Morten S. Olesen, Ph.D. - Publications

Affiliations: 
2009 Columbia University, New York, NY 

111 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Svendsen JH, Diederichsen SZ, Højberg S, Krieger DW, Graff C, Kronborg C, Olesen MS, Nielsen JB, Holst AG, Brandes A, Haugan KJ, Køber L. Implantable loop recorder detection of atrial fibrillation to prevent stroke (The LOOP Study): a randomised controlled trial. Lancet (London, England). PMID 34469766 DOI: 10.1016/S0140-6736(21)01698-6  1
2021 Ghouse J, Ahlberg G, Andreasen L, Banasik K, Brunak S, Schwinn M, Larsen IH, Petersen O, Sørensen E, Ullum H, Rasmussen ER, Eriksson N, Hallberg P, Wadelius M, Bundgaard H, ... Olesen MS, et al. Association of Variants Near the Bradykinin Receptor B Gene With Angioedema in Patients Taking ACE Inhibitors. Journal of the American College of Cardiology. 78: 696-709. PMID 34384552 DOI: 10.1016/j.jacc.2021.05.054  1
2021 Ahlberg G, Andreasen L, Ghouse J, Bertelsen L, Bundgaard H, Haunsø S, Svendsen JH, Olesen MS. Genome-wide association study identifies 18 novel loci associated with left atrial volume and function. European Heart Journal. PMID 34338756 DOI: 10.1093/eurheartj/ehab466  1
2021 Hicks SA, Isaksen JL, Thambawita V, Ghouse J, Ahlberg G, Linneberg A, Grarup N, Strümke I, Ellervik C, Olesen MS, Hansen T, Graff C, Holstein-Rathlou NH, Halvorsen P, Maleckar MM, et al. Explaining deep neural networks for knowledge discovery in electrocardiogram analysis. Scientific Reports. 11: 10949. PMID 34040033 DOI: 10.1038/s41598-021-90285-5  1
2021 Linscheid N, Santos A, Poulsen PC, Mills RW, Calloe K, Leurs U, Ye JZ, Stolte C, Thomsen MB, Bentzen BH, Lundegaard PR, Olesen MS, Jensen LJ, Olsen JV, Lundby A. Quantitative proteome comparison of human hearts with those of model organisms. Plos Biology. 19: e3001144. PMID 33872299 DOI: 10.1371/journal.pbio.3001144  1
2021 Bertelsen L, Diederichsen SZ, Haugan KJ, Brandes A, Graff C, Krieger D, Kronborg C, Køber L, Peters DC, Olesen MS, Højberg S, Vejlstrup N, Svendsen JH. The Authors Reply. Jacc. Cardiovascular Imaging. 14: 704-705. PMID 33663771 DOI: 10.1016/j.jcmg.2020.12.032  1
2020 Nielsen JB, Rom O, Surakka I, Graham SE, Zhou W, Roychowdhury T, Fritsche LG, Gagliano Taliun SA, Sidore C, Liu Y, Gabrielsen ME, Skogholt AH, Wolford B, Overton W, Zhao Y, ... ... Olesen MS, et al. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Nature Communications. 11: 6417. PMID 33339817 DOI: 10.1038/s41467-020-20086-3  1
2020 Isaksen JL, Ghouse J, Graff C, Olesen MS, Holst AG, Pietersen A, Nielsen JB, Skov MW, Kanters JK. Electrocardiographic T-wave morphology and risk of mortality. International Journal of Cardiology. PMID 33321127 DOI: 10.1016/j.ijcard.2020.12.016  1
2020 Andersen JH, Andreasen L, Olesen MS. Atrial fibrillation-a complex polygenetic disease. European Journal of Human Genetics : Ejhg. PMID 33279945 DOI: 10.1038/s41431-020-00784-8  1
2020 Vissing CR, Rasmussen TB, Dybro AM, Olesen MS, Pedersen LN, Jensen M, Bundgaard H, Christensen AH. Dilated cardiomyopathy caused by truncating titin variants: long-term outcomes, arrhythmias, response to treatment and sex differences. Journal of Medical Genetics. PMID 33106378 DOI: 10.1136/jmedgenet-2020-107178  1
2020 Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, Amin AS, Nannenberg EA, Ware JS, Whiffin N, Mazzarotto F, Škorić-Milosavljević D, Krijger C, Arbelo E, Babuty D, ... ... Olesen MS, et al. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32893267 DOI: 10.1038/S41436-020-00946-5  1
2020 Ghouse J, Blanche P, Skov MW, Lind B, Vaag A, Kanters JK, Svendsen JH, Køber L, Olesen MS, Gerds TA, Holst AG, Nielsen JB. Early glycemic changes after initiation of oral anti-diabetic medication and risk of major adverse cardiovascular events: results from a large primary care population of patients with type 2 diabetes. European Heart Journal. Cardiovascular Pharmacotherapy. PMID 32614428 DOI: 10.1093/Ehjcvp/Pvaa072  1
2020 Andreasen L, Bertelsen L, Ghouse J, Lundegaard PR, Ahlberg G, Refsgaard L, Rasmussen TB, Eiskjær H, Haunsø S, Vejlstrup N, Svendsen JH, Olesen MS. Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis. Scientific Reports. 10: 10039. PMID 32572052 DOI: 10.1038/s41598-020-66671-w  1
