| 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 | 406 | 2018 |
| 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 | 225 | 2013 |
| High prevalence of genetic variants previously associated with LQT syndrome in new exome data L Refsgaard, AG Holst, G Sadjadieh, S Haunsø, JB Nielsen, MS Olesen European Journal of Human Genetics 20 (8), 905-908, 2012 | 140 | 2012 |
| A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation MS Olesen, L Refsgaard, AG Holst, AP Larsen, S Grubb, S Haunsø, ... Cardiovascular research 98 (3), 488-495, 2013 | 110 | 2013 |
| High prevalence of genetic variants previously associated with Brugada syndrome in new exome data B Risgaard, R Jabbari, L Refsgaard, AG Holst, S Haunsø, A Sadjadieh, ... Clinical genetics 84 (5), 489-495, 2013 | 107 | 2013 |
| Genome-wide study of atrial fibrillation identifies seven risk loci and highlights biological pathways and regulatory elements involved in cardiac development JB Nielsen, LG Fritsche, W Zhou, TM Teslovich, OL Holmen, S Gustafsson, ... The American Journal of Human Genetics 102 (1), 103-115, 2018 | 88 | 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), 1-11, 2018 | 68 | 2018 |
| 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 | 66 | 2014 |
| Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data C Andreasen, L Refsgaard, JB Nielsen, A Sajadieh, BG Winkel, ... Canadian Journal of Cardiology 29 (9), 1104-1109, 2013 | 59 | 2013 |
| IKs Gain‐ and Loss‐of‐Function in Early‐Onset Lone Atrial Fibrillation AB Steffensen, L Refsgaard, MN Andersen, C Vallet, A Mujezinovic, ... Journal of cardiovascular electrophysiology 26 (7), 715-723, 2015 | 31 | 2015 |
| Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics AG Holst, S Saber, M Houshmand, EV Zaklyazminskaya, Y Wang, ... Canadian Journal of Cardiology 28 (2), 196-200, 2012 | 27 | 2012 |
| 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 |
| Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis L Andreasen, L Bertelsen, J Ghouse, PR Lundegaard, G Ahlberg, ... Scientific reports 10 (1), 1-8, 2020 | 7 | 2020 |
| A novel loss-of-function variant in the chloride ion channel gene CLCN2 associates with atrial fibrillation TH Hansen, Y Yan, G Ahlberg, OB Vad, L Refsgaard, JL Dos Santos, ... Scientific reports 10 (1), 1-10, 2020 | 7 | 2020 |
| Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p. M200V mutation C Mora, M Serzanti, A Giacomelli, S Beltramone, E Marchina, V Bertini, ... Stem Cell Research 24, 8-11, 2017 | 5 | 2017 |
| Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy L Refsgaard, MS Olesen, DV Møller, M Christiansen, S Haunsø, ... Applied & Translational Genomics 1, 44-46, 2012 | 5 | 2012 |
| Screening of the Ito Regulatory Subunit Klf15 in Patients with Early-Onset Lone Atrial Fibrillation MW Nielsen, MS Olesen, L Refsgaard, S Haunsø, JH Svendsen Frontiers in Genetics 4, 88, 2013 | 4 | 2013 |
| Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation OB Vad, Y Yan, F Denti, G Ahlberg, L Refsgaard, SH Bomholtz, JL Santos, ... Frontiers in Genetics 13, 2022 | | 2022 |
| 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 |
| Loss of function in cytoskeletal genes associates with early onset atrial fibrillation O Vad, G Ahlberg, L Refsgaard, JH Svendsen, A Tveit, IE Christophersen, ... EUROPEAN HEART JOURNAL 40, 687-687, 2019 | | 2019 |
Morten Salling OlesenProfessor, PhD, Head of Laboratory,Verified email at sund.ku.dk
