Connection

PAUL HOPKINS to Genotype

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

1.281
  1. Genotype-guided diagnosis in familial hypercholesterolemia: population burden and cascade screening. Curr Opin Lipidol. 2017 Apr; 28(2):136-143.
    View in: PubMed
    Score: 0.336
  2. Genotype-guided diagnosis in familial hypercholesterolemia: clinical management and concerns. Curr Opin Lipidol. 2017 Apr; 28(2):144-151.
    View in: PubMed
    Score: 0.336
  3. Hyperlipoproteinemia type 3: the forgotten phenotype. Curr Atheroscler Rep. 2014 Sep; 16(9):440.
    View in: PubMed
    Score: 0.070
  4. Molecular biology of atherosclerosis. Physiol Rev. 2013 Jul; 93(3):1317-542.
    View in: PubMed
    Score: 0.065
  5. Sodium bicarbonate cotransporter polymorphisms are associated with baseline and 10-year follow-up blood pressures. Hypertension. 2006 Mar; 47(3):532-6.
    View in: PubMed
    Score: 0.038
  6. Angiotensinogen genotype affects renal and adrenal responses to angiotensin II in essential hypertension. Circulation. 2002 Apr 23; 105(16):1921-7.
    View in: PubMed
    Score: 0.030
  7. Genetic Predictors of Salt Sensitivity of Blood Pressure: The Additive Impact of 2 Hits in the Same Biological Pathway. Hypertension. 2021 12; 78(6):1809-1817.
    View in: PubMed
    Score: 0.029
  8. Efficacy and Safety of Alirocumab in Patients With Autosomal Dominant Hypercholesterolemia Associated With Proprotein Convertase Subtilisin/Kexin Type 9 Gain-of-Function or Apolipoprotein B Loss-of-Function Mutations. Am J Cardiol. 2020 03 15; 125(6):880-886.
    View in: PubMed
    Score: 0.025
  9. Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindred. J Lipid Res. 1999 Jun; 40(6):1113-22.
    View in: PubMed
    Score: 0.024
  10. Epigenomics and metabolomics reveal the mechanism of the APOA2-saturated fat intake interaction affecting obesity. Am J Clin Nutr. 2018 07 01; 108(1):188-200.
    View in: PubMed
    Score: 0.023
  11. Striatin Gene Polymorphic Variants Are Associated With Salt Sensitive Blood Pressure in Normotensives and Hypertensives. Am J Hypertens. 2017 Dec 08; 31(1):124-131.
    View in: PubMed
    Score: 0.022
  12. Dysregulated aldosterone secretion in persons of African descent with endothelin-1 gene variants. JCI Insight. 2017 12 07; 2(23).
    View in: PubMed
    Score: 0.022
  13. Efficacy of alirocumab in 1191 patients with a wide spectrum of mutations in genes causative for familial hypercholesterolemia. J Clin Lipidol. 2017 Nov - Dec; 11(6):1338-1346.e7.
    View in: PubMed
    Score: 0.022
  14. Blunted renal vascular response to angiotensin II is associated with a common variant of the angiotensinogen gene and obesity. J Hypertens. 1996 Feb; 14(2):199-207.
    View in: PubMed
    Score: 0.019
  15. A prevalent caveolin-1 gene variant is associated with the metabolic syndrome in Caucasians and Hispanics. Metabolism. 2015 Dec; 64(12):1674-81.
    View in: PubMed
    Score: 0.019
  16. Variants in striatin gene are associated with salt-sensitive blood pressure in mice and humans. Hypertension. 2015 Jan; 65(1):211-217.
    View in: PubMed
    Score: 0.018
  17. Genome-wide association studies identified novel loci for non-high-density lipoprotein cholesterol and its postprandial lipemic response. Hum Genet. 2014 Jul; 133(7):919-30.
    View in: PubMed
    Score: 0.017
  18. Genetic analysis of 16 NMR-lipoprotein fractions in humans, the GOLDN study. Lipids. 2013 Feb; 48(2):155-65.
    View in: PubMed
    Score: 0.016
  19. 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: 0.014
  20. Apolipoprotein B genetic variants modify the response to fenofibrate: a GOLDN study. J Lipid Res. 2010 Nov; 51(11):3316-23.
    View in: PubMed
    Score: 0.013
  21. Identification of a pleiotropic locus on chromosome 7q for a composite left ventricular wall thickness factor and body mass index: the HyperGEN Study. BMC Med Genet. 2009 May 09; 10:40.
    View in: PubMed
    Score: 0.012
  22. The effect of IL6-174C/G polymorphism on postprandial triglyceride metabolism in the GOLDN studyboxs. J Lipid Res. 2008 Aug; 49(8):1839-45.
    View in: PubMed
    Score: 0.011
  23. Association of the FTO gene with BMI. Obesity (Silver Spring). 2008 Apr; 16(4):902-4.
    View in: PubMed
    Score: 0.011
  24. Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: the NHLBI Family Heart Study follow-up examination. Atherosclerosis. 2008 Jul; 199(1):172-8.
    View in: PubMed
    Score: 0.011
  25. Evidence of QTL on 15q21 for high-density lipoprotein cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study (NHLBI FHS). Atherosclerosis. 2007 Jan; 190(1):232-7.
    View in: PubMed
    Score: 0.010
  26. 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: 0.009
  27. TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart Study. Atherosclerosis. 2004 Jun; 174(2):357-62.
    View in: PubMed
    Score: 0.009
  28. The Arg16Gly polymorphism of the beta2-adrenergic receptor and left ventricular systolic function. Am J Hypertens. 2003 Nov; 16(11 Pt 1):945-51.
    View in: PubMed
    Score: 0.008
  29. Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes. 2003 Nov; 52(11):2840-7.
    View in: PubMed
    Score: 0.008
  30. A genome scan for loci influencing anti-atherogenic serum bilirubin levels. Eur J Hum Genet. 2002 Sep; 10(9):539-46.
    View in: PubMed
    Score: 0.008
  31. Linkage of left ventricular contractility to chromosome 11 in humans: The HyperGEN Study. Hypertension. 2001 Oct; 38(4):767-72.
    View in: PubMed
    Score: 0.007
  32. Evidence of linkage of familial hypoalphalipoproteinemia to a novel locus on chromosome 11q23. Am J Hum Genet. 2000 Jun; 66(6):1845-56.
    View in: PubMed
    Score: 0.006
  33. 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: 0.005
  34. 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
  35. A prospective study of sodium-lithium countertransport and hypertension in Utah. Hypertension. 1991 Jan; 17(1):1-7.
    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.