2020 Bertelsen L, Diederichsen SZ, Haugan KJ, Brandes A, Graff C, Krieger D, Kronborg C, Køber L, Peters DC, Olesen MS, Højberg S, Vejlstrup N, Svendsen JH. Left Atrial Late Gadolinium Enhancement is Associated With Incident Atrial Fibrillation as Detected by Continuous Monitoring With Implantable Loop Recorders. Jacc. Cardiovascular Imaging. PMID 32563642 DOI: 10.1016/j.jcmg.2020.03.024  1
2020 Ntalla I, Weng LC, Cartwright JH, Hall AW, Sveinbjornsson G, Tucker NR, Choi SH, Chaffin MD, Roselli C, Barnes MR, Mifsud B, Warren HR, Hayward C, Marten J, Cranley JJ, ... ... Olesen M, et al. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. Nature Communications. 11: 2542. PMID 32439900 DOI: 10.1038/S41467-020-15706-X  1
2020 Lahrouchi N, Tadros R, Crotti L, Mizusawa Y, Postema PG, Beekman L, Walsh R, Hasegawa K, Barc J, Ernsting M, Turkowski KL, Mazzanti A, Beckmann BM, Shimamoto K, Diamant UB, ... ... Olesen MS, et al. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation. PMID 32429735 DOI: 10.1161/Circulationaha.120.045956  1
2020 Linscheid N, Poulsen PC, Pedersen ID, Gregers E, Svendsen JH, Olesen MS, Olsen JV, Delmar M, Lundby A. Quantitative proteomics of human heart samples collected in vivo reveal the remodeled protein landscape of dilated left atrium without atrial fibrillation. Molecular & Cellular Proteomics : McP. PMID 32291283 DOI: 10.1074/mcp.RA119.001878  1
2020 Reese-Petersen AL, Olesen MS, Karsdal MA, Svendsen JH, Genovese F. Atrial fibrillation and cardiac fibrosis: A review on the potential of extracellular matrix proteins as biomarkers. Matrix Biology : Journal of the International Society For Matrix Biology. PMID 32205152 DOI: 10.1016/j.matbio.2020.03.005  1
2020 Hansen TH, Yan Y, Ahlberg G, Vad OB, Refsgaard L, Dos Santos JL, Mutsaers N, Svendsen JH, Olesen MS, Bentzen BH, Schmitt N. A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation. Scientific Reports. 10: 1453. PMID 31996765 DOI: 10.1038/s41598-020-58475-9  1
2019 Collins MM, Ahlberg G, Hansen CV, Guenther S, Marín-Juez R, Sokol AM, El-Sammak H, Piesker J, Hellsten Y, Olesen MS, Stainier DYR, Lundegaard PR. Early sarcomere and metabolic defects in a zebrafish cardiac arrhythmia model. Proceedings of the National Academy of Sciences of the United States of America. PMID 31704768 DOI: 10.1073/pnas.1913905116  1
2019 Ghouse J, Isaksen JL, Skov MW, Lind B, Svendsen JH, Kanters JK, Olesen MS, Holst AG, Nielsen JB. Effect of diabetes duration on the relationship between glycaemic control and risk of death in older adults with type 2 diabetes. Diabetes, Obesity & Metabolism. PMID 31596048 DOI: 10.1111/Dom.13891  1
2019 Benzoni P, Campostrini G, Landi S, Bertini V, Marchina E, Iascone M, Ahlberg G, Olesen MS, Crescini E, Mora C, Bisleri G, Muneretto C, Ronca R, Presta M, Poliani PL, et al. Human iPSC modeling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes. Cardiovascular Research. PMID 31504264 DOI: 10.1093/cvr/cvz217  1
2019 Ye JZ, Delmar M, Lundby A, Olesen MS. Reevaluation of Genetic Variants Previously Associated with Arrhythmogenic Right Ventricular Cardiomyopathy Integrating Population-based Cohorts and Proteomics Data. Clinical Genetics. PMID 31402444 DOI: 10.1111/cge.13621  1
2019 Seifert MB, Olesen MS, Christophersen IE, Nielsen JB, Carlson J, Holmqvist F, Tveit A, Haunsø S, Svendsen JH, Platonov PG. Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation. Annals of Noninvasive Electrocardiology : the Official Journal of the International Society For Holter and Noninvasive Electrocardiology, Inc. e12661. PMID 31152482 DOI: 10.1111/anec.12661  1
2019 Rasmussen PV, Skov MW, Ghouse J, Pietersen A, Hansen SM, Torp-Pedersen C, Køber L, Haunsø S, Olesen MS, Svendsen JH, Melgaard J, Graff C, Holst AG, Nielsen JB. Clinical implications of electrocardiographic bundle branch block in primary care. Heart (British Cardiac Society). PMID 31129608 DOI: 10.1136/heartjnl-2018-314295  1
2019 Hadji-Turdeghal K, Andreasen L, Hagen CM, Ahlberg G, Ghouse J, Bækvad-Hansen M, Bybjerg-Grauholm J, Hougaard DM, Hedley P, Haunsø S, Svendsen JH, Kanters JK, Jepps TA, Skov MW, Christiansen M, ... Olesen MS, et al. Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse. Cardiovascular Research. PMID 31049583 DOI: 10.1093/Cvr/Cvz106  1
