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Null Mutation in Human APOC3 Confers a Favorable Plasma Lipid Profile and Apparent Cardioprotection

Science (American Association for the Advancement of Science), 2008-12, Vol.322 (5908), p.1702-1705

2008

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Effects of novel capsinoid treatment on fatness and energy metabolism in humans: possible pharmacogenetic implications

The American journal of clinical nutrition, 2009-01, Vol.89 (1), p.45-50

2009

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Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the amish : Replication and evidence for a role in both insulin secretion and insulin resistance

Diabetes (New York, N.Y.), 2006-09, Vol.55 (9), p.2654-2659

2006

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Aspirin Resistance in Healthy Drug-Naive Men Versus Women (from the Heredity and Phenotype Intervention Heart Study)

The American journal of cardiology, 2009-08, Vol.104 (4), p.606-612

2009

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Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels

Journal of human genetics, 2011-11, Vol.56 (11), p.801-805

2011

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Decreased Bone Mineral Density in Subjects Carrying Familial Defective Apolipoprotein B-100

The journal of clinical endocrinology and metabolism, 2013-12, Vol.98 (12), p.E1999-E2005

2013

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Candidate Gene Association Study of Coronary Artery Calcification in Chronic Kidney Disease: Findings From the CRIC Study (Chronic Renal Insuiffciency Cohort)

Journal of the American College of Cardiology, 2013-08, Vol.62 (9), p.789-798

2013

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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.2648-2654

2010

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The genetic response to short-term interventions affecting cardiovascular function: Rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

The American heart journal, 2008-05, Vol.155 (5), p.823-828

2008

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Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

Circulation. Cardiovascular genetics, 2010-10, Vol.3 (5), p.445-453

2010

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The Association of Coronary Artery Calcification and Carotid Artery Intima-Media Thickness With Distinct, Traditional Coronary Artery Disease Risk Factors in Asymptomatic Adults

American journal of epidemiology, 2008-11, Vol.168 (9), p.1016-1023

2008

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Determinants of coronary artery and aortic calcification in the old order amish

Circulation (New York, N.Y.), 2007-02, Vol.115 (6), p.717-724

2007

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Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study

Human genetics, 2009-10, Vol.126 (4), p.567-574

2009

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Physical activity and the association of common FTO gene variants with body mass index and obesity

Archives of internal medicine (1960), 2008-09, Vol.168 (16), p.1791

2008

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Intragenic linkage disequilibrium structure of the human perilipin gene (PLIN) and haplotype association with increased obesity risk in a multiethnic Asian population

Journal of molecular medicine (Berlin, Germany), 2005-06, Vol.83 (6), p.448-456

2005

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A common variant in fibroblast growth factor binding protein 1 ( FGFBP1 ) is associated with bone mineral density and influences gene expression in vitro

Bone (New York, N.Y.), 2010-08, Vol.47 (2), p.272-280

2010

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Test-Retest Reproducibility for the Tau PET Imaging Agent Flortaucipir F 18

Journal of Nuclear Medicine, 2018-06, Vol.59 (6), p.937-943

2018

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Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction

Circulation (New York, N.Y.), 2011-12, Vol.124 (25), p.2855-2864

2011

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Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

Archives of internal medicine (1960), 2010-11, Vol.170 (20), p.1850

2010

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Physical activity modulates the combined effect of a common variant of the lipoprotein lipase gene and smoking on serum triglyceride levels and high-density lipoprotein cholesterol in men

Human genetics, 2001-10, Vol.109 (4), p.385-392

2001

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Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

Diabetes (New York, N.Y.), 2007-12, Vol.56 (12), p.3053-3062

2007

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Is IL12B a Potential Genetic Target for the Prevention of Type 1 Diabetes through Dietary Intervention?

Nutrition reviews, 2002-06, Vol.60 (6), p.182-186

2002

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VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification

Human genetics, 2013, Vol.132 (1), p.29-37

2013

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Gender-Specific Association of a Perilipin Gene Haplotype with Obesity Risk in a White Population

Obesity (Silver Spring, Md.), 2004-11, Vol.12 (11), p.1758-1765

2004

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Null Mutation in Human APOC3 Confers a Favorable Plasma Lipid Profile and Apparent Cardioprotection

Effects of novel capsinoid treatment on fatness and energy metabolism in humans: possible pharmacogenetic implications

Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the amish : Replication and evidence for a role in both insulin secretion and insulin resistance

Aspirin Resistance in Healthy Drug-Naive Men Versus Women (from the Heredity and Phenotype Intervention Heart Study)

Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels

Decreased Bone Mineral Density in Subjects Carrying Familial Defective Apolipoprotein B-100

Candidate Gene Association Study of Coronary Artery Calcification in Chronic Kidney Disease: Findings From the CRIC Study (Chronic Renal Insuiffciency Cohort)

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

The genetic response to short-term interventions affecting cardiovascular function: Rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease

The Association of Coronary Artery Calcification and Carotid Artery Intima-Media Thickness With Distinct, Traditional Coronary Artery Disease Risk Factors in Asymptomatic Adults

Determinants of coronary artery and aortic calcification in the old order amish

Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study

Physical activity and the association of common FTO gene variants with body mass index and obesity

Intragenic linkage disequilibrium structure of the human perilipin gene (PLIN) and haplotype association with increased obesity risk in a multiethnic Asian population

A common variant in fibroblast growth factor binding protein 1 ( FGFBP1 ) is associated with bone mineral density and influences gene expression in vitro

Test-Retest Reproducibility for the Tau PET Imaging Agent Flortaucipir F 18

Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

Common variants in the GDF5-UQCC region are associated with variation in human height

Physical activity modulates the combined effect of a common variant of the lipoprotein lipase gene and smoking on serum triglyceride levels and high-density lipoprotein cholesterol in men

Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations

Is IL12B a Potential Genetic Target for the Prevention of Type 1 Diabetes through Dietary Intervention?

VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification

Gender-Specific Association of a Perilipin Gene Haplotype with Obesity Risk in a White Population

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