ArticleJournal of the American Statistical Association2014
Identifying Genetic Variants for Addiction via Propensity Score Adjusted Generalized Kendall's Tau.
Article in Journal of the American Statistical Association, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- An integrative U method for joint analysis of multi-level omic data.BMC genetics · 2019Article
- Modeling Hybrid Traits for Comorbidity and Genetic Studies of Alcohol and Nicotine Co-Dependence.The annals of applied statistics · 2018Article
- Multisample adjusted U-statistics that account for confounding covariates.Statistics in medicine · 2018Article
- Conditional analysis of multiple quantitative traits based on marginal GWAS summary statistics.Genetic epidemiology · 2017Article
- Modeling Multiple Responses via Bootstrapping Margins with an Application to Genetic Association Testing.Statistics and its interfaceArticle
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3 authors.
Funding
Abstract
Identifying replicable genetic variants for addiction has been extremely challenging. Besides the common difficulties with genome-wide association studies (GWAS), environmental factors are known to be critical to addiction, and comorbidity is widely observed. Despite the importance of environmental factors and comorbidity for addiction study, few GWAS analyses adequately considered them due to the limitations of the existing statistical methods. Although parametric methods have been developed to adjust for covariates in association analysis, difficulties arise when the traits are multivariate because there is no ready-to-use model for them. Recent nonparametric development includes U-statistics to measure the phenotype-genotype association weighted by a similarity score of covariates. However, it is not clear how to optimize the similarity score. Therefore, we propose a semiparametric method to measure the association adjusted by covariates. In our approach, the nonparametric U-statistic is adjusted by parametric estimates of propensity scores using the idea of inverse probability weighting. The new measurement is shown to be asymptotically unbiased under our null hypothesis while the previous non-weighted and weighted ones are not. Simulation results show that our test improves power as opposed to the non-weighted and two other weighted U-statistic methods, and it is particularly powerful for detecting gene-environment interactions. Finally, we apply our proposed test to the Study of Addiction: Genetics and Environment (SAGE) to identify genetic variants for addiction. Novel genetic variants are found from our analysis, which warrant further investigation in the future.
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