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Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36[S]

Journal of lipid research, 2016-12, Vol.57 (12), p.2176-2184

2016

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High-fat meal effect on LDL, HDL, and VLDL particle size and number in the Genetics of Lipid-Lowering Drugs and Diet Network (GOLDN): an interventional study

Lipids in health and disease, 2011-10, Vol.10 (1), p.181-181, Article 181

2011

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Sex-Specific Association of the Putative Fructose Transporter SLC2A9 Variants With Uric Acid Levels Is Modified by BMI

Diabetes care, 2008-08, Vol.31 (8), p.1662-1667

2008

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Variants Identified in a GWAS Meta-Analysis for Blood Lipids Are Associated with the Lipid Response to Fenofibrate

PloS one, 2012-10, Vol.7 (10), p.e48663

2012

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Relation between Erythrocyte Trans Fat and Triglyceride, VLDL- and HDL-Cholesterol Concentrations Depends on Polyunsaturated Fat

PloS one, 2012-10, Vol.7 (10), p.e47430-e47430

2012

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Characterization of Autosomal Dominant Hypercholesterolemia Caused by PCSK9 Gain of Function Mutations and Its Specific Treatment With Alirocumab, a PCSK9 Monoclonal Antibody

Circulation. Cardiovascular genetics, 2015-12, Vol.8 (6), p.823-831

2015

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Salt Sensitivity of Blood Pressure Is Associated With Polymorphisms in the Sodium-Bicarbonate Cotransporter

Hypertension (Dallas, Tex. 1979), 2012-11, Vol.60 (5), p.1359-1366

2012

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Lipoprotein lipase S447X variant associated with VLDL, LDL and HDL diameter clustering in the MetS

Lipids in health and disease, 2011-08, Vol.10 (1), p.143-143

2011

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Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred

Arteriosclerosis, thrombosis, and vascular biology, 2000-04, Vol.20 (4), p.1089-1093

2000

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Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study

Circulation (New York, N.Y.), 2003-08, Vol.108 (5), p.519-523

2003

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Genetic Determinants of Nonmodulating Hypertension

Hypertension (Dallas, Tex. 1979), 2003-11, Vol.42 (5), p.901-908

2003

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Ala92 Type 2 Deiodinase Allele Increases Risk for the Development of Hypertension

Hypertension (Dallas, Tex. 1979), 2007-03, Vol.49 (3), p.461-466

2007

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Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity

Human genetics, 2013-04, Vol.132 (4), p.405-413

2013

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Genome-wide association studies identified novel loci for non-high-density lipoprotein cholesterol and its postprandial lipemic response

Human genetics, 2014-07, Vol.133 (7), p.919-930

2014

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Replication and meta-analysis of the gene-environment interaction between body mass index and the interleukin-6 promoter polymorphism with higher insulin resistance

Metabolism, clinical and experimental, 2012-05, Vol.61 (5), p.667-671

2012

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The Epithelial Sodium Channel γ-Subunit Gene and Blood Pressure: Family Based Association, Renal Gene Expression, and Physiological Analyses

Hypertension (Dallas, Tex. 1979), 2011-12, Vol.58 (6), p.1073-1078

2011

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Low-Renin Hypertension, Altered Sodium Homeostasis, and an α-Adducin Polymorphism

Hypertension (Dallas, Tex. 1979), 2002-02, Vol.39 (2), p.191-196

2002

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Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 1996-02, Vol.16 (2), p.250-255

1996

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Sodium Bicarbonate Cotransporter Polymorphisms Are Associated With Baseline and 10-Year Follow-Up Blood Pressures

Hypertension (Dallas, Tex. 1979), 2006-03, Vol.47 (3, Part 2 Suppl), p.532-536

2006

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INSIG2 Polymorphism Is Neither Associated With BMI Nor With Phenotypes of Lipoprotein Metabolism

Obesity (Silver Spring, Md.), 2008-04, Vol.16 (4), p.827-833

2008

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Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: Intra-familial association study in an eight-generation hyperlipidemic kindred

American journal of medical genetics, 2003-08, Vol.121A (2), p.136-140

2003

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Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait: the NHLBI family heart study

Atherosclerosis, 2001-02, Vol.154 (3), p.747-754

2001

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The genetic architecture of fasting plasma triglyceride response to fenofibrate treatment

European journal of human genetics : EJHG, 2008-05, Vol.16 (5), p.603-613

2008

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Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended Utah pedigrees

Hypertension (Dallas, Tex. 1979), 2003-09, Vol.42 (3), p.322-328

2003

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Angiotensinogen genotype affects renal and adrenal responses to angiotensin II in essential hypertension

Circulation (New York, N.Y.), 2002-04, Vol.105 (16), p.1921-1927

2002

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Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36[S]

High-fat meal effect on LDL, HDL, and VLDL particle size and number in the Genetics of Lipid-Lowering Drugs and Diet Network (GOLDN): an interventional study

Sex-Specific Association of the Putative Fructose Transporter SLC2A9 Variants With Uric Acid Levels Is Modified by BMI

Variants Identified in a GWAS Meta-Analysis for Blood Lipids Are Associated with the Lipid Response to Fenofibrate

Relation between Erythrocyte Trans Fat and Triglyceride, VLDL- and HDL-Cholesterol Concentrations Depends on Polyunsaturated Fat

Characterization of Autosomal Dominant Hypercholesterolemia Caused by PCSK9 Gain of Function Mutations and Its Specific Treatment With Alirocumab, a PCSK9 Monoclonal Antibody

Salt Sensitivity of Blood Pressure Is Associated With Polymorphisms in the Sodium-Bicarbonate Cotransporter

Lipoprotein lipase S447X variant associated with VLDL, LDL and HDL diameter clustering in the MetS

Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred

Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study

Genetic Determinants of Nonmodulating Hypertension

Ala92 Type 2 Deiodinase Allele Increases Risk for the Development of Hypertension

Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity

Genome-wide association studies identified novel loci for non-high-density lipoprotein cholesterol and its postprandial lipemic response

Replication and meta-analysis of the gene-environment interaction between body mass index and the interleukin-6 promoter polymorphism with higher insulin resistance

The Epithelial Sodium Channel γ-Subunit Gene and Blood Pressure: Family Based Association, Renal Gene Expression, and Physiological Analyses

Low-Renin Hypertension, Altered Sodium Homeostasis, and an α-Adducin Polymorphism

Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease

Sodium Bicarbonate Cotransporter Polymorphisms Are Associated With Baseline and 10-Year Follow-Up Blood Pressures

INSIG2 Polymorphism Is Neither Associated With BMI Nor With Phenotypes of Lipoprotein Metabolism

Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: Intra-familial association study in an eight-generation hyperlipidemic kindred

Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait: the NHLBI family heart study

The genetic architecture of fasting plasma triglyceride response to fenofibrate treatment

Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended Utah pedigrees

Angiotensinogen genotype affects renal and adrenal responses to angiotensin II in essential hypertension

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