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226 PR articles • 39,724 PR citations • Sorted by year • Download PDF (PDF by citations)
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1Premorbid predictors of death at initial presentation of coronary heart disease in the Women's Health Initiative study2.81Citations (PDF)
2Associations between accurate measures of adiposity and fitness, blood proteins, and insulin sensitivity among South Asians and Europeans3.91Citations (PDF)
3Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants4.03Citations (PDF)
4Plasma proteomic signatures for type 2 diabetes and related traits in the UK Biobank cohort5.92Citations (PDF)
5Bidirectional associations of zinc supplement intake with biological ageing interacted by metabolic equivalent of task: A large-scale population-based Biobank study
Clinical Nutrition, 2025, 50, 1-9
5.30Citations (PDF)
6Diet Quality and Epigenetic Aging in the Women’s Health Initiative1.517Citations (PDF)
7Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization2.923Citations (PDF)
8Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers13.722Citations (PDF)
9Mendelian randomization analyses clarify the effects of height on cardiovascular diseases
PLoS ONE, 2024, 19, e0298786
2.30Citations (PDF)
10Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Science, 2024, 385,
36.2250Citations (PDF)
11Rare variant contribution to the heritability of coronary artery disease13.79Citations (PDF)
12Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
Nature Genetics, 2024, 56, 2659-2671
25.224Citations (PDF)
13Genetic evidence for causal relationships between age at natural menopause and the risk of ageing-associated adverse health outcomes4.99Citations (PDF)
14Plasma proteomic signatures of a direct measure of insulin sensitivity in two population cohorts
Diabetologia, 2023, 66, 1643-1654
7.612Citations (PDF)
15Contemporary Polygenic Scores of Low-Density Lipoprotein Cholesterol and Coronary Artery Disease Predict Coronary Atherosclerosis in Adolescents and Young Adults2.93Citations (PDF)
16A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease
Nature Medicine, 2023, 29, 1793-1803
33.0200Citations (PDF)
17Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseases2.85Citations (PDF)
18Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts
Human Genetics, 2023, 142, 1477-1489
2.91Citations (PDF)
19Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Nature Genetics, 2023, 55, 1651-1664
25.279Citations (PDF)
20Genetic insights into resting heart rate and its role in cardiovascular disease13.725Citations (PDF)
21Plasma Protein Profiling of Incident Cardiovascular Diseases: A Multisample Evaluation2.99Citations (PDF)
22Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification
Nature Cardiovascular Research, 2023, 2, 1159-1172
8.417Citations (PDF)
23Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project
Stroke, 2022, 53, 875-885
6.033Citations (PDF)
24ZEB2 Shapes the Epigenetic Landscape of Atherosclerosis
Circulation, 2022, 145, 469-485
18.166Citations (PDF)
25APOL1 Risk Variants, Acute Kidney Injury, and Death in Participants With African Ancestry Hospitalized With COVID-19 From the Million Veteran Program
JAMA Internal Medicine, 2022, 182, 386
10.557Citations (PDF)
26Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program2.312Citations (PDF)
27Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci2.36Citations (PDF)
28Coronary Artery Disease Risk of Familial Hypercholesterolemia Genetic Variants Independent of Clinically Observed Longitudinal Cholesterol Exposure2.914Citations (PDF)
29Rare coding variants in RCN3 are associated with blood pressure
BMC Genomics, 2022, 23,
3.310Citations (PDF)
30Interactions of physical activity, muscular fitness, adiposity, and genetic risk for NAFLD
Hepatology Communications, 2022, 6, 1516-1526
4.513Citations (PDF)
31Genetic Landscape of the ACE2 Coronavirus Receptor
Circulation, 2022, 145, 1398-1411
18.134Citations (PDF)
32Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
Science Advances, 2022, 8,
10.973Citations (PDF)
33Gaseous air pollutants and DNA methylation in a methylome-wide association study of an ethnically and environmentally diverse population of U.S. adults
Environmental Research, 2022, 212, 113360
7.815Citations (PDF)
34Integration of rare expression outlier-associated variants improves polygenic risk prediction6.528Citations (PDF)
35Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program
PLoS ONE, 2022, 17, e0267900
2.36Citations (PDF)
36High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease
Nature Genetics, 2022, 54, 772-782
25.256Citations (PDF)
37A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Nature Genetics, 2022, 54, 761-771
25.2169Citations (PDF)
38A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program
PLoS Genetics, 2022, 18, e1010193
3.221Citations (PDF)
39Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits6.566Citations (PDF)
40Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait
JAMA Internal Medicine, 2022, 182, 796
10.520Citations (PDF)
41Use of Polygenic Risk Scores for Coronary Heart Disease in Ancestrally Diverse Populations
Current Cardiology Reports, 2022, 24, 1169-1177
2.920Citations (PDF)
42Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension
Hypertension, 2022, 79, 1656-1667
6.626Citations (PDF)
43Race and Ethnicity Stratification for Polygenic Risk Score Analyses May Mask Disparities in Hispanics
Circulation, 2022, 146, 265-267
18.122Citations (PDF)
44Broad clinical manifestations of polygenic risk for coronary artery disease in the Women’s Health Initiative4.55Citations (PDF)
45Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Nature Medicine, 2022, 28, 1679-1692
33.0302Citations (PDF)
46A translational genomics approach identifies IL10RB as the top candidate gene target for COVID-19 susceptibility4.315Citations (PDF)
47Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture2.915Citations (PDF)
48Genomics and phenomics of body mass index reveals a complex disease network13.7122Citations (PDF)
49Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease—Brief Report6.028Citations (PDF)
50Epigenome-wide association study of diet quality in the Women’s Health Initiative and TwinsUK cohort4.927Citations (PDF)
51Genetics of 35 blood and urine biomarkers in the UK Biobank
Nature Genetics, 2021, 53, 185-194
25.2680Citations (PDF)
52Multi-trait association studies discover pleiotropic loci between Alzheimer’s disease and cardiometabolic traits6.631Citations (PDF)
53Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices13.724Citations (PDF)
54Clonal hematopoiesis associated with epigenetic aging and clinical outcomes
Aging Cell, 2021, 20,
6.8121Citations (PDF)
55A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids13.732Citations (PDF)
56Association Between Genetic Variation in Blood Pressure and Increased Lifetime Risk of Peripheral Artery Disease6.033Citations (PDF)
57Epigenetically mediated electrocardiographic manifestations of sub-chronic exposures to ambient particulate matter air pollution in the Women's Health Initiative and Atherosclerosis Risk in Communities Study
Environmental Research, 2021, 198, 111211
7.87Citations (PDF)
58DXA Versus Clinical Measures of Adiposity as Predictors of Cardiometabolic Diseases and All-Cause Mortality in Postmenopausal Women
Mayo Clinic Proceedings, 2021, 96, 2831-2842
3.75Citations (PDF)
59Alcohol use and cardiometabolic risk in the UK Biobank: A Mendelian randomization study
PLoS ONE, 2021, 16, e0255801
2.344Citations (PDF)
60The Propagation of Racial Disparities in Cardiovascular Genomics Research2.926Citations (PDF)
61A Missense Variant in the IL-6 Receptor and Protection From Peripheral Artery Disease
Circulation Research, 2021, 129, 968-970
13.227Citations (PDF)
62Genetics of Smoking and Risk of Atherosclerotic Cardiovascular Diseases
JAMA Network Open, 2021, 4, e2034461
6.676Citations (PDF)
