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Items: 1 to 20 of 243


Visit-to-Visit Variability of Hemoglobin A1c in People Without Diabetes and Risk of Major Adverse Cardiovascular Events and All-Cause Mortality.

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.

Diabetes Care. 2019 Jan;42(1):134-141. doi: 10.2337/dc18-1396. Epub 2018 Oct 23.


Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation.

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, Holst AG, Svendsen JH, Olesen MS.

Nat Commun. 2018 Oct 17;9(1):4316. doi: 10.1038/s41467-018-06618-y.


Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest.

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.

Front Physiol. 2018 Jul 10;9:894. doi: 10.3389/fphys.2018.00894. eCollection 2018.


Risk Prediction of Atrial Fibrillation Based on Electrocardiographic Interatrial Block.

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, Kofoed KF, Svendsen JH, Holst AG, Nielsen JB.

J Am Heart Assoc. 2018 May 30;7(11). pii: e008247. doi: 10.1161/JAHA.117.008247.


Sudden Cardiac Death: Pharmacotherapy and Proarrhythmic Drugs: A Nationwide Cohort Study in Denmark.

Risgaard B, Winkel BG, Jabbari R, Lynge TH, Wissenberg M, Glinge C, Haunsø S, Behr ER, Fink-Jensen A, Gislason GH, Tfelt-Hansen J.

JACC Clin Electrophysiol. 2017 May;3(5):473-481. doi: 10.1016/j.jacep.2016.12.023. Epub 2017 Mar 29.


Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation.

Denti F, Paludan-Müller C, Olesen SP, Haunsø S, Svendsen JH, Olesen MS, Bentzen BH, Schmitt N.

Per Med. 2018 Mar;15(2):93-102. doi: 10.2217/pme-2017-0076. Epub 2018 Jan 31.


Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes.

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.

Eur J Hum Genet. 2018 May;26(5):660-668. doi: 10.1038/s41431-017-0092-0. Epub 2018 Feb 2.


Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease.

Paludan-Müller C, Ahlberg G, Ghouse J, Svendsen JH, Haunsø S, Olesen MS.

Circ Cardiovasc Genet. 2017 Dec;10(6). pii: e001878. doi: 10.1161/CIRCGENETICS.117.001878.


Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction.

Jabbari R, Jabbari J, Glinge C, Risgaard B, Sattler S, Winkel BG, Terkelsen CJ, Tilsted HH, Jensen LO, Hougaard M, Haunsø S, Engstrøm T, Albert CM, Tfelt-Hansen J.

BMC Med Genet. 2017 Nov 21;18(1):138. doi: 10.1186/s12881-017-0497-1.


Differences in clinical characteristics in patients with first ST-segment elevation myocardial infarction and ventricular fibrillation according to sex.

Jabbari R, Glinge C, Risgaard B, Lynge TH, Winkel BG, Haunsø S, Albert CM, Engstrøm T, Tfelt-Hansen J.

J Interv Card Electrophysiol. 2017 Oct;50(1):133-140. doi: 10.1007/s10840-017-0284-0. Epub 2017 Sep 22.


Sudden unexpected death caused by stroke: A nationwide study among children and young adults in Denmark.

Ågesen FN, Risgaard B, Zachariasardóttir S, Jabbari R, Lynge TH, Ingemann-Hansen O, Ottesen GL, Thomsen JL, Haunsø S, Krieger DW, Winkel BG, Tfelt-Hansen J.

Int J Stroke. 2018 Apr;13(3):285-291. doi: 10.1177/1747493017724625. Epub 2017 Aug 1.


Electrocardiographic Preexcitation and Risk of Cardiovascular Morbidity and Mortality: Results From the Copenhagen ECG Study.

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.

Circ Arrhythm Electrophysiol. 2017 Jun;10(6). pii: e004778. doi: 10.1161/CIRCEP.116.004778.


Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.

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.

Heart Rhythm. 2017 Oct;14(10):1531-1538. doi: 10.1016/j.hrthm.2017.05.027. Epub 2017 May 24.


Electrocardiographic PR Interval Duration and Cardiovascular Risk: Results From the Copenhagen ECG Study.

Rasmussen PV, Nielsen JB, Skov MW, Pietersen A, Graff C, Lind B, Struijk JJ, Olesen MS, Haunsø S, Køber L, Svendsen JH, Holst AG.

Can J Cardiol. 2017 May;33(5):674-681. doi: 10.1016/j.cjca.2017.02.015. Epub 2017 Mar 6.


Sudden cardiac death and coronary disease in the young: A nationwide cohort study in Denmark.

Zachariasardóttir S, Risgaard B, Ågesen FN, Jabbari R, Glinge C, Ingemann-Hansen O, Ottesen GL, Thomsen JL, Haunsø S, Banner J, Winkel BG, Tfelt-Hansen J.

Int J Cardiol. 2017 Jun 1;236:16-22. doi: 10.1016/j.ijcard.2017.01.118. Epub 2017 Jan 28.


A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.

Jabbari R, Glinge C, Jabbari J, Risgaard B, Winkel BG, Terkelsen CJ, Tilsted HH, Jensen LO, Hougaard M, Haunsø S, Engstrøm T, Albert CM, Tfelt-Hansen J.

PLoS One. 2017 Jan 13;12(1):e0170193. doi: 10.1371/journal.pone.0170193. eCollection 2017.


Gender differences in sudden cardiac death in the young-a nationwide study.

Winkel BG, Risgaard B, Bjune T, Jabbari R, Lynge TH, Glinge C, Bundgaard H, Haunsø S, Tfelt-Hansen J.

BMC Cardiovasc Disord. 2017 Jan 7;17(1):19. doi: 10.1186/s12872-016-0446-5.


Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy.

Nouhravesh N, Ahlberg G, Ghouse J, Andreasen C, Svendsen JH, Haunsø S, Bundgaard H, Weeke PE, Olesen MS.

Mol Genet Genomic Med. 2016 Sep 17;4(6):617-623. eCollection 2016 Nov.


Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality.

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, Kanters JK, Olesen MS.

Genet Med. 2017 May;19(5):521-528. doi: 10.1038/gim.2016.151. Epub 2016 Oct 6.


Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants.

Paludan-Müller C, Ahlberg G, Ghouse J, Herfelt C, Svendsen JH, Haunsø S, Kanters JK, Olesen MS.

Clin Genet. 2017 Jan;91(1):63-72. doi: 10.1111/cge.12847. Epub 2016 Sep 26.


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