2019 Paludan-Müller C, Ghouse J, Vad OB, Herfelt CB, Lundegaard P, Ahlberg G, Schmitt N, Svendsen JH, Haunsø S, Bundgaard H, Hansen T, Kanters JK, Olesen MS. Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts. European Journal of Human Genetics : Ejhg. PMID 31043699 DOI: 10.1038/S41431-019-0416-3  1
2019 Ghouse J, Isaksen JL, Skov MW, Lind B, Svendsen JH, Kanters JK, Olesen MS, Holst AG, Nielsen JB. Author response for "Effect of diabetes duration on the relationship between glycaemic control and risk of death in older adults with type 2 diabetes" Diabetes, Obesity and Metabolism. DOI: 10.1111/Dom.13891/V2/Response1  1
2019 Ahlberg G, Hadji-Turdeghal K, Andreasen L, Hagen CM, Ghouse J, Baekvad-Hansen M, Bybjerg-Grauholm J, Hougaard DM, Hedley P, Haunsoe S, Svendsen JH, Jepps TA, Skov MW, Christiansen M, Olesen MS. 4259Discovery of the first genome-wide significant risk loci for syncope and collapse European Heart Journal. 40. DOI: 10.1093/Eurheartj/Ehz745.0137  1
2018 Bundgaard H, Jøns C, Lodder EM, Izarzugaza JMG, Romero Herrera JA, Pehrson S, Tfelt-Hansen J, Ahlberg G, Olesen MS, Holst AG, Wellens H, de Villiers C, Hastings R, Stuart G, Brunak S, et al. A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression. The New England Journal of Medicine. 379: 1780-1781. PMID 30380381 DOI: 10.1056/Nejmc1807668  1
2018 Ghouse J, Skov MW, Kanters JK, Lind B, Isaksen JL, Blanche P, Haunsø S, Køber L, Svendsen JH, Olesen MS, Holst AG, Gerds TA, Nielsen JB. Visit-to-Visit Variability of Hemoglobin A in People Without Diabetes and Risk of Major Adverse Cardiovascular Events and All-Cause Mortality. Diabetes Care. PMID 30352898 DOI: 10.2337/Dc18-1396  1
2018 Ahlberg G, Refsgaard L, Lundegaard PR, Andreasen L, Ranthe MF, Linscheid N, Nielsen JB, Melbye M, Haunsø S, Sajadieh A, Camp L, Olesen SP, Rasmussen S, Lundby A, Ellinor PT, ... ... Olesen MS, et al. Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation. Nature Communications. 9: 4316. PMID 30333491 DOI: 10.1038/S41467-018-06618-Y  1
2018 Andreasen L, Ghouse J, Skov MW, Have CT, Ahlberg G, Rasmussen PV, Linneberg A, Pedersen O, Platonov PG, Haunsø S, Svendsen JH, Hansen T, Kanters JK, Olesen MS. Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest. Frontiers in Physiology. 9: 894. PMID 30042696 DOI: 10.3389/Fphys.2018.00894  1
2018 Roselli C, Chaffin MD, Weng LC, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG, Arking DE, Barnard J, Bartz TM, Benjamin EJ, Bihlmeyer NA, ... ... Olesen MS, et al. Multi-ethnic genome-wide association study for atrial fibrillation. Nature Genetics. PMID 29892015 DOI: 10.1038/S41588-018-0133-9  1
2018 Skov MW, Ghouse J, Kühl JT, Platonov PG, Graff C, Fuchs A, Rasmussen PV, Pietersen A, Nordestgaard BG, Torp-Pedersen C, Hansen SM, Olesen MS, Haunsø S, Køber L, Gerds TA, et al. Risk Prediction of Atrial Fibrillation Based on Electrocardiographic Interatrial Block. Journal of the American Heart Association. 7. PMID 29848496 DOI: 10.1161/JAHA.117.008247  1
2018 Denti F, Paludan-Müller C, Olesen SP, Haunsø S, Svendsen JH, Olesen MS, Bentzen BH, Schmitt N. Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation. Personalized Medicine. 15: 93-102. PMID 29714131 DOI: 10.2217/Pme-2017-0076  1
2018 Calloe K, Broendberg AK, Christensen AH, Pedersen LN, Olesen MS, de Los Angeles Tejada M, Friis S, Thomsen MB, Bundgaard H, Jensen HK. Multifocal atrial and ventricular premature contractions with an increased risk of dilated cardiomyopathy caused by a Na1.5 gain-of-function mutation (G213D). International Journal of Cardiology. 257: 160-167. PMID 29506689 DOI: 10.1016/j.ijcard.2017.11.095  1
2018 Andreasen L, Ahlberg G, Tang C, Andreasen C, Hartmann JP, Tfelt-Hansen J, Behr ER, Pehrson S, Haunsø S, LuCamp, Weeke PE, Jespersen T, Olesen MS, Svendsen JH. Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes. European Journal of Human Genetics : Ejhg. PMID 29396561 DOI: 10.1038/s41431-017-0092-0  1
2017 Nielsen JB, Fritsche LG, Zhou W, Teslovich TM, Holmen OL, Gustafsson S, Gabrielsen ME, Schmidt EM, Beaumont R, Wolford BN, Lin M, Brummett CM, Preuss MH, Refsgaard L, Bottinger EP, ... ... Olesen MS, et al. Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. American Journal of Human Genetics. PMID 29290336 DOI: 10.1016/J.Ajhg.2017.12.003  1
