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Journal Abstract Search

247 related items for PubMed ID: 18208878

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  • 2. Genetic variants of Complex I in multiple sclerosis.
    Vyshkina T, Banisor I, Shugart YY, Leist TP, Kalman B.
    J Neurol Sci; 2005 Jan 15; 228(1):55-64. PubMed ID: 15607211
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  • 3. Analyses of a MS-associated haplotype encompassing the CCL3 gene.
    Vyshkina T, Kalman B.
    J Neuroimmunol; 2006 Jul 15; 176(1-2):216-8. PubMed ID: 16712957
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  • 5. Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium.
    Chao MJ, Barnardo MC, Lui GZ, Lincoln MR, Ramagopalan SV, Herrera BM, Dyment DA, Sadovnick AD, Ebers GC.
    Hum Mol Genet; 2007 Aug 15; 16(16):1951-8. PubMed ID: 17584771
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  • 6. Risk alleles for multiple sclerosis in multiplex families.
    D'Netto MJ, Ward H, Morrison KM, Ramagopalan SV, Dyment DA, DeLuca GC, Handunnetthi L, Sadovnick AD, Ebers GC.
    Neurology; 2009 Jun 09; 72(23):1984-8. PubMed ID: 19506219
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  • 7. Association of haplotypes in the beta-chemokine locus with multiple sclerosis.
    Vyshkina T, Shugart YY, Birnbaum G, Leist TP, Kalman B.
    Eur J Hum Genet; 2005 Feb 09; 13(2):240-7. PubMed ID: 15494740
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  • 8. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping.
    Maniatis N, Collins A, Morton NE.
    Genet Epidemiol; 2007 Apr 09; 31(3):179-88. PubMed ID: 17285621
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  • 9. Genes on bovine chromosome 18 associated with bilateral convergent strabismus with exophthalmos in German Brown cattle.
    Fink S, Mömke S, Wöhlke A, Distl O.
    Mol Vis; 2008 Sep 22; 14():1737-51. PubMed ID: 18836565
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  • 10. Association of familial and sporadic rheumatoid arthritis with a single corticotropin-releasing hormone genomic region (8q12.3) haplotype.
    Fife M, Steer S, Fisher S, Newton J, McKay K, Worthington J, Shah C, Polley A, Rosenthal A, Ollier W, Lewis C, Wordsworth P, Lanchbury J.
    Arthritis Rheum; 2002 Jan 22; 46(1):75-82. PubMed ID: 11817611
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  • 13. Analysis of C1q polymorphisms suggests association with systemic lupus erythematosus, serum C1q and CH50 levels and disease severity.
    Martens HA, Zuurman MW, de Lange AH, Nolte IM, van der Steege G, Navis GJ, Kallenberg CG, Seelen MA, Bijl M.
    Ann Rheum Dis; 2009 May 22; 68(5):715-20. PubMed ID: 18504288
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  • 14. CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians.
    Gragnoli C.
    J Cell Physiol; 2008 Nov 22; 217(2):291-5. PubMed ID: 18680108
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  • 15. On the advantage of haplotype analysis in the presence of multiple disease susceptibility alleles.
    Morris RW, Kaplan NL.
    Genet Epidemiol; 2002 Oct 22; 23(3):221-33. PubMed ID: 12384975
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  • 17. Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14q.
    Giedraitis V, Modin H, Callander M, Landtblom AM, Fossdal R, Stefansson K, Hillert J, Gulcher J.
    Genes Immun; 2003 Dec 22; 4(8):559-63. PubMed ID: 14647195
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