Published in Am J Hypertens on November 01, 1993
Genetic and Environmental Determinants of Hypertension | NCT00005149
Coronary risk correlates with cerebral amyloid deposition. Neurobiol Aging (2011) 1.17
Genes for blood pressure: an opportunity to understand hypertension. Eur Heart J (2013) 1.07
Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22. J Clin Invest (1996) 0.99
The influence of family history of hypertension on disease prevalence and associated metabolic risk factors among Sri Lankan adults. BMC Public Health (2015) 0.86
Association of the angiotensinogen gene polymorphism with atherosclerosis and its risk traits in the Saudi population. BMC Cardiovasc Disord (2013) 0.86
Association between family risk of stroke and myocardial infarction with prevalent risk factors and coexisting diseases. Stroke (2012) 0.82
A common genetic mechanism determines plasma apolipoprotein B levels and dense LDL subfraction distribution in familial combined hyperlipidemia. Am J Hum Genet (1998) 0.80
Complex trait genetics: new methods yield a result for essential hypertension. J Clin Invest (1996) 0.75
A Novel Category of Anti-Hypertensive Drugs for Treating Salt-Sensitive Hypertension on the Basis of a New Development Concept. Pharmaceuticals (Basel) (2010) 0.75
Molecular basis of human hypertension: role of angiotensinogen. Cell (1992) 6.07
Genotyping and sequence analysis of apolipoprotein E isoforms. Genomics (1988) 3.20
Energy balance and colon cancer--beyond physical activity. Cancer Res (1997) 3.11
Iron overload in Africa. Interaction between a gene and dietary iron content. N Engl J Med (1992) 2.85
Problem drinking and medication adherence among persons with HIV infection. J Gen Intern Med (2001) 2.81
Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100. Proc Natl Acad Sci U S A (1989) 2.68
Familial and genetic determinants of systemic markers of inflammation: the NHLBI family heart study. Atherosclerosis (2001) 2.40
A comparison of positive family history definitions for defining risk of future disease. J Chronic Dis (1986) 2.30
NHLBI family blood pressure program: methodology and recruitment in the HyperGEN network. Hypertension genetic epidemiology network. Ann Epidemiol (2000) 2.28
Objective system for interviewer performance evaluation for use in epidemiologic studies. Am J Epidemiol (1994) 2.28
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro. J Clin Invest (1997) 2.23
Relation between dietary linolenic acid and coronary artery disease in the National Heart, Lung, and Blood Institute Family Heart Study. Am J Clin Nutr (2001) 2.22
Usefulness of cardiovascular family history data for population-based preventive medicine and medical research (the Health Family Tree Study and the NHLBI Family Heart Study). Am J Cardiol (2001) 2.14
Utah pedigree studies: design and preliminary data for premature male CHD deaths. Prog Clin Biol Res (1979) 2.11
A mixed-model likelihood approximation on large pedigrees. Comput Biomed Res (1982) 2.10
Statistical methods in epidemiology: a comparison of statistical methods to analyze dose-response and trend analysis in epidemiologic studies. J Clin Epidemiol (1998) 2.09
A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians. Diabetes (1999) 1.99
Comparison of occupation and industry information from death certificates and interviews. Am J Public Health (1986) 1.95
Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease. Arterioscler Thromb Vasc Biol (1996) 1.94
Complex segregation analysis of autism. Am J Hum Genet (1991) 1.89
Salt induces myocardial and renal fibrosis in normotensive and hypertensive rats. Circulation (1998) 1.87
Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. Am J Cardiol (1993) 1.87
A prospective cohort of American Indian and Alaska Native people: study design, methods, and implementation. Am J Epidemiol (2007) 1.86
Physical activity, diet, and risk of colon cancer in Utah. Am J Epidemiol (1988) 1.84
A survey of 246 suggested coronary risk factors. Atherosclerosis (1981) 1.76
Transcription factor 7-like 2 polymorphisms and type 2 diabetes, glucose homeostasis traits and gene expression in US participants of European and African descent. Diabetologia (2007) 1.73
Genetic heritability and common environmental components of resting and stressed blood pressures, lipids, and body mass index in Utah pedigrees and twins. Am J Epidemiol (1989) 1.73
A computerized diet history questionnaire for epidemiologic studies. J Am Diet Assoc (1994) 1.70
Influence of leisure time physical activity and television watching on atherosclerosis risk factors in the NHLBI Family Heart Study. Atherosclerosis (2000) 1.70
Effect of type 2 diabetes mellitus on left ventricular geometry and systolic function in hypertensive subjects: Hypertension Genetic Epidemiology Network (HyperGEN) study. Circulation (2001) 1.69
Blockade of the renin-angiotensin and endothelin systems on progressive renal injury. Hypertension (2000) 1.56
Evidence for major genes influencing pulmonary function in the NHLBI family heart study. Genet Epidemiol (2000) 1.54
Magnified risks from cigarette smoking for coronary prone families in Utah. West J Med (1984) 1.53
Health family trees: a tool for finding and helping young family members of coronary and cancer prone pedigrees in Texas and Utah. Am J Public Health (1988) 1.53
Validity of cigarette smoking habits in three epidemiologic studies in Utah. Prev Med (1989) 1.51
Irradiation-induced extracranial carotid stenosis in patients with head and neck malignancies. Am J Surg (1999) 1.48