2017 Paludan-Müller C, Ahlberg G, Ghouse J, Svendsen JH, Haunsø S, Olesen MS. Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease. Circulation. Cardiovascular Genetics. 10. PMID 29237690 DOI: 10.1161/CIRCGENETICS.117.001878  1
2017 Ghouse J, Skov MW, Bigseth RS, Ahlberg G, Kanters JK, Olesen MS. Distinguishing pathogenic mutations from background genetic noise in cardiology: the use of large genome databases for genetic interpretation. Clinical Genetics. PMID 28589536 DOI: 10.1111/Cge.13066  1
2017 Skov MW, Rasmussen PV, Ghouse J, Hansen SM, Graff C, Olesen MS, Pietersen A, Torp-Pedersen C, Haunsø S, Køber L, Svendsen JH, Holst AG, Nielsen JB. Electrocardiographic Preexcitation and Risk of Cardiovascular Morbidity and Mortality: Results From the Copenhagen ECG Study. Circulation. Arrhythmia and Electrophysiology. 10. PMID 28576781 DOI: 10.1161/CIRCEP.116.004778  1
2017 Gregers E, Ahlberg G, Christensen T, Jabbari J, Larsen KO, Herfelt CB, Henningsen KM, Andreasen L, Thiis JJ, Lund J, Holme S, Haunsø S, Bentzen BH, Schmitt N, Svendsen JH, ... Olesen MS, et al. Deep Sequencing of Atrial Fibrillation Patients with Mitral Valve Regurgitation Shows No Evidence of Mosaicism but Reveals Novel Rare Germline Variants. Heart Rhythm. PMID 28549997 DOI: 10.1016/j.hrthm.2017.05.027  1
2017 Rasmussen PV, Nielsen JB, Skov MW, Pietersen A, Graff C, Lind B, Struijk JJ, Olesen MS, Haunsø S, Køber L, Svendsen JH, Holst AG. Electrocardiographic PR Interval Duration and Cardiovascular Risk: Results From the Copenhagen ECG Study. The Canadian Journal of Cardiology. 33: 674-681. PMID 28449838 DOI: 10.1016/j.cjca.2017.02.015  1
2016 Nouhravesh N, Ahlberg G, Ghouse J, Andreasen C, Svendsen JH, Haunsø S, Bundgaard H, Weeke PE, Olesen MS. Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy. Molecular Genetics & Genomic Medicine. 4: 617-623. PMID 27896284 DOI: 10.1002/mgg3.245  1
2016 Ghouse J, Have CT, Skov MW, Andreasen L, Ahlberg G, Nielsen JB, Skaaby T, Olesen SP, Grarup N, Linneberg A, Pedersen O, Vestergaard H, Haunsø S, Svendsen JH, Hansen T, ... ... Olesen MS, et al. Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27711072 DOI: 10.1038/Gim.2016.151  1
2016 Paludan-Müller C, Svendsen JH, Olesen MS. The role of common genetic variants in atrial fibrillation. Journal of Electrocardiology. PMID 27624063 DOI: 10.1016/j.jelectrocard.2016.08.012  1
2016 Paludan-Müller C, Ahlberg G, Ghouse J, Herfelt C, Svendsen JH, Haunsø S, Kanters JK, Olesen MS. Integration of 60 000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia associated variants. Clinical Genetics. PMID 27538377 DOI: 10.1111/Cge.12847  1
2016 Manrai AK, Funke BH, Rehm HL, Olesen MS, Maron BA, Szolovits P, Margulies DM, Loscalzo J, Kohane IS. Genetic Misdiagnoses and the Potential for Health Disparities. The New England Journal of Medicine. 375: 655-65. PMID 27532831 DOI: 10.1056/Nejmsa1507092  0.01
2016 Skov MW, Bachmann TN, Rasmussen PV, Olesen MS, Pietersen A, Graff C, Lind B, Struijk JJ, Køber L, Haunsø S, Svendsen JH, Gerds TA, Holst AG, Nielsen JB. Association Between Heart Rate at Rest and Incident Atrial Fibrillation (from the Copenhagen Electrocardiographic Study). The American Journal of Cardiology. PMID 27394409 DOI: 10.1016/j.amjcard.2016.06.013  1
2016 Christensen AH, Chatelain FC, Huttner IG, Olesen MS, Soka M, Feliciangeli S, Horvat C, Santiago CF, Vandenberg JI, Schmitt N, Olesen SP, Lesage F, Fatkin D. The two-pore domain potassium channel, TWIK-1, has a role in the regulation of heart rate and atrial size. Journal of Molecular and Cellular Cardiology. PMID 27103460 DOI: 10.1016/J.Yjmcc.2016.04.006  1
2015 Kanters JK, Olesen MS, Christiansen M. KCNE1 G38S polymorphism is not the cause of long QT syndrome. Journal of Electrocardiology. PMID 26781364 DOI: 10.1016/J.Jelectrocard.2015.12.005  1
2015 Bachmann TN, Skov MW, Rasmussen PV, Graff C, Pietersen A, Lind B, Struijk JJ, Olesen MS, Haunsø S, Køber L, Svendsen JH, Holst AG, Nielsen JB. Electrocardiographic Tpeak-Tend interval and Risk of Cardiovascular Morbidity and Mortality: Results from the Copenhagen ECG Study. Heart Rhythm : the Official Journal of the Heart Rhythm Society. PMID 26707793 DOI: 10.1016/j.hrthm.2015.12.027  1
