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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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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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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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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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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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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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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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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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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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Two-dimensional, sex-specific autosomal linkage scan of the number of sodium pump sites

Journal of hypertension, 2010-04, Vol.28 (4), p.740-747

2010

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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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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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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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Increased Urinary Free Cortisol: A Potential Intermediate Phenotype of Essential Hypertension

Hypertension (Dallas, Tex. 1979), 1998-02, Vol.31 (2), p.569-574

1998

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Familial Aggregation of Low-Renin Hypertension

Hypertension (Dallas, Tex. 1979), 2002-04, Vol.39 (4), p.914-918

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]

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

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

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

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

Genetic Determinants of Nonmodulating Hypertension

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

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

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

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

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

Two-dimensional, sex-specific autosomal linkage scan of the number of sodium pump sites

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

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

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

Increased Urinary Free Cortisol: A Potential Intermediate Phenotype of Essential Hypertension

Familial Aggregation of Low-Renin Hypertension

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