ArticleHuman heredity2011
A dimension reduction approach for modeling multi-locus interaction in case-control studies.
Article in Human heredity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
6 citing papers in PubMed.
- [An improved association analysis pipeline for tumor susceptibility variant in haplotype amplification area].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020Article
- Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies.Computational and mathematical methods in medicine · 2017Article
- A Bayesian Partitioning Model for the Detection of Multilocus Effects in Case-Control Studies.Human heredity · 2015Article
- Weighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies.PloS one · 2015Article
- A novel kernel for correcting size bias in the logistic kernel machine test with an application to rheumatoid arthritis.Human heredity · 2012Article
- Adaptive tests for detecting gene-gene and gene-environment interactions.Human heredity · 2011Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Studying one locus or one single nucleotide polymorphism (SNP) at a time may not be sufficient to understand complex diseases because they are unlikely to result from the effect of only one SNP. Each SNP alone may have little or no effect on the risk of the disease, but together they may increase the risk substantially. Analyses focusing on individual SNPs ignore the possibility of interaction among SNPs. In this paper, we propose a parsimonious model to assess the joint effect of a group of SNPs in a case-control study. The model implements a data reduction strategy within a likelihood framework and uses a test to assess the statistical significance of the effect of the group of SNPs on the binary trait. The primary advantage of the proposed approach is that the dimension reduction technique produces a test statistic with degrees of freedom significantly lower than a multiple logistic regression with only main effects of the SNPs, and our parsimonious model can incorporate the possibility of interaction among the SNPs. Moreover, the proposed approach estimates the direction of association of each SNP with the disease and provides an estimate of the average effect of the group of SNPs positively and negatively associated with the disease in the given SNP set. We illustrate the proposed model on simulated and real data, and compare its performance with a few other existing approaches. Our proposed approach appeared to outperform the other approaches for independent SNPs in our simulation studies.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.