2015 Ghouse J, Have CT, Weeke P, Bille Nielsen J, Ahlberg G, Balslev-Harder M, Appel EV, Skaaby T, Olesen SP, Grarup N, Linneberg A, Pedersen O, Haunsø S, Hastrup Svendsen J, Hansen T, et al. Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval. European Heart Journal. 36: 2523-9. PMID 26159999 DOI: 10.1093/Eurheartj/Ehv297  1
2015 Nielsen JB, Kühl JT, Pietersen A, Graff C, Lind B, Struijk JJ, Olesen MS, Sinner MF, Bachmann TN, Haunsø S, Nordestgaard BG, Ellinor PT, Svendsen JH, Kofoed KF, Køber L, et al. P-wave duration and the risk of atrial fibrillation: Results from the Copenhagen ECG Study. Heart Rhythm : the Official Journal of the Heart Rhythm Society. PMID 25916567 DOI: 10.1016/j.hrthm.2015.04.026  1
2015 Steffensen AB, Refsgaard L, Andersen MN, Vallet C, Mujezinovic A, Haunsø S, Svendsen JH, Olesen SP, Olesen MS, Schmitt N. IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation. Journal of Cardiovascular Electrophysiology. 26: 715-23. PMID 25786344 DOI: 10.1111/jce.12666  1
2015 Winkel BG, Yuan L, Olesen MS, Sadjadieh G, Wang Y, Risgaard B, Jabbari R, Haunsø S, Holst AG, Hollegaard MV, Tfelt-Hansen J, Jespersen T. The role of the sodium current complex in a nonreferred nationwide cohort of sudden infant death syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 12: 1241-9. PMID 25757662 DOI: 10.1016/J.Hrthm.2015.03.013  1
2015 Jabbari J, Olesen MS, Yuan L, Nielsen JB, Liang B, Macri V, Christophersen IE, Nielsen N, Sajadieh A, Ellinor PT, Grunnet M, Haunsø S, Holst AG, Svendsen JH, Jespersen T. Common and rare variants in SCN10A modulate the risk of atrial fibrillation. Circulation. Cardiovascular Genetics. 8: 64-73. PMID 25691686 DOI: 10.1161/Circgenetics.113.000442  1
2015 Behr ER, Savio-Galimberti E, Barc J, Holst AG, Petropoulou E, Prins BP, Jabbari J, Torchio M, Berthet M, Mizusawa Y, Yang T, Nannenberg EA, Dagradi F, Weeke P, Bastiaenan R, ... ... Olesen M, et al. Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. Cardiovascular Research. 106: 520-9. PMID 25691538 DOI: 10.1093/Cvr/Cvv042  1
2015 Andreasen L, Nielsen JB, Olesen MS. Genetic aspects of lone atrial fibrillation: what do we know? Current Pharmaceutical Design. 21: 667-78. PMID 25175087  1
2014 Sinner MF, Tucker NR, Lunetta KL, Ozaki K, Smith JG, Trompet S, Bis JC, Lin H, Chung MK, Nielsen JB, Lubitz SA, Krijthe BP, Magnani JW, Ye J, Gollob MH, ... ... Olesen MS, et al. Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation. Circulation. 130: 1225-35. PMID 25124494 DOI: 10.1161/Circulationaha.114.009892  1
2014 Jabbari J, Olesen MS, Yuan L, Nielsen JB, Liang B, Macri V, Christophersen IE, Nielsen N, Sajadieh A, Ellinor PT, Grunnet M, Haunsø S, Holst AG, Svendsen JH, Jespersen T. Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation. Circulation. Cardiovascular Genetics. PMID 25085921 DOI: 10.1161/CIRCGENETICS.113.000442  1
2014 Savio-Galimberti E, Weeke P, Muhammad R, Blair M, Ansari S, Short L, Atack TC, Kor K, Vanoye CG, Olesen MS, LuCamp, Yang T, George AL, Roden DM, Darbar D. SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation. Cardiovascular Research. 104: 355-63. PMID 25053638 DOI: 10.1093/cvr/cvu170  1
2014 Yang RQ, Jabbari J, Cheng XS, Jabbari R, Nielsen JB, Risgaard B, Chen X, Sajadieh A, Haunsø S, Svendsen JH, Olesen MS, Tfelt-Hansen J. New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome. Bmc Genetics. 15: 74. PMID 24941995 DOI: 10.1186/1471-2156-15-74  1
2014 Rasmussen PV, Nielsen JB, Pietersen A, Graff C, Lind B, Struijk JJ, Olesen MS, Haunsø S, Køber L, Svendsen JH, Holst AG. Electrocardiographic precordial ST-segment deviations and the risk of cardiovascular death: results from the Copenhagen ECG Study. Journal of the American Heart Association. 3: e000549. PMID 24815495 DOI: 10.1161/JAHA.113.000549  1
2014 Nielsen JB, Bentzen BH, Olesen MS, David JP, Olesen SP, Haunsø S, Svendsen JH, Schmitt N. Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation. Biomarkers in Medicine. 8: 557-70. PMID 24796621 DOI: 10.2217/Bmm.13.137  1
