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Journal Abstract Search

103 related items for PubMed ID: 11840196

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  • 3. Genome-wide linkage analysis of 160 North American families with celiac disease.
    Garner CP, Ding YC, Steele L, Book L, Leiferman K, Zone JJ, Neuhausen SL.
    Genes Immun; 2007 Mar; 8(2):108-14. PubMed ID: 17136122
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  • 4. 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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  • 5. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
    Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
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  • 7. Analysis of candidate genes on chromosomes 5q and 19p in celiac disease.
    Latiano A, Mora B, Bonamico M, Megiorni F, Mazzilli MC, Cucchiara S, Palmieri O, Valvano MR, Annese V.
    J Pediatr Gastroenterol Nutr; 2007 Aug; 45(2):180-6. PubMed ID: 17667713
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  • 8. 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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  • 9. Suggestive genetic linkage to chromosome 11p11.2-q12.2 in hereditary prostate cancer families with primary kidney cancer.
    Johanneson B, Deutsch K, McIntosh L, Friedrichsen-Karyadi DM, Janer M, Kwon EM, Iwasaki L, Hood L, Ostrander EA, Stanford JL.
    Prostate; 2007 May 15; 67(7):732-42. PubMed ID: 17372923
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  • 12. Candidate gene regions and genetic heterogeneity in gluten sensitivity.
    Holopainen P, Mustalahti K, Uimari P, Collin P, Mäki M, Partanen J.
    Gut; 2001 May 15; 48(5):696-701. PubMed ID: 11302971
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  • 13. A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage.
    Thompson SD, Moroldo MB, Guyer L, Ryan M, Tombragel EM, Shear ES, Prahalad S, Sudman M, Keddache MA, Brown WM, Giannini EH, Langefeld CD, Rich SS, Nichols WC, Glass DN.
    Arthritis Rheum; 2004 Sep 15; 50(9):2920-30. PubMed ID: 15457461
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  • 16. Identification of susceptibility loci for cervical carcinoma by genome scan of affected sib-pairs.
    Engelmark MT, Ivansson EL, Magnusson JJ, Gustavsson IM, Beskow AH, Magnusson PK, Gyllensten UB.
    Hum Mol Genet; 2006 Nov 15; 15(22):3351-60. PubMed ID: 17035246
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  • 17. Evidence for multiple loci from a genome scan of autism kindreds.
    Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM.
    Mol Psychiatry; 2006 Nov 15; 11(11):1049-60, 979. PubMed ID: 16880825
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  • 18. Analysis of HLA and non-HLA alleles can identify individuals at high risk for celiac disease.
    Romanos J, van Diemen CC, Nolte IM, Trynka G, Zhernakova A, Fu J, Bardella MT, Barisani D, McManus R, van Heel DA, Wijmenga C.
    Gastroenterology; 2009 Sep 15; 137(3):834-40, 840.e1-3. PubMed ID: 19454285
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  • 19. 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; 15(9):980-7. PubMed ID: 17551518
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  • 20. A pedigree-based linkage study of coeliac disease: failure to replicate previous positive findings.
    Brett PM, Yiannakou JY, Morris MA, Bronson SR, Mathew C, Curtis D, Ciclitira PJ.
    Ann Hum Genet; 1998 Jan 15; 62(Pt 1):25-32. PubMed ID: 9659975
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