63Large‐Scale Plasma Protein Profiling of Incident Myocardial Infarction, Ischemic Stroke, and Heart Failure4.030Citations (PDF)
64The power of genetic diversity in genome-wide association studies of lipids
Nature, 2021, 600, 675-679
37.9845Citations (PDF)
65Associations between DNA methylation and BMI vary by metabolic health status: a potential link to disparate cardiovascular outcomes3.921Citations (PDF)
66Leukocyte Traits and Exposure to Ambient Particulate Matter Air Pollution in the Women’s Health Initiative and Atherosclerosis Risk in Communities Study8.422Citations (PDF)
67Cardioinformatics: the nexus of bioinformatics and precision cardiology
Briefings in Bioinformatics, 2020, 21, 2031-2051
6.620Citations (PDF)
68Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Circulation, 2020, 142, 1633-1646
18.1132Citations (PDF)
69Comprehensive Investigation of Circulating Biomarkers and Their Causal Role in Atherosclerosis-Related Risk Factors and Clinical Events2.927Citations (PDF)
70Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction13.785Citations (PDF)
71Genetic determinants of increased body mass index mediate the effect of smoking on increased risk for type 2 diabetes but not coronary artery disease
Human Molecular Genetics, 2020, 29, 3327-3337
2.910Citations (PDF)
72Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran program
PLoS ONE, 2020, 15, e0237430
2.325Citations (PDF)
73Transcriptomic signatures across human tissues identify functional rare genetic variation
Science, 2020, 369,
36.2139Citations (PDF)
74The relationship between circulating lipids and breast cancer risk: A Mendelian randomization study
PLoS Medicine, 2020, 17, e1003302
8.1105Citations (PDF)
75Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus2.910Citations (PDF)
76Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
Nature Genetics, 2020, 52, 680-691
25.2689Citations (PDF)
77The Project Baseline Health Study: a step towards a broader mission to map human health10.470Citations (PDF)
78Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study
PLoS Genetics, 2020, 16, e1008684
3.232Citations (PDF)
79Genotyping Array Design and Data Quality Control in the Million Veteran Program6.5201Citations (PDF)
80Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache4.946Citations (PDF)
81Urinary Albumin, Sodium, and Potassium and Cardiovascular Outcomes in the UK Biobank
Hypertension, 2020, 75, 714-722
6.646Citations (PDF)
82PCSK9 loss of function is protective against extra-coronary atherosclerotic cardiovascular disease in a large multi-ethnic cohort
PLoS ONE, 2020, 15, e0239752
2.316Citations (PDF)
83Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease
Circulation, 2019, 140, 645-657
18.1201Citations (PDF)
84Association of <i>APOL1</i> Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program
Circulation, 2019, 140, 1031-1040
18.145Citations (PDF)
85Genome-wide association study of peripheral artery disease in the Million Veteran Program
Nature Medicine, 2019, 25, 1274-1279
33.0280Citations (PDF)
86Association Between Heart Failure and Postoperative Mortality Among Patients Undergoing Ambulatory Noncardiac Surgery
JAMA Surgery, 2019, 154, 907
8.860Citations (PDF)
87Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
Nature Genetics, 2019, 51, 1574-1579
25.2222Citations (PDF)
88Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies6.5254Citations (PDF)
89Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
Human Genetics, 2019, 138, 199-210
2.934Citations (PDF)
90Methylome-wide association study provides evidence of particulate matter air pollution-associated DNA methylation
Environment International, 2019, 132, 104723
10.278Citations (PDF)
91An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis13.783Citations (PDF)
92HeartBioPortal2.98Citations (PDF)
93Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion
Kidney International, 2019, 95, 1197-1208
5.343Citations (PDF)
94Association of Left Ventricular Ejection Fraction and Symptoms With Mortality After Elective Noncardiac Surgery Among Patients With Heart Failure16.6122Citations (PDF)
