Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts.
- Authors
- Psaty, Bruce M; O'Donnell, Christopher J; Gudnason, Vilmundur; Lunetta, Kathryn L; Folsom, Aaron R; Rotter, Jerome I; Uitterlinden, AndrΓ© G; Harris, Tamara B; Witteman, Jacqueline C M; Boerwinkle, Eric; CHARGE Consortium
- Year
- 2009
- Journal
- Circulation. Cardiovascular genetics
- PMID
- 20031568
- DOI
- 10.1161/CIRCGENETICS.108.829747
- PMCID
- PMC2875693
BACKGROUND: The primary aim of genome-wide association studies is to identify novel genetic loci associated with interindividual variation in the levels of risk factors, the degree of subclinical disease, or the risk of clinical disease. The requirement for large sample sizes and the importance of replication have served as powerful incentives for scientific collaboration. Methods- The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium was formed to facilitate genome-wide association studies meta-analyses and replication opportunities among multiple large population-based cohort studies, which collect data in a standardized fashion and represent the preferred method for estimating disease incidence. The design of the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium includes 5 prospective cohort studies from the United States and Europe: the Age, Gene/Environment Susceptibility-Reykjavik Study, the Atherosclerosis Risk in Communities Study, the Cardiovascular Health Study, the Framingham Heart Study, and the Rotterdam Study. With genome-wide data on a total of about 38 000 individuals, these cohort studies have a large number of health-related phenotypes measured in similar ways. For each harmonized trait, within-cohort genome-wide association study analyses are combined by meta-analysis. A prospective meta-analysis of data from all 5 cohorts, with a properly selected level of genome-wide statistical significance, is a powerful approach to finding genuine phenotypic associations with novel genetic loci. CONCLUSIONS: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium and collaborating non-member studies or consortia provide an excellent framework for the identification of the genetic determinants of risk factors, subclinical-disease measures, and clinical events.
No figures extracted from this document.
No entities extracted from this document yet.
No uploaded files.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Association between DNA methylation at birth and cognitive outcomes from early childhood to adolescence: A systematic review. | Islam MR et al. | β | 2026 | β |
| Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants. | Noordam R et al. | β | 2026 | β |
| Historical review: more than two decades understanding the genetic architecture of hemostasis and thrombosis. | Sabater-Lleal M et al. | β | 2026 | β |
| UK Biobank at 20 - a growing, global resource for dementia research. | Matthews PM et al. | β | 2026 | β |
| Addressing global diversity in dementia research with the COSMIC collaboration. | Lipnicki DM et al. | β | 2025 | β |
| Advances in magnetic resonance imaging of the developing brain and its applications in pediatrics. | Chen RK et al. | β | 2025 | β |
| A multiomics approach reveals novel regulators of plasma factor V levels, highlighting CLEC4M as a clearance receptor. | Munsch G et al. | β | 2025 | β |
| Bidirectional Mendelian randomization and mediation analysis of million-scale data reveal causal relationships between thyroid-related phenotypes, smoking, and lung cancer. | Wang X et al. | β | 2025 | β |
| Biobanking with genetics shapes precision medicine and global health. | Gallagher CS et al. | β | 2025 | β |
| Data sharing in the PRIMED Consortium: Design, implementation, and recommendations for future policymaking. | Smith JL et al. | β | 2025 | β |
| Harnessing the power of genomics in hypertension: tip of the iceberg? | Naderi H et al. | β | 2025 | β |
| Measuring the Associations Between Brain Morphometry and Polygenic Risk Scores for Substance use Disorders in Drug-Naive Adolescents. | Kramer S et al. | β | 2025 | β |
| Missense variants in FRS3 affect body mass index in populations of diverse ancestries. | Jonsdottir AB et al. | β | 2025 | β |
| Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids. | Bentley AR et al. | β | 2025 | β |
| Network Interactions of Circulating FGF23, HRG-HMGB1, and Cardiac Disease in CKD. | Perwad F et al. | β | 2025 | β |
| Optimizing treatment of cardiovascular risk factors in cerebral small vessel disease using genetics. | Koohi F et al. | β | 2025 | β |
| Plasmalogen remodeling modulates macrophage response to cytotoxic oxysterols and atherosclerotic plaque vulnerability. | Jalil A et al. | β | 2025 | β |
| Plasma Proteomic Assessment of Calcific Aortic Valve Disease in Older Adults. | Bortnick AE et al. | β | 2025 | β |
| Relationship between cognitive abilities and mental health as represented by cognitive abilities at the neural and genetic levels of analysis. | Wang Y et al. | β | 2025 | β |
| The breadth and impact of the Global Lipids Genetics Consortium. | Dron JS et al. | β | 2025 | β |
| The evolution of lipid-lowering drugs in the management of cardiovascular disease risk: From the first cardiovascular disease risk-reducing therapies to the novel challenging strategies. | Henry D et al. | β | 2025 | β |
| WMH Contributions to Cognitive Impairment: Rationale and Design of the Diverse VCID Study. | DeCarli C et al. | β | 2025 | β |
| A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels. | de Vries PS et al. | β | 2024 | β |
| A genome wide search for non-additive allele effects identifies<i>PSKH2</i>as involved in the variability of Factor V activity | Gendre B et al. | β | 2024 | β |
| A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment. | Gallego-Fabrega C et al. | β | 2024 | β |
| Causal Effect of Lipoprotein-Associated Phospholipase A2 Activity on Ischemic Stroke: A Mendelian Randomization Study. | Zhang Y et al. | β | 2024 | β |
| Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases. | Brock DC et al. | β | 2024 | β |
| Does Thrombosis Play a Causal Role in Lacunar Stroke and Cerebral Small Vessel Disease? | Koohi F et al. | β | 2024 | β |
| Employing Informatics Strategies in Alzheimer's Disease Research: A Review from Genetics, Multiomics, and Biomarkers to Clinical Outcomes. | Bao J et al. | β | 2024 | β |
| Gene-environment interactions within a precision environmental health framework. | Motsinger-Reif AA et al. | β | 2024 | β |
| Generation Scotland: an update on Scotland's longitudinal family health study. | Milbourn H et al. | β | 2024 | β |
| Genetic architecture of brain morphology and overlap with neuropsychiatric traits. | Ge YJ et al. | β | 2024 | β |
| Genetic architectures of cerebral ventricles and their overlap with neuropsychiatric traits. | Ge YJ et al. | β | 2024 | β |
| Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia. | Sargurupremraj M et al. | β | 2024 | β |
| Genetic risk factors underlying white matter hyperintensities and cortical atrophy. | Patel Y et al. | β | 2024 | β |
| Genetic variants for head size share genes and pathways with cancer. | Knol MJ et al. | β | 2024 | β |
| Genome-Wide Interaction Analyses of Serum Calcium on Ventricular Repolarization Time in 125β393 Participants. | Young WJ et al. | β | 2024 | β |
| Genome-Wide Interaction Analysis With DASH Diet Score Identified Novel Loci for Systolic Blood Pressure. | Guirette M et al. | β | 2024 | β |
| Genome-Wide Search for Nonadditive Allele Effects Identifies <i>PSKH2</i> as Involved in the Variability of Factor V Activity. | Gendre B et al. | β | 2024 | β |
| Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries. | GarcΓa-MarΓn LM et al. | β | 2024 | β |
| Interaction between Continuous Pack-Years Smoked and Polygenic Risk Score on Lung Cancer Risk: Prospective Results from the Framingham Heart Study. | Duncan MS et al. | β | 2024 | β |
| Large-Scale Neuroimaging of Mental Illness. | Ching CRK et al. | β | 2024 | β |
| Long-term longitudinal analysis of 4,187 participants reveals insights into determinants of clonal hematopoiesis. | Uddin MM et al. | β | 2024 | β |
| National and international collaborations to advance research into vascular contributions to cognitive decline. | Saks DG et al. | β | 2024 | β |
| Population Neuroscience: Principles and Advances. | Paus T | β | 2024 | β |
| Proteomic prediction of incident heart failure and its main subtypes. | Emilsson V et al. | β | 2024 | β |
| The Danish Nationwide Electrocardiogram (ECG) Cohort. | Polcwiartek C et al. | β | 2024 | β |
| Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People With Type 2 Diabetes. | Kwak SH et al. | β | 2024 | β |
| Unsupervised deep representation learning enables phenotype discovery for genetic association studies of brain imaging. | Patel K et al. | β | 2024 | β |
| Validation of biomarkers of aging. | Moqri M et al. | β | 2024 | β |
| Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. | Huffman JE et al. | β | 2024 | β |
| Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels. | Ji Y et al. | β | 2023 | β |
| Biomedical consequences of elevated cholesterol-containing lipoproteins and apolipoproteins on cardiovascular and non-cardiovascular outcomes. | Schmidt AF et al. | β | 2023 | β |
| Cohort Network: A Knowledge Graph toward Data Dissemination and Knowledge-Driven Discovery for Cohort Studies. | Shen Y et al. | β | 2023 | β |
| Development and implementation of a distributed data network between an academic institution and state health departments to investigate variation in time to HIV viral suppression in the Deep South. | Bassler JR et al. | β | 2023 | β |
| Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. | Schmidt AF et al. | β | 2023 | β |
| Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. | Young WJ et al. | β | 2023 | β |
| Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts. | Yang C et al. | β | 2023 | β |
| Genomic approaches to identify and investigate genes associated with atrial fibrillation and heart failure susceptibility. | Patel KK et al. | β | 2023 | β |
| Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease. | Duperron MG et al. | β | 2023 | β |
| Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images. | Zhao B et al. | β | 2023 | β |
| Identification of circulating proteins associated with general cognitive function among middle-aged and older adults. | Tin A et al. | β | 2023 | β |
| Imaging genomics: data fusion in uncovering disease heritability. | Hartmann K et al. | β | 2023 | β |
| Importance of Diversity in Precision Medicine: Generalizability of Genetic Associations Across Ancestry Groups Toward Better Identification of Disease Susceptibility Variants. | Cruz LA et al. | β | 2023 | β |
| Linking Prenatal Environmental Exposures to Lifetime Health with Epigenome-Wide Association Studies: State-of-the-Science Review and Future Recommendations. | Bakulski KM et al. | β | 2023 | β |
| Mendelian randomization and the association of fibroblast growth factor-23 with heart failure with preserved ejection fraction. | Akwo EA et al. | β | 2023 | β |
| Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. | Kavousi M et al. | β | 2023 | β |
| Multiomics technologies: role in disease biomarker discoveries and therapeutics. | Dar MA et al. | β | 2023 | β |
| Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores. | Folsom AR et al. | β | 2023 | β |
| Protocol for Biospecimen Collection and Analysis Within the BACPAC Research Program. | Fields AJ et al. | β | 2023 | β |
| The Health, Aging, and Body Composition (Health ABC) Study-Ground-Breaking Science for 25 Years and Counting. | Newman AB et al. | β | 2023 | β |
| Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. | Young KL et al. | β | 2023 | β |
| A guide for researchers seeking training in retrospective data harmonization for population neuroscience studies of Alzheimer's disease and related dementias. | Shaaban CE et al. | β | 2022 | β |
| Association of Genetically Predicted Fibroblast Growth Factor-23 with Heart Failure: A Mendelian Randomization Study. | Akwo E et al. | β | 2022 | β |
| Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues. | Castaneda AB et al. | β | 2022 | β |
| Calcification of the abdominal aorta is an under-appreciated cardiovascular disease risk factor in the general population. | Sethi A et al. | β | 2022 | β |
| Collaborative Cohort of Cohorts for COVID-19 Research (C4R) Study: Study Design. | Oelsner EC et al. | β | 2022 | β |
| Elucidating the relationship between migraine risk and brain structure using genetic data. | Mitchell BL et al. | β | 2022 | β |
| Fully exploiting SNP arrays: a systematic review on the tools to extract underlying genomic structure. | BalaguΓ©-DobΓ³n L et al. | β | 2022 | β |
| Functional Studies of Genetic Variants Associated with Human Diseases in Notch Signaling-Related Genes Using Drosophila. | Yang SA et al. | β | 2022 | β |
| Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate. | Mishra A et al. | β | 2022 | β |
| Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. | Young WJ et al. | β | 2022 | β |
| Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study. | Portilla-Fernandez E et al. | β | 2022 | β |
| Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. | KDIGO Conference Participants | β | 2022 | β |
| Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation. | Longchamps RJ et al. | β | 2022 | β |
| Higher Coffee Consumption Is Associated With Reduced Cerebral Gray Matter Volume: A Mendelian Randomization Study. | Zheng BK et al. | β | 2022 | β |
| Host and gut microbial tryptophan metabolism and type 2 diabetes: an integrative analysis of host genetics, diet, gut microbiome and circulating metabolites in cohort studies. | Qi Q et al. | β | 2022 | β |
| Impact of SNP microarray analysis of compromised DNA on kinship classification success in the context of investigative genetic genealogy. | de Vries JH et al. | β | 2022 | β |
| Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels. | Sarnowski C et al. | β | 2022 | β |
| Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. | Temprano-Sagrera G et al. | β | 2022 | β |
| New insights into the genetic etiology of Alzheimer's disease and related dementias. | Bellenguez C et al. | β | 2022 | β |
| Nutritional and genetic determinants of essential hypertension among adult respondents of the 2013 national nutrition survey, Philippines: a preliminary observational study. | Zumaraga MPP et al. | β | 2022 | β |
| Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL Cholesterol. | Wu P et al. | β | 2022 | β |
| Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing. | Austin TR et al. | β | 2022 | β |
| Site effects how-to and when: An overview of retrospective techniques to accommodate site effects in multi-site neuroimaging analyses. | Bayer JMM et al. | β | 2022 | β |
| Strengthening Causal Inference in Exposomics Research: Application of Genetic Data and Methods. | Avery CL et al. | β | 2022 | β |
| Stroke Genetics: Discovery, Insight Into Mechanisms, and Clinical Perspectives. | Debette S et al. | β | 2022 | β |
