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Bailliere'S Clinical Endocrinology and Metabolism|October 1, 1995
The genetic determinants of plasma cholesterol and response to dietS E Humphries, R E Peacock, P J TalmudAnnals of Human Genetics|October 13, 2006
Polymorphisms in the angiotensin converting enzyme gene and growth in the first year of lifeP C Hindmarsh, C H Rodeck, S E HumphriesJournal of Medical Genetics|April 4, 2000
Universal primer quantitative fluorescent multiplex (UPQFM) PCR: a method to detect major and minor rearrangements of the low density lipoprotein receptor geneK E Heath, I N Day, S E HumphriesCiba Foundation Symposium|January 1, 1987
Use of DNA polymorphisms of the apolipoprotein genes to study the role of genetic variation in the determination of serum lipid levelsS E Humphries, P J Talmud, A M KesslingTrends in Endocrinology and Metabolism: TEM|November 25, 2000
The ACE I/D polymorphism and human physical performanceD R Woods, S E Humphries, H E MontgomeryAnnals of Human Genetics|December 18, 2002
Interaction between smoking and the stromelysin-1 (MMP3) gene 5A/6A promoter polymorphism and risk of coronary heart disease in healthy menS E Humphries, S Martin, J Cooper, et al.Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|September 11, 1992
Interaction between a polymorphism of the apo A-I promoter region and smoking determines plasma levels of HDL and apo A-IG Sigurdsson, V Gudnason, G Sigurdsson, et al.Pediatric Research|October 1, 1993
The molecular genetics of pediatric lipid disorders: recent progress and future research directionsS E Humphries, F Mailly, V Gudnason, et al.Human Mutation|January 1, 1997
Common founder mutation in the LDL receptor gene causing familial hypercholesterolaemia in the Icelandic populationV Gudnason, G Sigurdsson, H Nissen, et al.Biochemical and Biophysical Research Communications|October 14, 1987
Apolipoprotein CII (apo CII) gene expression defect in an individual with familial apo CII deficiencyP J Davison, A F Stalenhoef, S E HumphriesPageof 34