Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Evidence-based nutrition principles and recommendations for the treatment and prevention of diabetes and related complications.
|
Diabetes Care
|
2002
|
4.46
|
2
|
Detection and characterization of the heterozygote state for lipoprotein lipase deficiency.
|
Arteriosclerosis
|
1989
|
2.14
|
3
|
Apoproteins B and A-I and coronary artery disease in humans.
|
Arteriosclerosis
|
1984
|
1.73
|
4
|
Abdominal obesity and dyslipidemia in the metabolic syndrome: importance of type 2 diabetes and familial combined hyperlipidemia in coronary artery disease risk.
|
J Clin Endocrinol Metab
|
2004
|
1.70
|
5
|
Effect of ritonavir on lipids and post-heparin lipase activities in normal subjects.
|
AIDS
|
2000
|
1.60
|
6
|
Transcriptional activation of the lipoprotein lipase and apolipoprotein E genes accompanies differentiation in some human macrophage-like cell lines.
|
Biochemistry
|
1988
|
1.52
|
7
|
A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency.
|
Proc Natl Acad Sci U S A
|
1989
|
1.41
|
8
|
Body fat distribution and dyslipidemia.
|
Am J Med
|
1995
|
1.40
|
9
|
Human adipose tissue lipoprotein lipase: changes with feeding and relation to postheparin plasma enzyme.
|
Am J Physiol
|
1985
|
1.38
|
10
|
Partial gene duplication involving exon-Alu interchange results in lipoprotein lipase deficiency.
|
Am J Hum Genet
|
1990
|
1.31
|
11
|
Effect of hepatic lipase on LDL in normal men and those with coronary artery disease.
|
Arterioscler Thromb
|
1993
|
1.24
|
12
|
Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes.
|
J Lipid Res
|
1992
|
1.20
|
13
|
Analysis of techniques to obtain plasma for measurement of levels of free fatty acids.
|
J Lipid Res
|
1993
|
1.14
|
14
|
Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia.
|
Arteriosclerosis
|
1990
|
1.12
|
15
|
Weight loss leads to a marked decrease in nonresting energy expenditure in ambulatory human subjects.
|
Metabolism
|
1988
|
1.10
|
16
|
Evidence for a new pathophysiological mechanism for coronary artery disease regression: hepatic lipase-mediated changes in LDL density.
|
Circulation
|
1999
|
1.05
|
17
|
Human lipoprotein lipase. Analysis of the catalytic triad by site-directed mutagenesis of Ser-132, Asp-156, and His-241.
|
J Biol Chem
|
1992
|
1.04
|
18
|
Relationship between lipoprotein lipase activity and plasma sex steroid level in obese women.
|
J Clin Invest
|
1988
|
1.04
|
19
|
Molecular genetics of apolipoproteins and coronary heart disease.
|
Cold Spring Harb Symp Quant Biol
|
1986
|
1.03
|
20
|
Dyslipidemia of central obesity and insulin resistance.
|
Diabetes Care
|
1999
|
1.03
|
21
|
The contribution of intraabdominal fat to gender differences in hepatic lipase activity and low/high density lipoprotein heterogeneity.
|
J Clin Endocrinol Metab
|
2001
|
1.02
|
22
|
Characterization of low-density lipoprotein subclasses: methodologic approaches and clinical relevance.
|
Curr Opin Lipidol
|
1994
|
1.02
|
23
|
A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activity.
|
Proc Natl Acad Sci U S A
|
1995
|
1.01
|
24
|
Large buoyant LDL-like particles in hepatic lipase deficiency.
|
Arteriosclerosis
|
1989
|
1.01
|
25
|
Lipoprotein lipase gene expression in THP-1 cells.
|
Biochemistry
|
1989
|
0.99
|
26
|
Defective enzyme protein in lipoprotein lipase deficiency.
|
Eur J Clin Invest
|
1989
|
0.99
|
27
|
Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype.
|
Arterioscler Thromb
|
1994
|
0.96
|
28
|
A hepatic lipase gene promoter polymorphism attenuates the increase in hepatic lipase activity with increasing intra-abdominal fat in women.
|
Arterioscler Thromb Vasc Biol
|
1999
|
0.95
|
29
|
Coexistence of abnormalities of hepatic lipase and lipoprotein lipase in a large family.
|
Am J Hum Genet
|
1990
|
0.95
|
30
|
Conversion of plasma VLDL and IDL precursors into various LDL subpopulations using density gradient ultracentrifugation.
|
J Lipid Res
|
1990
|
0.94
|
31
|
Common hepatic lipase gene promoter variant determines clinical response to intensive lipid-lowering treatment.
|
Circulation
|
2001
|
0.93
|
32
|
Effect of weight loss with reduction of intra-abdominal fat on lipid metabolism in older men.
|
J Clin Endocrinol Metab
|
2000
|
0.93
|
33
|
The LPL gene in individuals with familial combined hyperlipidemia and decreased LPL activity.
|
Arterioscler Thromb
|
1994
|
0.92
|
34
|
Bile acid metabolism in hereditary forms of hypertriglyceridemia: evidence for an increased synthesis rate in monogenic familial hypertriglyceridemia.
