These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

242 related items for PubMed ID: 15069025

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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 15; 3(8):464-9. PubMed ID: 12486604
    [Abstract] [Full Text] [Related]

  • 3. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.
    Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, Green E, O'Mahony E, Nikolov I, Mulcahy T, Haque S, Bort S, Bennett P, Norton N, Owen MJ, Kirov G, Lendon C, Jones L, Jones I, Holmans P, Gill M, Craddock N.
    Mol Psychiatry; 2005 Sep 15; 10(9):831-41. PubMed ID: 15940300
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 46(4):612-6. PubMed ID: 10514098
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 4(8):559-63. PubMed ID: 14647195
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 13(4):472-6. PubMed ID: 8696345
    [Abstract] [Full Text] [Related]

  • 7. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
    Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.
    Arch Neurol; 2006 Nov 15; 63(11):1591-8. PubMed ID: 17101828
    [Abstract] [Full Text] [Related]

  • 8. Follow-up investigation of 12 proposed linkage regions in multiple sclerosis.
    Herrera BM, Cader MZ, Dyment DA, Bell JT, Ramagopalan SV, Lincoln MR, Orton S, Chao MJ, Sadovnick AD, Ebers GC.
    Genes Immun; 2006 Jul 15; 7(5):366-71. PubMed ID: 16738670
    [Abstract] [Full Text] [Related]

  • 9. Genetic susceptibility to MS: a second stage analysis in Canadian MS families.
    Dyment DA, Willer CJ, Scott B, Armstrong H, Ligers A, Hillert J, Paty DW, Hashimoto S, Devonshire V, Hooge J, Kastrukoff L, Oger J, Metz L, Warren S, Hader W, Power C, Auty A, Nath A, Nelson R, Freedman M, Brunet D, Paulseth JE, Rice G, O'Connor P, Duquette P, Lapierre Y, Francis G, Bouchard JP, Murray TJ, Bhan V, Maxner C, Pryse-Phillips W, Stefanelli M, Sadovnick AD, Risch N, Ebers GC.
    Neurogenetics; 2001 Jul 15; 3(3):145-51. PubMed ID: 11523565
    [Abstract] [Full Text] [Related]

  • 10. Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q.
    Chiu YF, McGrath JA, Thornquist MH, Wolyniec PS, Nestadt G, Swartz KL, Lasseter VK, Liang KY, Pulver AE.
    Mol Psychiatry; 2002 Jul 15; 7(6):658-64. PubMed ID: 12140791
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. 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 Jul 15; 17(1):51-63. PubMed ID: 10323184
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 12(4):376-84. PubMed ID: 17179998
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.