| Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk OB Vad, LM Monfort, C Paludan-Müller, K Kahnert, SZ Diederichsen, ... JAMA cardiology, 2024 | | 2024 |
| Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias LC Weng, S Khurshid, AW Hall, V Nauffal, VN Morrill, YV Sun, JT Rämö, ... Circulation: Genomic and Precision Medicine, e004320, 2024 | | 2024 |
| Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death C Paludan‐Müller, NK Stampe, LM Monfort, L Andreasen, OB Vad, ... Journal of the American Heart Association 13 (9), e034439, 2024 | | 2024 |
| Accessory Pathway Treated With Catheter Ablation Is Associated With Cardiomyopathy, Heart Failure, and Mortality C Paludan-Müller, NK Stampe, OB Vad, L Andreasen, C Torp-Pedersen, ... Clinical Electrophysiology 10 (5), 973-975, 2024 | | 2024 |
| Atrial fibrillation: age at diagnosis, incident cardiovascular events, and mortality C Paludan-Müller, OB Vad, NK Stampe, SZ Diederichsen, L Andreasen, ... European Heart Journal, ehae216, 2024 | 7 | 2024 |
| Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation OB Vad, E Angeli, M Liss, G Ahlberg, L Andreasen, IE Christophersen, ... Basic to Translational Science 9 (2), 163-180, 2024 | 4 | 2024 |
| Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications RBTM Sterenborg, I Steinbrenner, Y Li, MN Bujnis, T Naito, E Marouli, ... Nature communications 15 (1), 888, 2024 | 7 | 2024 |
| Therapeutic effects of ALK5i on pulmonary function and fibrosis in a high-fat diet+ bleomycin-induced and spirometry-confirmed mouse model of IPF AG Petersen, J Bousamaki, LJ Andreasen, D Oró, JD Schmidt, Y Nie, ... European Respiratory Journal 62 (suppl 67), 2023 | 1 | 2023 |
| Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci J Ghouse, V Tragante, A Muhammad, G Ahlberg, MW Skov, DM Roden, ... European Heart Journal 43 (45), 4707-4718, 2022 | 7 | 2022 |
| Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT L Andreasen, G Ahlberg, HM Ægisdottir, G Sveinbjörnsson, ... Circulation research 131 (10), 862-865, 2022 | 3 | 2022 |
| Genome-wide multi-trait analysis on cardioembolic stroke identifies 47 novel loci LM Monfort, G Ahlberg, L Andreasen, J Ghouse, S Haunso, H Bundgaard, ... EUROPEAN HEART JOURNAL 43, 2855-2855, 2022 | | 2022 |
| Genome-wide association study on cerebral white-matter hyperintensities in 36,577 individuals J Jespersen, G Ahlberg, L Andreasen, J Ghouse, KS Frederiksen, ... European Heart Journal 43 (Supplement_2), ehac544. 3019, 2022 | | 2022 |
| Loss-of-function variants in founder population highlight atrial myopathy as susceptibility to atrial fibrillation C Paludan-Muller, OB Vad, K Kahnert, G Ahlberg, LM Monfort, SA Rand, ... European Heart Journal 43 (Supplement_2), ehac544. 2875, 2022 | 1 | 2022 |
| Genome-wide multi-trait analysis on cardioembolic stroke identifies 47 novel loci L Meseguer Monfort, G Ahlberg, L Andreasen, J Ghouse, S Haunso, ... European Heart Journal 43 (Supplement_2), ehac544. 2855, 2022 | 1 | 2022 |
| Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways WJ Young, N Lahrouchi, A Isaacs, TV Duong, L Foco, F Ahmed, JA Brody, ... Nature communications 13 (1), 5144, 2022 | 21 | 2022 |
| Genome-wide association studies of the left atrium and supraventricular tachycardias (PhD). L Andreasen University of Copenhagen, 2022 | | 2022 |
| Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population C Paludan-Müller, S Larsen, G Ahlberg, L Andreasen, LM Monfort, ... Circulation: Genomic and Precision Medicine 15 (1), e003574, 2022 | 1 | 2022 |
| 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 42 (44), 4523-4534, 2021 | 37 | 2021 |
| Clinical Implications of SCN5A and SCN10A Loss of Function Variants in 169,610 Exomes Representing the General Population C Paludan-Mueller, S Larsen, G Ahlberg, L Andreasen, JHH Svendsen, ... Circulation 144 (Suppl_1), A12381-A12381, 2021 | | 2021 |
| Genetic Variants Close to NKX2-5 and MYH6 Are Associated With AV Nodal Reentry Tachycardia in First Genome-Wide Association Study L Andreasen, G Ahlberg, PR Lundegaard, H Ægisdottir, JP Hartmann, ... Circulation 144 (Suppl_1), A13222-A13222, 2021 | | 2021 |
Morten Salling OlesenProfessor, PhD在 sund.ku.dk 的电子邮件经过验证