| The combined impact of persistent infections and human genetic variation on C-reactive protein levels. | Hodel F et al. | β | 2022 | β |
| The Musical Abilities, Pleiotropy, Language, and Environment (MAPLE) Framework for Understanding Musicality-Language Links Across the Lifespan. | Nayak S et al. | β | 2022 | β |
| Whole-exome sequencing of 14β389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. | Pankratz N et al. | β | 2022 | β |
| Association of Genetic Variation With Cirrhosis: A Multi-Trait Genome-Wide Association and Gene-Environment Interaction Study. | Emdin CA et al. | β | 2021 | β |
| Association of low-frequency and rare coding variants with information processing speed. | Bressler J et al. | β | 2021 | β |
| Causal effect of Lipoprotein-associated phospholipase A2 activity on coronary artery disease and myocardial Infarction: A Two-Sample Mendelian Randomization study. | Sun L et al. | β | 2021 | β |
| Cholesteryl ester transfer protein (CETP) as a drug target for cardiovascular disease. | Schmidt AF et al. | β | 2021 | β |
| Emerging approaches to polypharmacy among older adults. | Mehta RS et al. | β | 2021 | β |
| Epigenome-wide association meta-analysis of DNA methylation with coffee and tea consumption. | KarabegoviΔ I et al. | β | 2021 | β |
| FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimer. | Thibord F et al. | β | 2021 | β |
| Framingham Heart Study: JACC Focus Seminar, 1/8. | Andersson C et al. | β | 2021 | β |
| Genetically regulated expression in late-onset Alzheimer's disease implicates risk genes within known and novel loci. | Chen HH et al. | β | 2021 | β |
| Genetic Determinants of Peripheral Artery Disease. | Klarin D et al. | β | 2021 | β |
| Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. | Francis M et al. | β | 2021 | β |
| Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. | Yang Y et al. | β | 2021 | β |
| Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease-Brief Report. | Small AM et al. | β | 2021 | β |
| Meta-analysis of epigenome-wide association studies of carotid intima-media thickness. | Portilla-FernΓ‘ndez E et al. | β | 2021 | β |
| Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. | Sun D et al. | β | 2021 | β |
| Multi-omics data integration and network-based analysis drives a multiplex drug repurposing approach to a shortlist of candidate drugs against COVID-19. | Tomazou M et al. | β | 2021 | β |
| Novel compound heterozygous missense variants (c.G955A and c.A1822C) of <i>CACNA2D4</i> likely causing autosomal recessive retinitis pigmentosa in a Chinese patient. | Cheng J et al. | β | 2021 | β |
| Pharmacogenomic Effects of Ξ²-Blocker Use on Femoral Neck Bone Mineral Density. | Nevola KT et al. | β | 2021 | β |
| Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function. | Yang T et al. | β | 2021 | β |
| SHIP-MR and Radiology: 12 Years of Whole-Body Magnetic Resonance Imaging in a Single Center. | Hosten N et al. | β | 2021 | β |
| Structural and functional brain alterations revealed by neuroimaging in CNV carriers. | Moreau CA et al. | β | 2021 | β |
| Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations. | Haslam DE et al. | β | 2021 | β |
| The ARIC (Atherosclerosis Risk In Communities) Study: JACC Focus Seminar 3/8. | Wright JD et al. | β | 2021 | β |
| Translating genetic association of lipid levels for biological and clinical application. | Crone B et al. | β | 2021 | β |
| Analysis on the polymorphisms of site RS4977574, and RS1333045 in region 9p21 and the susceptibility of coronary heart disease in Chinese population. | Hua L et al. | β | 2020 | β |
| Association of common genetic variants with brain microbleeds: A genome-wide association study. | Knol MJ et al. | β | 2020 | β |
| Association of Genetic Variation With Keratoconus. | McComish BJ et al. | β | 2020 | β |
| Cerebral small vessel disease genomics and its implications across the lifespan. | Sargurupremraj M et al. | β | 2020 | β |
| Challenge-comet assay, a functional and genomic biomarker for precision risk assessment and disease prevention among exposed workers. | Xu J et al. | β | 2020 | β |
| Circulating Protein Signatures and Causal Candidates for Type 2 Diabetes. | Gudmundsdottir V et al. | β | 2020 | β |
| Diet patterns and the incidence of age-related macular degeneration in the Atherosclerosis Risk in Communities (ARIC) study. | Dighe S et al. | β | 2020 | β |
| Embracing study heterogeneity for finding genetic interactions in large-scale research consortia. | Liu Y et al. | β | 2020 | β |
| Gene Variants Associated With Venous Thrombosis: A Replication Study in a Brazilian Multicentre Study. | Romano AVC et al. | β | 2020 | β |
| Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants. | Persyn E et al. | β | 2020 | β |
| Genotype imputation and variability in polygenic risk score estimation. | Chen SF et al. | β | 2020 | β |
| Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes. | Shin J et al. | β | 2020 | β |
| Investigation of the Causal Association between Long-Chain n-6 Polyunsaturated Fatty Acid Synthesis and the Risk of Type 2 Diabetes: A Mendelian Randomization Analysis. | Zulyniak MA et al. | β | 2020 | β |
| Multilevel omics for the discovery of biomarkers and therapeutic targets for stroke. | Montaner J et al. | β | 2020 | β |
| Opportunities, challenges and expectations management for translating biobank research to precision medicine. | O'Donnell CJ | β | 2020 | β |
| The Longitudinal Aging Study Amsterdam: cohort update 2019 and additional data collections. | Hoogendijk EO et al. | β | 2020 | β |
| The reliability and heritability of cortical folds and their genetic correlations across hemispheres. | Pizzagalli F et al. | β | 2020 | β |
| 70-year legacy of the Framingham Heart Study. | Andersson C et al. | β | 2019 | β |
| A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology. | de Vries PS et al. | β | 2019 | β |
| A large-scale exome array analysis of venous thromboembolism. | LindstrΓΆm S et al. | β | 2019 | β |
| Association of <i>FMO3</i> Variants with Blood Pressure in the Atherosclerosis Risk in Communities Study. | Bryant TS et al. | β | 2019 | β |
| Cohort profile: design and methods in the eye and vision consortium of UK Biobank. | Chua SYL et al. | β | 2019 | β |
| eQTL of KCNK2 regionally influences the brain sulcal widening: evidence from 15,597 UK Biobank participants with neuroimaging data. | Le Guen Y et al. | β | 2019 | β |
| Exome sequencing of 20,791Β cases of type 2 diabetes and 24,440Β controls. | Flannick J et al. | β | 2019 | β |
| Genetic architecture of hippocampal subfields on standard resolution MRI: How the parts relate to the whole. | Elman JA et al. | β | 2019 | β |
| Genetic architecture of subcortical brain structures in 38,851 individuals. | Satizabal CL et al. | β | 2019 | β |
| Genetic Overlap Between Alzheimer's Disease and Bipolar Disorder Implicates the MARK2 and VAC14 Genes. | Drange OK et al. | β | 2019 | β |
| Genetic risk for coronary heart disease alters the influence of Alzheimer's genetic risk on mild cognitive impairment. | Elman JA et al. | β | 2019 | β |
| Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment. | Nagtegaal AP et al. | β | 2019 | β |
| Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. | van Setten J et al. | β | 2019 | β |
| Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. | Sabater-Lleal M et al. | β | 2019 | β |
| Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans. | Do AN et al. | β | 2019 | β |
| Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry. | Irvin MR et al. | β | 2019 | β |
| HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype. | Malhotra R et al. | β | 2019 | β |