2014 Andreasen L, Nielsen JB, Darkner S, Christophersen IE, Jabbari J, Refsgaard L, Thiis JJ, Sajadieh A, Tveit A, Haunsø S, Svendsen JH, Schmitt N, Olesen MS. Brugada syndrome risk loci seem protective against atrial fibrillation. European Journal of Human Genetics : Ejhg. 22: 1357-61. PMID 24667784 DOI: 10.1038/ejhg.2014.46  1
2014 Nielsen JB, Graff C, Rasmussen PV, Pietersen A, Lind B, Olesen MS, Struijk JJ, Haunsø S, Svendsen JH, Køber L, Gerds TA, Holst AG. Risk prediction of cardiovascular death based on the QTc interval: evaluating age and gender differences in a large primary care population. European Heart Journal. 35: 1335-44. PMID 24603310 DOI: 10.1093/eurheartj/ehu081  1
2014 Yuan L, Koivumäki JT, Liang B, Lorentzen LG, Tang C, Andersen MN, Svendsen JH, Tfelt-Hansen J, Maleckar M, Schmitt N, Olesen MS, Jespersen T. Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant. American Journal of Physiology. Heart and Circulatory Physiology. 306: H1204-12. PMID 24561865 DOI: 10.1152/Ajpheart.00405.2013  1
2014 Sadjadieh G, Jabbari R, Risgaard B, Olesen MS, Haunsø S, Tfelt-Hansen J, Winkel BG. Nationwide (Denmark) study of symptoms preceding sudden death due to arrhythmogenic right ventricular cardiomyopathy. The American Journal of Cardiology. 113: 1250-4. PMID 24513468 DOI: 10.1016/j.amjcard.2013.12.038  1
2014 Liang B, Soka M, Christensen AH, Olesen MS, Larsen AP, Knop FK, Wang F, Nielsen JB, Andersen MN, Humphreys D, Mann SA, Huttner IG, Vandenberg JI, Svendsen JH, Haunsø S, et al. Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis. Journal of Molecular and Cellular Cardiology. 67: 69-76. PMID 24374141 DOI: 10.1016/J.Yjmcc.2013.12.014  1
2014 Olesen MS, Andreasen L, Jabbari J, Refsgaard L, Haunsø S, Olesen SP, Nielsen JB, Schmitt N, Svendsen JH. Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 246-51. PMID 24144883 DOI: 10.1016/J.Hrthm.2013.10.034  1
2014 Olesen MS, Nielsen MW, Haunsø S, Svendsen JH. Atrial fibrillation: the role of common and rare genetic variants. European Journal of Human Genetics : Ejhg. 22: 297-306. PMID 23838598 DOI: 10.1038/ejhg.2013.139  1
2013 Brodehl A, Dieding M, Klauke B, Dec E, Madaan S, Huang T, Gargus J, Fatima A, Saric T, Cakar H, Walhorn V, Tönsing K, Skrzipczyk T, Cebulla R, Gerdes D, ... ... Olesen MS, et al. The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death. Circulation. Cardiovascular Genetics. 6: 615-23. PMID 24200904 DOI: 10.1161/Circgenetics.113.000103  1
2013 Andreasen L, Nielsen JB, Christophersen IE, Holst AG, Sajadieh A, Tveit A, Haunsø S, Svendsen JH, Schmitt N, Olesen MS. Genetic modifier of the QTc interval associated with early-onset atrial fibrillation. The Canadian Journal of Cardiology. 29: 1234-40. PMID 24074973 DOI: 10.1016/j.cjca.2013.06.009  1
2013 Jabbari J, Jabbari R, Nielsen MW, Holst AG, Nielsen JB, Haunsø S, Tfelt-Hansen J, Svendsen JH, Olesen MS. New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia. Circulation. Cardiovascular Genetics. 6: 481-9. PMID 24025405 DOI: 10.1161/CIRCGENETICS.113.000118  1
2013 Nielsen MW, Holst AG, Olesen SP, Olesen MS. The genetic component of Brugada syndrome. Frontiers in Physiology. 4: 179. PMID 23874304 DOI: 10.3389/Fphys.2013.00179  1
2013 Bezzina CR, Barc J, Mizusawa Y, Remme CA, Gourraud JB, Simonet F, Verkerk AO, Schwartz PJ, Crotti L, Dagradi F, Guicheney P, Fressart V, Leenhardt A, Antzelevitch C, Bartkowiak S, ... ... Olesen MS, et al. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nature Genetics. 45: 1044-9. PMID 23872634 DOI: 10.1038/Ng.2712  1
2013 Nielsen JB, Pietersen A, Graff C, Lind B, Struijk JJ, Olesen MS, Haunsø S, Gerds TA, Ellinor PT, Køber L, Svendsen JH, Holst AG. Risk of atrial fibrillation as a function of the electrocardiographic PR interval: results from the Copenhagen ECG Study. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 10: 1249-56. PMID 23608590 DOI: 10.1016/j.hrthm.2013.04.012  1
2013 Nielsen JB, Graff C, Pietersen A, Lind B, Struijk JJ, Olesen MS, Haunsø S, Gerds TA, Svendsen JH, Køber L, Holst AG. J-shaped association between QTc interval duration and the risk of atrial fibrillation: results from the Copenhagen ECG study. Journal of the American College of Cardiology. 61: 2557-64. PMID 23583581 DOI: 10.1016/j.jacc.2013.03.032  1