|
Proc Natl Acad Sci U S A
|
1987
|
0.92
|
35
|
Adipose tissue fatty acid composition in humans with lipoprotein lipase deficiency.
|
J Investig Med
|
2001
|
0.92
|
36
|
Changes in LDL density across the menopausal transition.
|
J Investig Med
|
2000
|
0.91
|
37
|
Analysis of the ileal bile acid transporter gene, SLC10A2, in subjects with familial hypertriglyceridemia.
|
Arterioscler Thromb Vasc Biol
|
2001
|
0.90
|
38
|
In vivo evidence of a role for hepatic lipase in human apoB-containing lipoprotein metabolism, independent of its lipolytic activity.
|
J Lipid Res
|
2000
|
0.90
|
39
|
Plasma triglyceride and LDL heterogeneity in familial combined hyperlipidemia.
|
Arterioscler Thromb
|
1993
|
0.89
|
40
|
LDL physical and chemical properties in familial combined hyperlipidemia.
|
Arterioscler Thromb Vasc Biol
|
1995
|
0.89
|
41
|
Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency.
|
Am J Hum Genet
|
1999
|
0.89
|
42
|
Lipoprotein heterogeneity in end-stage renal disease.
|
Kidney Int
|
1993
|
0.89
|
43
|
PLTP activity in premenopausal women. Relationship with lipoprotein lipase, HDL, LDL, body fat, and insulin resistance.
|
J Lipid Res
|
2000
|
0.88
|
44
|
Bacterial lipopolysaccharide reduces macrophage lipoprotein lipase levels: an effect that is independent of tumor necrosis factor.
|
J Lipid Res
|
1988
|
0.88
|
45
|
Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex.
|
Arterioscler Thromb Vasc Biol
|
1998
|
0.87
|
46
|
Primary lipoprotein lipase deficiency.
|
Adv Exp Med Biol
|
1986
|
0.84
|
47
|
Relationship of insulin sensitivity and ApoB levels to intra-abdominal fat in subjects with familial combined hyperlipidemia.
|
Arterioscler Thromb Vasc Biol
|
2001
|
0.83
|
48
|
Regulatory mutations in the human lipoprotein lipase gene in patients with familial combined hyperlipidemia and coronary artery disease.
|
J Lipid Res
|
1996
|
0.83
|
49
|
Host and environmental effects on plasma apolipoprotein B.
|
Int J Clin Lab Res
|
1993
|
0.81
|
50
|
A missense mutation Pro157 Arg in lipoprotein lipase (LPLNijmegen) resulting in loss of catalytic activity.
|
Eur J Biochem
|
1992
|
0.80
|
51
|
Prevention of raised low-density lipoprotein cholesterol in a patient with familial hypercholesterolaemia and lipoprotein lipase deficiency.
|
Lancet
|
1993
|
0.79
|
52
|
Obesity and common genetic metabolic disorders.
|
Ann Intern Med
|
1985
|
0.79
|
53
|
Lipoprotein and apolipoprotein abnormalities in familial combined hyperlipidemia: a 20-year prospective study.
|
Atherosclerosis
|
2001
|
0.79
|
54
|
Low-density and high-density lipoprotein subspecies and risk for premature coronary artery disease.
|
Am J Med
|
1999
|
0.78
|
55
|
Hepatic lipase as a focal point for the development and treatment of coronary artery disease.
|
J Investig Med
|
2001
|
0.77
|
56
|
Lack of evidence for linkage between low-density lipoprotein subclass phenotypes and the apolipoprotein B locus in familial combined hyperlipidemia.
|
Genet Epidemiol
|
1991
|
0.77
|
57
|
Low density lipoprotein metabolism in familial combined hyperlipidemia and familial hypercholesterolemia: kinetic analysis using an integrated model.
|
Metabolism
|
1986
|
0.77
|
58
|
Evidence for kinetic heterogeneity among human low density lipoproteins.
|
Metabolism
|
1986
|
0.77
|
59
|
Two novel apolipoprotein A-IV variants in individuals with familial combined hyperlipidemia and diminished levels of lipoprotein lipase activity.
|
Hum Mutat
|
1996
|
0.76
|
60
|
Use of niacin, statins, and resins in patients with combined hyperlipidemia.
|
Am J Cardiol
|
1998
|
0.76
|
61
|
Relationships between LDL density and kinetic heterogeneity in subjects with normolipidemia and familial combined hyperlipidemia using density gradient ultracentrifugation.
|
J Lipid Res
|
1989
|
0.75
|
62
|
The effects of diuretics and adrenergic-blocking agents on plasma lipids.
|
West J Med
|
1986
|
0.75
|
63
|
Are all obese patients at risk for cardiovascular disease?
|
Int J Obes
|
1984
|
0.75
|
64
|
Individuality, hyperlipidemia, and premature coronary artery disease.
|
World Rev Nutr Diet
|
1990
|
0.75
|
65
|
Chylomicronemia induced by cimetidine.
|
Gastroenterology
|
1985
|
0.75
|
66
|
Association of apolipoprotein B gene variants with plasma apoB and low density lipoprotein (LDL) cholesterol levels.
|
Hum Genet
|
1992
|
0.75
|