| Innovation in Genomic Data Sharing at the NIH. | Psaty BM et al. | β | 2019 | β |
| Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease. | Ward-Caviness CK et al. | β | 2019 | β |
| Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. | de Vries PS et al. | β | 2019 | β |
| Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. | Bentley AR et al. | β | 2019 | β |
| Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. | Noordam R et al. | β | 2019 | β |
| Serum 25-Hydroxyvitamin D Concentrations and Incidence of Age-Related Macular Degeneration: The Atherosclerosis Risk in Communities Study. | Millen AE et al. | β | 2019 | β |
| The African Descent and Glaucoma Evaluation Study (ADAGES) III: Contribution of Genotype to Glaucoma Phenotype in African Americans: Study Design and Baseline Data. | Zangwill LM et al. | β | 2019 | β |
| The Effect of Pre-Analytical Conditions on Blood Metabolomics in Epidemiological Studies. | Santos Ferreira DL et al. | β | 2019 | β |
| Using Openly Accessible Resources to Strengthen Causal Inference in Epigenetic Epidemiology of Neurodevelopment and Mental Health. | Walton E et al. | β | 2019 | β |
| Validation and characterisation of a DNA methylation alcohol biomarker across the life course. | Yousefi PD et al. | β | 2019 | β |
| A genome-wide association study of red-blood cell fatty acids and ratios incorporating dietary covariates: Framingham Heart Study Offspring Cohort. | Kalsbeek A et al. | β | 2018 | β |
| Age-related DNA methylation and hemostatic factors. | de Andrade M | β | 2018 | β |
| Analyzing metabolomics data for association with genotypes using two-component Gaussian mixture distributions. | Westra J et al. | β | 2018 | β |
| A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS-based genetic diagnosis. | Fu J et al. | β | 2018 | β |
| Association of Methylation Signals With Incident Coronary Heart Disease in an Epigenome-Wide Assessment of Circulating Tumor Necrosis Factor Ξ±. | Aslibekyan S et al. | β | 2018 | β |
| Associations between polymorphisms of the CXCL12 and CNNM2 gene and hypertension risk: A case-control study. | Liu X et al. | β | 2018 | β |
| Associations of activated coagulation factor VII and factor VIIa-antithrombin levels with genome-wide polymorphisms and cardiovascular disease risk. | Olson NC et al. | β | 2018 | β |
| A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneys. | Ito YA et al. | β | 2018 | β |
| CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis. | Guo L et al. | β | 2018 | β |
| Cohort Profile: Pregnancy And Childhood Epigenetics (PACE) Consortium. | Felix JF et al. | β | 2018 | β |
| Collaborative, pooled and harmonized study designs for epidemiologic research: challenges and opportunities. | Lesko CR et al. | β | 2018 | β |
| Common Coding Variants in <i>SCN10A</i> Are Associated With the Nav1.8 Late Current and Cardiac Conduction. | Macri V et al. | β | 2018 | β |
| Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation. | Nandakumar P et al. | β | 2018 | β |
| DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis. | Ward-Caviness CK et al. | β | 2018 | β |
| Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging. | Jian X et al. | β | 2018 | β |
| FastSKAT: Sequence kernel association tests for very large sets of markers. | Lumley T et al. | β | 2018 | β |
| Genetic variants associated with earlier age at menopause increase the risk of cardiovascular events in women. | Sarnowski C et al. | β | 2018 | β |
| Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. | Ligthart S et al. | β | 2018 | β |
| Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume. | Vojinovic D et al. | β | 2018 | β |
| Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain. | Suri P et al. | β | 2018 | β |
| GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes. | Franceschini N et al. | β | 2018 | β |
| Harmonization of Respiratory Data From 9 US Population-Based Cohorts: The NHLBI Pooled Cohorts Study. | Oelsner EC et al. | β | 2018 | β |
| Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing. | Imani S et al. | β | 2018 | β |
| Integrated molecular analysis of Tamoxifen-resistant invasive lobular breast cancer cells identifies MAPK and GRM/mGluR signaling as therapeutic vulnerabilities. | Stires H et al. | β | 2018 | β |
| Integration of Drosophila and Human Genetics to Understand Notch Signaling Related Diseases. | Salazar JL et al. | β | 2018 | β |
| Large-Scale Genomic Biobanks and Cardiovascular Disease. | Small AM et al. | β | 2018 | β |
| Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group. | Floyd JS et al. | β | 2018 | β |
| Lp-PLA2, scavenger receptor class B type I gene (SCARB1) rs10846744 variant, and cardiovascular disease. | Manichaikul A et al. | β | 2018 | β |
| Neurogenomics - towards a more rigorous science. | Mitchell KJ | β | 2018 | β |
| Nutritional Genomics and Direct-to-Consumer Genetic Testing: An Overview. | Guasch-FerrΓ© M et al. | β | 2018 | β |
| Observational and Genetic Associations of Resting Heart Rate With Aortic Valve Calcium. | Whelton SP et al. | β | 2018 | β |
| Opportunities for an enhanced integration of neuroscience and genomics. | Moore AA et al. | β | 2018 | β |
| Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology. | Seyerle AA et al. | β | 2018 | β |
| Scientific Contributions of Population-Based Studies to Cardiovascular Epidemiology in the GWAS Era. | Lieb W et al. | β | 2018 | β |
| The genetics of retinopathy of prematurity: a model for neovascular retinal disease. | Swan R et al. | β | 2018 | β |
| Three Decades of Dementia Research: Insights from One Small Community ofΒ Indomitable Rotterdammers. | Wolters FJ et al. | β | 2018 | β |
| 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project. | Cai N et al. | β | 2017 | β |
| A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. | Noordam R et al. | β | 2017 | β |
| Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology. | Brody JA et al. | β | 2017 | β |
| Association between Dietary Xanthophyll (Lutein and Zeaxanthin) Intake and Early Age-Related Macular Degeneration: The Atherosclerosis Risk in Communities Study. | Lin H et al. | β | 2017 | β |
| Association of Triglyceride-Related Genetic Variants With MitralΒ AnnularΒ Calcification. | Afshar M et al. | β | 2017 | β |
| Brain imaging genetics in ADHD and beyond - Mapping pathways from gene to disorder at different levels of complexity. | Klein M et al. | β | 2017 | β |
| Building on a Legacy of Hypertension Research: Charting Our Future Together. | Mensah GA et al. | β | 2017 | β |
| Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases. | McAllister K et al. | β | 2017 | β |
| DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation. | Richard MA et al. | β | 2017 | β |
| Effect of handgrip on coronary artery disease and myocardial infarction: a Mendelian randomization study. | Xu L et al. | β | 2017 | β |
| Evidence for large-scale gene-by-smoking interaction effects on pulmonary function. | Aschard H et al. | β | 2017 | β |
| Extremely low-coverage whole genome sequencing in South Asians captures population genomics information. | Rustagi N et al. | β | 2017 | β |
| Four Decades of Research in Alzheimer's Disease (1975-2014): A Bibliometric and Scientometric Analysis. | Serrano-Pozo A et al. | β | 2017 | β |
| Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes. | Mandaviya PR et al. | β | 2017 | β |
| Genetic studies as a tool for identifying novel potential targets for treatment ofΒ COPD. | Manichaikul A et al. | β | 2017 | β |
| Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. | Veenstra J et al. | β | 2017 | β |
| <i>CEP78</i> is mutated in a distinct type of Usher syndrome. | Fu Q et al. | β | 2017 | β |
| Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants among exon-captured variants of uncertain significance. | Soens ZT et al. | β | 2017 | β |
| Local Ancestry and Clinical Cardiovascular Events Among African Americans From the Atherosclerosis Risk in Communities Study. | Shendre A et al. | β | 2017 | β |
| <i>PCSK9</i> Loss-of-Function Variants, Low-Density Lipoprotein Cholesterol, and Risk of Coronary Heart Disease and Stroke: Data From 9 Studies of Blacks and Whites. | Kent ST et al. | β | 2017 | β |
| Molecular Epidemiology of Heart Failure: Translational Challenges and Opportunities. | Smith JG | β | 2017 | β |
| Multiancestry Study of Gene-Lifestyle Interactions for Cardiovascular Traits in 610 475 Individuals From 124 Cohorts: Design and Rationale. | Rao DC et al. | β | 2017 | β |
| Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies. | Xu M et al. | β | 2017 | β |
| Neuroimaging genomics in psychiatry-a translational approach. | Mufford MS et al. | β | 2017 | β |
| On meta- and mega-analyses for gene-environment interactions. | Huang J et al. | β | 2017 | β |
| Rheumatoid Arthritis and Coronary Artery Disease: Genetic Analyses Do Not Support a Causal Relation. | Jansen H et al. | β | 2017 | β |
| STROKOG (stroke and cognition consortium): An international consortium to examine the epidemiology, diagnosis, and treatment of neurocognitive disorders in relation to cerebrovascular disease. | Sachdev PS et al. | β | 2017 | β |
| Studying neuroanatomy using MRI. | Lerch JP et al. | β | 2017 | β |
| Taller height as a risk factor for venous thromboembolism: a Mendelian randomization meta-analysis. | Roetker NS et al. | β | 2017 | β |
| The impact of rare and low-frequency genetic variants in common disease. | Bomba L et al. | β | 2017 | β |
| The integration of epigenetics and genetics in nutrition research for CVD risk factors. | Ma Y et al. | β | 2017 | β |
| The phenotypic variability of HK1-associated retinal dystrophy. | Yuan Z et al. | β | 2017 | β |
| The Rotterdam Study: 2018 update on objectives, design and main results. | Ikram MA et al. | β | 2017 | β |
| Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability. | Reijnders MRF et al. | β | 2017 | β |
| Vitamin D Status and Prevalent Early Age-Related Macular Degeneration in African Americans and Caucasians: The Atherosclerosis Risk in Communities (ARIC) Study. | Millen AE et al. | β | 2017 | β |
| Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation. | Eicher JD et al. | β | 2017 | β |
| A hybrid computational strategy to address WGS variant analysis in >5000 samples. | Huang Z et al. | β | 2016 | β |
| A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. | de Vries PS et al. | β | 2016 | β |
| An Empirical Comparison of Joint and Stratified Frameworks for Studying G Γ E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group. | Sung YJ et al. | β | 2016 | β |
| Association of the IGF1 gene with fasting insulin levels. | Willems SM et al. | β | 2016 | β |
| Building a Platform to Enable NCD Research to Address Population Health in Africa: CVD Working Group Discussion at the Sixth H3Africa Consortium Meeting in Zambia. | Peprah E et al. | β | 2016 | β |
| Contributions of the Framingham Heart Study to the Epidemiology of Coronary Heart Disease. | Chen G et al. | β | 2016 | β |
| Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia. | Khera AV et al. | β | 2016 | β |
| Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. | Smith JG et al. | β | 2016 | β |
| Discovery of rare variants for complex phenotypes. | Kosmicki JA et al. | β | 2016 | β |
| DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases. | Ligthart S et al. | β | 2016 | β |
| Fast set-based association analysis using summary data from GWAS identifies novel gene loci for human complex traits. | Bakshi A et al. | β | 2016 | β |
| Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies. | Allen NB et al. | β | 2016 | β |
| Genetic Risk Factors for Ischemic and Hemorrhagic Stroke. | Chauhan G et al. | β | 2016 | β |
| Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons. | Pilling LC et al. | β | 2016 | β |
| Genome-wide association studies identify genetic loci for low von Willebrand factor levels. | van Loon J et al. | β | 2016 | β |
| Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium. | Dehghan A et al. | β | 2016 | β |
| Genome-wide gene-environment interactions on quantitative traits using family data. | Sitlani CM et al. | β | 2016 | β |
| GWAS for executive function and processing speed suggests involvement of the CADM2 gene. | Ibrahim-Verbaas CA et al. | β | 2016 | β |
| ICC-dementia (International Centenarian Consortium - dementia): an international consortium to determine the prevalence and incidence of dementia in centenarians across diverse ethnoracial and sociocultural groups. | Brodaty H et al. | β | 2016 | β |
| Identifying genetic loci affecting antidepressant drug response in depression using drug-gene interaction models. | Noordam R et al. | β | 2016 | β |
| Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets. | Zhu Z et al. | β | 2016 | β |
| Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease. | Manousaki D et al. | β | 2016 | β |
| Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits. | CHARGE Consortium Hematology Working Group | β | 2016 | β |
| Million Veteran Program: A mega-biobank to study genetic influences on health and disease. | Gaziano JM et al. | β | 2016 | β |
| Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis. | Natarajan P et al. | β | 2016 | β |
| Multivariate Analysis of Anthropometric Traits Using Summary Statistics of Genome-Wide Association Studies from GIANT Consortium. | Park H et al. | β | 2016 | β |
| Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons. | Harding BN et al. | β | 2016 | β |
| Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicity. | Tajiguli A et al. | β | 2016 | β |
| Next-generation sequencing-based molecular diagnosis of 35 Hispanic retinitis pigmentosa probands. | Zhang Q et al. | β | 2016 | β |
| Novel Genetic Loci Associated With Retinal Microvascular Diameter. | Jensen RA et al. | β | 2016 | β |
| Novel genetic loci underlying human intracranial volume identified through genome-wide association. | Adams HH et al. | β | 2016 | β |
| Perioperative genomics: coming soon to (operating) theatres near you. | Sigurdsson MI et al. | β | 2016 | β |
| Rapid evaluation of phenotypes, SNPs and results through the dbGaP CHARGE Summary Results site. | Rich SS et al. | β | 2016 | β |
| Rare coding TTN variants are associated with electrocardiographic QT interval in the general population. | Kapoor A et al. | β | 2016 | β |
| Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk. | Yu B et al. | β | 2016 | β |
| Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease. | Jakobsdottir J et al. | β | 2016 | β |
| Reveel: large-scale population genotyping using low-coverage sequencing data. | Huang L et al. | β | 2016 | β |
| Serum calcium and incident type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) study. | Rooney MR et al. | β | 2016 | β |
| Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies. | Demirkan A et al. | β | 2016 | β |
| Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study. | Hsu YH et al. | β | 2016 | β |
| The Application of Genomics in Diabetes: Barriers to Discovery and Implementation. | Floyd JS et al. | β | 2016 | β |