2013 Andreasen C, Refsgaard L, Nielsen JB, Sajadieh A, Winkel BG, Tfelt-Hansen J, Haunsø S, Holst AG, Svendsen JH, Olesen MS. Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data. The Canadian Journal of Cardiology. 29: 1104-9. PMID 23465283 DOI: 10.1016/j.cjca.2012.12.002  1
2013 Olesen MS, Refsgaard L, Holst AG, Larsen AP, Grubb S, Haunsø S, Svendsen JH, Olesen SP, Schmitt N, Calloe K. A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation. Cardiovascular Research. 98: 488-95. PMID 23400760 DOI: 10.1093/Cvr/Cvt028  1
2013 Andreasen C, Nielsen JB, Refsgaard L, Holst AG, Christensen AH, Andreasen L, Sajadieh A, Haunsø S, Svendsen JH, Olesen MS. New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants. European Journal of Human Genetics : Ejhg. 21: 918-28. PMID 23299917 DOI: 10.1038/ejhg.2012.283  1
2013 Henningsen KM, Olesen MS, Sajadieh G, Haunsoe S, Svendsen JH. A polymorphism associated with increased levels of YKL-40 and the risk of early onset of lone atrial fibrillation. Journal of Negative Results in Biomedicine. 12: 1. PMID 23279705 DOI: 10.1186/1477-5751-12-1  1
2013 Christophersen IE, Olesen MS, Liang B, Andersen MN, Larsen AP, Nielsen JB, Haunsø S, Olesen SP, Tveit A, Svendsen JH, Schmitt N. Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation. European Heart Journal. 34: 1517-25. PMID 23264583 DOI: 10.1093/Eurheartj/Ehs442  1
2013 Christophersen IE, Budtz-Jørgensen E, Olesen MS, Haunsø S, Christensen K, Svendsen JH. Familial atrial fibrillation predicts increased risk of mortality: a study in Danish twins. Circulation. Arrhythmia and Electrophysiology. 6: 10-5. PMID 23255276 DOI: 10.1161/CIRCEP.112.971580  1
2013 Christophersen IE, Holmegard HN, Jabbari J, Sajadieh A, Haunsø S, Tveit A, Svendsen JH, Olesen MS. Rare variants in GJA5 are associated with early-onset lone atrial fibrillation. The Canadian Journal of Cardiology. 29: 111-6. PMID 23040431 DOI: 10.1016/j.cjca.2012.08.002  1
2013 Nielsen MW, Olesen MS, Refsgaard L, Haunsø S, Svendsen JH. Screening of the Ito regulatory subunit Klf15 in patients with early-onset lone atrial fibrillation Frontiers in Genetics. 4. DOI: 10.3389/fgene.2013.00088  1
2013 Bezzina CR, Barc J, Mizusawa Y, Remme CA, Gourraud JB, Simonet F, Verkerk AO, Schwartz PJ, Crotti L, Dagradi F, Guicheney P, Fressart V, Leenhardt A, Antzelevitch C, Bartkowiak S, ... ... Olesen MS, et al. Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death (Nature Genetics (2013) 45 (1044-1049)) Nature Genetics. 45. DOI: 10.1038/Ng1113-1409B  1
2013 Bidstrup S, Olesen MS, Svendsen JH, Nielsen JB. Role of PR-interval in predicting the occurrence of atrial fibrillation Journal of Atrial Fibrillation. 6: 90-94.  1
2012 Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunso S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, et al. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases Journal of Cardiovascular Electrophysiology. 23: 1092-1098. PMID 22882672 DOI: 10.1111/J.1540-8167.2012.02371.X  1
2012 Oyen N, Ranthe MF, Carstensen L, Boyd HA, Olesen MS, Olesen SP, Wohlfahrt J, Melbye M. Familial aggregation of lone atrial fibrillation in young persons. Journal of the American College of Cardiology. 60: 917-21. PMID 22726627 DOI: 10.1016/J.Jacc.2012.03.046  1
2012 Olesen MS, Yuan L, Liang B, Holst AG, Nielsen N, Nielsen JB, Hedley PL, Christiansen M, Olesen SP, Haunsø S, Schmitt N, Jespersen T, Svendsen JH. High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation. Circulation. Cardiovascular Genetics. 5: 450-9. PMID 22685113 DOI: 10.1161/Circgenetics.111.962597  1
2012 Olesen MS, Bentzen BH, Nielsen JB, Steffensen AB, David JP, Jabbari J, Jensen HK, Haunsø S, Svendsen JH, Schmitt N. Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation. Bmc Medical Genetics. 13: 24. PMID 22471742 DOI: 10.1186/1471-2350-13-24  1
2012 Refsgaard L, Holst AG, Sadjadieh G, Haunsø S, Nielsen JB, Olesen MS. High prevalence of genetic variants previously associated with LQT syndrome in new exome data. European Journal of Human Genetics : Ejhg. 20: 905-8. PMID 22378279 DOI: 10.1038/ejhg.2012.23  1
2012 Olesen MS, Holst AG, Jabbari J, Nielsen JB, Christophersen IE, Sajadieh A, Haunsø S, Svendsen JH. Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years. The Canadian Journal of Cardiology. 28: 191-5. PMID 22336519 DOI: 10.1016/j.cjca.2011.11.016  1
