review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Yibin Wang | Q40664206 |
Aldons Jake Lusis | Q60642067 | ||
P2093 | author name string | Christoph D Rau | |
P2860 | cites work | Heart Disease and Stroke Statistics--2013 Update: A Report From the American Heart Association | Q22306356 |
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy | Q24601469 | ||
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data | Q24612121 | ||
Biological, clinical and population relevance of 95 loci for blood lipids | Q24622541 | ||
Tnni3k modifies disease progression in murine models of cardiomyopathy | Q27349094 | ||
Heart failure and mouse models | Q27686849 | ||
Mapping genetic variants associated with beta-adrenergic responses in inbred mice | Q28481719 | ||
Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study | Q28704638 | ||
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium | Q28943463 | ||
Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality | Q29416992 | ||
Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes | Q33300816 | ||
Predictors of readmission among elderly survivors of admission with heart failure | Q33807660 | ||
Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study | Q33836293 | ||
Common variants in HSPB7 and FRMD4B associated with advanced heart failure | Q34096292 | ||
Progress and promise of genome-wide association studies for human complex trait genetics | Q34537519 | ||
Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium | Q34552350 | ||
A novel locus for dilated cardiomyopathy maps to canine chromosome 8 | Q34591160 | ||
Animal models of cardiovascular diseases | Q34591282 | ||
Mapping genetic contributions to cardiac pathology induced by Beta-adrenergic stimulation in mice | Q35102230 | ||
Endonuclease G is a novel determinant of cardiac hypertrophy and mitochondrial function | Q35294331 | ||
Efficient control of population structure in model organism association mapping | Q36515832 | ||
Genome-wide approach to identify novel candidate genes for beta blocker response in heart failure using an experimental model. | Q37051265 | ||
Small animal models of heart failure: development of novel therapies, past and present | Q37609676 | ||
Proportion of the decline in cardiovascular mortality disease due to prevention versus treatment: public health versus clinical care | Q37854652 | ||
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A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscher | Q44863885 | ||
FaST linear mixed models for genome-wide association studies | Q46661213 | ||
Multiple quantitative trait loci modify the heart failure phenotype in murine cardiomyopathy. | Q47594204 | ||
Heritability of left ventricular mass: the Framingham Heart Study. | Q50924384 | ||
A prospective genetic evaluation of familial dilated cardiomyopathy in the Doberman pinscher. | Q51108706 | ||
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A genetic linkage map of the Syrian hamster and localization of cardiomyopathy locus on chromosome 9qa2.1-b1 using RLGS spot-mapping | Q71167659 | ||
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Evaluation of tafazzin as candidate for dilated cardiomyopathy in Irish wolfhounds | Q80591072 | ||
QTL mapping in a mouse model of cardiomyopathy reveals an ancestral modifier allele affecting heart function and survival | Q80988562 | ||
Heart failure: advances through genomics | Q83667474 | ||
Direct detection of myocardial fibrosis by MRI | Q84938192 | ||
P433 | issue | 3 | |
P304 | page(s) | 222-227 | |
P577 | publication date | 2015-05-01 | |
P1433 | published in | Current Opinion in Cardiology | Q4626801 |
P1476 | title | Genetics of common forms of heart failure: challenges and potential solutions | |
P478 | volume | 30 |
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Q28267272 | Deletion of MLIP (muscle-enriched A-type lamin-interacting protein) leads to cardiac hyperactivation of Akt/mammalian target of rapamycin (mTOR) and impaired cardiac adaptation |
Q46406593 | Experimental Evolution and Heart Function in Drosophila. |
Q27309881 | Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred Strains |
Q36069291 | Genetic Dissection of Cardiac Remodeling in an Isoproterenol-Induced Heart Failure Mouse Model |
Q89294531 | Genetic Regulation of Fibroblast Activation and Proliferation in Cardiac Fibrosis |
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Q38774369 | Genomic translational research: Paving the way to individualized cardiac functional analyses and personalized cardiology |
Q41993432 | Shared genetic regulatory networks for cardiovascular disease and type 2 diabetes in multiple populations of diverse ethnicities in the United States |
Q37682494 | Systems Genetics Approach Identifies Gene Pathways and Adamts2 as Drivers of Isoproterenol-Induced Cardiac Hypertrophy and Cardiomyopathy in Mice |
Q63976707 | Variable outcomes of human heart attack recapitulated in genetically diverse mice |
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