ArticleGenetic epidemiology2017
Rare variant association test with multiple phenotypes.
Article in Genetic epidemiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.
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Who cites it
16 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Transethnic meta-analysis of exome-wide variants identifies new loci associated with male-specific metabolic syndrome.Genes & genomics · 2022Pooled it
- The sequence kernel association test for the proportional odds model.Bioinformatics (Oxford, England) · 2025Article
- A copula-based set-variant association test for bivariate continuous, binary or mixed phenotypes.The international journal of biostatistics · 2023Article
- A maximum kernel-based association test to detect the pleiotropic genetic effects on multiple phenotypes.Bioinformatics (Oxford, England) · 2023Article
- Bivariate quantitative Bayesian LASSO for detecting association of rare haplotypes with two correlated continuous phenotypes.Frontiers in genetics · 2023Article
- Computational Genomics in the Era of Precision Medicine: Applications to Variant Analysis and Gene Therapy.Journal of personalized medicine · 2022Review
- VCSEL: PRIORITIZING SNP-SET BY PENALIZED VARIANCE COMPONENT SELECTION.The annals of applied statistics · 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
- A fast and powerful aggregated Cauchy association test for joint analysis of multiple phenotypes.Genes & genomics · 2021Article
- Multi-trait analysis of rare-variant association summary statistics using MTAR.Nature communications · 2020Article
- Bivariate logistic Bayesian LASSO for detecting rare haplotype association with two correlated phenotypes.Genetic epidemiology · 2019Article
- Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test.Genetic epidemiology · 2019Article
- Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes.Genetic epidemiology · 2019Article
- Pathway-based approach using hierarchical components of rare variants to analyze multiple phenotypes.BMC bioinformatics · 2018Article
- New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population.Scientific reports · 2018Article
- Statistical methods to detect pleiotropy in human complex traits.Open biology · 2017Review
Corrections and comments
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7 authors.
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Abstract
Although genome-wide association studies (GWAS) have now discovered thousands of genetic variants associated with common traits, such variants cannot explain the large degree of "missing heritability," likely due to rare variants. The advent of next generation sequencing technology has allowed rare variant detection and association with common traits, often by investigating specific genomic regions for rare variant effects on a trait. Although multiple correlated phenotypes are often concurrently observed in GWAS, most studies analyze only single phenotypes, which may lessen statistical power. To increase power, multivariate analyses, which consider correlations between multiple phenotypes, can be used. However, few existing multivariant analyses can identify rare variants for assessing multiple phenotypes. Here, we propose Multivariate Association Analysis using Score Statistics (MAAUSS), to identify rare variants associated with multiple phenotypes, based on the widely used sequence kernel association test (SKAT) for a single phenotype. We applied MAAUSS to whole exome sequencing (WES) data from a Korean population of 1,058 subjects to discover genes associated with multiple traits of liver function. We then assessed validation of those genes by a replication study, using an independent dataset of 3,445 individuals. Notably, we detected the gene ZNF620 among five significant genes. We then performed a simulation study to compare MAAUSS's performance with existing methods. Overall, MAAUSS successfully conserved type 1 error rates and in many cases had a higher power than the existing methods. This study illustrates a feasible and straightforward approach for identifying rare variants correlated with multiple phenotypes, with likely relevance to missing heritability.
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