The lipoprotein lipase (Asn291 → Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia

Estimation of the Concentration of Low-Density Lipoprotein Cholesterol in Plasma, Without Use of the Preparative Ultracentrifuge

1972 • 31,801 citations

A simple salting out procedure for extracting DNA from human nucleated cells

1988 • 20,341 citations

Hyperlipidemia in Coronary Heart Disease II. GENETIC ANALYSIS OF LIPID LEVELS IN 176 FAMILIES AND DELINEATION OF A NEW INHERITED DISORDER, COMBINED HYPERLIPIDEMIA

1973 • 1,457 citations

Human Lipoprotein Lipase Complementary DNA Sequence

1987 • 484 citations

Extensions to pedigree analysis III. Variance components by the scoring method

1976 • 438 citations

Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia

1983 • 305 citations

Detection and characterization of the heterozygote state for lipoprotein lipase deficiency.

1989 • 295 citations

Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia.

1990 • 264 citations

A lipoprotein lipase mutation (Asn291Ser) is associated with reduced HDL cholesterol levels in premature atherosclerosis

1995 • 239 citations

A study of the use of polyethylene glycol in estimating cholesterol in high-density lipoprotein.

1980 • 218 citations

Familial Combined Hyperlipidemia Workshop

1989 • 215 citations

Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24

1991 • 188 citations

Linkage of atherogenic lipoprotein phenotype to the low density lipoprotein receptor locus on the short arm of chromosome 19.

1992 • 165 citations

Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation.

1990 • 164 citations

A Common Variant in the Gene for Lipoprotein Lipase (Asp9→Asn)

1995 • 153 citations

Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.

1993 • 145 citations

Familial combined hyperlipidemia and abnormal lipoprotein lipase.

1992 • 144 citations

Apolipoprotein, low density lipoprotein subfraction, and insulin associations with familial combined hyperlipidemia. Study of Utah patients with familial dyslipidemic hypertension.

1989 • 138 citations

High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: possible association with apolipoprotein E2 isoform.

1994 • 116 citations

Genetic and cultural inheritance of serum lipids, low and high density lipoprotein cholesterol and serum apolipoproteins A-I, A-II and B

1986 • 116 citations

Genetics and molecular biology of familial combined hyperlipidemia

1993 • 83 citations

The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity.

1994 • 77 citations

Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia.

1994 • 72 citations

Bimodality of plasma apolipoprotein B levels in familial combined hyperlipidemia

1992 • 70 citations

Complex segregation analysis provides evidence for a major gene acting on serum triglyceride levels in 55 British families with familial combined hyperlipidemia.

1994 • 67 citations

Hyperapobetalipoproteinemia in a kindred with familial combined hyperlipidemia and familial hypercholesterolemia.

1987 • 60 citations

Evaluation of the dual-precipitation method by comparison with the ultracentrifugation method for measurement of lipoproteins in serum.

1977 • 53 citations

The effects of generation and gender on the joint distributions of lipid and apolipoprotein phenotypes in the population at large

1990 • 37 citations