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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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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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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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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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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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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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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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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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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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Model-fitting and linkage analysis of sodium-lithium countertransport

European journal of human genetics : EJHG, 2004-12, Vol.12 (12), p.1055-1061, Article 1055

2004

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Non-Modulation as an Intermediate Phenotype in Essential Hypertension

Hypertension (Dallas, Tex. 1979), 1992-12, Vol.20 (6), p.788-796

1992

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Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees

European journal of human genetics : EJHG, 2002-06, Vol.10 (6), p.367-374

2002

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Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics

The American journal of cardiology, 1993-07, Vol.72 (2), p.171-176

1993

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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

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

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

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

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

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

The genetic architecture of fasting plasma triglyceride response to fenofibrate treatment

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

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

Model-fitting and linkage analysis of sodium-lithium countertransport

Non-Modulation as an Intermediate Phenotype in Essential Hypertension

Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees

Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics

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