| Genetic misdiagnoses and the potential for health disparities AK Manrai, BH Funke, HL Rehm, MS Olesen, BA Maron, P Szolovits, ... New England Journal of Medicine 375 (7), 655-665, 2016 | 713 | 2016 |
| 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 | 621 | 2018 |
| Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ... Nature genetics 45 (9), 1044-1049, 2013 | 552 | 2013 |
| Implantable loop recorder detection of atrial fibrillation to prevent stroke (The LOOP Study): a randomised controlled trial JH Svendsen, SZ Diederichsen, S Højberg, DW Krieger, C Graff, ... The Lancet 398 (10310), 1507-1516, 2021 | 352 | 2021 |
| 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 | 239 | 2013 |
| 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 | 223 | 2015 |
| 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 | 220 | 2014 |
| 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 34 (20), 1517-1525, 2013 | 162 | 2013 |
| Familial Aggregation of Lone Atrial Fibrillation in Young Persons N Øyen, MF Ranthe, L Carstensen, HA Boyd, MS Olesen, SP Olesen, ... Journal of the American College of Cardiology, 2012 | 158 | 2012 |
| 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 5 (4), 450-459, 2012 | 150 | 2012 |
| 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 | 147 | 2012 |
| Atrial fibrillation: the role of common and rare genetic variants MS Olesen, MW Nielsen, S Haunsø, JH Svendsen European Journal of Human Genetics 22 (3), 297-306, 2014 | 145 | 2014 |
| 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 | 144 | 2013 |
| 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 | 139 | 2013 |
| 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 | 136 | 2011 |
| 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 | 131 | 2014 |
| Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study ER Behr, E Savio-Galimberti, J Barc, AG Holst, E Petropoulou, BP Prins, ... Cardiovascular research 106 (3), 520-529, 2015 | 128 | 2015 |
| 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 | 126 | 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 | 116 | 2013 |
| 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, 1-9, 2012 | 113 | 2012 |
Jesper Hastrup SvendsenProfessor, MD, DMSc, FESC, FEHRA在 regionh.dk 的电子邮件经过验证
