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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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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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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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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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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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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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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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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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The Arg16Gly polymorphism of the β2-adrenergic receptor and left ventricular systolic function

American journal of hypertension, 2003-11, Vol.16 (11), p.945-951

2003

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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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OR-36: Linkage of serum creatinine and creatinine clearance to chromosome 2 in Utah pedigrees

American journal of hypertension, 2003-05, Vol.16 (S1), p.16A-16A

2003

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Are There Interactions and Relations Between Genetic and Environmental Factors Predisposing to High Blood Pressure?

Hypertension (Dallas, Tex. 1979), 1991-09, Vol.18 (3 Suppl I), p.I-29-I-37

1991

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Genetic Traits Related to Hypertension and Electrolyte Metabolism

Hypertension (Dallas, Tex. 1979), 1991-01, Vol.17 (1 Suppl I), p.I-69-I-73

1991

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Primordial Prevention of Cardiovascular Disease through Applied Genetics

Preventive medicine, 1999-12, Vol.29 (6), p.S41-S49

1999

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Evidence for single gene contributions to hypertension and lipid disturbances: definition, genetics, and clinical significance

Clinical genetics, 1994-07, Vol.46 (1), p.80-87

1994

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A genome-wide linkage and association scan reveals novel loci for autism

Nature (London), 2009-10, Vol.461 (7265), p.802-808

2009

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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

Putting Into Perspective the Hazards of Untreated Familial Hypercholesterolemia

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

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

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

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

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

Sodium Bicarbonate Cotransporter Polymorphisms Are Associated With Baseline and 10-Year Follow-Up Blood Pressures

The Arg16Gly polymorphism of the β2-adrenergic receptor and left ventricular systolic function

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

OR-36: Linkage of serum creatinine and creatinine clearance to chromosome 2 in Utah pedigrees

Are There Interactions and Relations Between Genetic and Environmental Factors Predisposing to High Blood Pressure?

Genetic Traits Related to Hypertension and Electrolyte Metabolism

Primordial Prevention of Cardiovascular Disease through Applied Genetics

Evidence for single gene contributions to hypertension and lipid disturbances: definition, genetics, and clinical significance

A genome-wide linkage and association scan reveals novel loci for autism

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