A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
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2008, Classification of the cardiomyopathies: a position statement from the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases, Eur Heart J, 29, 270
2007, Dilated Cardiomyopathy Overview
2008, Cardiac transplantation in the United States: an analysis of the UNOS registry, Clin Transpl, 35
1989, Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975–1984, Circulation, 80, 564, 10.1161/01.CIR.80.3.564
2010, Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy, Circ Cardiovasc Genet, 3, 155, 10.1161/CIRCGENETICS.109.912345
2010, Common susceptibility variants examined for association with dilated cardiomyopathy, Ann Hum Genet, 74, 110, 10.1111/j.1469-1809.2010.00566.x
2000, Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy: the CARDIGENE study, J Am Coll Cardiol, 35, 29, 10.1016/S0735-1097(99)00522-7
2007, Genomewide association analysis of coronary artery disease, N Engl J Med, 357, 443, 10.1056/NEJMoa072366
2010, Genome-wide association study of intracranial aneurysm identifies three new risk loci, Nat Genet, 42, 420, 10.1038/ng.563
1999, Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy, Eur Heart J, 20, 93
1999, Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE group, Eur Heart J, 20, 1587, 10.1053/euhj.1999.1696
2009, Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy, Eur Heart J, 30, 2128, 10.1093/eurheartj/ehp225
1992, A case-control study of lipoprotein particles in two populations at contrasting risk for coronary heart disease. The ECTIM Study, Arterioscler Thromb, 12, 701, 10.1161/01.ATV.12.6.701
2009, Prevalence of factor V Leiden and prothrombin G20210A mutation in a large French population selected for nonthrombotic history: geographical and age distribution, Blood Coagul Fibrinolysis, 20, 503, 10.1097/MBC.0b013e32832f5d7a
R Development Core Team, 2008, R: A Language and Environment for Statistical Computing
2008, WGAViewer: software for genomic annotation of whole genome association studies, Genome Res, 18, 640, 10.1101/gr.071571.107
2010, LocusZoom: regional visualization of genome-wide association scan results, Bioinformatics, 26, 2336, 10.1093/bioinformatics/btq419
2005, Population structure, differential bias and genomic control in a large-scale, case-control association study, Nat Genet, 37, 1243, 10.1038/ng1653
2010, Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy, PLoS Genet, 6, e1001167, 10.1371/journal.pgen.1001167
2007, A new JAVA interface implementation of THESIAS: testing haplotype effects in association studies, Bioinformatics, 23, 1038, 10.1093/bioinformatics/btm058
1999, Identification and characterization of cvHsp. A novel human small stress protein selectively expressed in cardiovascular and insulin-sensitive tissues, J Biol Chem, 274, 36592, 10.1074/jbc.274.51.36592
2010, Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease, J Clin Invest, 120, 280, 10.1172/JCI39085
2010, Genetics and beyond—the transcriptome of human monocytes and disease susceptibility, PLoS ONE, 5, e10693, 10.1371/journal.pone.0010693
2010, A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk, Nature, 467, 460, 10.1038/nature09386
2011, Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation, Proc Natl Acad Sci USA, 108, 2456, 10.1073/pnas.1017494108
2006, A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25–26, J Am Coll Cardiol, 48, 106, 10.1016/j.jacc.2006.01.079
2003, Genomewide distribution of high-frequency, completely mismatching SNP haplotype pairs observed to be common across human populations, Am J Hum Genet, 73, 1073, 10.1086/379154
2008, Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption, Hum Hered, 65, 33, 10.1159/000106060
2003, The human genome encodes 10 alpha-crystallin-related small heat shock proteins: HspB1–10, Cell Stress Chaperones, 8, 53, 10.1379/1466-1268(2003)8<53:THGECS>2.0.CO;2
2008, Autophagy is an adaptive response in desmin-related cardiomyopathy, Proc Natl Acad Sci USA, 105, 9745, 10.1073/pnas.0706802105
2010, Common variants in HSPB7 and FRMD4B associated with advanced heart failure, Circ Cardiovasc Genet, 3, 147, 10.1161/CIRCGENETICS.109.898395
2009, Protein quality control during aging involves recruitment of the macroautophagy pathway by BAG3, EMBO J, 28, 889, 10.1038/emboj.2009.29
2006, BAG3 deficiency results in fulminant myopathy and early lethality, Am J Pathol, 169, 761, 10.2353/ajpath.2006.060250
2010, Chaperone-assisted selective autophagy is essential for muscle maintenance, Curr Biol, 20, 143, 10.1016/j.cub.2009.11.022
2010, Identification of the key structural motifs involved in HspB8/HspB6-Bag3 interaction, Biochem J, 425, 245, 10.1042/BJ20090907
2009, Mutation in BAG3 causes severe dominant childhood muscular dystrophy, Ann Neurol, 65, 83, 10.1002/ana.21553
2010, BAG3 and Hsc70 interact with actin capping protein CapZ to maintain myofibrillar integrity under mechanical stress, Circ Res, 107, 1220, 10.1161/CIRCRESAHA.110.225649
2008, Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays, Nucleic Acids Res, 36, e35, 10.1093/nar/gkm1060
2009, Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans, Hum Genet, 125, 305, 10.1007/s00439-009-0626-9