Connection

PAUL HOPKINS to Cholesterol, LDL

This is a "connection" page, showing publications PAUL HOPKINS has written about Cholesterol, LDL.
Connection Strength

1.018
  1. A comparative study of four independent methods to measure LDL particle concentration. Atherosclerosis. 2015 Nov; 243(1):99-106.
    View in: PubMed
    Score: 0.366
  2. Pharmacokinetic and pharmacodynamic assessment of alirocumab in patients with familial hypercholesterolemia associated with proprotein convertase subtilisin/kexin type 9 gain-of-function or apolipoprotein B loss-of-function mutations. J Clin Lipidol. 2019 Nov - Dec; 13(6):970-978.
    View in: PubMed
    Score: 0.122
  3. Familial hypercholesterolemias: prevalence, genetics, diagnosis and screening recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. J Clin Lipidol. 2011 Jun; 5(3 Suppl):S9-17.
    View in: PubMed
    Score: 0.067
  4. Evaluation of the gene-age interactions in HDL cholesterol, LDL cholesterol, and triglyceride levels: the impact of the SORT1 polymorphism on LDL cholesterol levels is age dependent. Atherosclerosis. 2011 Jul; 217(1):139-41.
    View in: PubMed
    Score: 0.067
  5. Defining the challenges of familial hypercholesterolemia screening: introduction. J Clin Lipidol. 2010 Sep-Oct; 4(5):342-5.
    View in: PubMed
    Score: 0.065
  6. Altered composition of triglyceride-rich lipoproteins and coronary artery disease in a large case-control study. Atherosclerosis. 2009 Dec; 207(2):559-66.
    View in: PubMed
    Score: 0.059
  7. Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides. Hum Genet. 2005 Sep; 117(5):444-51.
    View in: PubMed
    Score: 0.045
  8. Evaluation of coronary risk factors in patients with heterozygous familial hypercholesterolemia. Am J Cardiol. 2001 Mar 01; 87(5):547-53.
    View in: PubMed
    Score: 0.034
  9. Alirocumab efficacy in patients with double heterozygous, compound heterozygous, or homozygous familial hypercholesterolemia. J Clin Lipidol. 2018 Mar - Apr; 12(2):390-396.e8.
    View in: PubMed
    Score: 0.027
  10. The association between hypercholesterolemia and sitosterolemia, and report of a sitosterolemia kindred. J Clin Lipidol. 2018 Jan - Feb; 12(1):152-161.
    View in: PubMed
    Score: 0.027
  11. Plasma homocyst(e)ine as a risk factor for early familial coronary artery disease. Clin Chem. 1994 Apr; 40(4):552-61.
    View in: PubMed
    Score: 0.021
  12. Variants identified in a GWAS meta-analysis for blood lipids are associated with the lipid response to fenofibrate. PLoS One. 2012; 7(10):e48663.
    View in: PubMed
    Score: 0.019
  13. Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction. Arterioscler Thromb. 1991 Sep-Oct; 11(5):1137-46.
    View in: PubMed
    Score: 0.017
  14. Association of gene variants with lipid levels in response to fenofibrate is influenced by metabolic syndrome status. Atherosclerosis. 2011 Apr; 215(2):435-9.
    View in: PubMed
    Score: 0.017
  15. Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populations. J Hum Genet. 2008; 53(3):193-200.
    View in: PubMed
    Score: 0.013
  16. Efficacy and safety of lovastatin therapy in adolescent girls with heterozygous familial hypercholesterolemia. Pediatrics. 2005 Sep; 116(3):682-8.
    View in: PubMed
    Score: 0.011
  17. Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study. Arterioscler Thromb Vasc Biol. 2001 Dec; 21(12):1969-76.
    View in: PubMed
    Score: 0.009
  18. Remnant-like particle cholesterol and triglyceride levels of hypertriglyceridemic patients in the fed and fasted state. J Lipid Res. 2000 Sep; 41(9):1428-36.
    View in: PubMed
    Score: 0.008
  19. Association of genetic variations in apolipoprotein B with hypercholesterolemia, coronary artery disease, and receptor binding of low density lipoproteins. J Lipid Res. 1997 Jul; 38(7):1361-73.
    View in: PubMed
    Score: 0.006
  20. Genetic basis of familial dyslipidemia and hypertension: 15-year results from Utah. Am J Hypertens. 1993 Nov; 6(11 Pt 2):319S-327S.
    View in: PubMed
    Score: 0.005
  21. Effects of three genetic loci in a pedigree with multiple lipoprotein phenotypes. Arterioscler Thromb. 1991 Sep-Oct; 11(5):1349-55.
    View in: PubMed
    Score: 0.004
  22. Apolipoprotein, low density lipoprotein subfraction, and insulin associations with familial combined hyperlipidemia. Study of Utah patients with familial dyslipidemic hypertension. Arteriosclerosis. 1989 May-Jun; 9(3):335-44.
    View in: PubMed
    Score: 0.004
  23. Familial dyslipidemic hypertension. Evidence from 58 Utah families for a syndrome present in approximately 12% of patients with essential hypertension. JAMA. 1988 Jun 24; 259(24):3579-86.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.