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Journal Abstract Search

135 related items for PubMed ID: 17059418

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  • 24. Estrogen receptor alpha gene polymorphisms and risk of myocardial infarction.
    Schuit SC, Oei HH, Witteman JC, Geurts van Kessel CH, van Meurs JB, Nijhuis RL, van Leeuwen JP, de Jong FH, Zillikens MC, Hofman A, Pols HA, Uitterlinden AG.
    JAMA; 2004 Jun 23; 291(24):2969-77. PubMed ID: 15213208
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  • 26. Coagulation factor VII, R353Q polymorphism, and serum choline-containing phospholipids in males at high risk for coronary heart disease.
    Lindman AS, Pedersen JI, Arnesen H, Hjerkinn EM, Veierød MB, Prydz H, Seljeflot I.
    Thromb Res; 2004 Jun 23; 113(1):57-65. PubMed ID: 15081566
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  • 27. Cardiovascular risk factor profile in subjects with familial predisposition to myocardial infarction in Denmark.
    Hippe M, Vestbo J, Bjerg AM, Borch-Johnsen K, Appleyard M, Hein HO, Andersen PK, Jensen G, Sørensen TI.
    J Epidemiol Community Health; 1997 Jun 23; 51(3):266-71. PubMed ID: 9229055
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  • 28. Association of genetic variants with myocardial infarction in Japanese individuals with chronic kidney disease.
    Fujimaki T, Kato K, Yoshida T, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Kimura G, Yamada Y.
    Thromb Haemost; 2009 May 23; 101(5):963-8. PubMed ID: 19404551
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  • 30. R353Q polymorphism in the factor VII gene and cardiovascular risk in Heterozygous Familial Hypercholesterolemia: a case-control study.
    Criado-García J, Fuentes F, Cruz-Teno C, García-Rios A, Jiménez-Morales A, Delgado-Lista J, Mata P, Alonso R, López-Miranda J, Pérez-Jiménez F, Spanish Group for the Study of Familiar Hypercholesterolemia.
    Lipids Health Dis; 2011 Apr 09; 10():50. PubMed ID: 21477332
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  • 31. Human F7 sequence is split into three deep clades that are related to FVII plasma levels.
    Sabater-Lleal M, Soria JM, Bertranpetit J, Almasy L, Blangero J, Fontcuberta J, Calafell F.
    Hum Genet; 2006 Feb 09; 118(6):741-51. PubMed ID: 16292673
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  • 32. Associations of activated coagulation factor VII and factor VIIa-antithrombin levels with genome-wide polymorphisms and cardiovascular disease risk.
    Olson NC, Raffield LM, Lange LA, Lange EM, Longstreth WT, Chauhan G, Debette S, Seshadri S, Reiner AP, Tracy RP.
    J Thromb Haemost; 2018 Jan 09; 16(1):19-30. PubMed ID: 29112333
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  • 33. Associations between common fibrinogen gene polymorphisms and cardiovascular disease in older adults. The Cardiovascular Health Study.
    Carty CL, Cushman M, Jones D, Lange LA, Hindorff LA, Rice K, Jenny NS, Durda JP, Walston J, Carlson CS, Nickerson D, Tracy RP, Reiner AP.
    Thromb Haemost; 2008 Feb 09; 99(2):388-95. PubMed ID: 18278190
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  • 34. Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.
    Baessler A, Fischer M, Mayer B, Koehler M, Wiedmann S, Stark K, Doering A, Erdmann J, Riegger G, Schunkert H, Kwitek AE, Hengstenberg C.
    Hum Mol Genet; 2007 Apr 15; 16(8):887-99. PubMed ID: 17324965
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  • 35. Lack of association between a common polymorphism near the INSIG2 gene and BMI, myocardial infarction, and cardiovascular risk factors.
    Wiedmann S, Neureuther K, Stark K, Reinhard W, Kallmünzer B, Baessler A, Fischer M, Linsel-Nitschke P, Erdmann J, Schunkert H, Hengstenberg C.
    Obesity (Silver Spring); 2009 Jul 15; 17(7):1390-5. PubMed ID: 19197259
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  • 36. Cholesterol ester transfer protein, interleukin-8, peroxisome proliferator activator receptor alpha, and Toll-like receptor 4 genetic variations and risk of incident nonfatal myocardial infarction and ischemic stroke.
    Enquobahrie DA, Smith NL, Bis JC, Carty CL, Rice KM, Lumley T, Hindorff LA, Lemaitre RN, Williams MA, Siscovick DS, Heckbert SR, Psaty BM.
    Am J Cardiol; 2008 Jun 15; 101(12):1683-8. PubMed ID: 18549840
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  • 37. The role of neuromedin U in adiposity regulation. Haplotype analysis in European children from the IDEFICS Cohort.
    Gianfagna F, Grippi C, Ahrens W, Bailey ME, Börnhorst C, De Henauw S, Foraita R, Koni AC, Krogh V, Mårild S, Molnár D, Moreno L, Pitsiladis Y, Russo P, Siani A, Tornaritis M, Veidebaum T, Iacoviello L.
    PLoS One; 2017 Jun 15; 12(2):e0172698. PubMed ID: 28235053
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  • 38. Factor VII levels, R353Q and -323P0/10 Factor VII variants, and the risk of acute coronary syndrome among Arab-African Tunisians.
    Ben-Hadj-Khalifa S, Lakhal B, Nsiri B, Mahjoub T, Almawi WY.
    Mol Biol Rep; 2013 May 15; 40(5):3793-8. PubMed ID: 23275237
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  • 40. Coagulation gene polymorphisms as risk factors for myocardial infarction in young Indian Asians.
    Pegoraro RJ, Ranjith N, Rom L.
    Cardiovasc J S Afr; 2005 May 15; 16(3):152-7. PubMed ID: 16049588
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