Literature DB >> 9529360

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.

C R Weinberg1, A J Wilcox, R T Lie.   

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.

Mesh:

Year:  1998        PMID: 9529360      PMCID: PMC1377041          DOI: 10.1086/301802

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  10 in total

1.  On estimating HLA/disease association with application to a study of aplastic anemia.

Authors:  S G Self; G Longton; K J Kopecky; K Y Liang
Journal:  Biometrics       Date:  1991-03       Impact factor: 2.571

Review 2.  The TDT and other family-based tests for linkage disequilibrium and association.

Authors:  R S Spielman; W J Ewens
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

3.  General score tests for associations of genetic markers with disease using cases and their parents.

Authors:  D J Schaid
Journal:  Genet Epidemiol       Date:  1996       Impact factor: 2.135

4.  Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium.

Authors:  L E Mitchell
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

5.  Genotype relative risks: methods for design and analysis of candidate-gene association studies.

Authors:  D J Schaid; S S Sommer
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

6.  Variation in HLA-associated risks of childhood insulin-dependent diabetes in the Finnish population: I. Allele effects at A, B, and DR loci. DiMe Study Group. Childhood Diabetes in Finland.

Authors:  B Langholz; E Tuomilehto-Wolf; D Thomas; J Pitkäniemi; J Tuomilehto
Journal:  Genet Epidemiol       Date:  1995       Impact factor: 2.135

7.  Variation in HLA-associated risks of childhood insulin-dependent diabetes in the Finnish population: II. Haplotype effects. DiMe Study Group. Childhood Diabetes in Finland.

Authors:  D Thomas; J Pitkäniemi; B Langholz; E Tuomilehto-Wolf; J Tuomilehto
Journal:  Genet Epidemiol       Date:  1995       Impact factor: 2.135

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

Authors:  C T Falk; P Rubinstein
Journal:  Ann Hum Genet       Date:  1987-07       Impact factor: 1.670

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

Authors:  R S Spielman; R E McGinnis; W J Ewens
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

10.  Mapping disease genes: family-based association studies.

Authors:  G Thomson
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

  10 in total
  183 in total

1.  Methods for detection of parent-of-origin effects in genetic studies of case-parents triads.

Authors:  C R Weinberg
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

2.  The use of case-parent triads to study joint effects of genotype and exposure.

Authors:  D M Umbach; C R Weinberg
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

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

Authors:  G R Abecasis; L R Cardon; W O Cookson
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

4.  Allowing for missing parents in genetic studies of case-parent triads.

Authors:  C R Weinberg
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

5.  Informative missingness in genetic association studies: case-parent designs.

Authors:  Andrew S Allen; Paul J Rathouz; Glen A Satten
Journal:  Am J Hum Genet       Date:  2003-02-14       Impact factor: 11.025

6.  Regarding "parental genotypes in the risk of a complex disease".

Authors:  Clarice R Weinberg; Laura Mitchell
Journal:  Am J Hum Genet       Date:  2002-11       Impact factor: 11.025

7.  Family-based association tests incorporating parental genotypes.

Authors:  Peter Kraft; Melissa Wilson
Journal:  Am J Hum Genet       Date:  2002-11       Impact factor: 11.025

8.  The FGF and FGFR Gene Family and Risk of Cleft Lip With or Without Cleft Palate.

Authors:  Hong Wang; Tianxiao Zhang; Tao Wu; Jacqueline B Hetmanski; Ingo Ruczinski; Holger Schwender; Kung Yee Liang; Tanda Murray; M Daniele Fallin; Richard J Redett; Gerald V Raymond; Sheng-Chih Jin; Yah-Huei Wu Chou; Philip Kuo-Ting Chen; Vincent Yeow; Samuel S Chong; Felicia S H Cheah; Sun Ha Jee; Ethylin W Jabs; Alan F Scott; Terri H Beaty
Journal:  Cleft Palate Craniofac J       Date:  2011-11-10

9.  Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.

Authors:  Ming Li; Stephen W Erickson; Charlotte A Hobbs; Jingyun Li; Xinyu Tang; Todd G Nick; Stewart L Macleod; Mario A Cleves
Journal:  Genet Epidemiol       Date:  2014-03-02       Impact factor: 2.135

Review 10.  The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.

Authors:  Anne M Molloy; Lawrence C Brody; James L Mills; John M Scott; Peadar N Kirke
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-04
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