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Long-term use of antihypertensive drugs and risk of cancer.
- Published in:
- Pharmacoepidemiology & Drug Safety, 2008, v. 17, n. 11, p. 1039, doi. 10.1002/pds.1656
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- Publication type:
- Article
The Project Baseline Health Study: a step towards a broader mission to map human health.
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- NPJ Digital Medicine, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s41746-020-0290-y
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- Publication type:
- Article
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease.
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- Human Genetics, 2008, v. 123, n. 4, p. 399, doi. 10.1007/s00439-008-0489-5
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- Publication type:
- Article
Genomics and phenomics of body mass index reveals a complex disease network.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-35553-2
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- Publication type:
- Article
The combination of 9p21.3 genotype and biomarker profile improves a peripheral artery disease risk prediction model.
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- Vascular Medicine, 2014, v. 19, n. 1, p. 3, doi. 10.1177/1358863X13514791
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- Publication type:
- Article
Sex differences in the prevalence of peripheral artery disease in patients undergoing coronary catheterization.
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- Vascular Medicine, 2010, v. 15, n. 6, p. 443, doi. 10.1177/1358863X10388345
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- Publication type:
- Article
COMMENTARY: Cardiac outcomes occurred more frequently with PCIthan CABG or medical therapy in coronary artery disease.
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- ACP Journal Club, 2004, v. 141, n. 3, p. 57, doi. 10.7326/acpjc-2004-141-3-057
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- Publication type:
- Article
Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.
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- Human Molecular Genetics, 2014, v. 23, n. 8, p. 1957
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- Publication type:
- Article
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 15, p. 2320, doi. 10.1093/hmg/ddn132
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- Publication type:
- Article
Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci.
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- Nature Communications, 2016, v. 7, n. 7, p. 12092, doi. 10.1038/ncomms12092
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- Publication type:
- Article
Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program.
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- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0267900
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- Publication type:
- Article
Alcohol use and cardiometabolic risk in the UK Biobank: A Mendelian randomization study.
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- PLoS ONE, 2021, p. 1, doi. 10.1371/journal.pone.0255801
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- Publication type:
- Article
Genome-Wide Association Studies of Coronary Artery Disease: Recent Progress and Challenges Ahead.
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- Current Atherosclerosis Reports, 2018, v. 20, n. 9, p. 1, doi. 10.1007/s11883-018-0748-4
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- Article
Dissecting the Causal Genetic Mechanisms of Coronary Heart Disease.
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- Current Atherosclerosis Reports, 2014, v. 16, n. 5, p. 1, doi. 10.1007/s11883-014-0406-4
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- Publication type:
- Article
Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity.
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- Diabetes, 2014, v. 63, n. 6, p. 2158, doi. 10.2337/db13-0949
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- Publication type:
- Article
Genetic Variants Associated With Glycine Metabolism and Their Role in Insulin Sensitivity and Type 2 Diabetes.
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- Diabetes, 2013, v. 62, n. 6, p. 2141, doi. 10.2337/db12-0876
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- Publication type:
- Article
A Bivariate Genome-Wide Approach to Metabolic Syndrome.
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- Diabetes, 2011, v. 60, n. 4, p. 1329, doi. 10.2337/db10-1011
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- Publication type:
- Article
Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans.
- Published in:
- Diabetes, 2010, v. 59, n. 5, p. 1266, doi. 10.2337/DB09-1568
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- Publication type:
- Article
Corrigendum: Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example.
- Published in:
- 2015
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- Publication type:
- Correction Notice
Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00254
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- Publication type:
- Article
Association of Left Ventricular Ejection Fraction and Symptoms With Mortality After Elective Noncardiac Surgery Among Patients With Heart Failure.
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- 2019
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- Publication type:
- journal article
Mendelian randomization analyses suggest a causal role for circulating GIP and IL-1RA levels in homeostatic model assessment-derived measures of β-cell function and insulin sensitivity in Africans without type 2 diabetes.
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- Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01263-7
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- Publication type:
- Article
Mendelian randomization analyses clarify the effects of height on cardiovascular diseases.
- Published in:
- PLoS ONE, 2024, v. 19, n. 7, p. 1, doi. 10.1371/journal.pone.0298786
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- Publication type:
- Article
Defining the role of common variation in the genomic and biological architecture of adult human height.
- Published in:
- Nature Genetics, 2014, v. 46, n. 11, p. 1173, doi. 10.1038/ng.3097
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- Publication type:
- Article
Large-scale association analysis identifies new risk loci for coronary artery disease.
