Evidence map›Paper›PMID 31625595›Full record

ArticleBiometrics2020

Gene-based association analysis for bivariate time-to-event data through functional regression with copula models.

Yue Wei, Yi Liu, Tao Sun, Wei Chen, Ying Ding

Abstract read
In one paragraph

Article in Biometrics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Multimodal Genotype and Phenotype Data Integration to Improve Partial Data-Based Longitudinal Prediction.Journal of computational biology : a journal of computational molecular cell biology · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yue WeiDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania.ORCID 0000-0002-9922-3479
Yi LiuDepartment of Biostatistics and Data Sciences, Boehringer Ingelheim, Ridgefield, Connecticut.
Tao SunDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania.
Wei ChenDepartment of Pediatrics, Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.
Ying DingDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, Pennsylvania.ORCID 0000-0003-1352-1000

Funding

Statistical methods for population and family-based whole-genome sequence dataR01HG007358 · NHGRI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHEN, WEI · 2014 to 2018
$1.7M
AMD genetics: methods and analysis for progression, prediction, and associationR01EY024226 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHEN, WEI · 2014 to 2016
$899k
NEI NIH HHS R01 EY024226NHGRI NIH HHS R01 HG007358
6 · The paper itself

Abstract

Several gene-based association tests for time-to-event traits have been proposed recently to detect whether a gene region (containing multiple variants), as a set, is associated with the survival outcome. However, for bivariate survival outcomes, to the best of our knowledge, there is no statistical method that can be directly applied for gene-based association analysis. Motivated by a genetic study to discover the gene regions associated with the progression of a bilateral eye disease, age-related macular degeneration (AMD), we implement a novel functional regression (FR) method under the copula framework. Specifically, the effects of variants within a gene region are modeled through a functional linear model, which then contributes to the marginal survival functions within the copula. Generalized score test statistics are derived to test for the association between bivariate survival traits and the genetic region. Extensive simulation studies are conducted to evaluate the type I error control and power performance of the proposed approach, with comparisons to several existing methods for a single survival trait, as well as the marginal Cox FR model using the robust sandwich estimator for bivariate survival traits. Finally, we apply our method to a large AMD study, the Age-related Eye Disease Study, and to identify the gene regions that are associated with AMD progression.

Indexed as

Linear ModelsRegression AnalysisAnalysis of VarianceBiometryComputer SimulationDisease ProgressionGenetic Association StudiesGenetic VariationGenome-Wide Association StudyHumansMacular DegenerationModels, GeneticPolymorphism, Single NucleotideProportional Hazards ModelsSurvival AnalysisTime FactorsAMD progressionbivariate time-to-eventcopulafunctional regressiongene-based association analysis

Identifiers

PMID31625595
PMCPMC7165069

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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.