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155 related items for PubMed ID: 17697822

  • 1. Usefulness of combining complement factor H and C-reactive protein genetic profiles for predicting myocardial infarction (from the Rotterdam Study).
    Kardys I, de Maat MP, Klaver CC, Despriet DD, Uitterlinden AG, Hofman A, de Jong PT, Witteman JC.
    Am J Cardiol; 2007 Aug 15; 100(4):646-8. PubMed ID: 17697822
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  • 2. A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study.
    Kardys I, Klaver CC, Despriet DD, Bergen AA, Uitterlinden AG, Hofman A, Oostra BA, Van Duijn CM, de Jong PT, Witteman JC.
    J Am Coll Cardiol; 2006 Apr 18; 47(8):1568-75. PubMed ID: 16630992
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  • 3. The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factors.
    Stark K, Neureuther K, Sedlacek K, Hengstenberg W, Fischer M, Baessler A, Wiedmann S, Jeron A, Holmer S, Erdmann J, Schunkert H, Hengstenberg C.
    Clin Sci (Lond); 2007 Aug 18; 113(4):213-8. PubMed ID: 17472578
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  • 4. Host polymorphisms in interleukin 4, complement factor H, and C-reactive protein associated with nasal carriage of Staphylococcus aureus and occurrence of boils.
    Emonts M, Uitterlinden AG, Nouwen JL, Kardys I, Maat MP, Melles DC, Witteman J, Jong PT, Verbrugh HA, Hofman A, Hermans PW, Belkum Av.
    J Infect Dis; 2008 May 01; 197(9):1244-53. PubMed ID: 18422436
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  • 5. Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration.
    Despriet DD, Klaver CC, Witteman JC, Bergen AA, Kardys I, de Maat MP, Boekhoorn SS, Vingerling JR, Hofman A, Oostra BA, Uitterlinden AG, Stijnen T, van Duijn CM, de Jong PT.
    JAMA; 2006 Jul 19; 296(3):301-9. PubMed ID: 16849663
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  • 6. Complement Factor H polymorphism Y402H associates with inflammation, visual acuity, and cardiovascular mortality in the elderly population at large.
    Mooijaart SP, Koeijvoets KM, Sijbrands EJ, Daha MR, Westendorp RG.
    Exp Gerontol; 2007 Nov 19; 42(11):1116-22. PubMed ID: 17869048
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  • 7. Polymorphism of the C-reactive protein (CRP) gene is related to serum CRP Level and arterial pulse wave velocity in healthy elderly Japanese.
    Morita A, Nakayama T, Doba N, Hinohara S, Soma M.
    Hypertens Res; 2006 May 19; 29(5):323-31. PubMed ID: 16832152
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  • 9. The cholesteryl ester transfer protein I405V polymorphism is associated with increased high-density lipoprotein levels and decreased risk of myocardial infarction: the Rotterdam Study.
    Isaacs A, Sayed-Tabatabaei FA, Hofman A, Oostra BA, Klungel OH, Maitland-Vander Zee AH, Stricker BH, Witteman JC, van Duijn CM.
    Eur J Cardiovasc Prev Rehabil; 2007 Jun 19; 14(3):419-21. PubMed ID: 17568242
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  • 11. C-reactive protein gene C1444T polymorphism and risk of recurrent ischemic events in patients with symptomatic intracranial atherostenoses.
    Arenillas JF, Massot A, Alvarez-Sabín J, Fernandez-Cadenas I, del Rio-Espinola A, Chacon P, Quintana M, Molina CA, Rovira A, Montaner J.
    Cerebrovasc Dis; 2009 Jun 19; 28(1):95-102. PubMed ID: 19494488
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  • 12. Genetic variation, C-reactive protein levels, and incidence of diabetes.
    Dehghan A, Kardys I, de Maat MP, Uitterlinden AG, Sijbrands EJ, Bootsma AH, Stijnen T, Hofman A, Schram MT, Witteman JC.
    Diabetes; 2007 Mar 19; 56(3):872-8. PubMed ID: 17327459
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  • 13. Interleukin-6 gene polymorphism is an age-dependent risk factor for myocardial infarction in men.
    Chiappelli M, Tampieri C, Tumini E, Porcellini E, Caldarera CM, Nanni S, Branzi A, Lio D, Caruso M, Hoffmann E, Caruso C, Licastro F.
    Int J Immunogenet; 2005 Dec 19; 32(6):349-53. PubMed ID: 16313298
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  • 14. Complement factor H Y402H decreases cardiovascular disease risk in patients with familial hypercholesterolaemia.
    Koeijvoets KC, Mooijaart SP, Dallinga-Thie GM, Defesche JC, Steyerberg EW, Westendorp RG, Kastelein JJ, van Hagen PM, Sijbrands EJ.
    Eur Heart J; 2009 Mar 19; 30(5):618-23. PubMed ID: 19098018
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  • 17. Decreased risk for myocardial infarction and lower tumor necrosis factor-alpha levels in carriers of variants of the PDCD1 gene.
    Bennet AM, Alarcón-Riquelme M, Wiman B, de Faire U, Prokunina-Olsson L.
    Hum Immunol; 2006 Sep 19; 67(9):700-5. PubMed ID: 17002900
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  • 19. The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms.
    Liu J, Colville D, Wang YY, Baird PN, Guymer RH, Savige J.
    Br J Ophthalmol; 2009 Mar 19; 93(3):379-82. PubMed ID: 19019939
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  • 20. The HR2 haplotype of factor V is not associated with the risk of myocardial infarction.
    Doggen CJ, de Visser MC, Vos HL, Bertina RM, Cats VM, Rosendaal FR.
    Thromb Haemost; 2000 Nov 19; 84(5):815-8. PubMed ID: 11127862
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