| The effect of hematocrit and hemoglobin on the risk of ischemic heart disease: A Mendelian randomization study. | Zhong Y et al. | β | 2016 | β |
| Uromodulin gene variants and their association with renal function and blood pressure in cats: a pilot study. | Jepson RE et al. | β | 2016 | β |
| Whole Exome Sequencing in Atrial Fibrillation. | Lubitz SA et al. | β | 2016 | β |
| Ο-3 Polyunsaturated Fatty Acid Biomarkers and Coronary Heart Disease: Pooling Project of 19 Cohort Studies. | Del Gobbo LC et al. | β | 2016 | β |
| A genome-wide association study of saturated, mono- and polyunsaturated red blood cell fatty acids in the Framingham Heart Offspring Study. | Tintle NL et al. | β | 2015 | β |
| A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing. | Wang Q et al. | β | 2015 | β |
| Circadian clock genes and risk of fatal prostate cancer. | Markt SC et al. | β | 2015 | β |
| Coagulation factorΒ XII genetic variation, exΒ vivo thrombin generation, and stroke risk in the elderly: results from the Cardiovascular Health Study. | Olson NC et al. | β | 2015 | β |
| Consumption of meat is associated with higher fasting glucose and insulin concentrations regardless of glucose and insulin genetic risk scores: a meta-analysis of 50,345 Caucasians. | Fretts AM et al. | β | 2015 | β |
| Dietary Patterns, Genes, and Health: Challenges and Obstacles to be Overcome. | Frazier-Wood AC | β | 2015 | β |
| Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. | Bis JC et al. | β | 2015 | β |
| Generalized estimating equations for genome-wide association studies using longitudinal phenotype data. | Sitlani CM et al. | β | 2015 | β |
| Genetic analyses benefit from using less heterogeneous phenotypes: an illustration with the hospital anxiety and depression scale (HADS). | Laurin CA et al. | β | 2015 | β |
| Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. | Mozaffarian D et al. | β | 2015 | β |
| Genetics and brain morphology. | Strike LT et al. | β | 2015 | β |
| Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk. | Jansen H et al. | β | 2015 | β |
| Genome-wide association study for endothelial growth factors. | Lieb W et al. | β | 2015 | β |
| GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy. | Broer L et al. | β | 2015 | β |
| Imaging genetics and psychiatric disorders. | Hashimoto R et al. | β | 2015 | β |
| Invited commentary: future of population studies--defining research priorities and processes. | Vasan RS et al. | β | 2015 | β |
| Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. | Wessel J et al. | β | 2015 | β |
| Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. | Gottlieb DJ et al. | β | 2015 | β |
| Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions. | Yu F et al. | β | 2015 | β |
| Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. | Huffman JE et al. | β | 2015 | β |
| Recent developments in genome and exome-wide analyses of plasma lipids. | Lange LA et al. | β | 2015 | β |
| The role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African Americans. | Sung YJ et al. | β | 2015 | β |
| The Rotterdam Study: 2016 objectives and design update. | Hofman A et al. | β | 2015 | β |
| Use of electronic health records to ascertain, validate and phenotype acute myocardial infarction: A systematic review and recommendations. | Rubbo B et al. | β | 2015 | β |
| White Matter Lesion Progression: Genome-Wide Search for Genetic Influences. | Hofer E et al. | β | 2015 | β |
| ADAM19 and HTR4 variants and pulmonary function: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. | London SJ et al. | β | 2014 | β |
| A genome-wide association meta-analysis of plasma AΞ² peptides concentrations in the elderly. | Chouraki V et al. | β | 2014 | β |
| Aging and cardiovascular diseases: the role of gene-diet interactions. | Corella D et al. | β | 2014 | β |
| An empirical comparison of meta-analysis and mega-analysis of individual participant data for identifying gene-environment interactions. | Sung YJ et al. | β | 2014 | β |
| Association of CDKN2BAS polymorphism rs4977574 with coronary heart disease: a case-control study and a meta-analysis. | Huang Y et al. | β | 2014 | β |
| Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. | Cornes BK et al. | β | 2014 | β |
| Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis. | Smith JG et al. | β | 2014 | β |
| Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. | Peloso GM et al. | β | 2014 | β |
| Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium. | Bis JC et al. | β | 2014 | β |
| A three-stage genome-wide association study combining multilocus test and gene expression analysis for young-onset hypertension in Taiwan Han Chinese. | Chiang KM et al. | β | 2014 | β |
| Biobanks for cardiovascular epidemiology and prevention. | Iacoviello L et al. | β | 2014 | β |
| Calibrating longitudinal cognition in Alzheimer's disease across diverse test batteries and datasets. | Gross AL et al. | β | 2014 | β |
| Challenges in elucidating the genetics of diabetic retinopathy. | Kuo JZ et al. | β | 2014 | β |
| Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest. | Lemaitre RN et al. | β | 2014 | β |
| Dementia Prevention: optimizing the use of observational data for personal, clinical, and public health decision-making. | Dacks PA et al. | β | 2014 | β |
| Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. | Avery CL et al. | β | 2014 | β |
| Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. | Ganesh SK et al. | β | 2014 | β |
| Following-up genome-wide association study signals: lessons learned from Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. | Boerwinkle E et al. | β | 2014 | β |
| Genetic determinants influencing human serum metabolome among African Americans. | Yu B et al. | β | 2014 | β |
| Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study. | Restrepo NA et al. | β | 2014 | β |
| Genetic variants related to height and risk of atrial fibrillation: the cardiovascular health study. | Rosenberg MA et al. | β | 2014 | β |
| Genome-wide association studies on serum sex steroid levels. | Vandenput L et al. | β | 2014 | β |
| Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium. | Guan W et al. | β | 2014 | β |
| Heritability of and mortality prediction with a longevity phenotype: the healthy aging index. | Sanders JL et al. | β | 2014 | β |
| Illumina human exome genotyping array clustering and quality control. | Guo Y et al. | β | 2014 | β |
| In silico tools for splicing defect prediction: a survey from the viewpoint of end users. | Jian X et al. | β | 2014 | β |
| Integrated genomics and metabolomics in nephrology. | Atzler D et al. | β | 2014 | β |
| Integrative DNA, RNA, and protein evidence connects TREML4 to coronary artery calcification. | Sen SK et al. | β | 2014 | β |
| Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. | Nalls MA et al. | β | 2014 | β |
| Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies. | Malik R et al. | β | 2014 | β |
| No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects. | Baumert J et al. | β | 2014 | β |
| Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans. | Jiang L et al. | β | 2014 | β |
| Personalized nutrition and cardiovascular disease prevention: From Framingham to PREDIMED. | Konstantinidou V et al. | β | 2014 | β |
| Predicting stroke through genetic risk functions: the CHARGE Risk Score Project. | Ibrahim-Verbaas CA et al. | β | 2014 | β |
| Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study. | Morrison AC et al. | β | 2014 | β |
| Sequence variation in TMEM18 in association with body mass index: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. | Liu CT et al. | β | 2014 | β |
