Morten Salling Olesen
Morten Salling Olesen
Associate professor, PhD, Head of Laboratory,
Verified email at sund.ku.dk
TitleCited byYear
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, 2013
3102013
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
2562016
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, 2013
1882013
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
1342014
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, 2012
1232012
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, 2010
1112010
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, 2012
1022012
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
1012012
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
972012
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, 2014
902014
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
882013
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
862013
The genetic component of Brugada syndrome
MW Nielsen, AG Holst, SP Olesen, MS Olesen
Frontiers in physiology 4, 179, 2013
792013
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
782015
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
782012
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
762015
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
742013
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
682013
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
672013
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, 2018
662018
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