关注
Morten Salling Olesen
Morten Salling Olesen
Professor, PhD
在 sund.ku.dk 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
7132016
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
6212018
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
5522013
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
3522021
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
2392013
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
2232015
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
2202014
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
1622013
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
1582012
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
1502012
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
1472012
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
1452014
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
1442013
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
1392013
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
1362011
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
1312014
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
1282015
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
1262013
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
1162013
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
1132012
系统目前无法执行此操作,请稍后再试。
文章 1–20