BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 10323184)

  • 1. Exploring the dense mapping of a region of potential linkage in complex disease: an example in multiple sclerosis.
    Feakes R; Sawcer S; Chataway J; Coraddu F; Broadley S; Gray J; Jones HB; Clayton D; Goodfellow PN; Compston A
    Genet Epidemiol; 1999; 17(1):51-63. PubMed ID: 10323184
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage and association analysis of susceptibility regions on chromosomes 5 and 6 in 106 Scandinavian sibling pair families with multiple sclerosis.
    Oturai A; Larsen F; Ryder LP; Madsen HO; Hillert J; Fredrikson S; Sandberg-Wollheim M; Laaksonen M; Koch-Henriksen N; Sawcer S; Fugger L; Sorensen PS; Svejgaard A
    Ann Neurol; 1999 Oct; 46(4):612-6. PubMed ID: 10514098
    [TBL] [Abstract][Full Text] [Related]  

  • 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;
    Hum Mol Genet; 2004 May; 13(10):1005-15. PubMed ID: 15069025
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 170(1-2):122-33. PubMed ID: 16169605
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A genome screen for linkage in Australian sibling-pairs with multiple sclerosis.
    Ban M; Stewart GJ; Bennetts BH; Heard R; Simmons R; Maranian M; Compston A; Sawcer SJ
    Genes Immun; 2002 Dec; 3(8):464-9. PubMed ID: 12486604
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 4(8):559-63. PubMed ID: 14647195
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 1(7):456-9. PubMed ID: 11196677
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.
    Zeiger JS; Hetmanski JB; Beaty TH; VanderKolk CA; Wyszynski DF; Bailey-Wilson JE; de Luna RO; Perandones C; Tolarova MM; Mosby T; Bennun R; Segovia M; Calda P; Pugh EW; Doheny K; McIntosh I
    Eur J Hum Genet; 2003 Nov; 11(11):835-9. PubMed ID: 14571267
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dense genome-wide linkage analysis of rheumatoid arthritis, including covariates.
    Osorio Y Fortéa J; Bukulmez H; Petit-Teixeira E; Michou L; Pierlot C; Cailleau-Moindrault S; Lemaire I; Lasbleiz S; Alibert O; Quillet P; Bardin T; Prum B; Olson JM; Cornélis F
    Arthritis Rheum; 2004 Sep; 50(9):2757-65. PubMed ID: 15457443
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families.
    Swinburne JE; Boursnell M; Hill G; Pettitt L; Allen T; Chowdhary B; Hasegawa T; Kurosawa M; Leeb T; Mashima S; Mickelson JR; Raudsepp T; Tozaki T; Binns M
    Genomics; 2006 Jan; 87(1):1-29. PubMed ID: 16314071
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Finer linkage mapping of a primary hip osteoarthritis susceptibility locus on chromosome 6.
    Loughlin J; Mustafa Z; Dowling B; Southam L; Marcelline L; Räinä SS; Ala-Kokko L; Chapman K
    Eur J Hum Genet; 2002 Sep; 10(9):562-8. PubMed ID: 12173034
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification by denaturing high-performance liquid chromatography of numerous polymorphisms in a candidate region for multiple sclerosis susceptibility.
    Giordano M; Oefner PJ; Underhill PA; Cavalli Sforza LL; Tosi R; Richiardi PM
    Genomics; 1999 Mar; 56(3):247-53. PubMed ID: 10087191
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Finer linkage mapping of primary hip osteoarthritis susceptibility on chromosome 11q in a cohort of affected female sibling pairs.
    Chapman K; Mustafa Z; Dowling B; Southam L; Carr A; Loughlin J
    Arthritis Rheum; 2002 Jul; 46(7):1780-3. PubMed ID: 12124861
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage analysis in multiple sclerosis of chromosomal regions syntenic to experimental autoimmune disease loci.
    Xu C; Dai Y; Lorentzen JC; Dahlman I; Olsson T; Hillert J
    Eur J Hum Genet; 2001 Jun; 9(6):458-63. PubMed ID: 11436128
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Linkage and allelic association of chromosome 5 cytokine cluster genetic markers with atopy and asthma associated traits.
    Walley AJ; Wiltshire S; Ellis CM; Cookson WO
    Genomics; 2001 Feb; 72(1):15-20. PubMed ID: 11247662
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.
    Haines JL; Ter-Minassian M; Bazyk A; Gusella JF; Kim DJ; Terwedow H; Pericak-Vance MA; Rimmler JB; Haynes CS; Roses AD; Lee A; Shaner B; Menold M; Seboun E; Fitoussi RP; Gartioux C; Reyes C; Ribierre F; Gyapay G; Weissenbach J; Hauser SL; Goodkin DE; Lincoln R; Usuku K; Oksenberg JR
    Nat Genet; 1996 Aug; 13(4):469-71. PubMed ID: 8696344
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
    Salmon B; Hallmayer J; Rogers T; Kalaydjieva L; Petersen PB; Nicholas P; Pingree C; McMahon W; Spiker D; Lotspeich L; Kraemer H; McCague P; Dimiceli S; Nouri N; Pitts T; Yang J; Hinds D; Myers RM; Risch N
    Am J Med Genet; 1999 Oct; 88(5):551-6. PubMed ID: 10490715
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genome screen for linkage disequilibrium in HLA-DRB1*15-positive Germans with multiple sclerosis based on 4666 microsatellite markers.
    Goedde R; Sawcer S; Boehringer S; Miterski B; Sindern E; Haupts M; Schimrigk S; Compston A; Epplen JT
    Hum Genet; 2002 Sep; 111(3):270-7. PubMed ID: 12215840
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23.
    Cantor RM; Yuan J; Napier S; Kono N; Grossman JM; Hahn BH; Tsao BP
    Arthritis Rheum; 2004 Oct; 50(10):3203-10. PubMed ID: 15476245
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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(9):1433-41. PubMed ID: 16520807
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.