2012 Holst AG, Saber S, Houshmand M, Zaklyazminskaya EV, Wang Y, Jensen HK, Refsgaard L, Haunsø S, Svendsen JH, Olesen MS, Tfelt-Hansen J. Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics. The Canadian Journal of Cardiology. 28: 196-200. PMID 22284586 DOI: 10.1016/j.cjca.2011.11.011  1
2012 Olesen MS, Holst AG, Svendsen JH, Haunsø S, Tfelt-Hansen J. SCN1Bb R214Q found in 3 patients: 1 with Brugada syndrome and 2 with lone atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 9: 770-3. PMID 22155598 DOI: 10.1016/j.hrthm.2011.12.005  1
2012 Refsgaard L, Olesen MS, Møller DV, Christiansen M, Haunsø S, Svendsen JH, Christensen AH. Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy Applied and Translational Genomics. 1: 44-46. DOI: 10.1016/j.atg.2012.06.001  1
2011 Olesen MS, Holst AG, Schmitt N. Letter by Olesen et al regarding article, "MOG1: a new susceptibility gene for Brugada syndrome". Circulation. Cardiovascular Genetics. 4: e22; author reply e2. PMID 22010171 DOI: 10.1161/CIRCGENETICS.111.960799  1
2011 Henningsen KM, Olesen MS, Haunsoe S, Svendsen JH. Association of rs2200733 at 4q25 with early onset of lone atrial fibrillation in young patients. Scandinavian Cardiovascular Journal : Scj. 45: 324-6. PMID 21793630 DOI: 10.3109/14017431.2011.594081  1
2011 Olesen MS, Jensen NF, Holst AG, Nielsen JB, Tfelt-Hansen J, Jespersen T, Sajadieh A, Haunsø S, Lund JT, Calloe K, Schmitt N, Svendsen JH. A novel nonsense variant in Nav1.5 cofactor MOG1 eliminates its sodium current increasing effect and may increase the risk of arrhythmias. The Canadian Journal of Cardiology. 27: 523.e17-23. PMID 21621375 DOI: 10.1016/J.Cjca.2011.01.003  1
2011 Jabbari J, Olesen MS, Holst AG, Nielsen JB, Haunso S, Svendsen JH. Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians. Cardiology. 118: 116-20. PMID 21555883 DOI: 10.1159/000323840  1
2011 Olesen MS, Jabbari J, Holst AG, Nielsen JB, Steinbrüchel DA, Jespersen T, Haunsø S, Svendsen JH. Screening of KCNN3 in patients with early-onset lone atrial fibrillation. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 13: 963-7. PMID 21398315 DOI: 10.1093/Europace/Eur007  1
2011 Winkel BG, Hollegaard MV, Olesen MS, Svendsen JH, Haunsø S, Hougaard DM, Tfelt-Hansen J. Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis. Bmc Medical Genetics. 12: 22. PMID 21306642 DOI: 10.1186/1471-2350-12-22  1
2011 Nielsen JB, Olesen MS, Tangø M, Haunsø S, Holst AG, Svendsen JH. Incomplete right bundle branch block: a novel electrocardiographic marker for lone atrial fibrillation. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 13: 182-7. PMID 21138928 DOI: 10.1093/europace/euq436  1
2011 Henningsen KM, Olesen MS, Ravn LS, Dixen U, Haunsoe S, Bruunsgaard H, Svendsen JH. Inflammatory single nucleotide polymorphisms and the risk of atrial fibrillation: a case control study. Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]. 60: 209-11. PMID 21132345 DOI: 10.1007/s00011-010-0285-2  1
2011 Olesen MS, Jespersen T, Nielsen JB, Liang B, Møller DV, Hedley P, Christiansen M, Varró A, Olesen SP, Haunsø S, Schmitt N, Svendsen JH. Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation. Cardiovascular Research. 89: 786-93. PMID 21051419 DOI: 10.1093/Cvr/Cvq348  1
2011 Holmqvist F, Olesen MS, Tveit A, Enger S, Tapanainen J, Jurkko R, Havmöller R, Haunsø S, Carlson J, Svendsen JH, Platonov PG. Abnormal atrial activation in young patients with lone atrial fibrillation. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 13: 188-92. PMID 20864492 DOI: 10.1093/europace/euq352  1
2010 Holst AG, Tfelt-Hansen J, Olesen MS, Theilade J, Winkel BG, Christensen AH, Bundgaard H, Haunsø S, Svendsen JH. [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease]. Ugeskrift For Laeger. 172: 2140-4. PMID 20670590  1
2010 Henningsen KM, Olesen MS, Pedersen M, Nielsen L, Haunsø S, Bruunsgaard H, Svendsen JH. Single nucleotide polymorphisms in inflammatory genes and the risk of early onset of lone atrial fibrillation. Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]. 59: 965-9. PMID 20490891 DOI: 10.1007/s00011-010-0210-8  1
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