| Item Type | Name |
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Academic Article
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Generalized T2 test for genome association studies.
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Academic Article
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Autosomal genome-wide scan for coronary artery calcification loci in sibships at high risk for hypertension.
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Academic Article
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Interaction effects of high-density lipoprotein metabolism gene variation and alcohol consumption on coronary heart disease risk: the atherosclerosis risk in communities study.
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Academic Article
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Evaluating the context-dependent effect of family history of stroke in a genome scan for hypertension.
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Academic Article
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Five common gene variants identify elevated genetic risk for coronary heart disease.
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Academic Article
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Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.
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Academic Article
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Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships.
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Academic Article
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Pharmacogenetic associations of MMP9 and MMP12 variants with cardiovascular disease in patients with hypertension.
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Academic Article
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Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.
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Academic Article
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Contrasting multi-site genotypic distributions among discordant quantitative phenotypes: the APOA1/C3/A4/A5 gene cluster and cardiovascular disease risk factors.
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Academic Article
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The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions.
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Academic Article
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A common allele on chromosome 9 associated with coronary heart disease.
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Academic Article
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Consistent effects of genes involved in reverse cholesterol transport on plasma lipid and apolipoprotein levels in CARDIA participants.
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Academic Article
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A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease.
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Academic Article
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Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study.
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Academic Article
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Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls.
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Academic Article
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Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans.
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Academic Article
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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
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Academic Article
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A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.
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Academic Article
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Sequence polymorphism at the human apolipoprotein AII gene ( APOA2): unexpected deficit of variation in an African-American sample.
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Academic Article
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Sequence variations in PCSK9, low LDL, and protection against coronary heart disease.
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Academic Article
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Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD.
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Academic Article
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Variation in PCSK9, low LDL cholesterol, and risk of peripheral arterial disease.
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Academic Article
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Genetic predisposition to higher blood pressure increases coronary artery disease risk.
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Academic Article
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Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.
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Concept
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Genetic Diseases, Inborn
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Academic Article
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Small dense low-density lipoprotein-cholesterol concentrations predict risk for coronary heart disease: the Atherosclerosis Risk In Communities (ARIC) study.
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Academic Article
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Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study.
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Academic Article
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A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases.
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Academic Article
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Molecular findings among patients referred for clinical whole-exome sequencing.
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Academic Article
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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
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Academic Article
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PLD3 variants in population studies.
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Academic Article
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The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities.
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Academic Article
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Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease.
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Academic Article
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Whole-Exome Sequencing in Familial Parkinson Disease.
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Academic Article
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Molecular diagnostic experience of whole-exome sequencing in adult patients.
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Academic Article
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Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.
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Academic Article
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Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections.
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Academic Article
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Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.
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Academic Article
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Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease.
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Academic Article
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Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort.
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Academic Article
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Lessons learned from additional research analyses of unsolved clinical exome cases.
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Academic Article
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Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study.
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Academic Article
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
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Academic Article
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Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation.
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Academic Article
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
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Academic Article
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GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.
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Academic Article
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Insights into genetics, human biology and disease gleaned from family based genomic studies.
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Academic Article
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ACAT: A Fast and Powerful p Value Combination Method for Rare-Variant Analysis in Sequencing Studies.
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Academic Article
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Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
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Academic Article
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Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
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Academic Article
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A Genocentric Approach to Discovery of Mendelian Disorders.
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Academic Article
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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
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Academic Article
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Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.
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Academic Article
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Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
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Academic Article
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Genetic diversity fuels gene discovery for tobacco and alcohol use.
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