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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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Aldosterone Stimulation by Angiotensin II: Influence of Gender, Plasma Renin, and Familial Resemblance

Hypertension (Dallas, Tex. 1979), 2000-03, Vol.35 (3), p.710-716

2000

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Angiotensinogen genotype affects renal and adrenal responses to angiotensin II in essential hypertension

Circulation (New York, N.Y.), 2002-04, Vol.105 (16), p.1921-1927

2002

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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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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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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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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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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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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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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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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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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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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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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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Erythrocyte Fatty Acid Composition and the Metabolic Syndrome: A National Heart, Lung, and Blood Institute GOLDN Study

Clinical chemistry (Baltimore, Md.), 2008-01, Vol.54 (1), p.154-162

2008

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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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Evidence for a major gene elevating serum bilirubin concentration in Utah pedigrees

Arteriosclerosis, thrombosis, and vascular biology, 1996-08, Vol.16 (8), p.912-917

1996

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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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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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Familial Aggregation of Low-Renin Hypertension

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

2002

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Familial factors in the antihypertensive response to lisinopril

American journal of hypertension, 2001-03, Vol.14 (3), p.218-223

2001

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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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Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

Nature communications, 2020-09, Vol.11 (1), p.4796-16, Article 4796

2020

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

Aldosterone Stimulation by Angiotensin II: Influence of Gender, Plasma Renin, and Familial Resemblance

Angiotensinogen genotype affects renal and adrenal responses to angiotensin II in essential hypertension

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

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

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

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

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

Carbohydrate and fat intake associated with risk of metabolic diseases through epigenetics of CPT1A

Characterization of Autosomal Dominant Hypercholesterolemia Caused by PCSK9 Gain of Function Mutations and Its Specific Treatment With Alirocumab, a PCSK9 Monoclonal Antibody

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

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

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

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

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

Erythrocyte Fatty Acid Composition and the Metabolic Syndrome: A National Heart, Lung, and Blood Institute GOLDN Study

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

Evidence for a major gene elevating serum bilirubin concentration in Utah pedigrees

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

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

Familial Aggregation of Low-Renin Hypertension

Familial factors in the antihypertensive response to lisinopril

The genetic architecture of fasting plasma triglyceride response to fenofibrate treatment

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

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