| 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), 918-928, 2013 | 216 | 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 | 60 | 2014 |
| 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), 1-11, 2018 | 49 | 2018 |
| 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), 521-528, 2017 | 21 | 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 | 15 | 2015 |
| 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), 1357-1361, 2014 | 15 | 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 | 12 | 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), 660-668, 2018 | 8 | 2018 |
| Loss-of-function variants in cytoskeletal genes are associated with early-onset atrial fibrillation OB Vad, C Paludan-Müller, G Ahlberg, SM Kalstø, J Ghouse, L Andreasen, ... Journal of clinical medicine 9 (2), 372, 2020 | 7 | 2020 |
| 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 | 7 | 2017 |
| 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 116 (1), 138-148, 2020 | 6 | 2020 |
| Atrial fibrillation—a complex polygenetic disease JH Andersen, L Andreasen, MS Olesen European Journal of Human Genetics, 1-10, 2020 | 2 | 2020 |
| Verification of threshold for image intensity ratio analyses of late gadolinium enhancement magnetic resonance imaging of left atrial fibrosis in 1.5 T scans L Bertelsen, F Alarcón, L Andreasen, E Benito, MS Olesen, N Vejlstrup, ... The international journal of cardiovascular imaging 36 (3), 513-520, 2020 | 2 | 2020 |
| 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 | 2 | 2018 |
| Association of Variants Near the Bradykinin Receptor B2 Gene With Angioedema in Patients Taking ACE Inhibitors J Ghouse, G Ahlberg, L Andreasen, K Banasik, S Brunak, M Schwinn, ... Journal of the American College of Cardiology 78 (7), 696-709, 2021 | 1 | 2021 |
| Genome-wide association study identifies 18 novel loci associated with left atrial volume and function G Ahlberg, L Andreasen, J Ghouse, L Bertelsen, H Bundgaard, S Haunsø, ... European Heart Journal, 2021 | 1 | 2021 |
| Cardiac magnetic resonance systematically overestimates mitral regurgitations by the indirect method L Bertelsen, N Vejlstrup, L Andreasen, MS Olesen, JH Svendsen Open heart 7 (2), e001323, 2020 | 1 | 2020 |
| Mendelian randomization—a powerful tool to study the causal effects of atrial fibrillation on loss of brain volume L Andreasen BMC medicine 19 (1), 1-2, 2021 | | 2021 |
| Rare coding variants in MYH6 are associated with atrial fibrillation: results from 45,596 exomes representing the general population OB Vad, C Paludan-Muller, G Ahlberg, L Andreasen, L Refsgaard, ... European Heart Journal 41 (Supplement_2), ehaa946. 0342, 2020 | | 2020 |
| Genome-wide association study of patients with atrioventricular nodal reentry tachycardia L Andreasen, G Ahlberg, J Hartmann, C Paludan-Mueller, HK Jensen, ... European Heart Journal 41 (Supplement_2), ehaa946. 3687, 2020 | | 2020 |
Morten Salling OlesenProfessor, PhD, Head of Laboratory,Verified email at sund.ku.dk