| Sequencing of 2 subclinical atherosclerosis candidate regions in 3669 individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. | Bis JC et al. | β | 2014 | β |
| Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. | Lin H et al. | β | 2014 | β |
| Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study. | Lin H et al. | β | 2014 | β |
| The emerging era of pharmacogenomics: current successes, future potential, and challenges. | Lee JW et al. | β | 2014 | β |
| The role of environmental heterogeneity in meta-analysis of gene-environment interactions with quantitative traits. | Li S et al. | β | 2014 | β |
| Variant association tools for quality control and analysis of large-scale sequence and genotyping array data. | Wang GT et al. | β | 2014 | β |
| Whole-genome analyses of whole-brain data: working within an expanded search space. | Medland SE et al. | β | 2014 | β |
| A genome-wide association study of depressive symptoms. | Hek K et al. | β | 2013 | β |
| Association of heat shock proteins with all-cause mortality. | Broer L et al. | β | 2013 | β |
| Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. | Grove ML et al. | β | 2013 | β |
| Candidate gene association study of BMI-related loci, weight, and adiposity in old age. | Murphy RA et al. | β | 2013 | β |
| De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome. | Bainbridge MN et al. | β | 2013 | β |
| Development and evaluation of a genetic risk score for obesity. | Belsky DW et al. | β | 2013 | β |
| Estimation and partition of heritability in human populations using whole-genome analysis methods. | Vinkhuyzen AA et al. | β | 2013 | β |
| Gain-of-function lipoprotein lipase variant rs13702 modulates lipid traits through disruption of a microRNA-410 seed site. | Richardson K et al. | β | 2013 | β |
| Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus. | Li X et al. | β | 2013 | β |
| Genetic associations with valvular calcification and aortic stenosis. | Thanassoulis G et al. | β | 2013 | β |
| Genetic loci for retinal arteriolar microcirculation. | Sim X et al. | β | 2013 | β |
| Genetic risk factors for BMI and obesity in an ethnically diverse population: results from the population architecture using genomics and epidemiology (PAGE) study. | Fesinmeyer MD et al. | β | 2013 | β |
| Genetics and genomics for the prevention and treatment of cardiovascular disease: update: a scientific statement from the American Heart Association. | Ganesh SK et al. | β | 2013 | β |
| Genome-wide association study of retinopathy in individuals without diabetes. | Jensen RA et al. | β | 2013 | β |
| Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study. | Zhang L et al. | β | 2013 | β |
| Novel locus including FGF21 is associated with dietary macronutrient intake. | Chu AY et al. | β | 2013 | β |
| Pitfalls of predicting complex traits from SNPs. | Wray NR et al. | β | 2013 | β |
| Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium. | Shah T et al. | β | 2013 | β |
| Principal components methods for narrow-sense heritability in the analysis of multidimensional longitudinal cognitive phenotypes. | Fung WL et al. | β | 2013 | β |
| Quantifying diet for nutrigenomic studies. | Tucker KL et al. | β | 2013 | β |
| Simple risk model predicts incidence of atrial fibrillation in a racially and geographically diverse population: the CHARGE-AF consortium. | Alonso A et al. | β | 2013 | β |
| Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes. | Meschia JF et al. | β | 2013 | β |
| The 1000 Genomes Project: paving the way for personalized genomic medicine. | Gibson IB et al. | β | 2013 | β |
| The Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium as a model of collaborative science. | Psaty BM et al. | β | 2013 | β |
| The Contribution of the Framingham Heart Study to Gene Identification for Cardiovascular Risk Factors and Coronary Heart Disease. | Ehret GB | β | 2013 | β |
| The epidemiology of longevity and exceptional survival. | Newman AB et al. | β | 2013 | β |
| The molecular genetic architecture of self-employment. | van der Loos MJ et al. | β | 2013 | β |
| The Rotterdam Study: 2014 objectives and design update. | Hofman A et al. | β | 2013 | β |
| Value and challenges of measuring left ventricular mass in clinical research: implications for the practitioner. | Gottdiener JS | β | 2013 | β |
| A genetic risk score is associated with incident cardiovascular disease and coronary artery calcium: the Framingham Heart Study. | Thanassoulis G et al. | β | 2012 | β |
| A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. | Li X et al. | β | 2012 | β |
| Analysis of family- and population-based samples in cohort genome-wide association studies. | Manichaikul A et al. | β | 2012 | β |
| Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. | Murabito JM et al. | β | 2012 | β |
| Common genetic factors for hematological traits in humans. | Okada Y et al. | β | 2012 | β |
| Common variants at 12q14 and 12q24 are associated with hippocampal volume. | Bis JC et al. | β | 2012 | β |
| Common variants at 12q15 and 12q24 are associated with infant head circumference. | Taal HR et al. | β | 2012 | β |
| Common variants at 6q22 and 17q21 are associated with intracranial volume. | Ikram MA et al. | β | 2012 | β |
| Decreases in Casz1 mRNA by an siRNA Complex Do not Alter Blood Pressure in Mice. | Ji SM et al. | β | 2012 | β |
| Early menopause predicts future coronary heart disease and stroke: the Multi-Ethnic Study of Atherosclerosis. | Wellons M et al. | β | 2012 | β |
| 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. | Grallert H et al. | β | 2012 | β |
| Genetic, physiological, and lifestyle predictors of mortality in the general population. | Walter S et al. | β | 2012 | β |
| Genetic variants and associations of 25-hydroxyvitamin D concentrations with major clinical outcomes. | Levin GP et al. | β | 2012 | β |
| Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. | Hancock DB et al. | β | 2012 | β |
| Genomics and successful aging: grounds for renewed optimism? | Pilling LC et al. | β | 2012 | β |
| Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. | Yang HC et al. | β | 2012 | β |
| Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis. | Iliev ID et al. | β | 2012 | β |
| Methods of data collection and definitions of cardiac outcomes in the Rotterdam Study. | Leening MJ et al. | β | 2012 | β |
| Pharmacogenetics of statins: achievements, whole-genome analyses and future perspectives. | Postmus I et al. | β | 2012 | β |
| Population-based case-control association studies. | Hancock DB et al. | β | 2012 | β |
| Randomized trial of personal genomics for preventive cardiology: design and challenges. | Knowles JW et al. | β | 2012 | β |
| Relations of long-term and contemporary lipid levels and lipid genetic risk scores with coronary artery calcium in the framingham heart study. | Tsao CW et al. | β | 2012 | β |
| Research guidelines in the era of large-scale collaborations: an analysis of Genome-wide Association Study Consortia. | Austin MA et al. | β | 2012 | β |
| The Promises and Pitfalls of Genoeconomics* | Benjamin DJ et al. | β | 2012 | β |
| The search for longevity and healthy aging genes: insights from epidemiological studies and samples of long-lived individuals. | Murabito JM et al. | β | 2012 | β |
| Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies. | Bykhovskaya Y et al. | β | 2012 | β |
| A genome-wide association study of aging. | Walter S et al. | β | 2011 | β |
