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Putting Into Perspective the Hazards of Untreated Familial Hypercholesterolemia

Journal of the American Heart Association, 2017-06, Vol.6 (6)

Hopkins, Paul N

2017

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A High Intake of Saturated Fatty Acids Strengthens the Association between the Fat Mass and Obesity-Associated Gene and BMI

The Journal of nutrition, 2011-12, Vol.141 (12), p.2219-2225

2011

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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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Carbohydrate and fat intake associated with risk of metabolic diseases through epigenetics of CPT1A

The American journal of clinical nutrition, 2020-11, Vol.112 (5), p.1200-1211

2020

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An Exome-Wide Sequencing Study of the GOLDN Cohort Reveals Novel Associations of Coding Variants and Fasting Plasma Lipids

Frontiers in genetics, 2019-02, Vol.10, p.158-158

2019

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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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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

2015

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Salivary AMY1 Copy Number Variation Modifies Age-Related Type 2 Diabetes Risk

Clinical chemistry (Baltimore, Md.), 2020-05, Vol.66 (5), p.718-726

2020

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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

2000

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Striatin Gene Polymorphic Variants Are Associated With Salt Sensitive Blood Pressure in Normotensives and Hypertensives

American journal of hypertension, 2018-01, Vol.31 (1), p.124-131

2018

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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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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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Lysine-Specific Demethylase 1: An Epigenetic Regulator of Salt-Sensitive Hypertension

American journal of hypertension, 2012-07, Vol.25 (7), p.812-817

2012

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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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Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred

Journal of human genetics, 2002-12, Vol.47 (12), p.656-664

2002

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

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

2002

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

GENETIC HERITABILITY AND COMMON ENVIRONMENTAL COMPONENTS OF RESTING AND STRESSED BLOOD PRESSURES, LIPIDS, AND BODY MASS INDEX IN UTAH PEDIGREES AND TWINS

American journal of epidemiology, 1989-03, Vol.129 (3), p.625-638

1989

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Putting Into Perspective the Hazards of Untreated Familial Hypercholesterolemia

A High Intake of Saturated Fatty Acids Strengthens the Association between the Fat Mass and Obesity-Associated Gene and BMI

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

Carbohydrate and fat intake associated with risk of metabolic diseases through epigenetics of CPT1A

An Exome-Wide Sequencing Study of the GOLDN Cohort Reveals Novel Associations of Coding Variants and Fasting Plasma Lipids

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

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

Salivary AMY1 Copy Number Variation Modifies Age-Related Type 2 Diabetes Risk

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

Striatin Gene Polymorphic Variants Are Associated With Salt Sensitive Blood Pressure in Normotensives and Hypertensives

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

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

Lysine-Specific Demethylase 1: An Epigenetic Regulator of Salt-Sensitive 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

Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred

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

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

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

GENETIC HERITABILITY AND COMMON ENVIRONMENTAL COMPONENTS OF RESTING AND STRESSED BLOOD PRESSURES, LIPIDS, AND BODY MASS INDEX IN UTAH PEDIGREES AND TWINS

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