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- Nature Genetics, 2013, v. 45, n. 1, p. 25, doi. 10.1038/ng.2480
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- Publication type:
- Article
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
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- Nature Genetics, 2011, v. 43, n. 4, p. 333, doi. 10.1038/ng.784
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- Publication type:
- Article
Genome-wide meta-analyses identify multiple loci associated with smoking behavior.
- Published in:
- Nature Genetics, 2010, v. 42, n. 5, p. 441, doi. 10.1038/ng.571
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- Publication type:
- Article
Characterization of TCF21 Downstream Target Regions Identifies a Transcriptional Network Linking Multiple Independent Coronary Artery Disease Loci.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 5, p. 1, doi. 10.1371/journal.pgen.1005202
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- Publication type:
- Article
Coronary Heart Disease-Associated Variation in <i>TCF21</i> Disrupts a miR-224 Binding Site and miRNA-Mediated Regulation.
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- PLoS Genetics, 2014, v. 10, n. 3, p. 1, doi. 10.1371/journal.pgen.1004263
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- Publication type:
- Article
Disease-Related Growth Factor and Embryonic Signaling Pathways Modulate an Enhancer of <i>TCF21</i> Expression at the 6q23.2 Coronary Heart Disease Locus.
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- PLoS Genetics, 2013, v. 9, n. 7, p. 1, doi. 10.1371/journal.pgen.1003652
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- Publication type:
- Article
Cardioinformatics: the nexus of bioinformatics and precision cardiology.
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- Briefings in Bioinformatics, 2020, v. 21, n. 6, p. 2031, doi. 10.1093/bib/bbz119
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- Publication type:
- Article
Cardiorespiratory fitness and risk of heart failure with preserved ejection fraction.
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- European Journal of Heart Failure, 2024, v. 26, n. 5, p. 1163, doi. 10.1002/ejhf.3117
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- Publication type:
- Article
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22339-1
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- Publication type:
- Article
Insulin Resistance: Regression and Clustering.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0094129
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- Publication type:
- Article
Long-Term Use of Angiotensin Receptor Blockers and the Risk of Cancer.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0050893
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- Publication type:
- Article
Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035651
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- Publication type:
- Article
Detecting clinically meaningful biomarkers with repeated measurements: An illustration with electronic health records.
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- Biometrics, 2015, v. 71, n. 2, p. 478, doi. 10.1111/biom.12283
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- Publication type:
- Article
Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts.
- Published in:
- Human Genetics, 2023, v. 142, n. 10, p. 1477, doi. 10.1007/s00439-023-02593-7
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- Publication type:
- Article
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
- Published in:
- Human Genetics, 2019, v. 138, n. 2, p. 199, doi. 10.1007/s00439-019-01975-0
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- Publication type:
- Article
No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis.
- Published in:
- Scientific Reports, 2016, p. 35278, doi. 10.1038/srep35278
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- Publication type:
- Article
Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program.
- Published in:
- Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.777076
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- Publication type:
- Article
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci.
- Published in:
- Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.787545
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- Publication type:
- Article
PCSK9 loss of function is protective against extra-coronary atherosclerotic cardiovascular disease in a large multi-ethnic cohort.
- Published in:
- PLoS ONE, 2020, v. 15, n. 11, p. 1, doi. 10.1371/journal.pone.0239752
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- Publication type:
- Article
Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran program.
- Published in:
- PLoS ONE, 2020, v. 15, n. 8, p. 1, doi. 10.1371/journal.pone.0237430
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- Publication type:
- Article
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene.
- Published in:
- 2016
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- Publication type:
- corrected article
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene.
- Published in:
- Journal of Clinical Investigation, 2015, v. 125, n. 4, p. 1739, doi. 10.1172/JCI74692
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- Publication type:
- Article
Trans-ethnic fine mapping identifies a novel independent locus at the 3′ end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population.
- Published in:
- Diabetologia, 2013, v. 56, n. 12, p. 2619, doi. 10.1007/s00125-013-3047-1
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- Publication type:
- Article
Development and utility of a clinical research informatics application for participant recruitment and workflow management for a return of results pilot trial in familial hypercholesterolemia in the Million Veteran Program.
- Published in:
- JAMIA Open, 2024, v. 7, n. 1, p. 1, doi. 10.1093/jamiaopen/ooae020
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- Publication type:
- Article
Genetics of Smoking and Risk of Atherosclerotic Cardiovascular Diseases: A Mendelian Randomization Study.
- Published in:
- JAMA Network Open, 2021, v. 4, n. 1, p. 1, doi. 10.1001/jamanetworkopen.2020.34461
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- Publication type:
- Article
Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91113-6
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- Publication type:
- Article