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Journal Abstract Search

137 related items for PubMed ID: 16342180

  • 1. Genotyping errors, pedigree errors, and missing data.
    Hinrichs AL, Suarez BK.
    Genet Epidemiol; 2005; 29 Suppl 1():S120-4. PubMed ID: 16342180
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  • 2. Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels.
    Goode EL, Jarvik GP.
    Genet Epidemiol; 2005; 29 Suppl 1():S72-6. PubMed ID: 16342185
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  • 3. Characteristics of replicated single-nucleotide polymorphism genotypes from COGA: Affymetrix and Center for Inherited Disease Research.
    Tintle NL, Ahn K, Mendell NR, Gordon D, Finch SJ.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S154. PubMed ID: 16451615
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  • 7. Estimation of genotype error rate using samples with pedigree information--an application on the GeneChip Mapping 10K array.
    Hao K, Li C, Rosenow C, Hung Wong W.
    Genomics; 2004 Oct 30; 84(4):623-30. PubMed ID: 15475239
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  • 8. Singleton SNPs in the human genome and implications for genome-wide association studies.
    Ke X, Taylor MS, Cardon LR.
    Eur J Hum Genet; 2008 Apr 30; 16(4):506-15. PubMed ID: 18197193
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  • 11. Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference.
    Saunders IW, Brohede J, Hannan GN.
    Genomics; 2007 Sep 30; 90(3):291-6. PubMed ID: 17587543
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  • 12. A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.
    Xiao Y, Segal MR, Yang YH, Yeh RF.
    Bioinformatics; 2007 Jun 15; 23(12):1459-67. PubMed ID: 17459966
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  • 14. Alcoholism and related traits: a summary of Group 13 contributions.
    Rice JP, Saccone SF.
    Genet Epidemiol; 2005 Jun 15; 29 Suppl 1():S96-S102. PubMed ID: 16342188
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  • 15. Bayesian trio models for association in the presence of genotyping errors.
    Bernardinelli L, Berzuini C, Seaman S, Holmans P.
    Genet Epidemiol; 2004 Jan 15; 26(1):70-80. PubMed ID: 14691958
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  • 16. Summary report: Missing data and pedigree and genotyping errors.
    Badzioch MD, Thomas DC, Jarvik GP.
    Genet Epidemiol; 2003 Jan 15; 25 Suppl 1():S36-42. PubMed ID: 14635167
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  • 17. Dissection of heterogeneous phenotypes for quantitative trait mapping.
    Bickeböller H, Bailey JN, Papanicolaou GJ, Rosenberger A, Viel KR.
    Genet Epidemiol; 2005 Jan 15; 29 Suppl 1():S41-7. PubMed ID: 16342183
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  • 18. Detection of genotyping errors by Hardy-Weinberg equilibrium testing.
    Hosking L, Lumsden S, Lewis K, Yeo A, McCarthy L, Bansal A, Riley J, Purvis I, Xu CF.
    Eur J Hum Genet; 2004 May 15; 12(5):395-9. PubMed ID: 14872201
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  • 20. Quantifying the amount of missing information in genetic association studies.
    Nicolae DL.
    Genet Epidemiol; 2006 Dec 15; 30(8):703-17. PubMed ID: 16986163
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