Nielsen, L Refsgaard, AG Holst, AH Christensen, ... European Journal of Human Genetics 21 (9), 918, 2013 | 188 | 2013 |
| Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation MS Olesen, L Andreasen, J Jabbari, L Refsgaard, S Haunsø, SP Olesen, ... Heart Rhythm 11 (2), 246-251, 2014 | 44 | 2014 |
| Numerous Brugada syndrome–associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality J Ghouse, CT Have, MW Skov, L Andreasen, G Ahlberg, JB Nielsen, ... Genetics in Medicine 19 (5), 521, 2017 | 15 | 2017 |
| Genetic aspects of lone atrial fibrillation: what do we know? L Andreasen, J B Nielsen, M S Olesen Current pharmaceutical design 21 (5), 667-678, 2015 | 13 | 2015 |
| Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation G Ahlberg, L Refsgaard, PR Lundegaard, L Andreasen, MF Ranthe, ... Nature communications 9 (1), 4316, 2018 | 11 | 2018 |
| Brugada syndrome risk loci seem protective against atrial fibrillation L Andreasen, JB Nielsen, S Darkner, IE Christophersen, J Jabbari, ... European Journal of Human Genetics 22 (12), 1357, 2014 | 11 | 2014 |
| Genetic modifier of the QTc interval associated with early-onset atrial fibrillation L Andreasen, JB Nielsen, IE Christophersen, AG Holst, A Sajadieh, ... Canadian Journal of Cardiology 29 (10), 1234-1240, 2013 | 11 | 2013 |
| Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes L Andreasen, G Ahlberg, C Tang, C Andreasen, JP Hartmann, ... European Journal of Human Genetics 26 (5), 660, 2018 | 3 | 2018 |
| Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants E Gregers, G Ahlberg, T Christensen, J Jabbari, KO Larsen, CB Herfelt, ... Heart rhythm 14 (10), 1531-1538, 2017 | 3 | 2017 |
| 4259 Discovery of the first genome-wide significant risk loci for syncope and collapse G Ahlberg, K Hadji-Turdeghal, L Andreasen, CM Hagen, J Ghouse, ... European Heart Journal 40 (Supplement_1), ehz745. 0137, 2019 | | 2019 |
| Genome-wide association study identifies locus at chromosome 2q32. 1 associated with syncope and collapse K Hadji-Turdeghal, L Andreasen, CM Hagen, G Ahlberg, J Ghouse, ... Cardiovascular research, 2019 | | 2019 |
| Titin-truncating variants associates with atrial fibrillation, compromises assembly of the sarcomere: 195 M Olesen, P Lundegaard, G Ahlberg, L Refsgaard, L Andreasen, ... European Heart Journal 39, 2018 | | 2018 |
| 195 Titin-truncating variants associates with atrial fibrillation, compromises assembly of the sarcomere MS Olesen, P Lundegaard, G Ahlberg, L Refsgaard, L Andreasen, ... European Heart Journal 39 (suppl_1), ehy564. 195, 2018 | | 2018 |
| Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest L Andreasen, J Ghouse, MW Skov, CT Have, G Ahlberg, PV Rasmussen, ... Frontiers in physiology 9, 894, 2018 | | 2018 |
| Patients with valvular heart disease and atrial fibrillation carry a high number of germline mutations E Gregers, GA Ahlberg, KO Larsen, J Jabbari, CB Herfelt, KM Henningsen, ... EUROPEAN HEART JOURNAL 37, 302-302, 2016 | | 2016 |
| Spectrum and prevalence of rare mutations involving 13 susceptible genes associated with AF in a cohort of unrelated early-onset lone AF patients MS Olesen, L Andreasen, JB Nielsen, AG Holst, J Jabbari, SP Olesen, ... European Heart Journal 34 (suppl_1), 2013 | | 2013 |
| Heriditary Atrial Fibrillation L Andreasen | | 2013 |
Morten Salling OlesenAssociate professor, PhD, Head of Laboratory,Verified email at sund.ku.dk
