## Abstract Maternal‐fetal genotype (MFG) incompatibility is an interaction between the genes of a mother and offspring at a particular locus that adversely affects the developing fetus, thereby increasing susceptibility to disease. Statistical methods for examining MFG incompatibility as a disease
Restricted parameter space models for testing gene-gene interaction
✍ Scribed by Minsun Song; Dan L. Nicolae
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 123 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
There is a growing recognition that interactions (gene‐gene and gene‐environment) can play an important role in common disease etiology. The development of cost‐effective genotyping technologies has made genome‐wide association studies the preferred tool for searching for loci affecting disease risk. These studies are characterized by a large number of investigated SNPs, and efficient statistical methods are even more important than in classical association studies that are done with a small number of markers. In this article we propose a novel gene‐gene interaction test that is more powerful than classical methods. The increase in power is due to the fact that the proposed method incorporates reasonable constraints in the parameter space. The test for both association and interaction is based on a likelihood ratio statistic that has a x̄^2^ distribution asymptotically. We also discuss the definitions used for “no interaction” and argue that tests for pure interaction are useful in genome‐wide studies, especially when using two‐stage strategies where the analyses in the second stage are done on pairs of loci for which at least one is associated with the trait. Genet. Epidemiol. 33:386–393, 2009. © 2008 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract Genetic association studies achieve an unprecedented level of resolution in mapping disease genes by genotyping dense single nucleotype polymorphisms (SNPs) in a gene region. Meanwhile, these studies require new powerful statistical tools that can optimally handle a large amount of info
## Abstract When testing for genetic effects, failure to account for a gene‐environment interaction can mask the true association effects of a genetic marker with disease. Family‐based association tests are popular because they are completely robust to population substructure and model misspecifica
Hereditary nonpolyposis colorectal cancer (Lynch syndrome) is an autosomal dominant disease caused by mutations in the mismatch repair genes in particular in MLH1, MSH2 and MSH6. The disease is characterized by the development of colorectal, endometrial cancer and several other cancers. There is evi