Jonas Bille Nielsen
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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
2892019
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), 1758-1766, 2017
2442017
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), 1752-1757, 2017
2082017
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
2072013
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
1952018
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
1612014
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
1402018
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
1282012
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
1172011
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
1152012
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
1132012
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
1072013
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
1062015
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
1022014
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
962013
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), 1-9, 2012
912012
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
862013
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
852014
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
712013
Biological and clinical insights from genetics of insomnia symptoms
JM Lane, SE Jones, HS Dashti, AR Wood, KG Aragam, VT van Hees, ...
Nature genetics 51 (3), 387-393, 2019
662019
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