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Altered composition of triglyceride-rich lipoproteins and coronary artery disease in a large case–control study

Atherosclerosis, 2009-12, Vol.207 (2), p.559-566

2009

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Plasma triglycerides and type III hyperlipidemia are independently associated with premature familial coronary artery disease

Journal of the American College of Cardiology, 2005-04, Vol.45 (7), p.1003-1012

2005

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Establishment of an in-house ELISA and the reference range for serum amyloid A (SAA): complementarity between SAA and C-reactive protein as markers of inflammation

Clinica chimica acta, 2007-02, Vol.376 (1-2), p.72-76

2007

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Apolipoprotein H Variant Modifies Plasma Triglyceride Phenotype in Familial Hypercholesterolemia: A Molecular Study in an Eight-generation Hyperlipidemic Family

Journal of Atherosclerosis and Thrombosis, 2003, Vol.10(2), pp.79-84

2003

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Evaluation of coronary risk factors in patients with heterozygous familial hypercholesterolemia

The American journal of cardiology, 2001-03, Vol.87 (5), p.547-553

2001

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Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 1996-02, Vol.16 (2), p.250-255

1996

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Development of an ELISA for myeloperoxidase on microplate: Normal reference values and effect of temperature on specimen preparation

Clinica chimica acta, 2006-11, Vol.373 (1), p.158-163

2006

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A panel of multiple markers associated with chronic systemic inflammation and the risk of atherogenesis is detectable in asthma and chronic obstructive pulmonary disease

Journal of clinical laboratory analysis, 2007, Vol.21 (6), p.367-371

2007

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Lipoprotein(a) interactions with lipid and nonlipid risk factors in early familial coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 1997-11, Vol.17 (11), p.2783-2792

1997

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Enhanced blood pressure response to mild sodium reduction in subjects with the 235T variant of the angiotensinogen gene

American journal of hypertension, 1999-05, Vol.12 (5), p.460-466

1999

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Higher plasma homocyst(e)ine and increased susceptibility to adverse effects of low folate in early familial coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 1995-09, Vol.15 (9), p.1314-1320

1995

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Apolipoprotein polymorphisms fail to define risk of coronary artery disease : results of a prospective, angiographically controlled study

Circulation (New York, N.Y.), 1994-02, Vol.89 (2), p.567-577

1994

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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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A Gene for High Urinary Kallikrein May Protect Against Hypertension in Utah Kindreds

Hypertension (Dallas, Tex. 1979), 1989-01, Vol.13 (1), p.3-8

1989

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Atherogenic Lipids and Lipoproteins in Hemodialysis Patients

American journal of kidney diseases, 1993-08, Vol.22 (2), p.271-276

1993

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A Gene-Environment Interaction Between Inferred Kallikrein Genotype and Potassium

Hypertension (Dallas, Tex. 1979), 1993-08, Vol.22 (2), p.161-168

1993

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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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Plasma homocyst(e)ine as a risk factor for early familial coronary artery disease

Clinical chemistry (Baltimore, Md.), 1994-04, Vol.40 (4), p.552-561

1994

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Risk Factors for Cardiovascular Disease Predict the Development of Diabetes among Utah Families

Epidemiology (Cambridge, Mass.), 1992-09, Vol.3 (5), p.459-463

1992

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Familial dyslipidemic hypertension. Evidence from 58 Utah families for a syndrome present in approximately 12% of patients with essential hypertension

JAMA : the journal of the American Medical Association, 1988-06, Vol.259 (24), p.3579

1988

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Molecular Genetic Diagnosis of a Family with Hypercholesterolemia by a Mismatched PCR-RFLP Method for Genotyping Single Base Substitution of the LDL Receptor Gene

Japanese Heart Journal, 1998, Vol.39(5), pp.681-686

1998

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Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction

Arteriosclerosis and thrombosis, 1991-09, Vol.11 (5), p.1137-1146

1991

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A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia

Journal of human genetics, 1999-01, Vol.44 (6), p.364-367

1999

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Familial Hypercholesterolemia in Utah Kindred with Novel R103W Mutations in Exon 4 of the LDL Receptor Gene

Japanese Heart Journal, 1999, Vol.40(4), pp.443-449

1999

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Environmental Determinants of Urinary Kallikrein Excretion

American journal of hypertension, 1993-03, Vol.6 (3-Pt-1), p.226-233

1993

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Altered composition of triglyceride-rich lipoproteins and coronary artery disease in a large case–control study

Plasma triglycerides and type III hyperlipidemia are independently associated with premature familial coronary artery disease

Establishment of an in-house ELISA and the reference range for serum amyloid A (SAA): complementarity between SAA and C-reactive protein as markers of inflammation

Apolipoprotein H Variant Modifies Plasma Triglyceride Phenotype in Familial Hypercholesterolemia: A Molecular Study in an Eight-generation Hyperlipidemic Family

Evaluation of coronary risk factors in patients with heterozygous familial hypercholesterolemia

Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease

Development of an ELISA for myeloperoxidase on microplate: Normal reference values and effect of temperature on specimen preparation

A panel of multiple markers associated with chronic systemic inflammation and the risk of atherogenesis is detectable in asthma and chronic obstructive pulmonary disease

Lipoprotein(a) interactions with lipid and nonlipid risk factors in early familial coronary artery disease

Enhanced blood pressure response to mild sodium reduction in subjects with the 235T variant of the angiotensinogen gene

Higher plasma homocyst(e)ine and increased susceptibility to adverse effects of low folate in early familial coronary artery disease

Apolipoprotein polymorphisms fail to define risk of coronary artery disease : results of a prospective, angiographically controlled study

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

A Gene for High Urinary Kallikrein May Protect Against Hypertension in Utah Kindreds

Atherogenic Lipids and Lipoproteins in Hemodialysis Patients

A Gene-Environment Interaction Between Inferred Kallikrein Genotype and Potassium

Genetic Traits Related to Hypertension and Electrolyte Metabolism

Plasma homocyst(e)ine as a risk factor for early familial coronary artery disease

Risk Factors for Cardiovascular Disease Predict the Development of Diabetes among Utah Families

Familial dyslipidemic hypertension. Evidence from 58 Utah families for a syndrome present in approximately 12% of patients with essential hypertension

Molecular Genetic Diagnosis of a Family with Hypercholesterolemia by a Mismatched PCR-RFLP Method for Genotyping Single Base Substitution of the LDL Receptor Gene

Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction

A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia

Familial Hypercholesterolemia in Utah Kindred with Novel R103W Mutations in Exon 4 of the LDL Receptor Gene

Environmental Determinants of Urinary Kallikrein Excretion

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