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Journal Abstract Search

121 related items for PubMed ID: 17971050

  • 1. Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32.
    Adamovic S, Amundsen SS, Lie BA, Hellqvist A, Gudjónsdóttir AH, Ek J, Nilsson S, Wahlström J, Ascher H, Sollid LM, Naluai AT.
    Tissue Antigens; 2008 Jan; 71(1):27-34. PubMed ID: 17971050
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  • 2. Linkage and association analyses of microsatellites and single-nucleotide polymorphisms in nuclear families.
    Lin J, Liu KY.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S25. PubMed ID: 16451634
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  • 3. Fine mapping of a region on chromosome 21q21.11-q22.3 showing linkage to type 1 diabetes.
    Bergholdt R, Nerup J, Pociot F.
    J Med Genet; 2005 Jan 30; 42(1):17-25. PubMed ID: 15635070
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  • 4. Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.
    Sutton BS, Langefeld CD, Campbell JK, Haffner SM, Norris JM, Scherzinger AL, Wagenknecht LE, Bowden DW.
    Int J Obes (Lond); 2006 Sep 30; 30(9):1433-41. PubMed ID: 16520807
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  • 5. A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish/Norwegian celiac disease families.
    Amundsen SS, Adamovic S, Hellqvist A, Nilsson S, Gudjónsdóttir AH, Ascher H, Ek J, Larsson K, Wahlström J, Lie BA, Sollid LM, Naluai AT.
    Eur J Hum Genet; 2007 Sep 30; 15(9):980-7. PubMed ID: 17551518
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  • 6. Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.
    Koskinen LL, Einarsdottir E, Korponay-Szabo IR, Kurppa K, Kaukinen K, Sistonen P, Pocsai Z, Széles G, Adány R, Mäki M, Kere J, Saavalainen P.
    Tissue Antigens; 2009 Nov 30; 74(5):408-16. PubMed ID: 19845895
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  • 7. Association study of IL2/IL21 and FcgRIIa: significant association with the IL2/IL21 region in Scandinavian coeliac disease families.
    Adamovic S, Amundsen SS, Lie BA, Gudjónsdóttir AH, Ascher H, Ek J, van Heel DA, Nilsson S, Sollid LM, Torinsson Naluai A.
    Genes Immun; 2008 Jun 30; 9(4):364-7. PubMed ID: 18418394
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  • 8. Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.
    Petryshen TL, Middleton FA, Tahl AR, Rockwell GN, Purcell S, Aldinger KA, Kirby A, Morley CP, McGann L, Gentile KL, Waggoner SG, Medeiros HM, Carvalho C, Macedo A, Albus M, Maier W, Trixler M, Eichhammer P, Schwab SG, Wildenauer DB, Azevedo MH, Pato MT, Pato CN, Daly MJ, Sklar P.
    Mol Psychiatry; 2005 Dec 30; 10(12):1074-88, 1057. PubMed ID: 16172613
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  • 12. Localization of a susceptibility locus for hepatocellular carcinoma to chromosome 4q in a hepatitis B hyperendemic area.
    Shih WL, Yu MW, Chen PJ, Yeh SH, Lo MT, Chang HC, Liaw YF, Lin SM, Liu CJ, Lee SD, Lin CL, Hsiao CK, Yang SY, Chen CJ.
    Oncogene; 2006 May 25; 25(22):3219-24. PubMed ID: 16407824
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  • 15. Genome scan linkage analysis comparing microsatellites and single-nucleotide polymorphisms markers for two measures of alcoholism in chromosomes 1, 4, and 7.
    Chen G, Adeyemo A, Zhou J, Yuan A, Chen Y, Rotimi C.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S4. PubMed ID: 16451650
    [Abstract] [Full Text] [Related]

  • 16. Microsatellite linkage analysis, single-nucleotide polymorphisms, and haplotype associations with ECB21 in the COGA data.
    Kraja AT, Borecki IB, Province MA.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S94. PubMed ID: 16451710
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  • 17. A genome-wide scan maps a novel high myopia locus to 5p15.
    Lam CY, Tam PO, Fan DS, Fan BJ, Wang DY, Lee CW, Pang CP, Lam DS.
    Invest Ophthalmol Vis Sci; 2008 Sep 30; 49(9):3768-78. PubMed ID: 18421076
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  • 18. Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort.
    Amundsen SS, Rundberg J, Adamovic S, Gudjónsdóttir AH, Ascher H, Ek J, Nilsson S, Lie BA, Naluai AT, Sollid LM.
    Genes Immun; 2010 Jan 30; 11(1):79-86. PubMed ID: 19693089
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  • 20. Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia.
    Sillén A, Brohede J, Lilius L, Forsell C, Andrade J, Odeberg J, Ebise H, Winblad B, Graff C.
    J Hum Genet; 2010 Oct 30; 55(10):649-55. PubMed ID: 20596041
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