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A Bivariate Genome-Wide Approach to Metabolic Syndrome: STAMPEED Consortium

Diabetes (New York, N.Y.), 2011-04, Vol.60 (4), p.1329-1339

2011

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Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

Arteriosclerosis, thrombosis, and vascular biology, 2010-12, Vol.30 (12), p.2648

2010

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Multiple Genes for Essential-Hypertension Susceptibility on Chromosome 1q

American journal of human genetics, 2007-02, Vol.80 (2), p.253-264

2007

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Epigenetic age acceleration is associated with cardiometabolic risk factors and clinical cardiovascular disease risk scores in African Americans

Clinical epigenetics, 2021-03, Vol.13 (1), p.55-55, Article 55

2021

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Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

Nature genetics, 2017-01, Vol.49 (1), p.125-130

2017

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Applying Novel Methods for Assessing Individual- and Neighborhood-Level Social and Psychosocial Environment Interactions with Genetic Factors in the Prediction of Depressive Symptoms in the Multi-Ethnic Study of Atherosclerosis

Behavior genetics, 2016-01, Vol.46 (1), p.89-99

2016

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Genetic Structure, Self-Identified Race/Ethnicity, and Confounding in Case-Control Association Studies

American journal of human genetics, 2005-02, Vol.76 (2), p.268-275

2005

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A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction

Scientific reports, 2016-01, Vol.6 (1), p.18812-18812, Article 18812

2016

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Epigenetics of single-site and multi-site atherosclerosis in African Americans from the Genetic Epidemiology Network of Arteriopathy (GENOA)

Clinical epigenetics, 2022-01, Vol.14 (1), p.10, Article 10

2022

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5' and 3' region variability in the dopamine transporter gene (SLC6A3), pesticide exposure and Parkinson's disease risk : a hypothesis-generating study

Human molecular genetics, 2006-10, Vol.15 (20), p.3055-3062

2006

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Genomic Susceptibility Loci for Brain Atrophy in Hypertensive Sibships From the GENOA Study

Hypertension (Dallas, Tex. 1979), 2005-04, Vol.45 (4, Part 2 Suppl), p.793-798

2005

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Matrix gla protein gene polymorphism is associated with increased coronary artery calcification progression

Arteriosclerosis, thrombosis, and vascular biology, 2013-03, Vol.33 (3), p.645

2013

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The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region

BMC medical genomics, 2015-05, Vol.8 (1), p.21-21, Article 21

2015

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Novel DNA methylation sites associated with cigarette smoking among African Americans

Epigenetics, 2019-04, Vol.14 (4), p.383-391

2019

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Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury

Human genetics, 2007, Vol.120 (5), p.671-680

2007

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Classification and Clustering Methods for Multiple Environmental Factors in Gene–Environment Interaction: Application to the Multi-Ethnic Study of Atherosclerosis

Epidemiology (Cambridge, Mass.), 2016-11, Vol.27 (6), p.870-878

2016

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Heritability of dietary traits that contribute to nephrolithiasis in a cohort of adult sibships

Journal of nephrology, 2016-02, Vol.29 (1), p.45-51

2016

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Copy Number Variations Associated With Obesity‐Related Traits in African Americans: A Joint Analysis Between GENOA and HyperGEN

Obesity (Silver Spring, Md.), 2012-12, Vol.20 (12), p.2431-2437

2012

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Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population

BMC genetics, 2014-10, Vol.15, p.113

2014

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Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Nature genetics, 2018-11, Vol.50 (11), p.1505-1513

2018

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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

PLoS genetics, 2019-12, Vol.15 (12), p.e1008500

2019

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Hypertrophy-Associated Polymorphisms Ascertained in a Founder Cohort Applied to Heart Failure Risk and Mortality

Clinical and translational science, 2011-02, Vol.4 (1), p.17-23

2011

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Genome-wide linkage analysis for smoking-related regions, with replication in two ethnically diverse populations

Nicotine & tobacco research, 2007-09, Vol.9 (9), p.955-958

2007

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Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships

American journal of hypertension, 2005, Vol.18 (1), p.99-103

2005

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A Bivariate Genome-Wide Approach to Metabolic Syndrome: STAMPEED Consortium

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

Multiple Genes for Essential-Hypertension Susceptibility on Chromosome 1q

Epigenetic age acceleration is associated with cardiometabolic risk factors and clinical cardiovascular disease risk scores in African Americans

Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

Applying Novel Methods for Assessing Individual- and Neighborhood-Level Social and Psychosocial Environment Interactions with Genetic Factors in the Prediction of Depressive Symptoms in the Multi-Ethnic Study of Atherosclerosis

Genetic Structure, Self-Identified Race/Ethnicity, and Confounding in Case-Control Association Studies

A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction

Epigenetics of single-site and multi-site atherosclerosis in African Americans from the Genetic Epidemiology Network of Arteriopathy (GENOA)

5' and 3' region variability in the dopamine transporter gene (SLC6A3), pesticide exposure and Parkinson's disease risk : a hypothesis-generating study

Genomic Susceptibility Loci for Brain Atrophy in Hypertensive Sibships From the GENOA Study

Matrix gla protein gene polymorphism is associated with increased coronary artery calcification progression

The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region

Novel DNA methylation sites associated with cigarette smoking among African Americans

Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury

Classification and Clustering Methods for Multiple Environmental Factors in Gene–Environment Interaction: Application to the Multi-Ethnic Study of Atherosclerosis

Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores

Heritability of dietary traits that contribute to nephrolithiasis in a cohort of adult sibships

Copy Number Variations Associated With Obesity‐Related Traits in African Americans: A Joint Analysis Between GENOA and HyperGEN

Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

Hypertrophy-Associated Polymorphisms Ascertained in a Founder Cohort Applied to Heart Failure Risk and Mortality

Genome-wide linkage analysis for smoking-related regions, with replication in two ethnically diverse populations

Pleiotropic genetic effects contribute to the correlation between HDL cholesterol, triglycerides, and LDL particle size in hypertensive sibships

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