| Multi-ethnic genome-wide association study for atrial fibrillation C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ... Nature genetics 50 (9), 1225-1233, 2018 | 698 | 2018 |
| 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 | 119 | 2018 |
| Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism J Ghouse, V Tragante, G Ahlberg, SA Rand, JB Jespersen, EB Leinøe, ... Nature genetics 55 (3), 399-409, 2023 | 89 | 2023 |
| DeepFake electrocardiograms using generative adversarial networks are the beginning of the end for privacy issues in medicine V Thambawita, JL Isaksen, SA Hicks, J Ghouse, G Ahlberg, A Linneberg, ... Scientific reports 11 (1), 21896, 2021 | 78 | 2021 |
| Explaining deep neural networks for knowledge discovery in electrocardiogram analysis SA Hicks, JL Isaksen, V Thambawita, J Ghouse, G Ahlberg, A Linneberg, ... Scientific reports 11 (1), 10949, 2021 | 75 | 2021 |
| Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes P Benzoni, G Campostrini, S Landi, V Bertini, E Marchina, M Iascone, ... Cardiovascular Research 116 (6), 1147-1160, 2020 | 66 | 2020 |
| Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval J Ghouse, CT Have, P Weeke, J Bille Nielsen, G Ahlberg, ... European heart journal 36 (37), 2523-2529, 2015 | 60 | 2015 |
| Early sarcomere and metabolic defects in a zebrafish pitx2c cardiac arrhythmia model MM Collins, G Ahlberg, CV Hansen, S Guenther, R Marín-Juez, AM Sokol, ... Proceedings of the National Academy of Sciences 116 (48), 24115-24121, 2019 | 43 | 2019 |
| 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 | 42 | 2021 |
| Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia‐associated variants C Paludan‐Müller, G Ahlberg, J Ghouse, C Herfelt, JH Svendsen, ... Clinical Genetics 91 (1), 63-72, 2017 | 35 | 2017 |
| 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 | 32 | 2022 |
| Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy N Nouhravesh, G Ahlberg, J Ghouse, C Andreasen, JH Svendsen, ... Molecular genetics & genomic medicine 4 (6), 617-623, 2016 | 32 | 2016 |
| 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 | 28 | 2017 |
| A novel familial cardiac arrhythmia syndrome with widespread ST-segment depression H Bundgaard, C Jøns, EM Lodder, JMG Izarzugaza, JA Romero Herrera, ... New England Journal of Medicine 379 (18), 1780-1781, 2018 | 25 | 2018 |
| Distinguishing pathogenic mutations from background genetic noise in cardiology: the use of large genome databases for genetic interpretation J Ghouse, MW Skov, RS Bigseth, G Ahlberg, JK Kanters, MS Olesen Clinical Genetics 93 (3), 459-466, 2018 | 25 | 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 | 22 | 2020 |
| 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 | 20 | 2018 |
| Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis J Ghouse, G Sveinbjörnsson, M Vujkovic, AS Seidelin, ... Nature Genetics, 1-11, 2024 | 17 | 2024 |
| 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 | 17 | 2021 |
| 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 | 17 | 2020 |