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Journal Abstract Search

225 related items for PubMed ID: 8696345

  • 1. A full genome search in multiple sclerosis.
    Ebers GC, Kukay K, Bulman DE, Sadovnick AD, Rice G, Anderson C, Armstrong H, Cousin K, Bell RB, Hader W, Paty DW, Hashimoto S, Oger J, Duquette P, Warren S, Gray T, O'Connor P, Nath A, Auty A, Metz L, Francis G, Paulseth JE, Murray TJ, Pryse-Phillips W, Nelson R, Freedman M, Brunet D, Bouchard JP, Hinds D, Risch N.
    Nat Genet; 1996 Aug; 13(4):472-6. PubMed ID: 8696345
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  • 3. An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group.
    Dyment DA, Sadovnick AD, Willer CJ, Armstrong H, Cader ZM, Wiltshire S, Kalman B, Risch N, Ebers GC, Canadian Collaborative Study Group.
    Hum Mol Genet; 2004 May 15; 13(10):1005-15. PubMed ID: 15069025
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  • 7. Genetic studies in familial ankylosing spondylitis susceptibility.
    Zhang G, Luo J, Bruckel J, Weisman MA, Schumacher HR, Khan MA, Inman RD, Mahowald M, Maksymowych WP, Martin TM, Yu DT, Stone M, Rosenbaum JT, Newman P, Lee J, McClain JA, West OC, Jin L, Reveille JD.
    Arthritis Rheum; 2004 Jul 15; 50(7):2246-54. PubMed ID: 15248224
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  • 8. Fine mapping of the multiple sclerosis susceptibility locus on 5p14-p12.
    Riise Stensland HM, Saarela J, Bronnikov DO, Parkkonen M, Jokiaho AJ, Palotie A, Tienari PJ, Sumelahti ML, Elovaara I, Koivisto K, Pirttilä T, Reunanen M, Sobel E, Peltonen L.
    J Neuroimmunol; 2005 Dec 30; 170(1-2):122-33. PubMed ID: 16169605
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  • 10. Linkage analysis of a candidate region in Scandinavian sib pairs with multiple sclerosis reveals linkage to chromosome 17q.
    Larsen F, Oturai A, Ryder LP, Madsen HO, Hillert J, Fredrikson S, Sandberg-Wollheim M, Laaksonen M, Harbo HF, Sawcer S, Fugger L, Sorensen PS, Svejgaard A.
    Genes Immun; 2000 Oct 30; 1(7):456-9. PubMed ID: 11196677
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  • 11. 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 30; 4(8):559-63. PubMed ID: 14647195
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  • 15. A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.
    Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen-White KR, Rosso A, Donald JA, Adams LJ, Schofield PR.
    Mol Psychiatry; 2002 Dec 30; 7(8):851-9. PubMed ID: 12232778
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  • 16. [HLA and familial multiple sclerosis].
    Barroche G, Perrier P, Raffoux C, Gehin P, Streiff F, Weber M.
    Rev Neurol (Paris); 1986 Dec 30; 142(10):738-45. PubMed ID: 3823705
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  • 17. Association and linkage analysis of candidate chromosomal regions in multiple sclerosis: indication of disease genes in 12q23 and 7ptr-15.
    Xu C, Dai Y, Fredrikson S, Hillert J.
    Eur J Hum Genet; 1999 Dec 30; 7(2):110-6. PubMed ID: 10196692
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  • 19. Multiple sclerosis.
    Compston A, Kellar-Wood H, Wood N.
    Baillieres Clin Neurol; 1994 Aug 30; 3(2):353-71. PubMed ID: 7952852
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