Literature DB >> 19178434

Testing for genetic association with constrained models using triads.

J F Troendle1, K F Yu, J L Mills.   

Abstract

It has been shown that it is preferable to use a robust model that incorporated constraints on the genotype relative risk rather than rely on a model that assumes the disease operates in a recessive or dominant fashion. Previous methods are applicable to case-control studies, but not to family based studies of case children along with their parents (triads). We show here how to implement analogous constraints while analyzing triad data. The likelihood, conditional on the parents genotype, is maximized over the appropriately constrained parameter space. The asymptotic distribution for the maximized likelihood ratio statistic is found and used to estimate the null distribution of the test statistics. The properties of several methods of testing for association are compared by simulation. The constrained method provides higher power across a wide range of genetic models with little cost when compared to methods that restrict to a dominant, recessive, or multiplicative model, or make no modeling restriction. The methods are applied to two SNPs on the methylenetetrahydrofolate reductase (MTHFR) gene with neural tube defect (NTD) triads.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19178434      PMCID: PMC2657230          DOI: 10.1111/j.1469-1809.2008.00494.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  8 in total

1.  Testing for association with a case-parents design in the presence of genotyping errors.

Authors:  Richard W Morris; Norman L Kaplan
Journal:  Genet Epidemiol       Date:  2004-02       Impact factor: 2.135

2.  Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study.

Authors:  Peadar N Kirke; James L Mills; Anne M Molloy; Lawrence C Brody; Valerie B O'Leary; Leslie Daly; Sharon Murray; Mary Conley; Philip D Mayne; Owen Smith; John M Scott
Journal:  BMJ       Date:  2004-05-21

3.  A constrained-likelihood approach to marker-trait association studies.

Authors:  Kai Wang; Val C Sheffield
Journal:  Am J Hum Genet       Date:  2005-09-14       Impact factor: 11.025

4.  Simple formulas for gauging the potential impacts of population stratification bias.

Authors:  Wen-Chung Lee; Liang-Yi Wang
Journal:  Am J Epidemiol       Date:  2007-09-19       Impact factor: 4.897

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

Review 6.  5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review.

Authors:  L D Botto; Q Yang
Journal:  Am J Epidemiol       Date:  2000-05-01       Impact factor: 4.897

7.  Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defects.

Authors:  Anne Parle-McDermott; James L Mills; Peadar N Kirke; Valerie B O'Leary; Deborah A Swanson; Faith Pangilinan; Mary Conley; Anne M Molloy; Christopher Cox; John M Scott; Lawrence C Brody
Journal:  J Hum Genet       Date:  2003-03-05       Impact factor: 3.172

8.  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

  8 in total
  2 in total

1.  Incorporating parental information into family-based association tests.

Authors:  Zhaoxia Yu; Daniel Gillen; Carey F Li; Michael Demetriou
Journal:  Biostatistics       Date:  2012-12-23       Impact factor: 5.899

2.  Association analysis of complex diseases using triads, parent-child dyads and singleton monads.

Authors:  Ruzong Fan; Annie Lee; Zhaohui Lu; Aiyi Liu; James F Troendle; James L Mills
Journal:  BMC Genet       Date:  2013-09-04       Impact factor: 2.797

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.