95The role of epigenetic aging in education and racial/ethnic mortality disparities among older U.S. Women
Psychoneuroendocrinology, 2019, 104, 18-24
2.767Citations (PDF)
96Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection2.3180Citations (PDF)
97Breastfeeding Duration and the Risk of Coronary Artery Disease
Journal of Women's Health, 2019, 28, 30-36
2.134Citations (PDF)
98Melanoma risk prediction using a multilocus genetic risk score in the Women's Health Initiative cohort1.823Citations (PDF)
99GWAS of epigenetic aging rates in blood reveals a critical role for TERT13.7187Citations (PDF)
100Genome‐wide scan for circulating vascular adhesion protein‐1 levels: MACROD2 as a potential transcriptional regulator of adipogenesis2.717Citations (PDF)
101Hypermetabolic macrophages in rheumatoid arthritis and coronary artery disease due to glycogen synthase kinase 3b inactivation6.9103Citations (PDF)
102Effects of Genetic Variants Associated with Familial Hypercholesterolemia on Low-Density Lipoprotein-Cholesterol Levels and Cardiovascular Outcomes in the Million Veteran Program2.920Citations (PDF)
103Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Nature Genetics, 2018, 50, 1514-1523
25.2611Citations (PDF)
104Evaluation of 71 Coronary Artery Disease Risk Variants in a Multiethnic Cohort2.519Citations (PDF)
105Genome-Wide Association Studies of Coronary Artery Disease: Recent Progress and Challenges Ahead4.726Citations (PDF)
106Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study
Human Molecular Genetics, 2018, 27, 2940-2953
2.920Citations (PDF)
107Coffee consumption is associated with DNA methylation levels of human blood3.039Citations (PDF)
108Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci
Human Genetics, 2017, 136, 771-800
2.936Citations (PDF)
109Leveraging information from genetic risk scores of coronary atherosclerosis4.013Citations (PDF)
110Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms
Nature Genetics, 2017, 49, 1113-1119
25.2306Citations (PDF)
111Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Human Molecular Genetics, 2017, 26, 1770-1784
2.9154Citations (PDF)
112Exome-wide association study of plasma lipids in &gt;300,000 individuals
Nature Genetics, 2017, 49, 1758-1766
25.2543Citations (PDF)
113Leveraging Multi-ethnic Evidence for Risk Assessment of Quantitative Traits in Minority Populations6.583Citations (PDF)
114Association analyses based on false discovery rate implicate new loci for coronary artery disease
Nature Genetics, 2017, 49, 1385-1391
25.2679Citations (PDF)
115DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation6.5198Citations (PDF)
116Epigenetic Aging and Immune Senescence in Women With Insomnia Symptoms: Findings From the Women’s Health Initiative Study
Biological Psychiatry, 2017, 81, 136-144
5.4148Citations (PDF)
117Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study2.553Citations (PDF)
118Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
Nature Genetics, 2017, 49, 1450-1457
25.2250Citations (PDF)
119The associations of leptin, adiponectin and resistin with incident atrial fibrillation in women
Heart, 2016, 102, 1354-1362
4.036Citations (PDF)
120Genetics: Implications for Prevention and Management of Coronary Artery Disease2.3104Citations (PDF)
121DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases
Genome Biology, 2016, 17,
8.1317Citations (PDF)
122An epigenetic clock analysis of race/ethnicity, sex, and coronary heart disease
Genome Biology, 2016, 17,
8.1681Citations (PDF)
123Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci13.7142Citations (PDF)
124The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Nature Genetics, 2016, 48, 1171-1184
25.2410Citations (PDF)
125Menopause accelerates biological aging7.5468Citations (PDF)
126No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis3.430Citations (PDF)
127Genetic cardiovascular risk prediction: are we already there?
