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Journal Abstract Search

756 related items for PubMed ID: 16032531

  • 21. Linkage disequilibrium assessment via log-linear modeling of SNP haplotype frequencies.
    Morris A, Pedder A, Ayres K.
    Genet Epidemiol; 2003 Sep; 25(2):106-14. PubMed ID: 12916019
    [Abstract] [Full Text] [Related]

  • 22. Dynamin-binding protein gene on chromosome 10q is associated with late-onset Alzheimer's disease.
    Kuwano R, Miyashita A, Arai H, Asada T, Imagawa M, Shoji M, Higuchi S, Urakami K, Kakita A, Takahashi H, Tsukie T, Toyabe S, Akazawa K, Kanazawa I, Ihara Y, Japanese Genetic Study Consortium for Alzeheimer's Disease.
    Hum Mol Genet; 2006 Jul 01; 15(13):2170-82. PubMed ID: 16740596
    [Abstract] [Full Text] [Related]

  • 23. Efficiency and power in genetic association studies.
    de Bakker PI, Yelensky R, Pe'er I, Gabriel SB, Daly MJ, Altshuler D.
    Nat Genet; 2005 Nov 01; 37(11):1217-23. PubMed ID: 16244653
    [Abstract] [Full Text] [Related]

  • 24. Testing for association with a case-parents design in the presence of genotyping errors.
    Morris RW, Kaplan NL.
    Genet Epidemiol; 2004 Feb 01; 26(2):142-54. PubMed ID: 14748014
    [Abstract] [Full Text] [Related]

  • 25. 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 01; 69(Pt 1):102-12. PubMed ID: 15638831
    [Abstract] [Full Text] [Related]

  • 26. Quantifying bias due to allele misclassification in case-control studies of haplotypes.
    Govindarajulu US, Spiegelman D, Miller KL, Kraft P.
    Genet Epidemiol; 2006 Nov 01; 30(7):590-601. PubMed ID: 16830341
    [Abstract] [Full Text] [Related]

  • 27. Using tree-based recursive partitioning methods to group haplotypes for increased power in association studies.
    Yu K, Xu J, Rao DC, Province M.
    Ann Hum Genet; 2005 Sep 01; 69(Pt 5):577-89. PubMed ID: 16138916
    [Abstract] [Full Text] [Related]

  • 28. Hidden population substructures in an apparently homogeneous population bias association studies.
    Berger M, Stassen HH, Köhler K, Krane V, Mönks D, Wanner C, Hoffmann K, Hoffmann MM, Zimmer M, Bickeböller H, Lindner TH.
    Eur J Hum Genet; 2006 Feb 01; 14(2):236-44. PubMed ID: 16333311
    [Abstract] [Full Text] [Related]

  • 29. [A related analysis for alpha, beta fibrinogen gene haplotypes and nucleotide polymorphisms associated with the ischemic stroke in Hainan Han population].
    Liang L, Sun C, Liao XP, Xiao F, Chen XD, Huang SX, Tang XL, Wen GQ, Long ZG, Wang XY, Liu GX, Cheng S, Cai WW.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun 01; 23(3):316-9. PubMed ID: 16767673
    [Abstract] [Full Text] [Related]

  • 30. Haplotype block structures show significant variation among populations.
    Liu N, Sawyer SL, Mukherjee N, Pakstis AJ, Kidd JR, Kidd KK, Brookes AJ, Zhao H.
    Genet Epidemiol; 2004 Dec 01; 27(4):385-400. PubMed ID: 15389924
    [Abstract] [Full Text] [Related]

  • 31. [Screening susceptibility genes of type 2 diabetes in Chinese population by single nucleotide polymorphism analysis].
    Li Y, Wu GD, Zuo J, Meng Y, Fang FD.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Jun 01; 27(3):274-9. PubMed ID: 16038259
    [Abstract] [Full Text] [Related]

  • 32. Inference of missing SNPs and information quantity measurements for haplotype blocks.
    Su SC, Kuo CC, Chen T.
    Bioinformatics; 2005 May 01; 21(9):2001-7. PubMed ID: 15699029
    [Abstract] [Full Text] [Related]

  • 33. Testing association between disease and multiple SNPs in a candidate gene.
    Gauderman WJ, Murcray C, Gilliland F, Conti DV.
    Genet Epidemiol; 2007 Jul 01; 31(5):383-95. PubMed ID: 17410554
    [Abstract] [Full Text] [Related]

  • 34. 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]

  • 35. Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.
    Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG.
    Hum Mutat; 2006 Aug 01; 27(8):778-85. PubMed ID: 16835882
    [Abstract] [Full Text] [Related]

  • 36. Fibrinogen genes and myocardial infarction: a haplotype analysis.
    Koch W, Hoppmann P, Biele J, Mueller JC, Schömig A, Kastrati A.
    Arterioscler Thromb Vasc Biol; 2008 Apr 01; 28(4):758-63. PubMed ID: 18202324
    [Abstract] [Full Text] [Related]

  • 37. Susceptibility of biallelic haplotype and genotype frequencies to genotyping error.
    Moskvina V, Schmidt KM.
    Biometrics; 2006 Dec 01; 62(4):1116-23. PubMed ID: 17156286
    [Abstract] [Full Text] [Related]

  • 38. A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations.
    Zhang C, Bailey DK, Awad T, Liu G, Xing G, Cao M, Valmeekam V, Retief J, Matsuzaki H, Taub M, Seielstad M, Kennedy GC.
    Bioinformatics; 2006 Sep 01; 22(17):2122-8. PubMed ID: 16845142
    [Abstract] [Full Text] [Related]

  • 39. Association of ApoE genetic variants with obstructive sleep apnea in children.
    Kalra M, Pal P, Kaushal R, Amin RS, Dolan LM, Fitz K, Kumar S, Sheng X, Guha S, Mallik J, Deka R, Chakraborty R.
    Sleep Med; 2008 Mar 01; 9(3):260-5. PubMed ID: 17658295
    [Abstract] [Full Text] [Related]

  • 40. Detecting susceptibility genes in case-control studies using set association.
    Kim S, Zhang K, Sun F.
    BMC Genet; 2003 Dec 31; 4 Suppl 1(Suppl 1):S9. PubMed ID: 14975077
    [Abstract] [Full Text] [Related]

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