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Petretta M, Pirozzi F, Sasso L, Paglia A, Bonaduce D. Review and metaanalysis of the frequency of familial dilated cardiomyopathy. <i>Am J Cardiol<\/i> 2011; 108: 1171\u20131176.","DOI":"10.1016\/j.amjcard.2011.06.022"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Baig MK, Goldman JH, Caforio AL, Coonar AS, Keeling PJ, McKenna WJ. Familial dilated cardiomyopathy: Cardiac abnormalities are common in asymptomatic relatives and may represent early disease. <i>J Am Coll Cardiol<\/i> 1998; 31: 195\u2013201.","DOI":"10.1016\/S0735-1097(97)00433-6"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Michels VV, Moll PP, Miller FA, Tajik AJ, Chu JS, Driscoll DJ, et al. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. <i>N Engl J Med<\/i> 1992; 326: 77\u201382.","DOI":"10.1056\/NEJM199201093260201"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. 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Mortality and sudden cardiac death risk stratification using the noninvasive combination of wide QRS duration and late gadolinium enhancement in idiopathic dilated cardiomyopathy. <i>Circ Arrhythm Electrophysiol<\/i> 2018; 11: e006233.","DOI":"10.1161\/CIRCEP.117.006233"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Richardson P, McKenna W, Bristow M, Maisch B, Mautner B, O\u2019Connell J, et al. Report of the 1995 World Health Organization\/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyopathies. <i>Circulation<\/i> 1996; 93: 841\u2013842.","DOI":"10.1161\/01.CIR.93.5.841"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Felker GM, Shaw LK, O\u2019Connor CM. A standardized definition of ischemic cardiomyopathy for use in clinical research. <i>J Am Coll Cardiol<\/i> 2002; 39: 210\u2013218.","DOI":"10.1016\/S0735-1097(01)01738-7"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. 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Temporal trends and factors associated with cardiac rehabilitation referral among patients hospitalized with heart failure: Findings from Get With The Guidelines-Heart Failure Registry. <i>J Am Coll Cardiol<\/i> 2015; 66: 917\u2013926.","DOI":"10.1016\/j.jacc.2015.06.1089"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Klem I, Weinsaft JW, Bahnson TD, Hegland D, Kim HW, Hayes B, et al. Assessment of myocardial scarring improves risk stratification in patients evaluated for cardiac defibrillator implantation. <i>J Am Coll Cardiol<\/i> 2012; 60: 408\u2013420.","DOI":"10.1016\/j.jacc.2012.02.070"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Gulati A, Jabbour A, Ismail TF, Guha K, Khwaja J, Raza S, et al. Association of fibrosis with mortality and sudden cardiac death in patients with nonischemic dilated cardiomyopathy. <i>JAMA<\/i> 2013; 309: 896\u2013908.","DOI":"10.1001\/jama.2013.1363"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Hicks KA, Tcheng JE, Bozkurt B, Chaitman BR, Cutlip DE, Farb A, et al. 2014 ACC\/AHA key data elements and definitions for cardiovascular endpoint events in clinical trials: A report of the American College of Cardiology\/American Heart Association Task Force on Clinical Data Standards (Writing Committee to Develop Cardiovascular Endpoints Data Standards). <i>Circulation<\/i> 2015; 132: 302\u2013361.","DOI":"10.1161\/CIR.0000000000000156"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Buxton AE, Calkins H, Callans DJ, DiMarco JP, Fisher JD, Greene HL, et al. 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Use of cardiovascular magnetic resonance for risk stratification in chronic heart failure: Prognostic value of late gadolinium enhancement in patients with non-ischaemic dilated cardiomyopathy. <i>Heart<\/i> 2011; 97: 727\u2013732.","DOI":"10.1136\/hrt.2010.205542"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22. Bezzina CR, Lahrouchi N, Priori SG. Genetics of sudden cardiac death. <i>Circ Res<\/i> 2015; 116: 1919\u20131936.","DOI":"10.1161\/CIRCRESAHA.116.304030"},{"key":"23","doi-asserted-by":"crossref","unstructured":"23. Cho KW, Lee J, Kim Y. Genetic variations leading to familial dilated cardiomyopathy. <i>Mol Cells<\/i> 2016; 39: 722\u2013727.","DOI":"10.14348\/molcells.2016.0061"},{"key":"24","doi-asserted-by":"crossref","unstructured":"24. McNally EM, Mestroni L. Dilated cardiomyopathy: Genetic determinants and mechanisms. <i>Circ Res<\/i> 2017; 121: 731\u2013748.","DOI":"10.1161\/CIRCRESAHA.116.309396"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25. Hershberger RE, Hedges DJ, Morales A. Dilated cardiomyopathy: The complexity of a diverse genetic architecture. <i>Nat Rev Cardiol<\/i> 2013; 10: 531\u2013547.","DOI":"10.1038\/nrcardio.2013.105"},{"key":"26","doi-asserted-by":"crossref","unstructured":"26. Herman DS, Lam L, Taylor MR, Wang L, Teekakirikul P, Christodoulou D, et al. Truncations of titin causing dilated cardiomyopathy. <i>N Engl J Med<\/i> 2012; 366: 619\u2013628.","DOI":"10.1056\/NEJMoa1110186"},{"key":"27","doi-asserted-by":"crossref","unstructured":"27. Tobita T, Nomura S, Fujita T, Morita H, Asano Y, Onoue K, et al. Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling. <i>Sci Rep<\/i> 2018; 8: 1998.","DOI":"10.1038\/s41598-018-20114-9"},{"key":"28","doi-asserted-by":"crossref","unstructured":"28. Haas J, Frese KS, Peil B, Kloos W, Keller A, Nietsch R, et al. 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