European Heart Journal, 2016, 37, 3279-3281
2.26Citations (PDF)
128Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci
Human Molecular Genetics, 2016, 25, 5500-5512
2.932Citations (PDF)
129Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans
EBioMedicine, 2016, 4, 153-161
9.717Citations (PDF)
130Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
Science, 2016, 351, 1166-1171
36.2506Citations (PDF)
131The glycolytic enzyme PKM2 bridges metabolic and inflammatory dysfunction in coronary artery disease9.2518Citations (PDF)
132Lean body mass and risk of incident atrial fibrillation in post-menopausal women
European Heart Journal, 2016, 37, 1606-1613
2.235Citations (PDF)
133Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi Consortium
PLoS ONE, 2016, 11, e0138014
2.336Citations (PDF)
134Associations between a Genetic Risk Score for Clinical CAD and Early Stage Lesions in the Coronary Artery and the Aorta
PLoS ONE, 2016, 11, e0166994
2.32Citations (PDF)
135Detecting Clinically Meaningful Biomarkers with Repeated Measurements: An Illustration with Electronic Health Records
Biometrics, 2015, 71, 478-486
1.613Citations (PDF)
136The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
PLoS Genetics, 2015, 11, e1005378
3.2393Citations (PDF)
137Effect of Common Genetic Variants of Growth Arrest-Specific 6 Gene on Insulin Resistance, Obesity and Type 2 Diabetes in an Asian Population
PLoS ONE, 2015, 10, e0135681
2.38Citations (PDF)
138Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene
Journal of Clinical Investigation, 2015, 125, 1739-1751
10.6111Citations (PDF)
139Systems Genetics Analysis of Genome-Wide Association Study Reveals Novel Associations Between Key Biological Processes and Coronary Artery Disease6.079Citations (PDF)
140Leukocyte Telomere Length and Risks of Incident Coronary Heart Disease and Mortality in a Racially Diverse Population of Postmenopausal Women6.058Citations (PDF)
141Dissecting the Roles of MicroRNAs in Coronary Heart Disease via Integrative Genomic Analyses6.056Citations (PDF)
142New genetic loci link adipose and insulin biology to body fat distribution
Nature, 2015, 518, 187-196
37.91,561Citations (PDF)
143Genetic studies of body mass index yield new insights for obesity biology
Nature, 2015, 518, 197-206
37.94,431Citations (PDF)
144Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk
Atherosclerosis, 2015, 241, 419-426
1.528Citations (PDF)
145Characterization of TCF21 Downstream Target Regions Identifies a Transcriptional Network Linking Multiple Independent Coronary Artery Disease Loci
PLoS Genetics, 2015, 11, e1005202
3.244Citations (PDF)
146Genetically Determined Height and Coronary Artery Disease
New England Journal of Medicine, 2015, 372, 1608-1618
34.6244Citations (PDF)
147Susceptibility Loci for Clinical Coronary Artery Disease and Subclinical Coronary Atherosclerosis Throughout the Life-Course3.836Citations (PDF)
148A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Nature Genetics, 2015, 47, 1121-1130
25.22,461Citations (PDF)
149Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity
Diabetes, 2014, 63, 2158-2171
4.2333Citations (PDF)
150Multiple Nonglycemic Genomic Loci Are Newly Associated With Blood Level of Glycated Hemoglobin in East Asians
Diabetes, 2014, 63, 2551-2562
4.265Citations (PDF)
151The combination of 9p21.3 genotype and biomarker profile improves a peripheral artery disease risk prediction model
Vascular Medicine, 2014, 19, 3-8
2.48Citations (PDF)
152Obesity, Physical Activity, and Their Interaction in Incident Atrial Fibrillation in Postmenopausal Women4.098Citations (PDF)
153Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Human Molecular Genetics, 2014, 23, 5492-5504
2.9209Citations (PDF)
154Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example2.347Citations (PDF)
155Integrative Genomics Reveals Novel Molecular Pathways and Gene Networks for Coronary Artery Disease
PLoS Genetics, 2014, 10, e1004502
3.2199Citations (PDF)
156Coronary Heart Disease-Associated Variation in TCF21 Disrupts a miR-224 Binding Site and miRNA-Mediated Regulation
PLoS Genetics, 2014, 10, e1004263
3.2114Citations (PDF)
157Study of Exonic Variation Identifies Incremental Information Regarding Lipid-Related and Coronary Heart Disease Genes
Circulation Research, 2014, 115, 478-480
13.22Citations (PDF)
158Near-Term Prediction of Sudden Cardiac Death in Older Hemodialysis Patients Using Electronic Health Records4.232Citations (PDF)
