ArticleGenetic epidemiology2012
Multivariate phenotype association analysis by marker-set kernel machine regression.
Article in Genetic epidemiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 2 of them syntheses that pooled it.
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Who cites it
54 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models.European journal of human genetics : EJHG · 2017Pooled it
- Pooled it
- RKMR: A Rapid Kernel Machine Regression Framework for Optimal Marker Detection in Spatial Omics Data.bioRxiv : the preprint server for biology · 2026Article
- CBKMR: A Copula-based Bayesian Kernel Machine Regression Framework for Optimal Marker Detection in Omics Data.bioRxiv : the preprint server for biology · 2025Article
- Multiple phenotype association tests based on sliced inverse regression.BMC bioinformatics · 2024Article
- Statistical Inference for High-Dimensional Pathway Analysis with Multiple Responses.Computational statistics & data analysis · 2022Article
- Compositional Data Analysis using Kernels in mass cytometry data.Bioinformatics advances · 2022Article
- VCSEL: PRIORITIZING SNP-SET BY PENALIZED VARIANCE COMPONENT SELECTION.The annals of applied statistics · 2021Article
- Random effect based tests for multinomial logistic regression in genetic association studies.Genetic epidemiology · 2021Article
- Unpaired data empowers association tests.Bioinformatics (Oxford, England) · 2021Article
- Quantitative trait locus mapping analysis of multiple traits when using genotype data with potential errors.PeerJ · 2021Article
- Associating Multivariate Traits with Genetic Variants Using Collapsing and Kernel Methods with Pedigree- or Population-Based Studies.Computational and mathematical methods in medicine · 2021Article
- Robust kernel association testing (RobKAT).Genetic epidemiology · 2020Article
- Article
- Genome-Wide Gene-Based Multi-Trait Analysis.Frontiers in genetics · 2020Article
- Pleiotropy informed adaptive association test of multiple traits using genome-wide association study summary data.Biometrics · 2019Article
- Integrate multiple traits to detect novel trait-gene association using GWAS summary data with an adaptive test approach.Bioinformatics (Oxford, England) · 2019Article
- Powerful and efficient SNP-set association tests across multiple phenotypes using GWAS summary data.Bioinformatics (Oxford, England) · 2019Article
- A review of kernel methods for genetic association studies.Genetic epidemiology · 2019Review
- Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes.Genetic epidemiology · 2019Article
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Authors and funding
3 authors.
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Abstract
Genetic studies of complex diseases often collect multiple phenotypes relevant to the disorders. As these phenotypes can be correlated and share common genetic mechanisms, jointly analyzing these traits may bring more power to detect genes influencing individual or multiple phenotypes. Given the advancement brought by the multivariate phenotype approaches and the multimarker kernel machine regression, we construct a multivariate regression based on kernel machine to facilitate the joint evaluation of multimarker effects on multiple phenotypes. The kernel machine serves as a powerful dimension-reduction tool to capture complex effects among markers. The multivariate framework incorporates the potentially correlated multidimensional phenotypic information and accommodates common or different environmental covariates for each trait. We derive the multivariate kernel machine test based on a score-like statistic, and conduct simulations to evaluate the validity and efficacy of the method. We also study the performance of the commonly adapted strategies for kernel machine analysis on multiple phenotypes, including the multiple univariate kernel machine tests with original phenotypes or with their principal components. Our results suggest that none of these approaches has the uniformly best power, and the optimal test depends on the magnitude of the phenotype correlation and the effect patterns. However, the multivariate test retains to be a reasonable approach when the multiple phenotypes have none or mild correlations, and gives the best power once the correlation becomes stronger or when there exist genes that affect more than one phenotype. We illustrate the utility of the multivariate kernel machine method through the Clinical Antipsychotic Trails of Intervention Effectiveness antibody study.
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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.