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A Log-Linear Approach to Case-Parent–Triad Data: Assessing Effects of Disease Genes That Act Either Directly or through Maternal Effects and That May Be Subject to Parental Imprinting

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TLDR
A log-linear method for analysis of case-parent-triad data, based on maximum likelihood with stratification on parental mating type, which generalizes easily to accommodate maternal effects on risk and produces powerful and orthogonal tests of the contribution of fetal versus maternal genetic factors.
Abstract
We describe a log-linear method for analysis of case-parent-triad data, based on maximum likelihood with stratification on parental mating type. The method leads to estimates of association parameters, such as relative risks, for a single allele, and also to likelihood ratio chi2 tests (LRTs) of linkage disequilibrium. Hardy-Weinberg equilibrium need not be assumed. Our simulations suggest that the LRT has power similar to that of the chi2 "score" test proposed by Schaid and Sommer and that both can outperform the transmission/disequilibrium test (TDT), although the TDT can perform better under an additive model of inheritance. Because a restricted version of the LRT is asymptotically equivalent to the TDT, the proposed test can be regarded as a generalization of the TDT. The method that we describe generalizes easily to accommodate maternal effects on risk and, in fact, produces powerful and orthogonal tests of the contribution of fetal versus maternal genetic factors. We further generalize the model to allow for effects of parental imprinting. Imprinting effects can be fitted by a simple, iterative procedure that relies on the expectation-maximization algorithm and that uses standard statistical software for the maximization steps. Simulations reveal that LRT tests for detection of imprinting have very good operating characteristics. When a single allele is under study, the proposed method can yield powerful tests for detection of linkage disequilibrium and is applicable to a broader array of causal scenarios than is the TDT.

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Journal ArticleDOI

A general test of association for quantitative traits in nuclear families.

TL;DR: A general approach that can accommodate nuclear families of any size, with or without parental information, is constructed, and it is shown that, when siblings are available, the total number of genotypes required in order to achieve comparable power is smaller if parents are not genotyped.
Journal ArticleDOI

Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.

Frank Dudbridge
- 31 Mar 2008 - 
TL;DR: A novel likelihood for nuclear families is proposed, in which distinct sets of association parameters are used to model the parental genotypes and the offspring genotypes, which is robust to population structure when the data are complete, and has only minor loss of robustness when there are missing data.
Journal ArticleDOI

Sample Size Requirements for Association Studies of Gene-Gene Interaction

TL;DR: The author investigates sample size requirements for studies of G x G interaction, focusing on four study designs: the matched-case-control design, the case-sibling design,The case-parent design, and the cases-only design, which provide an estimate of interaction on a multiplicative scale.
Journal ArticleDOI

Genetic association studies

TL;DR: The rationale behind and methods of design and analysis of genetic association studies are reviewed, including the need to account for different underlying genetic mechanisms, and the effect of population history.
References
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Journal Article

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

TL;DR: The statistical basis for this "transmission test for linkage disequilibrium" (transmission/disequilibrium test] is described and the relationship of this test to tests of cosegregation that are based on the proportion of haplotypes or genes identical by descent in affected sibs is shown.
Journal Article

The TDT and other family-based tests for linkage disequilibrium and association.

TL;DR: The properties of the TDT are compared with those of family-based tests of association, and issues regarding the use of these tests are commented on.
Journal ArticleDOI

The GLIM System Release 3.

Journal ArticleDOI

Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations

TL;DR: The formulation of a haplotype relative risk (HRR) thus eliminates the problems of sampling from the same homogeneous population to form both the disease sample and an appropriate control in calculating the risk of disease in the presence of particular antigens or phenotypes.
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