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Journal Abstract Search

231 related items for PubMed ID: 9759477

  • 1. Hidden linkage: a comparison of the affected sib pair (ASP) test and transmission/disequilibrium test (TDT).
    McGinnis RE.
    Ann Hum Genet; 1998 Mar; 62(Pt 2):159-79. PubMed ID: 9759477
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  • 3. Informative-transmission disequilibrium test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring.
    Guo CY, Lunetta KL, DeStefano AL, Ordovas JM, Cupples LA.
    Genet Epidemiol; 2007 Feb; 31(2):115-33. PubMed ID: 17123304
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  • 9. Affected sib pair identity by state analyses.
    Thomson G, Motro U.
    Genet Epidemiol; 1994 Feb; 11(4):353-64. PubMed ID: 7813897
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  • 10. Transmission disequilibrium test with discordant sib pairs when parents are available.
    Deng HW, Chen WM, Recker RR.
    Hum Genet; 2002 May; 110(5):451-61. PubMed ID: 12073016
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  • 11. The Sib TDT adjusted for age of disease onset.
    Ghosh S, Reich T.
    Ann Hum Genet; 2004 May; 68(Pt 3):249-56. PubMed ID: 15180705
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  • 12. Linkage detection adaptive to linkage disequilibrium: the disequilibrium maximum-likelihood-binomial test for affected-sibship data.
    Huang J, Jiang Y.
    Am J Hum Genet; 1999 Dec; 65(6):1741-59. PubMed ID: 10577929
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  • 13. Affected-sib-pair test for linkage based on constraints for identical-by-descent distributions corresponding to disease models with imprinting.
    Knapp M, Strauch K.
    Genet Epidemiol; 2004 May; 26(4):273-85. PubMed ID: 15095387
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  • 14. Evaluating linkage and linkage disequilibrium: use of excess sharing and transmission disequilibrium methods in affected sib pairs.
    Wicks J, Wilson SR.
    Ann Hum Genet; 2000 Sep; 64(Pt 5):419-32. PubMed ID: 11281280
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  • 18. Transmission/disequilibrium tests for quantitative traits.
    Zhu X, Elston RC.
    Genet Epidemiol; 2001 Jan; 20(1):57-74. PubMed ID: 11119297
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  • 19. Linkage and association studies of QTL for nuclear families by mixed models.
    Fan R, Xiong M.
    Biostatistics; 2003 Jan; 4(1):75-95. PubMed ID: 12925331
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  • 20. A remark on rare variants.
    Oexle K.
    J Hum Genet; 2010 Apr; 55(4):219-26. PubMed ID: 20203695
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