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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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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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An exome-wide sequencing study of lipid response to high-fat meal and fenofibrate in Caucasians from the GOLDN cohort

Journal of lipid research, 2018-04, Vol.59 (4), p.722-729

2018

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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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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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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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Efficacy of alirocumab in 1191 patients with a wide spectrum of mutations in genes causative for familial hypercholesterolemia

Journal of clinical lipidology, 2017-11, Vol.11 (6), p.1338-1346.e7

2017

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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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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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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 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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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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Association of the melanocortin-4 receptor V103I polymorphism with dietary intake in severely obese persons

The American journal of clinical nutrition, 2008-09, Vol.88 (3), p.797-800

2008

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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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Lack of Association of Glutamate Decarboxylase 2 Gene Polymorphisms with Severe Obesity in Utah

Obesity (Silver Spring, Md.), 2006-04, Vol.14 (4), p.650-655

2006

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Estrogen receptor 1 variants and coronary artery disease: shedding light into a murky pool

JAMA : the journal of the American Medical Association, 2003-11, Vol.290 (17), p.2317

2003

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Blunted renal vascular response to angiotensin II is associated with a common variant of the angiotensinogen gene and obesity

Journal of hypertension, 1996-02, Vol.14 (2), p.199-207

1996

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A genome scan for loci influencing anti-atherogenic serum bilirubin levels

European journal of human genetics : EJHG, 2002-09, Vol.10 (9), p.539-546

2002

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Putting Into Perspective the Hazards of Untreated Familial Hypercholesterolemia

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

An exome-wide sequencing study of lipid response to high-fat meal and fenofibrate in Caucasians from the GOLDN cohort

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

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

Efficacy of alirocumab in 1191 patients with a wide spectrum of mutations in genes causative for familial hypercholesterolemia

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

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

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

Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations[S]

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

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

Association of the melanocortin-4 receptor V103I polymorphism with dietary intake in severely obese persons

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

Lack of Association of Glutamate Decarboxylase 2 Gene Polymorphisms with Severe Obesity in Utah

Estrogen receptor 1 variants and coronary artery disease: shedding light into a murky pool

Blunted renal vascular response to angiotensin II is associated with a common variant of the angiotensinogen gene and obesity

A genome scan for loci influencing anti-atherogenic serum bilirubin levels

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