Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data - Test2 - elhamkhani - TriplyDB

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

http://www.wikidata.org/entity/Q24612121

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Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study Genome-wide association analysis identifies multiple loci related to resting heart rate Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation The Rotterdam Study: 2010 objectives and design update Advances in the epidemiology of heart failure and left ventricular remodeling Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes A comprehensive genetic study on left atrium size in Caribbean Hispanics identifies potential candidate genes in 17p10 Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy Prioritizing causal disease genes using unbiased genomic features Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.Genetic determinants of myocardial dysfunction.Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.[A cohort study investigating risk factors for cardiovascular disease in an urban elderly East-German population (CARLA study)].Validation study of candidate single nucleotide polymorphisms associated with left ventricular hypertrophy in the Korean population.An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.Genetic Variation in Kruppel like Factor 15 Is Associated with Left Ventricular Hypertrophy in Patients with Type 2 Diabetes: Discovery and Replication Cohorts.WWOX gene is associated with HDL cholesterol and triglyceride levels.Identification and validation of genes affecting aortic lesions in mice Association of an intronic, but not any exonic, FRMD4B sequence variant and heart failure Common variants in HSPB7 and FRMD4B associated with advanced heart failure WWOX at the crossroads of cancer, metabolic syndrome related traits and CNS pathologies.Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure.Genetic loci associated with atrial fibrillation: relation to left atrial structure in the Framingham Heart Study.Common variation neighbouring micro-RNA 22 is associated with increased left ventricular mass The phenotype of recurrent 10q22q23 deletions and duplications.Genetics of hypertension and cardiovascular disease and their interconnected pathways: lessons from large studies.Genome-wide association study of gene by smoking interactions in coronary artery calcification.The WWOX gene modulates high-density lipoprotein and lipid metabolism.WW domain-containing oxidoreductase in neuronal injury and neurological diseases.Renin-angiotensin-aldosterone genotype influences ventricular remodeling in infants with single ventricle.Functional genomics applied to cardiovascular medicine.Large-scale gene-centric analysis identifies polymorphisms for resistant hypertension.The Rotterdam Study: 2012 objectives and design update.Endonuclease G is a novel determinant of cardiac hypertrophy and mitochondrial function.Genetics of common forms of heart failure: challenges and potential solutions.Genome-wide association study for endothelial growth factors A systematic eQTL study of cis-trans epistasis in 210 HapMap individuals.What can genetic studies of left ventricular mass tell us?

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Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

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Functional conservation of the telomerase protein Est1p in humans

A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

A common variant of HMGA2 is associated with adult and childhood height in the general population

Cep120 and TACCs control interkinetic nuclear migration and the neural progenitor pool.

Altered phosphodiesterase 3-mediated cAMP hydrolysis contributes to a hypermotile phenotype in obese JCR:LA-cp rat aortic vascular smooth muscle cells: implications for diabetes-associated cardiovascular disease

Cardiac-specific overexpression of sarcolipin inhibits sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA2a) activity and impairs cardiac function in mice

Mutation responsible for the mouse pygmy phenotype in the developmentally regulated factor HMGI-C

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

A new multipoint method for genome-wide association studies by imputation of genotypes

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Heinz Erich Wichmann

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