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Journal Abstract Search

143 related items for PubMed ID: 12006406

  • 1. Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2.
    Harrap SB, Zammit KS, Wong ZY, Williams FM, Bahlo M, Tonkin AM, Anderson ST.
    Arterioscler Thromb Vasc Biol; 2002 May 01; 22(5):874-8. PubMed ID: 12006406
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  • 2. A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.
    Francke S, Manraj M, Lacquemant C, Lecoeur C, Leprêtre F, Passa P, Hebe A, Corset L, Yan SL, Lahmidi S, Jankee S, Gunness TK, Ramjuttun US, Balgobin V, Dina C, Froguel P.
    Hum Mol Genet; 2001 Nov 15; 10(24):2751-65. PubMed ID: 11734540
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  • 4. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
    Hoffmann K, Mattheisen M, Dahm S, Nürnberg P, Roe C, Johnson J, Cox NJ, Wichmann HE, Wienker TF, Schulze J, Schwarz PE, Lindner TH.
    Diabetologia; 2007 Jul 15; 50(7):1418-22. PubMed ID: 17464498
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  • 5. Fine mapping and SNP analysis of positional candidates at the preeclampsia susceptibility locus (PREG1) on chromosome 2.
    Fitzpatrick E, Göring HH, Liu H, Borg A, Forrest S, Cooper DW, Brennecke SP, Moses EK.
    Hum Biol; 2004 Dec 15; 76(6):849-62. PubMed ID: 15974297
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  • 6. Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.
    Paterson AD, Liu XQ, Wang K, Magistroni R, Song X, Kappel J, Klassen J, Cattran D, St George-Hyslop P, Pei Y.
    J Am Soc Nephrol; 2007 Aug 15; 18(8):2408-15. PubMed ID: 17634434
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  • 8. A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study.
    Samani NJ, Burton P, Mangino M, Ball SG, Balmforth AJ, Barrett J, Bishop T, Hall A, BHF Family Heart Study Research Group.
    Am J Hum Genet; 2005 Dec 15; 77(6):1011-20. PubMed ID: 16380912
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  • 10. Comparison of linkage analysis methods for genome-wide scanning of extended pedigrees, with application to the TG/HDL-C ratio in the Framingham Heart Study.
    Horne BD, Malhotra A, Camp NJ, Framingham Heart Study.
    BMC Genet; 2003 Dec 31; 4 Suppl 1(Suppl 1):S93. PubMed ID: 14975161
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  • 11. A comprehensive linkage analysis for myocardial infarction and its related risk factors.
    Broeckel U, Hengstenberg C, Mayer B, Holmer S, Martin LJ, Comuzzie AG, Blangero J, Nürnberg P, Reis A, Riegger GA, Jacob HJ, Schunkert H.
    Nat Genet; 2002 Feb 31; 30(2):210-4. PubMed ID: 11818963
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  • 12. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.
    Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T, Parkinson Study Group.
    Am J Hum Genet; 2002 Jul 31; 71(1):124-35. PubMed ID: 12058349
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  • 13. A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.
    Hauser ER, Crossman DC, Granger CB, Haines JL, Jones CJ, Mooser V, McAdam B, Winkelmann BR, Wiseman AH, Muhlestein JB, Bartel AG, Dennis CA, Dowdy E, Estabrooks S, Eggleston K, Francis S, Roche K, Clevenger PW, Huang L, Pedersen B, Shah S, Schmidt S, Haynes C, West S, Asper D, Booze M, Sharma S, Sundseth S, Middleton L, Roses AD, Hauser MA, Vance JM, Pericak-Vance MA, Kraus WE.
    Am J Hum Genet; 2004 Sep 31; 75(3):436-47. PubMed ID: 15272420
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  • 14. Coincident linkage of type 2 diabetes, metabolic syndrome, and measures of cardiovascular disease in a genome scan of the diabetes heart study.
    Bowden DW, Rudock M, Ziegler J, Lehtinen AB, Xu J, Wagenknecht LE, Herrington D, Rich SS, Freedman BI, Carr JJ, Langefeld CD.
    Diabetes; 2006 Jul 31; 55(7):1985-94. PubMed ID: 16804067
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  • 16. Comparison of the linkage results of two phenotypic constructs from longitudinal data in the Framingham Heart Study: analyses on data measured at three time points and on the average of three measurements.
    Cheng R, Park N, Hodge SE, Juo SH, Framingham Heart Study.
    BMC Genet; 2003 Dec 31; 4 Suppl 1(Suppl 1):S20. PubMed ID: 14975088
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  • 17. Genome-wide scan for premature hypertension supports linkage to chromosome 2 in a large Kyrgyz family.
    Kalmyrzaev B, Aldashev A, Khalmatov M, Polupanov A, Jumagulova A, Mamanova L, Wilkins MR, Town M.
    Hypertension; 2006 Nov 31; 48(5):908-13. PubMed ID: 17000929
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  • 20. Identification of a novel locus for triglyceride on chromosome 1p31-32 in families with premature CAD and MI.
    Seidelmann SB, Li L, Shen GQ, Topol EJ, Wang QK.
    J Lipid Res; 2008 May 31; 49(5):1034-8. PubMed ID: 18245017
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