Blood pressure response to angiotensin II, low-density lipoprotein cholesterol and polymorphisms of the angiotensin II type 1 receptor gene in hypertensive sibling pairs. J Mol Med (Berl) (2001) 1.43
Environmental determinants of urinary kallikrein excretion. Am J Hypertens (1993) 1.42
Evidence that men with familial hypercholesterolemia can avoid early coronary death. An analysis of 77 gene carriers in four Utah pedigrees. JAMA (1986) 1.39
Planning parental leave. Ann Intern Med (1990) 1.37
Renal expression of transforming growth factor-beta inducible gene-h3 (beta ig-h3) in normal and diabetic rats. Kidney Int (1998) 1.36
Effect of angiotensin II type 1 receptor blockade on experimental hepatic fibrogenesis. J Hepatol (2001) 1.35
Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension. Nat Genet (1992) 1.34
A DNA probe for the LDL receptor gene is tightly linked to hypercholesterolemia in a pedigree with early coronary disease. Am J Hum Genet (1986) 1.32
A genome scan for renal function among hypertensives: the HyperGEN study. Am J Hum Genet (2000) 1.31
Genetic linkage between lipoprotein(a) phenotype and a DNA polymorphism in the plasminogen gene. Genomics (1988) 1.31
Aortic root dilatation at sinuses of valsalva and aortic regurgitation in hypertensive and normotensive subjects: The Hypertension Genetic Epidemiology Network Study . Hypertension (2001) 1.29
Vascular endothelial growth factor and its receptors in control and diabetic rat eyes. Lab Invest (1998) 1.29
Occupation, cadmium exposure, and prostate cancer. Epidemiology (1990) 1.26
Familial dyslipidemic hypertension. Evidence from 58 Utah families for a syndrome present in approximately 12% of patients with essential hypertension. JAMA (1988) 1.25
Sibling correlation of left ventricular mass and geometry in hypertensive African Americans and whites: the HyperGEN study. Hypertension Genetic Epidemiology Network. Am J Hypertens (2001) 1.24
Plasma homocyst(e)ine as a risk factor for early familial coronary artery disease. Clin Chem (1994) 1.24
Identification and relative weight of cardiovascular risk factors. Cardiol Clin (1986) 1.24
The impact of RFLPs on human gene mapping. Prog Clin Biol Res (1984) 1.24
Possible locus on chromosome 18q influencing postural systolic blood pressure changes. Hypertension (2000) 1.24
Genome-wide meta-analyses of smoking behaviors in African Americans. Transl Psychiatry (2012) 1.23
Spinal dysraphia as an autosomal dominant defect in four families. Am J Med Genet (1982) 1.22
Quantitative trait linkage analysis of lipid-related traits in familial type 2 diabetes: evidence for linkage of triglyceride levels to chromosome 19q. Diabetes (2002) 1.21
Dietary fats and colon cancer: assessment of risk associated with specific fatty acids. Int J Cancer (1997) 1.20
Heritability of pancreatic beta-cell function among nondiabetic members of Caucasian familial type 2 diabetic kindreds. J Clin Endocrinol Metab (1999) 1.20
Segregation analysis of serum uric acid in the NHLBI Family Heart Study. Hum Genet (2000) 1.19
Pathological expression of renin and angiotensin II in the renal tubule after subtotal nephrectomy. Implications for the pathogenesis of tubulointerstitial fibrosis. Am J Pathol (1999) 1.19
Lack of association of diagonal earlobe crease with other cardiovascular risk factors. West J Med (1984) 1.18
Symptomatic lower extremity deep venous thrombosis: accuracy, limitations, and role of color duplex flow imaging in diagnosis. Radiology (1990) 1.18
Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindred. J Lipid Res (1999) 1.17
Predictors of an increased risk of future hypertension in Utah. A screening analysis. Hypertension (1991) 1.15
Development and implementation of a computer-generated reminder system for diabetes preventive care. Proc Annu Symp Comput Appl Med Care (1994) 1.14
Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study. Arterioscler Thromb Vasc Biol (2001) 1.13
Hypertension and sodium-lithium countertransport in Utah pedigrees: evidence for major-locus inheritance. Am J Hum Genet (1988) 1.13
Insulin resistance in hypertensives: effect of salt sensitivity, renin status and sodium intake. J Hypertens (2001) 1.12
Prevalence of primary hyperaldosteronism in mild to moderate hypertension without hypokalaemia. J Hum Hypertens (2006) 1.12
X-linked inheritance of Alport syndrome: family P revisited. Am J Hum Genet (1983) 1.11
Evidence for multiple determinants of the body mass index: the National Heart, Lung, and Blood Institute Family Heart Study. Obes Res (1998) 1.11
Antibody-dependent enhancement (ADE) of porcine reproductive and respiratory syndrome virus (PRRSV) infection in pigs. Viral Immunol (1996) 1.10
Mapping of Alport syndrome to the long arm of the X chromosome. Am J Hum Genet (1988) 1.10
Familial aggregation of QT-interval variability in a general population: results from the NHLBI Family Heart Study. Clin Genet (2001) 1.07
Identification of uterine leiomyoma genes developmentally reprogrammed by neonatal exposure to diethylstilbestrol. Reprod Sci (2008) 1.07
Association between the alpha-adducin gene and hypertension in the HyperGEN Study. Am J Hypertens (2000) 1.07
A rare case of ambiguous genitalia. Singapore Med J (2007) 1.06
Sex-specific findings from a genome-wide linkage analysis of human fatness in non-Hispanic whites and African Americans: the HyperGEN study. Int J Obes (Lond) (2005) 1.06
Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait: the NHLBI family heart study. Atherosclerosis (2001) 1.06