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Journal Abstract Search

515 related items for PubMed ID: 19716196

  • 1. Understanding cardiovascular disease through the lens of genome-wide association studies.
    Arking DE, Chakravarti A.
    Trends Genet; 2009 Sep; 25(9):387-94. PubMed ID: 19716196
    [Abstract] [Full Text] [Related]

  • 2. Complement factor H gene polymorphism and risk of cardiovascular disease in end-stage renal disease patients.
    Buraczynska M, Ksiazek P, Zukowski P, Benedyk-Lorens E, Orlowska-Kowalik G.
    Clin Immunol; 2009 Aug; 132(2):285-90. PubMed ID: 19428307
    [Abstract] [Full Text] [Related]

  • 3. Review of recent genome-wide association scans in lupus.
    Graham RR, Hom G, Ortmann W, Behrens TW.
    J Intern Med; 2009 Jun; 265(6):680-8. PubMed ID: 19493061
    [Abstract] [Full Text] [Related]

  • 4. Genome-wide association studies identify new targets in cardiovascular disease.
    Calkin AC, Tontonoz P.
    Sci Transl Med; 2010 Sep 08; 2(48):48ps46. PubMed ID: 20826839
    [Abstract] [Full Text] [Related]

  • 5. Genome-wide association studies of bladder cancer risk: a field synopsis of progress and potential applications.
    Wu X, Hildebrandt MA, Chang DW.
    Cancer Metastasis Rev; 2009 Dec 08; 28(3-4):269-80. PubMed ID: 20016998
    [Abstract] [Full Text] [Related]

  • 6. The pursuit of genome-wide association studies: where are we now?
    Ku CS, Loy EY, Pawitan Y, Chia KS.
    J Hum Genet; 2010 Apr 08; 55(4):195-206. PubMed ID: 20300123
    [Abstract] [Full Text] [Related]

  • 7. [Genome-wide association studies in hepatology].
    Weber S, Grünhage F, Hall R, Lammert F.
    Z Gastroenterol; 2010 Jan 08; 48(1):56-64. PubMed ID: 20072997
    [Abstract] [Full Text] [Related]

  • 8. Gene polymorphism association studies in dialysis: cardiovascular disease.
    Rao M, Jaber BL, Balakrishnan VS, DialGene Consortium.
    Semin Dial; 2005 Jan 08; 18(3):217-25. PubMed ID: 15934969
    [Abstract] [Full Text] [Related]

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  • 10. Association of genetic risk variants with expression of proximal genes identifies novel susceptibility genes for cardiovascular disease.
    Folkersen L, van't Hooft F, Chernogubova E, Agardh HE, Hansson GK, Hedin U, Liska J, Syvänen AC, Paulsson-Berne G, Franco-Cereceda A, Hamsten A, Gabrielsen A, Eriksson P, BiKE and ASAP study groups.
    Circ Cardiovasc Genet; 2010 Aug 08; 3(4):365-73. PubMed ID: 20562444
    [Abstract] [Full Text] [Related]

  • 11. Using genome-wide pathway analysis to unravel the etiology of complex diseases.
    Elbers CC, van Eijk KR, Franke L, Mulder F, van der Schouw YT, Wijmenga C, Onland-Moret NC.
    Genet Epidemiol; 2009 Jul 08; 33(5):419-31. PubMed ID: 19235186
    [Abstract] [Full Text] [Related]

  • 12. Association of OSBPL11 gene polymorphisms with cardiovascular disease risk factors in obesity.
    Bouchard L, Faucher G, Tchernof A, Deshaies Y, Marceau S, Lescelleur O, Biron S, Bouchard C, Pérusse L, Vohl MC.
    Obesity (Silver Spring); 2009 Jul 08; 17(7):1466-72. PubMed ID: 19325544
    [Abstract] [Full Text] [Related]

  • 13. A neurologist's guide to genome-wide association studies.
    Mullen SA, Crompton DE, Carney PW, Helbig I, Berkovic SF.
    Neurology; 2009 Feb 10; 72(6):558-65. PubMed ID: 19204266
    [Abstract] [Full Text] [Related]

  • 14. From candidate gene to genome-wide association studies in cardiovascular disease.
    Gianfagna F, Cugino D, Santimone I, Iacoviello L.
    Thromb Res; 2012 Mar 10; 129(3):320-4. PubMed ID: 22154244
    [Abstract] [Full Text] [Related]

  • 15. The common variants/multiple disease hypothesis of common complex genetic disorders.
    Becker KG.
    Med Hypotheses; 2004 Mar 10; 62(2):309-17. PubMed ID: 14962646
    [Abstract] [Full Text] [Related]

  • 16. Progress and challenges in genome-wide association studies in humans.
    Donnelly P.
    Nature; 2008 Dec 11; 456(7223):728-31. PubMed ID: 19079049
    [Abstract] [Full Text] [Related]

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  • 19. Genetic architecture of the F7 gene in a Spanish population: implication for mapping complex diseases and for functional assays.
    Sabater-Lleal M, Almasy L, Martínez-Marchán E, Martínez-Sánchez E, Souto R, Blangero J, Souto J, Fontcuberta J, Soria JM.
    Clin Genet; 2006 May 11; 69(5):420-8. PubMed ID: 16650081
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