| Association of coagulation-related and inflammation-related genes and factor VIIc levels with stroke: the Cardiovascular Health Study. | Zakai NA et al. | β | 2011 | β |
| Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study. | Franceschini N et al. | β | 2011 | β |
| Association of HSP70 and its co-chaperones with Alzheimer's disease. | Broer L et al. | β | 2011 | β |
| Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals. | Johnson AD et al. | β | 2011 | β |
| Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus. | Burdon KP et al. | β | 2011 | β |
| Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. | Lemaitre RN et al. | β | 2011 | β |
| Genetic predictors of fibrin D-dimer levels in healthy adults. | Smith NL et al. | β | 2011 | β |
| Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease. | Schmidt H et al. | β | 2011 | β |
| Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis. | Smith NL et al. | β | 2011 | β |
| Genome partitioning of genetic variation for complex traits using common SNPs. | Yang J et al. | β | 2011 | β |
| Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. | ParΓ© G et al. | β | 2011 | β |
| Genome-wide association studies of atrial fibrillation: past, present, and future. | Sinner MF et al. | β | 2011 | β |
| Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium. | Fornage M et al. | β | 2011 | β |
| Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. | O'Donnell CJ et al. | β | 2011 | β |
| Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele. | Tin A et al. | β | 2011 | β |
| Grid-enabled measures: using Science 2.0 to standardize measures and share data. | Moser RP et al. | β | 2011 | β |
| How pleiotropic genetics of the musculoskeletal system can inform genomics and phenomics of aging. | Karasik D | β | 2011 | β |
| Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. | Okada Y et al. | β | 2011 | β |
| Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. | Schunkert H et al. | β | 2011 | β |
| Meta-analysis of gene-environment interaction: joint estimation of SNP and SNP Γ environment regression coefficients. | Manning AK et al. | β | 2011 | β |
| Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. | Bis JC et al. | β | 2011 | β |
| Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. | Dehghan A et al. | β | 2011 | β |
| Molecular Genetics and Economics. | Beauchamp JP et al. | β | 2011 | β |
| Multiple loci are associated with white blood cell phenotypes. | Nalls MA et al. | β | 2011 | β |
| Phenotype harmonization and cross-study collaboration in GWAS consortia: the GENEVA experience. | Bennett SN et al. | β | 2011 | β |
| Post-genomic update on a classical candidate gene for coronary artery disease: ESR1. | Lucas G et al. | β | 2011 | β |
| PRIMe: a method for characterization and evaluation of pleiotropic regions from multiple genome-wide association studies. | Huang J et al. | β | 2011 | β |
| The Rotterdam Study: 2012 objectives and design update. | Hofman A et al. | β | 2011 | β |
| Total zinc intake may modify the glucose-raising effect of a zinc transporter (SLC30A8) variant: a 14-cohort meta-analysis. | Kanoni S et al. | β | 2011 | β |
| Unraveling the biological mechanisms in Alzheimer's disease--lessons from genomics. | Borovecki F et al. | β | 2011 | β |
| Utility of genetic determinants of lipids and cardiovascular events in assessing risk. | Holmes MV et al. | β | 2011 | β |
| A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. | Newman AB et al. | β | 2010 | β |
| 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. | Smith NL et al. | β | 2010 | β |
| Common genetic variants associate with serum phosphorus concentration. | Kestenbaum B et al. | β | 2010 | β |
| Common variants in HSPB7 and FRMD4B associated with advanced heart failure. | Cappola TP et al. | β | 2010 | β |
| Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. | O'Seaghdha CM et al. | β | 2010 | β |
| 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. | Preuss M et al. | β | 2010 | β |
| Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. | Ikram MK et al. | β | 2010 | β |
| Genetic predictors of medically refractory ulcerative colitis. | Haritunians T et al. | β | 2010 | β |
| Genetics studies in ischaemic stroke. | Markus HS | β | 2010 | β |
| Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. | Qi L et al. | β | 2010 | β |
| Genome-wide analysis of genetic loci associated with Alzheimer disease. | Seshadri S et al. | β | 2010 | β |
| Genome-wide association analysis identifies multiple loci related to resting heart rate. | Eijgelsheim M et al. | β | 2010 | β |
| Genome-wide association studies and large-scale collaborations in epidemiology. | Psaty BM et al. | β | 2010 | β |
| Genome-wide association studies and the genetics of entrepreneurship. | van der Loos MJ et al. | β | 2010 | β |
| Genome-wide association studies in nephrology research. | KΓΆttgen A | β | 2010 | β |
| Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium. | Debette S et al. | β | 2010 | β |
| Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels. | Meyer TE et al. | β | 2010 | β |
| Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. | Tang W et al. | β | 2010 | β |
| 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. | Morrison AC et al. | β | 2010 | β |
| Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies. | Nettleton JA et al. | β | 2010 | β |
| Is coronary artery calcification at the intersection of vitamin D and coronary artery disease? | Dastani Z et al. | β | 2010 | β |
| Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. | Barbalic M et al. | β | 2010 | β |
| Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. | Hancock DB et al. | β | 2010 | β |
| Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. | Yang Q et al. | β | 2010 | β |
| Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. | Smith NL et al. | β | 2010 | β |
| Phenomics: the next challenge. | Houle D et al. | β | 2010 | β |
| Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. | Dehghan A et al. | β | 2009 | β |
| Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture. | Richards JB et al. | β | 2009 | β |
| Common variants at ten loci influence QT interval duration in the QTGEN Study. | Newton-Cheh C et al. | β | 2009 | β |
| Dissecting complex traits: recent advances in hypertension genomics. | O'Shaughnessy KM | β | 2009 | β |
| Genetic scoring analysis: a way forward in genome wide association studies? | Amin N et al. | β | 2009 | β |
| Genetics of stroke. | Fornage M | β | 2009 | β |
| Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. | Vasan RS et al. | β | 2009 | β |
| Genome-wide association meta-analysis for total serum bilirubin levels. | Johnson AD et al. | β | 2009 | β |
| Genome-wide association studies of cardiovascular risk factors: design, conduct and interpretation. | Bis JC et al. | β | 2009 | β |
| Genomewide association studies of stroke. | Ikram MA et al. | β | 2009 | β |
| Genome-wide association study of blood pressure and hypertension. | Levy D et al. | β | 2009 | β |
| GRIMP: a web- and grid-based tool for high-speed analysis of large-scale genome-wide association using imputed data. | Estrada K et al. | β | 2009 | β |
| Multiple loci associated with indices of renal function and chronic kidney disease. | KΓΆttgen A et al. | β | 2009 | β |
| Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. | Ganesh SK et al. | β | 2009 | β |
| Recent trends in cardiovascular epidemiology. | Hofman A | β | 2009 | β |
| The Rotterdam Study: 2010 objectives and design update. | Hofman A et al. | β | 2009 | β |
| Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. | Benjamin EJ et al. | β | 2009 | β |