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Journal of Human Hypertension|January 19, 2007
Urinary albumin excretion is associated with impaired flow- and nitroglycerin-mediated brachial artery dilatation in hypertensive adultsA R Malik, S Sultan, S T Turner, et al.
Annals of Human Genetics|March 14, 2001
Analysis of lipoprotein lipase haplotypes reveals associations not apparent from analysis of the constituent lociD M Hallman, B E Groenemeijer, J W Jukema, et al.
Diabetologia|April 26, 2008
TCF7L2 single nucleotide polymorphisms, cardiovascular disease and all-cause mortality: the Atherosclerosis Risk in Communities (ARIC) studyS J Bielinski, J S Pankow, A R Folsom, et al.
Molecular Biology and Evolution|September 1, 1995
A novel measure of genetic distance for highly polymorphic tandem repeat lociM D Shriver, L Jin, E Boerwinkle, et al.
Diabetes|November 1, 1991
Signal peptide-length variation in human apolipoprotein B gene. Molecular characteristics and association with plasma glucose levelsE Boerwinkle, S H Chen, S Visvikis, et al.
Human Genetics|March 1, 1990
Frequency and effect of human apolipoprotein A-IV polymorphism on lipid and lipoprotein levels in an Icelandic populationH J Menzel, G Sigurdsson, E Boerwinkle, et al.
Atherosclerosis|December 4, 2001
Influence of lipoprotein lipase serine 447 stop polymorphism on tracking of triglycerides and HDL cholesterol from childhood to adulthood and familial risk of coronary artery disease: the Bogalusa heart studyW Chen, S R Srinivasan, A Elkasabany, et al.
American Journal of Hypertension|November 17, 2001
Combined effects of endothelial nitric oxide synthase gene polymorphism (G894T) and insulin resistance status on blood pressure and familial risk of hypertension in young adults: the Bogalusa Heart StudyW Chen, S R Srinivasan, A Elkasabany, et al.
Annals of Human Genetics|December 18, 2002
Power of a simplified multivariate test for genetic linkageO Y Gorlova, C I Amos, D K Zhu, et al.
The New England Journal of Medicine|May 24, 1990
Relation of serum lipoprotein(a) concentration and apolipoprotein(a) phenotype to coronary heart disease in patients with familial hypercholesterolemiaM Seed, F Hoppichler, D Reaveley, et al.
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