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    Results: 1 to 20 of 104

    4.

    Haplotype-based quantitative trait mapping using a clustering algorithm.

    Li J, Zhou Y, Elston RC.

    BMC Bioinformatics. 2006 May 18;7:258.

    PMID:
    16709248
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    5.

    Role of STAT4 polymorphisms in systemic lupus erythematosus in a Japanese population: a case-control association study of the STAT1-STAT4 region.

    Kawasaki A, Ito I, Hikami K, Ohashi J, Hayashi T, Goto D, Matsumoto I, Ito S, Tsutsumi A, Koga M, Arinami T, Graham RR, Hom G, Takasaki Y, Hashimoto H, Behrens TW, Sumida T, Tsuchiya N.

    Arthritis Res Ther. 2008;10(5):R113. Epub 2008 Sep 19.

    PMID:
    18803832
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    7.

    Fast and robust association tests for untyped SNPs in case-control studies.

    Allen AS, Satten GA, Bray SL, Dudbridge F, Epstein MP.

    Hum Hered. 2010;70(3):167-76. Epub 2010 Jul 30.

    PMID:
    20689309
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    An evaluation of the performance of HapMap SNP data in a Shanghai Chinese population: analyses of allele frequency, linkage disequilibrium pattern and tagging SNPs transferability on chromosome 1q21-q25.

    Hu C, Jia W, Zhang W, Wang C, Zhang R, Wang J, Ma X; International Type 2 Diabetes 1q Consortium, Xiang K.

    BMC Genet. 2008 Feb 27;9:19.

    PMID:
    18302794
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    9.

    Combining an evolution-guided clustering algorithm and haplotype-based LRT in family association studies.

    Lee MH, Tzeng JY, Huang SY, Hsiao CK.

    BMC Genet. 2011 May 19;12:48.

    PMID:
    21592403
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    10.

    Parallel and serial computing tools for testing single-locus and epistatic SNP effects of quantitative traits in genome-wide association studies.

    Ma L, Runesha HB, Dvorkin D, Garbe JR, Da Y.

    BMC Bioinformatics. 2008 Jul 21;9:315.

    PMID:
    18644146
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    11.

    A haplotype inference algorithm for trios based on deterministic sampling.

    Iliadis A, Watkinson J, Anastassiou D, Wang X.

    BMC Genet. 2010 Aug 23;11:78.

    PMID:
    20727218
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    12.

    Performance of single nucleotide polymorphisms versus haplotypes for genome-wide association analysis in barley.

    Lorenz AJ, Hamblin MT, Jannink JL.

    PLoS One. 2010 Nov 22;5(11):e14079.

    PMID:
    21124933
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    13.

    Making a haplotype catalog with estimated frequencies based on SNP homozygotes.

    Yamaguchi-Kabata Y, Tsunoda T, Takahashi A, Hosono N, Kubo M, Nakamura Y, Kamatani N.

    J Hum Genet. 2010 Aug;55(8):500-6. Epub 2010 May 20.

    PMID:
    20485442
    [PubMed - indexed for MEDLINE]
    14.

    Robust relationship inference in genome-wide association studies.

    Manichaikul A, Mychaleckyj JC, Rich SS, Daly K, Sale M, Chen WM.

    Bioinformatics. 2010 Nov 15;26(22):2867-73. Epub 2010 Oct 5.

    PMID:
    20926424
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    15.

    Prediction of disease-associated single nucleotide polymorphisms using virtual genomes constructed from a public haplotype database.

    Toyabe S, Miyashita A, Kitamura N, Kuwano R, Akazawa K.

    Methods Inf Med. 2008;47(6):522-8.

    PMID:
    19057809
    [PubMed - indexed for MEDLINE]
    16.

    Whole genome association mapping by incompatibilities and local perfect phylogenies.

    Mailund T, Besenbacher S, Schierup MH.

    BMC Bioinformatics. 2006 Oct 16;7:454.

    PMID:
    17042942
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    17.

    SNPassoc: an R package to perform whole genome association studies.

    González JR, Armengol L, Solé X, Guinó E, Mercader JM, Estivill X, Moreno V.

    Bioinformatics. 2007 Mar 1;23(5):644-5. Epub 2007 Jan 31.

    PMID:
    17267436
    [PubMed - indexed for MEDLINE]
    Free Article
    18.
    19.

    A novel haplotype-sharing approach for genome-wide case-control association studies implicates the calpastatin gene in Parkinson's disease.

    Allen AS, Satten GA.

    Genet Epidemiol. 2009 Dec;33(8):657-67.

    PMID:
    19365859
    [PubMed - indexed for MEDLINE]
    20.

    Accounting for haplotype uncertainty in matched association studies: a comparison of simple and flexible techniques.

    Kraft P, Cox DG, Paynter RA, Hunter D, De Vivo I.

    Genet Epidemiol. 2005 Apr;28(3):261-72.

    PMID:
    15637718
    [PubMed - indexed for MEDLINE]

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