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Genetics of inherited cardiomyopathies

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Pages 683-697 | Published online: 10 Jan 2014

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JS Munday, CB Dyer, AC Hartman & GMB Orbell. (2006) A possible predisposition to dilated cardiomyopathy in Huntaway dogs. New Zealand Veterinary Journal 54:5, pages 231-234.
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Nzali V. Campbell, David A. Weitzenkamp, Ian L. Campbell, Ronald F. Schmidt, Chindo Hicks, Michael J. Morgan, David C. Irwin & John J. Tentler. (2018) “Omics” data integration and functional analyses link Enoyl-CoA hydratase, short chain 1 to drug refractory dilated cardiomyopathy. BMC Medical Genomics 11:1.
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Wei Wang, Fuyang Zhang, Yunlong Xia, Shihao Zhao, Wenjun Yan, Helin Wang, Yan Lee, Congye Li, Ling Zhang, Kun Lian, Erhe Gao, Hexiang Cheng & Ling Tao. (2016) Defective branched chain amino acid catabolism contributes to cardiac dysfunction and remodeling following myocardial infarction. American Journal of Physiology-Heart and Circulatory Physiology 311:5, pages H1160-H1169.
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Haipeng Sun & Yibin Wang. 2015. Branched Chain Amino Acids in Clinical Nutrition. Branched Chain Amino Acids in Clinical Nutrition 81 88 .
Thenappan Thenappan, Allen S. Anderson & Savitri Fedson. 2015. Management of Heart Failure. Management of Heart Failure 31 45 .
Alessandra Medeiros, Diogo G. Biagi, Tiago J.P. Sobreira, Paulo Sérgio L. de Oliveira, Carlos Eduardo Negrão, Alfredo J. Mansur, José Eduardo Krieger, Patricia C. Brum & Alexandre C. Pereira. (2011) Mutations in the human phospholamban gene in patients with heart failure. American Heart Journal 162:6, pages 1088-1095.e1.
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Y. Huang, M. Zhou, H. Sun & Y. Wang. (2011) Branched-chain amino acid metabolism in heart disease: an epiphenomenon or a real culprit?. Cardiovascular Research 90:2, pages 220-223.
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Tomás Ripoll Vera, Lorenzo Monserrat Iglesias, Manuel Hermida Prieto, Martin Ortiz, Isabel Rodriguez Garcia, Nancy Govea Callizo, Carlos Gómez Navarro, Jordi Rosell Andreo, José María Gámez Martínez, Guillermo Pons Lladó, David Cremer Luengos & Joan Torres Marqués. (2010) The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans. International Journal of Cardiology 145:2, pages 405-407.
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Diogo GB Santos, Alessandra Medeiros, Patrícia C Brum, José G Mill, Alfredo J Mansur, José E Krieger & Alexandre C Pereira. (2009) No evidence for an association between the -36A>C phospholamban gene polymorphism and a worse prognosis in heart failure. BMC Cardiovascular Disorders 9:1.
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Kenneth B. Margulies, Daniel P. Bednarik & Daniel L. Dries. (2009) Genomics, Transcriptional Profiling, and Heart Failure. Journal of the American College of Cardiology 53:19, pages 1752-1759.
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Wilma P. van der Roest, José M. Pennings, Marian Bakker, Maarten P. van den Berg & J. Peter van Tintelen. (2009) Family letters are an effective way to inform relatives about inherited cardiac disease. American Journal of Medical Genetics Part A 149A:3, pages 357-363.
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Enkhsaikhan Purevjav, David P. Nelson, Jacquelin J. Varela, Shinawe Jimenez, Debra L. Kearney, Ximena V. Sanchez, Gilberto DeFreitas, Blasé Carabello, Michael D. Taylor, Matteo Vatta, William T. Shearer, Jeffrey A. Towbin & Neil E. Bowles. (2007) Myocardial Fas Ligand Expression Increases Susceptibility to AZT-Induced Cardiomyopathy. Cardiovascular Toxicology 7:4, pages 255-263.
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Jorieke E.H. Bergman, Hermine E. Veenstra-Knol, Anthonie J. van Essen, Conny M.A. van Ravenswaaij, Wilfred F.A. den Dunnen, Arthur van den Wijngaard & J. Peter van Tintelen. (2007) Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene. European Journal of Medical Genetics 50:5, pages 355-366.
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Elly Hoedemaekers, Jan P.C. Jaspers & J. Peter Van Tintelen. (2007) The influence of coping styles and perceived control on emotional distress in persons at risk for a hereditary heart disease. American Journal of Medical Genetics Part A 143A:17, pages 1997-2005.
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Rebecca Sparkes, David Patton & Francois Bernier. (2007) Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein. Cardiology in the Young 17:2, pages 215-217.
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Anita M. Arola, Ximena Sanchez, Ross T. Murphy, Erika Hasle, Hua Li, Perry M. Elliott, William J. McKenna, Jeffrey A. Towbin & Neil E. Bowles. (2007) Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathy. Molecular Genetics and Metabolism 90:4, pages 435-440.
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Megan M. DeWitt, Heather M. MacLeod, Betty Soliven & Elizabeth M. McNally. (2006) Phospholamban R14 Deletion Results in Late-Onset, Mild, Hereditary Dilated Cardiomyopathy. Journal of the American College of Cardiology 48:7, pages 1396-1398.
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Stacie B. Peddy, Luca A. Vricella, Jane E. Crosson, Gretchen L. Oswald, Ronald D. Cohn, Duke E. Cameron, David Valle & Bart L. Loeys. (2006) Infantile Restrictive Cardiomyopathy Resulting From a Mutation in the Cardiac Troponin T Gene. Pediatrics 117:5, pages 1830-1833.
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STEVEN D. COLAN. 2006. Nadas' Pediatric Cardiology. Nadas' Pediatric Cardiology 415 458 .
Rafal M. SmigrodzkiShaharyar M. Khan. (2005) Mitochondrial Microheteroplasmy and a Theory of Aging and Age-Related Disease. Rejuvenation Research 8:3, pages 172-198.
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Despina Sanoudou, Elizabeth Vafiadaki, Demetrios A. Arvanitis, Evangelia Kranias & Aikaterini Kontrogianni-Konstantopoulos. (2005) Array lessons from the heart: focus on the genome and transcriptome of cardiomyopathies. Physiological Genomics 21:2, pages 131-143.
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