ArticleHuman heredity2010
A unified framework for detecting genetic association with multiple SNPs in a candidate gene or region: contrasting genotype scores and LD patterns between cases and controls.
Article in Human heredity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Two-phase SSU and SKAT in genetic association studies.Journal of genetics · 2020Article
- Reflections on the Field of Human Genetics: A Call for Increased Disease Genetics Theory.Frontiers in genetics · 2016Article
- Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection.Genetic epidemiology · 2015Article
- A Bayesian Partitioning Model for the Detection of Multilocus Effects in Case-Control Studies.Human heredity · 2015Article
- A Bayesian approach to identify genes and gene-level SNP aggregates in a genetic analysis of cancer data.Statistics and its interface · 2015Article
- A composite likelihood approach to latent multivariate Gaussian modeling of SNP data with application to genetic association testing.Biometrics · 2012Article
- Powerful multi-marker association tests: unifying genomic distance-based regression and logistic regression.Genetic epidemiology · 2010Article
- Test selection with application to detecting disease association with multiple SNPs.Human heredity · 2010Article
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Abstract
It is critical to develop and apply powerful statistical tests for genetic association studies due to typically weak associations with complex human diseases or phenotypes. For population-based case-control studies with unphased multilocus genotype data, most of the existing methods are based on comparing genotype scores, e.g. allele frequencies, between the case and control groups. Another class of approaches are motivated to contrast linkage disequilibrium (LD) patterns between the two groups. It is expected that no single test can be uniformly most powerful across all situations, and different tests may perform better under different scenarios. A recent effort has been devoted to combining the above two classes of approaches, which however has some potential drawbacks. Here we propose a general and simple framework to unify the above two classes of approaches: it is based on the simple idea to incorporate LD measurements, in addition to genotype scores, as covariates in a logistic regression model, from which various tests can be constructed by taking advantage of the nice properties of the score statistics for the logistic model. It also has an advantage in easily accommodating covariates and other study designs. We use simulated data to show that our proposed tests performed well across several scenarios. In particular, in contrast to either of the two classes of the tests that is only powerful in detecting only one, but not both, of the two types of the distributional differences between cases and controls, our proposed tests are sensitive to both.
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