Further evidence for the increased power of LOD scores compared with nonparametric methods.
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[1] S E Hodge,et al. The power to detect linkage in complex disease by means of simple LOD-score analyses. , 1998, American journal of human genetics.
[2] S. Hodge. Exact elods and exact power for affected sib pairs analyzed for linkage under simple right and wrong models. , 1998, American journal of medical genetics.
[3] D. Weeks,et al. Comparison of nonparametric statistics for detection of linkage in nuclear families: single-marker evaluation. , 1997, American journal of human genetics.
[4] K. Kidd. Editorial: Can we find genes for schizophrenia? , 1997 .
[5] S E Hodge,et al. Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study. , 1997, American journal of human genetics.
[6] K. Kidd. Can we find genes for schizophrenia? , 1997, American journal of medical genetics.
[7] L Kruglyak,et al. Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.
[8] M. Babron,et al. Conclusion of LOD-score analysis for family data generated under two-locus models. , 1996, American journal of human genetics.
[9] S E Hodge,et al. Affecteds-only linkage methods are not a panacea. , 1996, American journal of human genetics.
[10] Elliot S. Gershon,et al. Genetic approaches to mental disorders , 1994 .
[11] S A Seuchter,et al. Linkage analysis in nuclear families. 1: Optimality criteria for affected sib-pair tests. , 1994, Human heredity.
[12] S A Seuchter,et al. Linkage analysis in nuclear families. 2: Relationship between affected sib-pair tests and lod score analysis. , 1994, Human heredity.
[13] R C Elston,et al. Lods, wrods, and mods: The interpretation of lod scores calculated under different models , 1994, Genetic epidemiology.
[14] C. Bonaïti‐pellié,et al. Conclusions of segregation analysis for family data generated under two-locus models. , 1993, American journal of human genetics.
[15] V. Vieland,et al. Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures. , 1993, Human heredity.
[16] D. Weeks,et al. Two-locus models of disease: comparison of likelihood and nonparametric linkage methods. , 1993, American journal of human genetics.
[17] S. Hodge,et al. Inter- and intrafamilial heterogeneity: effective sampling strategies and comparison of analysis methods. , 1992, American journal of human genetics.
[18] D. Greenberg,et al. Effect of heterogeneity and assumed mode of inheritance on lod scores. , 1992, American journal of medical genetics.
[19] V. Vieland,et al. Adequacy of single‐locus approximations for linkage analyses of oligogenic traits , 1992, Genetic epidemiology.
[20] D. Rao,et al. Linkage analysis assuming a single‐locus mode of inheritance for traits determined by two loci: Inferring mode of inheritance and estimating penetrance , 1990, Genetic epidemiology.
[21] S. Hodge,et al. Linkage analysis under “random” and “genetic” reduced penetrance , 1989, Genetic epidemiology.
[22] Greenberg Da. The effect of proband designation on segregation analysis. , 1986 .
[23] C. Bonaïti‐pellié,et al. Effects of misspecifying genetic parameters in lod score analysis. , 1986, Biometrics.
[24] D. Greenberg,et al. The effect of proband designation on segregation analysis. , 1986, American journal of human genetics.
[25] Blackwelder Wc,et al. A comparison of sib-pair linkage tests for disease susceptibility loci , 1985 .
[26] R. Elston,et al. A comparison of sib‐pair linkage tests for disease susceptibility loci , 1985, Genetic epidemiology.
[27] J. Ott. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. , 1974, American journal of human genetics.
[28] G. Dahlberg,et al. Genetics of human populations. , 1948, Advances in genetics.