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Journal Abstract Search

197 related items for PubMed ID: 19845895

  • 1. 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; 74(5):408-16. PubMed ID: 19845895
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  • 3. Linkage and association study of FcgammaR polymorphisms in celiac disease.
    Sareneva I, Koskinen LL, Korponay-Szabo IR, Kaukinen K, Kurppa K, Ziberna F, Vatta S, Not T, Ventura A, Adány R, Pocsai Z, Széles G, Mäki M, Saavalainen P, Einarsdottir E.
    Tissue Antigens; 2009 Jan; 73(1):54-8. PubMed ID: 19140833
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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; 15(9):980-7. PubMed ID: 17551518
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  • 6. 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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  • 7. Genome-wide analysis of extended pedigrees confirms IL2-IL21 linkage and shows additional regions of interest potentially influencing coeliac disease risk.
    Einarsdottir E, Koskinen LL, de Kauwe AL, Dukes E, Mustalahti K, Balogh M, Korponay-Szabo IR, Kaukinen K, Kurppa K, Adány R, Pocsai Z, Széles G, Mäki M, Kere J, Saavalainen P.
    Tissue Antigens; 2011 Dec; 78(6):428-37. PubMed ID: 22077623
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  • 8. Genetics of celiac disease.
    Clot F, Babron MC.
    Mol Genet Metab; 2000 Dec; 71(1-2):76-80. PubMed ID: 11001799
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  • 9. Cytokine gene polymorphisms and genetic association with coeliac disease in the Finnish population.
    Woolley N, Mustalahti K, Mäki M, Partanen J.
    Scand J Immunol; 2005 Jan; 61(1):51-6. PubMed ID: 15644122
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  • 11. Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19.
    Tello-Ruiz MK, Curley C, DelMonte T, Giallourakis C, Kirby A, Miller K, Wild G, Cohen A, Langelier D, Latiano A, Wedemeyer N, Lander E, Schreiber S, Annese V, Daly MJ, Rioux JD.
    Eur J Hum Genet; 2006 Jun; 14(6):780-90. PubMed ID: 16570073
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  • 12. Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations.
    Einarsdottir E, Bevova MR, Zhernakova A, Monsuur A, Koskinen LL, van't Slot R, Mulder C, Mearin ML, Korponay-Szabo IR, Kaukinen K, Kurppa K, Kere J, Mäki M, Wijmenga C, Saavalainen P.
    Eur J Hum Genet; 2011 Jun; 19(6):682-6. PubMed ID: 21326284
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  • 15. A genomewide screen in a four-generation Dutch family with celiac disease: evidence for linkage to chromosomes 6 and 9.
    van Belzen MJ, Vrolijk MM, Meijer JW, Crusius JB, Pearson PL, Sandkuijl LA, Houwen RH, Wijmenga C.
    Am J Gastroenterol; 2004 Mar; 99(3):466-71. PubMed ID: 15056087
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  • 16. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.
    Rioux JD, Daly MJ, Silverberg MS, Lindblad K, Steinhart H, Cohen Z, Delmonte T, Kocher K, Miller K, Guschwan S, Kulbokas EJ, O'Leary S, Winchester E, Dewar K, Green T, Stone V, Chow C, Cohen A, Langelier D, Lapointe G, Gaudet D, Faith J, Branco N, Bull SB, McLeod RS, Griffiths AM, Bitton A, Greenberg GR, Lander ES, Siminovitch KA, Hudson TJ.
    Nat Genet; 2001 Oct; 29(2):223-8. PubMed ID: 11586304
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  • 17. Genomewide linkage scan for nicotine dependence: identification of a chromosome 5 risk locus.
    Gelernter J, Panhuysen C, Weiss R, Brady K, Poling J, Krauthammer M, Farrer L, Kranzler HR.
    Biol Psychiatry; 2007 Jan 01; 61(1):119-26. PubMed ID: 17081504
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  • 18. Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association.
    Koskinen LL, Korponay-Szabo IR, Viiri K, Juuti-Uusitalo K, Kaukinen K, Lindfors K, Mustalahti K, Kurppa K, Adány R, Pocsai Z, Széles G, Einarsdottir E, Wijmenga C, Mäki M, Partanen J, Kere J, Saavalainen P.
    J Med Genet; 2008 Apr 01; 45(4):222-7. PubMed ID: 18077767
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  • 19. Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.
    Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG.
    Hum Mutat; 2006 Aug 01; 27(8):778-85. PubMed ID: 16835882
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