| 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 | 190 | 2013 |
| Exome-wide association study of plasma lipids in> 300,000 individuals DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ... Nature genetics 49 (12), 1758, 2017 | 163 | 2017 |
| Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation MF Sinner, NR Tucker, KL Lunetta, K Ozaki, JG Smith, S Trompet, JC Bis, ... Circulation 130 (15), 1225-1235, 2014 | 143 | 2014 |
| Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology MA Ferreira, JM Vonk, H Baurecht, I Marenholz, C Tian, JD Hoffman, ... Nature genetics 49 (12), 1752, 2017 | 129 | 2017 |
| 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 | 123 | 2012 |
| Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation MS Olesen, T Jespersen, JB Nielsen, B Liang, DV Møller, P Hedley, ... Cardiovascular research 89 (4), 786-793, 2011 | 111 | 2011 |
| High Prevalence of Long QT Syndrome Associated SCN5A Variants in Patients with Early-Onset Lone Atrial Fibrillation MS Olesen, L Yuan, B Liang, AG Holst, N Nielsen, JB Nielsen, PL Hedley, ... Circulation: Cardiovascular Genetics, 2012 | 103 | 2012 |
| Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation IE Christophersen, MS Olesen, B Liang, MN Andersen, AP Larsen, ... European Heart Journal, 2012 | 102 | 2012 |
| Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use M Liu, Y Jiang, R Wedow, Y Li, DM Brazel, F Chen, G Datta, ... Nature genetics 51 (2), 237-244, 2019 | 97 | 2019 |
| Epilepsy and risk of death and sudden unexpected death in the young: a nationwide study AG Holst, BG Winkel, B Risgaard, JB Nielsen, PV Rasmussen, S Haunsø, ... Epilepsia 54 (9), 1613-1620, 2013 | 93 | 2013 |
| J-shaped association between QTc interval duration and the risk of atrial fibrillation: results from the Copenhagen ECG study JB Nielsen, C Graff, A Pietersen, B Lind, JJ Struijk, MS Olesen, S Haunsø, ... Journal of the American College of Cardiology 61 (25), 2557-2564, 2013 | 91 | 2013 |
| Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies W Zhou, JB Nielsen, LG Fritsche, R Dey, ME Gabrielsen, BN Wolford, ... Nature genetics 50 (9), 1335-1341, 2018 | 89 | 2018 |
| Recurrence of arrhythmia following short-term oral AMIOdarone after CATheter ablation for atrial fibrillation: a double-blind, randomized, placebo-controlled study (AMIO-CAT trial) S Darkner, X Chen, J Hansen, S Pehrson, A Johannessen, JB Nielsen, ... European heart journal 35 (47), 3356-3364, 2014 | 84 | 2014 |
| P-wave duration and the risk of atrial fibrillation: Results from the Copenhagen ECG Study JB Nielsen, JT Kühl, A Pietersen, C Graff, B Lind, JJ Struijk, MS Olesen, ... Heart Rhythm 12 (9), 1887-1895, 2015 | 81 | 2015 |
| Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation MS Olesen, BH Bentzen, JB Nielsen, AB Steffensen, JP David, J Jabbari, ... BMC medical genetics 13 (1), 24, 2012 | 78 | 2012 |
| Risk of atrial fibrillation as a function of the electrocardiographic PR interval: results from the Copenhagen ECG Study JB Nielsen, A Pietersen, C Graff, B Lind, JJ Struijk, MS Olesen, S Haunsø, ... Heart Rhythm 10 (9), 1249-1256, 2013 | 76 | 2013 |
| Biobank-driven genomic discovery yields new insight into atrial fibrillation biology JB Nielsen, RB Thorolfsdottir, LG Fritsche, W Zhou, MW Skov, SE Graham, ... Nature genetics 50 (9), 1234-1239, 2018 | 70 | 2018 |
| New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia J Jabbari, R Jabbari, MW Nielsen, AG Holst, JB Nielsen, S Haunsø, ... Circulation: Cardiovascular Genetics 6 (5), 481-489, 2013 | 68 | 2013 |
| Risk prediction of cardiovascular death based on the QTc interval: evaluating age and gender differences in a large primary care population JB Nielsen, C Graff, PV Rasmussen, A Pietersen, B Lind, MS Olesen, ... European heart journal 35 (20), 1335-1344, 2014 | 63 | 2014 |
| Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years MS Olesen, AG Holst, J Jabbari, JB Nielsen, IE Christophersen, ... Canadian Journal of Cardiology 28 (2), 191-195, 2012 | 52 | 2012 |
Jesper Hastrup SvendsenProfessor, MD, DMSc, FESC, FEHRAVerified email at regionh.dk
