Strauss DG, Vicente J, Johannesen L, et al. Common Genetic Variant Risk Score Is Associated With Drug-Induced QT Prolongation and Torsade de Pointes Risk: A Pilot Study. Circulation. 2017;135(14):1300-1310. doi:10.1161/CIRCULATIONAHA.116.023980.

Lubitz SA. Clockwork and Arrhythmias in Catecholaminergic Polymorphic Ventricular Tachycardia. JACC Clin Electrophysiol. 2017;3(11):1318-1320. doi:10.1016/j.jacep.2017.08.010.

Smith G, Lowe JK, Kovvali S, et al. Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. Heart Rhythm. 2009;6(5):634-41. doi:10.1016/j.hrthm.2009.02.022.

Newton-Cheh C, Shah R. Genetic determinants of QT interval variation and sudden cardiac death. Curr Opin Genet Dev. 2007;17(3):213-21. doi:10.1016/j.gde.2007.04.010.

Arking DE, Pulit SL, Crotti L, et al. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat Genet. 2014;46(8):826-36. doi:10.1038/ng.3014.

Lubitz SA, Ellinor PT. Next-generation sequencing for the diagnosis of cardiac arrhythmia syndromes. Heart Rhythm. 2015;12(5):1062-70. doi:10.1016/j.hrthm.2015.01.011.

Smith G, Newton-Cheh C. Genome-wide association studies of late-onset cardiovascular disease. J Mol Cell Cardiol. 2015;83:131-41. doi:10.1016/j.yjmcc.2015.04.004.

Kenttä TV, Nearing BD, Porthan K, et al. Prediction of sudden cardiac death with automated high-throughput analysis of heterogeneity in standard resting 12-lead electrocardiograms. Heart Rhythm. 2016;13(3):713-20. doi:10.1016/j.hrthm.2015.11.035.

MacRae CA. In vitro and in vivo reprogramming for the conduction system. Trends Cardiovasc Med. 2016;26(1):21-2. doi:10.1016/j.tcm.2015.08.005.