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Molecular biology of atherosclerosis

Physiological reviews, 2013-07, Vol.93 (3), p.1317-1542

Hopkins, Paul N

2013

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Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred

Journal of human genetics, 2004, Vol.49 (1), p.29-34

2004

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Age‐related differences in lean mass, protein synthesis and skeletal muscle markers of proteolysis after bed rest and exercise rehabilitation

The Journal of physiology, 2015-09, Vol.593 (18), p.4259-4273

2015

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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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Methylation at CPT1A locus is associated with lipoprotein subfraction profiles[S]

Journal of lipid research, 2014-07, Vol.55 (7), p.1324-1330

2014

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A comparative study of four independent methods to measure LDL particle concentration

Atherosclerosis, 2015-11, Vol.243 (1), p.99-106

2015

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A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree

Human genetics, 2004-03, Vol.114 (4), p.349-353

2004

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Genotype-guided diagnosis in familial hypercholesterolemia: population burden and cascade screening

Current opinion in lipidology, 2017-04, Vol.28 (2), p.136-143

Hopkins, Paul N

2017

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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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Colesevelam Hydrochloride: Efficacy and Safety in Pediatric Subjects with Heterozygous Familial Hypercholesterolemia

The Journal of pediatrics, 2010-02, Vol.156 (2), p.231-236.e3

2010

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Relationship between Aldosterone and Progesterone in the Human Menstrual Cycle

The journal of clinical endocrinology and metabolism, 2006-10, Vol.91 (10), p.3981-3987

2006

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Efficacy and Safety of Alirocumab in Patients With Autosomal Dominant Hypercholesterolemia Associated With Proprotein Convertase Subtilisin/Kexin Type 9 Gain-of-Function or Apolipoprotein B Loss-of-Function Mutations

The American journal of cardiology, 2020-03, Vol.125 (6), p.880-886

2020

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Downregulation of E3 ubiquitin ligases and mitophagy-related genes in skeletal muscle of physically inactive, frail older women: a cross-sectional comparison

The journals of gerontology. Series A, Biological sciences and medical sciences, 2014-08, Vol.69 (8), p.1040-1048

2014

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Higher urinary cortisol levels associate with increased cardiovascular risk

Endocrine Connections, 2019-06, Vol.8 (6), p.634-640

2019

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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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A candidate locus in the renalase gene and susceptibility to blood pressure responses to the dietary salt

Journal of hypertension, 2023-05, Vol.41 (5), p.723

2023

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Salt Sensitivity of Blood Pressure and Aldosterone: Interaction Between the Lysine-specific Demethylase 1 Gene, Sex, and Age

The journal of clinical endocrinology and metabolism, 2022-04, Vol.107 (5), p.1294-1302

2022

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Hyperlipoproteinemia Type 3: The Forgotten Phenotype

Current atherosclerosis reports, 2014-09, Vol.16 (9), p.440-440, Article 440

2014

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Do inflammation and procoagulation biomarkers contribute to the metabolic syndrome cluster?

Nutrition & metabolism, 2007-12, Vol.4 (1), p.28-28

2007

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Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia

Journal of clinical lipidology, 2011-05, Vol.5 (3), p.133-140

2011

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Genotype-guided diagnosis in familial hypercholesterolemia: clinical management and concerns

Current opinion in lipidology, 2017-04, Vol.28 (2), p.144-151

2017

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Time trends for injuries and illness, and their relation to performance in the National Basketball Association

Journal of science and medicine in sport, 2015-05, Vol.18 (3), p.278-282

2015

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Cardiovascular responses to rhythmic handgrip exercise in heart failure with preserved ejection fraction

Journal of applied physiology (1985), 2020-12, Vol.129 (6), p.1267-1276

2020

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Persistent vascular dysfunction following an acute nonpharmacological reduction in blood pressure in hypertensive patients

Journal of hypertension, 2022-06, Vol.40 (6), p.1115-1125

2022

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Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia

Journal of clinical lipidology, 2011-06, Vol.5 (3 Suppl), p.S1-S8

2011

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Molecular biology of atherosclerosis

Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred

Age‐related differences in lean mass, protein synthesis and skeletal muscle markers of proteolysis after bed rest and exercise rehabilitation

Putting Into Perspective the Hazards of Untreated Familial Hypercholesterolemia

Methylation at CPT1A locus is associated with lipoprotein subfraction profiles[S]

A comparative study of four independent methods to measure LDL particle concentration

A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree

Genotype-guided diagnosis in familial hypercholesterolemia: population burden and cascade screening

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

Colesevelam Hydrochloride: Efficacy and Safety in Pediatric Subjects with Heterozygous Familial Hypercholesterolemia

Relationship between Aldosterone and Progesterone in the Human Menstrual Cycle

Efficacy and Safety of Alirocumab in Patients With Autosomal Dominant Hypercholesterolemia Associated With Proprotein Convertase Subtilisin/Kexin Type 9 Gain-of-Function or Apolipoprotein B Loss-of-Function Mutations

Downregulation of E3 ubiquitin ligases and mitophagy-related genes in skeletal muscle of physically inactive, frail older women: a cross-sectional comparison

Higher urinary cortisol levels associate with increased cardiovascular risk

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

A candidate locus in the renalase gene and susceptibility to blood pressure responses to the dietary salt

Salt Sensitivity of Blood Pressure and Aldosterone: Interaction Between the Lysine-specific Demethylase 1 Gene, Sex, and Age

Hyperlipoproteinemia Type 3: The Forgotten Phenotype

Do inflammation and procoagulation biomarkers contribute to the metabolic syndrome cluster?

Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia

Genotype-guided diagnosis in familial hypercholesterolemia: clinical management and concerns

Time trends for injuries and illness, and their relation to performance in the National Basketball Association

Cardiovascular responses to rhythmic handgrip exercise in heart failure with preserved ejection fraction

Persistent vascular dysfunction following an acute nonpharmacological reduction in blood pressure in hypertensive patients

Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia

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