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PUBMED FOR HANDHELDS

Journal Abstract Search


170 related items for PubMed ID: 16451697

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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. Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.
    Boyles AL, Scott WK, Martin ER, Schmidt S, Li YJ, Ashley-Koch A, Bass MP, Schmidt M, Pericak-Vance MA, Speer MC, Hauser ER.
    Hum Hered; 2005; 59(4):220-7. PubMed ID: 16093727
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  • 4. Handling linkage disequilibrium in qualitative trait linkage analysis using dense SNPs: a two-step strategy.
    Cho K, Dupuis J.
    BMC Genet; 2009 Aug 10; 10():44. PubMed ID: 19664279
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  • 6. Evaluation of linkage disequilibrium and its effect on non-parametric multipoint linkage analysis using two high density single-nucleotide polymorphism mapping panels.
    Murray SS.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S85. PubMed ID: 16451700
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  • 9. Comparison of the power between microsatellite and single-nucleotide polymorphism markers for linkage and linkage disequilibrium mapping of an electrophysiological phenotype.
    Lin HF, Juo SH, Cheng R.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S7. PubMed ID: 16451683
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  • 14. SNPLINK: multipoint linkage analysis of densely distributed SNP data incorporating automated linkage disequilibrium removal.
    Webb EL, Sellick GS, Houlston RS.
    Bioinformatics; 2005 Jul 01; 21(13):3060-1. PubMed ID: 15840706
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  • 15. Examining the effect of linkage disequilibrium between markers on the Type I error rate and power of nonparametric multipoint linkage analysis of two-generation and multigenerational pedigrees in the presence of missing genotype data.
    Kim Y, Duggal P, Gillanders EM, Kim H, Bailey-Wilson JE.
    Genet Epidemiol; 2008 Jan 01; 32(1):41-51. PubMed ID: 17685456
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  • 16. Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease.
    Sieh W, Yu CE, Bird TD, Schellenberg GD, Wijsman EM.
    Hum Hered; 2007 Jan 01; 63(1):26-34. PubMed ID: 17215579
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  • 17. Simulation studies of detection of a complex disease in a partially isolated population.
    Levinson DF, Kirby A, Slepner S, Nolte I, Spijker GT, te Meerman G.
    Am J Med Genet; 2001 Jan 08; 105(1):65-70. PubMed ID: 11425003
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  • 20. Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits.
    Klein AP, Tsai YY, Duggal P, Gillanders EM, Barnhart M, Mathias RA, Dusenberry IP, Turiff A, Chines PS, Goldstein J, Wojciechowski R, Hening W, Pugh EW, Bailey-Wilson JE.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S20. PubMed ID: 16451629
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