Connection

PAUL HOPKINS to Pedigree

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

0.679
  1. Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees. Am J Hypertens. 2004 Jun; 17(6):511-5.
    View in: PubMed
    Score: 0.165
  2. 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: 0.046
  3. Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred. J Hum Genet. 2004; 49(1):29-34.
    View in: PubMed
    Score: 0.040
  4. Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat. Kidney Int. 2002 Oct; 62(4):1143-8.
    View in: PubMed
    Score: 0.037
  5. Usefulness of cardiovascular family history data for population-based preventive medicine and medical research (the Health Family Tree Study and the NHLBI Family Heart Study). Am J Cardiol. 2001 Jan 15; 87(2):129-35.
    View in: PubMed
    Score: 0.033
  6. 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: 0.029
  7. A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia. J Hum Genet. 1999; 44(6):364-7.
    View in: PubMed
    Score: 0.028
  8. 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: 0.023
  9. Hemodynamic and echocardiographic profiles in African American compared with White offspring of hypertensive parents: the HyperGEN study. Am J Hypertens. 2014 Jan; 27(1):21-6.
    View in: PubMed
    Score: 0.020
  10. Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. Am J Cardiol. 1993 Jul 15; 72(2):171-6.
    View in: PubMed
    Score: 0.019
  11. Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity. Hum Genet. 2013 Apr; 132(4):405-13.
    View in: PubMed
    Score: 0.019
  12. 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
  13. Lipoprotein lipase S447X variant associated with VLDL, LDL and HDL diameter clustering in the MetS. Lipids Health Dis. 2011 Aug 19; 10:143.
    View in: PubMed
    Score: 0.017
  14. Two-dimensional, sex-specific autosomal linkage scan of the number of sodium pump sites. J Hypertens. 2010 Apr; 28(4):740-7.
    View in: PubMed
    Score: 0.015
  15. Family history as an independent risk factor for incident coronary artery disease in a high-risk cohort in Utah. Am J Cardiol. 1988 Oct 01; 62(10 Pt 1):703-7.
    View in: PubMed
    Score: 0.014
  16. Association of the FTO gene with BMI. Obesity (Silver Spring). 2008 Apr; 16(4):902-4.
    View in: PubMed
    Score: 0.013
  17. 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: 0.011
  18. A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree. Hum Genet. 2004 Mar; 114(4):349-53.
    View in: PubMed
    Score: 0.010
  19. Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees. Hypertension. 2003 Sep; 42(3):322-8.
    View in: PubMed
    Score: 0.010
  20. 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: 0.009
  21. Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees. Eur J Hum Genet. 2002 Jun; 10(6):367-74.
    View in: PubMed
    Score: 0.009
  22. Identification of a common variant in the lipoprotein lipase gene in a large Utah kindred ascertained for coronary heart disease: the -93G/D9N variant predisposes to low HDL-C/high triglycerides. Clin Genet. 2001 Feb; 59(2):88-98.
    View in: PubMed
    Score: 0.008
  23. 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: 0.008
  24. Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred. Arterioscler Thromb Vasc Biol. 2000 Apr; 20(4):1089-93.
    View in: PubMed
    Score: 0.008
  25. Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities. J Hum Genet. 2000; 45(3):154-8.
    View in: PubMed
    Score: 0.008
  26. Primordial prevention of cardiovascular disease through applied genetics. Prev Med. 1999 Dec; 29(6 Pt 2):S41-9.
    View in: PubMed
    Score: 0.008
  27. 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
  28. Evidence for a major gene elevating serum bilirubin concentration in Utah pedigrees. Arterioscler Thromb Vasc Biol. 1996 Aug; 16(8):912-7.
    View in: PubMed
    Score: 0.006
  29. 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
  30. Familial dyslipidaemic hypertension and other multiple metabolic syndromes. Ann Med. 1992 Dec; 24(6):469-75.
    View in: PubMed
    Score: 0.005
  31. Molecular basis of human hypertension: role of angiotensinogen. Cell. 1992 Oct 02; 71(1):169-80.
    View in: PubMed
    Score: 0.005
  32. 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
  33. Family-oriented nutrition intervention for a lipid clinic population. J Am Diet Assoc. 1991 Jan; 91(1):57-65.
    View in: PubMed
    Score: 0.004
  34. Genetic traits related to hypertension and electrolyte metabolism. Hypertension. 1991 Jan; 17(1 Suppl):I69-73.
    View in: PubMed
    Score: 0.004
  35. Multigenic human hypertension: evidence for subtypes and hope for haplotypes. J Hypertens Suppl. 1990 Dec; 8(7):S39-46.
    View in: PubMed
    Score: 0.004
  36. Population-based frequency of dyslipidemia syndromes in coronary-prone families in Utah. Arch Intern Med. 1990 Mar; 150(3):582-8.
    View in: PubMed
    Score: 0.004
  37. Genetics of hypertension: what we know and don't know. Clin Exp Hypertens A. 1990; 12(5):865-76.
    View in: PubMed
    Score: 0.004
  38. Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemia. Am J Cardiol. 1989 Jan 01; 63(1):109-12.
    View in: PubMed
    Score: 0.004
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.