ArticleBiostatistics (Oxford, England)2022
Integrative functional linear model for genome-wide association studies with multiple traits.
Article in Biostatistics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Research on multi-trait genome association study method based on Shannon information entropy.BMC bioinformatics · 2026Article
- High-Dimensional Gene-Environment Interaction Analysis.Annual review of statistics and its application · 2025Article
- Article
- Prior information-assisted integrative analysis of multiple datasets.Bioinformatics (Oxford, England) · 2023Article
- Article
- Article
- Gene Region Association Analysis of Longitudinal Quantitative Traits Based on a Function-On-Function Regression Model.Frontiers in genetics · 2022Article
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4 authors.
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Abstract
In recent biomedical research, genome-wide association studies (GWAS) have demonstrated great success in investigating the genetic architecture of human diseases. For many complex diseases, multiple correlated traits have been collected. However, most of the existing GWAS are still limited because they analyze each trait separately without considering their correlations and suffer from a lack of sufficient information. Moreover, the high dimensionality of single nucleotide polymorphism (SNP) data still poses tremendous challenges to statistical methods, in both theoretical and practical aspects. In this article, we innovatively propose an integrative functional linear model for GWAS with multiple traits. This study is the first to approximate SNPs as functional objects in a joint model of multiple traits with penalization techniques. It effectively accommodates the high dimensionality of SNPs and correlations among multiple traits to facilitate information borrowing. Our extensive simulation studies demonstrate the satisfactory performance of the proposed method in the identification and estimation of disease-associated genetic variants, compared to four alternatives. The analysis of type 2 diabetes data leads to biologically meaningful findings with good prediction accuracy and selection stability.
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