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

294 related items for PubMed ID: 15638831

  • 1. Fine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs.
    Cheng R, Ma JZ, Elston RC, Li MD.
    Ann Hum Genet; 2005 Jan; 69(Pt 1):102-12. PubMed ID: 15638831
    [Abstract] [Full Text] [Related]

  • 2. HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination.
    Zhang K, Sun F, Zhao H.
    Bioinformatics; 2005 Jan 01; 21(1):90-103. PubMed ID: 15231536
    [Abstract] [Full Text] [Related]

  • 3. Nonparametric disequilibrium mapping of functional sites using haplotypes of multiple tightly linked single-nucleotide polymorphism markers.
    Cheng R, Ma JZ, Wright FA, Lin S, Gao X, Wang D, Elston RC, Li MD.
    Genetics; 2003 Jul 01; 164(3):1175-87. PubMed ID: 12871923
    [Abstract] [Full Text] [Related]

  • 4. A novel method to express SNP-based genetic heterogeneity, Psi, and its use to measure linkage disequilibrium for multiple SNPs, D(g), and to estimate absolute maximum of haplotype frequency.
    Yamada R, Matsuda F.
    Genet Epidemiol; 2007 Nov 01; 31(7):709-26. PubMed ID: 17508358
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Estimating haplotype frequencies and standard errors for multiple single nucleotide polymorphisms.
    Li SS, Khalid N, Carlson C, Zhao LP.
    Biostatistics; 2003 Oct 01; 4(4):513-22. PubMed ID: 14557108
    [Abstract] [Full Text] [Related]

  • 7. Genome-wide selection of tag SNPs using multiple-marker correlation.
    Hao K.
    Bioinformatics; 2007 Dec 01; 23(23):3178-84. PubMed ID: 18006555
    [Abstract] [Full Text] [Related]

  • 8. Tag SNP selection for association studies.
    Stram DO.
    Genet Epidemiol; 2004 Dec 01; 27(4):365-74. PubMed ID: 15372618
    [Abstract] [Full Text] [Related]

  • 9. 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 01; 31(3):179-88. PubMed ID: 17285621
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information.
    Rohde K, Fuerst R.
    Hum Mutat; 2001 Apr 01; 17(4):289-95. PubMed ID: 11295827
    [Abstract] [Full Text] [Related]

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

  • 13. Maximum-likelihood estimation of haplotype frequencies in nuclear families.
    Becker T, Knapp M.
    Genet Epidemiol; 2004 Jul 01; 27(1):21-32. PubMed ID: 15185400
    [Abstract] [Full Text] [Related]

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

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Imputation methods to improve inference in SNP association studies.
    Dai JY, Ruczinski I, LeBlanc M, Kooperberg C.
    Genet Epidemiol; 2006 Dec 01; 30(8):690-702. PubMed ID: 16986162
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels.
    Goode EL, Jarvik GP.
    Genet Epidemiol; 2005 Dec 01; 29 Suppl 1():S72-6. PubMed ID: 16342185
    [Abstract] [Full Text] [Related]

  • 20. On the use of DNA pooling to estimate haplotype frequencies.
    Wang S, Kidd KK, Zhao H.
    Genet Epidemiol; 2003 Jan 01; 24(1):74-82. PubMed ID: 12508258
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.