159Use of Medicare Data to Identify Coronary Heart Disease Outcomes in the Women’s Health Initiative4.181Citations (PDF)
160Clinical Interpretation and Implications of Whole-Genome Sequencing16.6430Citations (PDF)
161Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol6.5205Citations (PDF)
162Dissecting the Causal Genetic Mechanisms of Coronary Heart Disease4.711Citations (PDF)
163Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease
Stroke, 2014, 45, 24-36
6.0324Citations (PDF)
164Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset
Human Molecular Genetics, 2014, 23, 1957-1963
2.984Citations (PDF)
165Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
New England Journal of Medicine, 2014, 371, 2072-2082
34.6405Citations (PDF)
166The relationship of lipoprotein(a), C-reactive protein and homocysteine with metabolic syndrome in South Asians0.23Citations (PDF)
167Defining the role of common variation in the genomic and biological architecture of adult human height
Nature Genetics, 2014, 46, 1173-1186
25.21,965Citations (PDF)
168Loss-of-Function Mutations inAPOC3,Triglycerides, and Coronary Disease34.61,054Citations (PDF)
169Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
Nature, 2014, 518, 102-106
37.9623Citations (PDF)
170Insulin Resistance: Regression and Clustering
PLoS ONE, 2014, 9, e94129
2.33Citations (PDF)
171The shared allelic architecture of adiponectin levels and coronary artery disease
Atherosclerosis, 2013, 229, 145-148
1.531Citations (PDF)
172Discovery and refinement of loci associated with lipid levels
Nature Genetics, 2013, 45, 1274-1283
25.22,993Citations (PDF)
173Common variants associated with plasma triglycerides and risk for coronary artery disease
Nature Genetics, 2013, 45, 1345-1352
25.2833Citations (PDF)
174Genetic Variants Associated With Glycine Metabolism and Their Role in Insulin Sensitivity and Type 2 Diabetes
Diabetes, 2013, 62, 2141-2150
4.280Citations (PDF)
175Trans-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
Diabetologia, 2013, 56, 2619-2628
7.627Citations (PDF)
176Genetics and Genomics for the Prevention and Treatment of Cardiovascular Disease: Update
Circulation, 2013, 128, 2813-2851
18.1119Citations (PDF)
177Association Between the Chromosome 9p21 Locus and Angiographic Coronary Artery Disease Burden2.359Citations (PDF)
178Measurement of insulin-mediated glucose uptake: Direct comparison of the modified insulin suppression test and the euglycemic, hyperinsulinemic clamp9.158Citations (PDF)
179Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Nature Genetics, 2013, 45, 501-512
25.2645Citations (PDF)
180Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders
Nature Genetics, 2013, 45, 621-631
25.2308Citations (PDF)
181A Systems Biology Framework Identifies Molecular Underpinnings of Coronary Heart Disease6.0167Citations (PDF)
182Genetic Predisposition to Higher Blood Pressure Increases Coronary Artery Disease Risk
Hypertension, 2013, 61, 995-1001
6.674Citations (PDF)
183Disease-Related Growth Factor and Embryonic Signaling Pathways Modulate an Enhancer of TCF21 Expression at the 6q23.2 Coronary Heart Disease Locus
PLoS Genetics, 2013, 9, e1003652
3.269Citations (PDF)
184Trans-Ethnic Fine-Mapping of Lipid Loci Identifies Population-Specific Signals and Allelic Heterogeneity That Increases the Trait Variance Explained
PLoS Genetics, 2013, 9, e1003379
3.2114Citations (PDF)
185Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits
PLoS Genetics, 2013, 9, e1003500
3.2416Citations (PDF)
186Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes
Diabetes, 2013, 62, 3589-3598
4.2121Citations (PDF)
187Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies
Lancet, The, 2012, 379, 1205-1213
62.3768Citations (PDF)
188Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies3.8111Citations (PDF)
189Central obesity is important but not essential component of the metabolic syndrome for predicting diabetes mellitus in a hypertensive family-based cohort. Results from the Stanford Asia-pacific program for hypertension and insulin resistance (SAPPHIRe) Taiwan follow-up study9.421Citations (PDF)
190FTO genotype is associated with phenotypic variability of body mass index
Nature, 2012, 490, 267-272
37.9426Citations (PDF)
191Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study
PLoS ONE, 2012, 7, e35651
2.373Citations (PDF)
192Long-Term Use of Angiotensin Receptor Blockers and the Risk of Cancer
PLoS ONE, 2012, 7, e50893
2.370Citations (PDF)
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