Effects of dietary cholesterol on serum cholesterol : a meta-analysis and reviewHOPKINS, P. N.The American journal of clinical nutrition. 1992, Vol 55, Num 6, pp 1060-1070, issn 0002-9165Article

Identification of a common variant in the lipoprotein lipase gene in a large Utah kindred ascertained for coronary heart disease : the - 93G/D9N variant predisposes to low HDL-C/high triglyceridesSAMUELS, M. E; FORBEY, K. C; SKOLNICK, M. H et al.Clinical genetics. 2001, Vol 59, Num 2, pp 88-98, issn 0009-9163Article

Molecular genetic diagnosis of a family with hypercholesterolemia by a mismatched PCR-FFLP method for genotyping single base substitution of the LDL receptor geneYAMAKI, E; HIRAYAMA, T; WU, L. L et al.Japanese heart journal. 1998, Vol 39, Num 5, pp 681-686, issn 0021-4868Article

Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular geneticsWILLIAMS, R. R; HUNT, S. C; SCHUMACHER, C et al.The American journal of cardiology. 1993, Vol 72, Num 2, pp 171-176, issn 0002-9149Article

Non-modulation as an intermediate phenotype in essential hypertensionWILLIAMS, G. H; DLUHY, R. G; LIFTON, R. P et al.Hypertension (Dallas, Tex. 1979). 1992, Vol 20, Num 6, pp 788-796, issn 0194-911XArticle

Human genetics and coronary heart disease: a public health perspectiveHOPKINS, P. N; WILLIAMS, R. R.Annual review of nutrition. 1989, Vol 9, pp 303-345, issn 0199-9885, 43 p.Article

Ratio of remnant-like particle-cholesterol to serum total triglycerides is an effective alternative to ultracentrifugal and electrophoretic methods in the diagnosis of familial type III hyperlipoproteinemiaWANG, T; NAKAJIMA, K; LEARY, E. T et al.Clinical chemistry (Baltimore, Md.). 1999, Vol 45, Num 11, pp 1981-1987, issn 0009-9147Conference Paper

Evidence for a major gene elevating serum bilirubin concentration in Utah pedigreesHUNT, S. C; WU, L. L; HOPKINS, P. N et al.Arteriosclerosis, thrombosis, and vascular biology. 1996, Vol 16, Num 8, pp 912-917, issn 1079-5642Article

Higher serum bilirubin is associated with decreased risk for early familial coronary artery diseaseHOPKINS, P. N; WU, L. L; HUNT, S. C et al.Arteriosclerosis, thrombosis, and vascular biology. 1996, Vol 16, Num 2, pp 250-255, issn 1079-5642Article

Evidence for single gene contributions to hypertension and lipid disturbances : definition, genetics, and clinical significanceWILLIAMS, R. R; HUNT, S. C; HOPKINS, P. N et al.Clinical genetics. 1994, Vol 46, Num 1, pp 80-87, issn 0009-9163Conference Paper

Genetic basis of familial dyslipidemia and hypertension : 15-year results from UtahWILLIAMS, R. R; HUNT, S. C; ELBEIN, S. C et al.American journal of hypertension. 1993, Vol 6, Num 11, pp 319S-327S, issn 0895-7061, 2Conference Paper

Are there interactions and relations between genetic and environmental factors predisposing to high blood pressure ?WILLIAMS, R. R; HUNT, S. C; LALOUEL, J. M et al.Hypertension (Dallas, Tex. 1979). 1991, Vol 18, Num 3, pp I29-I37, issn 0194-911X, SUPConference Paper

Prevalence of primary hyperaldosteronism in mild to moderate hypertension without hypokalaemiaWILLIAMS, J. S; WILLIAMS, G. H; RAJI, A et al.Journal of human hypertension. 2006, Vol 20, Num 2, pp 129-136, issn 0950-9240, 8 p.Article

Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindredHUNT, S. C; HOPKINS, P. N; BULKA, K et al.Arteriosclerosis, thrombosis, and vascular biology. 2000, Vol 20, Num 4, pp 1089-1093, issn 1079-5642Article

Familial hypercholesterolemia in Utah kindred with novel R103W mutations in exon 4 of the LDL receptor geneKATSUMATA, H; EMI, M; NOBE, Y et al.Japanese heart journal. 1999, Vol 40, Num 4, pp 443-449, issn 0021-4868Article

Lipoprotein(a) interactions with lipid and non-lipid risk factors in patients with early onset coronary artery disease : Results from the NHLBI Family Heart StudyHOPKINS, P. N; HUNT, S. C; SCHREINER, P. J et al.Atherosclerosis. 1998, Vol 141, Num 2, pp 333-345, issn 0021-9150Article

Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2 : evidence for a gene-gene interactionHOPKINS, P. N; WU, L. L; SCHUMACHER, M. C et al.Arteriosclerosis and thrombosis. 1991, Vol 11, Num 5, pp 1137-1146Article

Current knowledge regarding the genetics of human hypertensionWILLIAMS, R. R; HUNT, S. C; HASSTEDT, S. J et al.Journal of hypertension. 1989, Vol 7, pp S8-S13, issn 0263-6352, suppl. 6Conference Paper

Familial aggregation of QT-interval variability in a general population : Results from the NHLBI Family Heart StudyHONG, Y; RAUTAHARJU, P. M; HOPKINS, P. N et al.Clinical genetics. 2001, Vol 59, Num 3, pp 171-177, issn 0009-9163Article

Familial hypercholesterolemia kindred in Utah with novel C54S mutations of the LDL receptor geneEMI, M; YAMAKI, E; HIRAYAMA, T et al.Japanese heart journal. 1998, Vol 39, Num 6, pp 785-789, issn 0021-4868Article

Plasma homocyst(e)ine as a risk factor for early familial coronary artery diseaseWU, L. L; WU, J; HUNT, S. C et al.Clinical chemistry (Baltimore, Md.). 1994, Vol 40, Num 4, pp 552-561, issn 0009-9147Conference Paper

Molecular basis of human hypertension : role of angiotensinogenJEUNEMAITRE, X; SOUBRIER, F; CORVOL, P et al.Cell (Cambridge). 1992, Vol 71, Num 1, pp 169-180, issn 0092-8674Article

Effects of three genetic loci in a pedigree with multiple lipoprotein phenotypesEMI, M; HEGELE, R. M; HOPKINS, P. N et al.Arteriosclerosis and thrombosis. 1991, Vol 11, Num 5, pp 1349-1355Article

Genetic heritability and common environmental components of resting and stressed blood pressures, lipids, and body mass index in Utah pedigrees and twinsHUNT, S. C; HASSTEDT, S. J; KUIDA, H et al.American journal of epidemiology. 1989, Vol 129, Num 3, pp 625-638, issn 0002-9262Article

Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemiaHEGELE, R. A; EMI, M; WU, L. L et al.The American journal of cardiology. 1989, Vol 63, Num 1, pp 109-112, issn 0002-9149Article