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Journal Abstract Search

158 related items for PubMed ID: 20568256

  • 21. Accurate power approximations for chi2-tests in case-control association studies of complex disease genes.
    Jackson MR, Genin E, Knapp M, Escary JL.
    Ann Hum Genet; 2002 Jul; 66(Pt 4):307-21. PubMed ID: 12418971
    [Abstract] [Full Text] [Related]

  • 22. Linkage analysis of a complex disease through use of admixed populations.
    Zhu X, Cooper RS, Elston RC.
    Am J Hum Genet; 2004 Jun; 74(6):1136-53. PubMed ID: 15131754
    [Abstract] [Full Text] [Related]

  • 23. Genetic association mapping under founder heterogeneity via weighted haplotype similarity analysis in candidate genes.
    Yu K, Gu CC, Province M, Xiong CJ, Rao DC.
    Genet Epidemiol; 2004 Nov; 27(3):182-91. PubMed ID: 15389925
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  • 24. 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; 69(Pt 5):577-89. PubMed ID: 16138916
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  • 25. Sporadic, Global Linkage Disequilibrium Between Unlinked Segregating Sites.
    Skelly DA, Magwene PM, Stone EA.
    Genetics; 2016 Feb; 202(2):427-37. PubMed ID: 26715671
    [Abstract] [Full Text] [Related]

  • 26. The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests.
    Liu W, Zhao W, Chase GA.
    Hum Hered; 2006 Feb; 61(1):31-44. PubMed ID: 16557026
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  • 28. The expected power of genome-wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low-frequency disease variant.
    Ohashi J, Tokunaga K.
    Ann Hum Genet; 2002 Jul; 66(Pt 4):297-306. PubMed ID: 12418970
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  • 32. A systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure.
    Yang Y, Li SS, Chien JW, Andriesen J, Zhao LP.
    BMC Genet; 2008 Dec 22; 9():90. PubMed ID: 19102730
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  • 35. The single-nucleotide polymorphism lottery: how useful are a few common SNPs in identifying disease-associated alleles?
    Barton A, Chapman P, Myerscough A, Pinel T, Davies N, Worthington J, John S.
    Genet Epidemiol; 2001 Dec 22; 21 Suppl 1():S384-9. PubMed ID: 11793704
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  • 37. Where is the causal variant? On the advantage of the family design over the case-control design in genetic association studies.
    Dandine-Roulland C, Perdry H.
    Eur J Hum Genet; 2015 Oct 22; 23(10):1357-63. PubMed ID: 25585700
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  • 39. A statistical method for identification of polymorphisms that explain a linkage result.
    Sun L, Cox NJ, McPeek MS.
    Am J Hum Genet; 2002 Feb 22; 70(2):399-411. PubMed ID: 11791210
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