ArticlePloS one2015
Region-Based Association Test for Familial Data under Functional Linear Models.
Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.
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Who cites it
18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.
- Systematic review of gastric cancer-associated genetic variants, gene-based meta-analysis, and gene-level functional analysis to identify candidate genes for drug development.Frontiers in genetics · 2022Pooled it
- Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models.European journal of human genetics : EJHG · 2017Pooled it
- Research on multi-trait genome association study method based on Shannon information entropy.BMC bioinformatics · 2026Article
- Introduction of FixFRM package for gene-based association test and its innovative application to mixture exposure analysis.Scientific reports · 2025Article
- The integration of quantile regression with 3VmrMLM identifies more QTNs and QTN-by-environment interactions using SNP- and haplotype-based markers.Plant communications · 2025Article
- Article
- sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics.PLoS computational biology · 2022Article
- Article
- Gene Region Association Analysis of Longitudinal Quantitative Traits Based on a Function-On-Function Regression Model.Frontiers in genetics · 2022Article
- Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration.Journal of the American Statistical Association · 2021Article
- Gene-based association analysis of survival traits via functional regression-based mixed effect cox models for related samples.Genetic epidemiology · 2019Article
- A generalized model for combining dependent SNP-level summary statistics and its extensions to statistics of other levels.Scientific reports · 2019Article
- Linear mixed models for association analysis of quantitative traits with next-generation sequencing data.Genetic epidemiology · 2019Article
- Article
- A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing.Genetic epidemiology · 2017Article
- A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits.Genetic epidemiology · 2016Article
- Some pitfalls in application of functional data analysis approach to association studies.Scientific reports · 2016Article
- Uncovering Local Trends in Genetic Effects of Multiple Phenotypes via Functional Linear Models.Genetic epidemiology · 2016Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Region-based association analysis is a more powerful tool for gene mapping than testing of individual genetic variants, particularly for rare genetic variants. The most powerful methods for regional mapping are based on the functional data analysis approach, which assumes that the regional genome of an individual may be considered as a continuous stochastic function that contains information about both linkage and linkage disequilibrium. Here, we extend this powerful approach, earlier applied only to independent samples, to the samples of related individuals. To this end, we additionally include a random polygene effects in functional linear model used for testing association between quantitative traits and multiple genetic variants in the region. We compare the statistical power of different methods using Genetic Analysis Workshop 17 mini-exome family data and a wide range of simulation scenarios. Our method increases the power of regional association analysis of quantitative traits compared with burden-based and kernel-based methods for the majority of the scenarios. In addition, we estimate the statistical power of our method using regions with small number of genetic variants, and show that our method retains its advantage over burden-based and kernel-based methods in this case as well. The new method is implemented as the R-function 'famFLM' using two types of basis functions: the B-spline and Fourier bases. We compare the properties of the new method using models that differ from each other in the type of their function basis. The models based on the Fourier basis functions have an advantage in terms of speed and power over the models that use the B-spline basis functions and those that combine B-spline and Fourier basis functions. The 'famFLM' function is distributed under GPLv3 license and is freely available at http://mga.bionet.nsc.ru/soft/famFLM/.
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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.