Morten Salling Olesen
Morten Salling Olesen
Associate professor, PhD, Head of Laboratory,
Dirección de correo verificada de sund.ku.dk
TítuloCitado porAño
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
3052013
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
2442016
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
1862013
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
1292014
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
1092010
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
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
962012
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
952012
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
872014
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
872013
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
852013
The genetic component of Brugada syndrome
MW Nielsen, AG Holst, SP Olesen, MS Olesen
Frontiers in physiology 4, 179, 2013
792013
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
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
762015
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
732013
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
672013
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
652013
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
612014
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20