Evidence map›Paper›PMID 26139508›Full record

ArticleGenetic epidemiology2015

A Fast Multiple-Kernel Method With Applications to Detect Gene-Environment Interaction.

Rachel Marceau, Wenbin Lu, Shannon Holloway, Michèle M Sale, Bradford B Worrall, Stephen R Williams, Fang-Chi Hsu, Jung-Ying Tzeng

Open access · greenAbstract read
In one paragraph

Article in Genetic epidemiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. High-Dimensional Gene-Environment Interaction Analysis.Annual review of statistics and its application · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Robust genetic interaction analysis.Briefings in bioinformatics · 2019
    Review
  7. Article
  8. Set-Based Tests for the Gene-Environment Interaction in Longitudinal Studies.Journal of the American Statistical Association · 2017
    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

8 authors at 4 institutions in 2 countries.

Rachel MarceauDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
Wenbin LuDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
Shannon HollowayDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
Michèle M SaleCenter for Public Health Genomics, University of Virginia, Charlottesville, Virginia, United States of America.
Bradford B WorrallCenter for Public Health Genomics, University of Virginia, Charlottesville, Virginia, United States of America.
Stephen R WilliamsCenter for Public Health Genomics, University of Virginia, Charlottesville, Virginia, United States of America.
Fang-Chi HsuDepartment of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America.
Jung-Ying TzengDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
North Carolina State University · USUniversity of Virginia · USNational Cheng Kung University · TWWake Forest University · US

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
Vitamin Intervention for Stroke Prevention (VISP)R01NS034447 · NINDS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI TOOLE, JAMES F · 1996 to 2006
$18.0M
Biostatistics Training in the Omics EraT32GM081057 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MUSE, SPENCER V. · 2007 to 2019
$2.5M
Pharmacogenomic studies in VISP: results & implications for clinical trial designU01HG005160 · NHGRI · UNIVERSITY OF VIRGINIA · PI SALE, MICHELE M, WORRALL, BRADFORD B · 2009 to 2011
$1.9M
Genome-wide Haplotype Association Analysis in Mental DisordersR01MH084022 · NIMH · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI TZENG, JUNG-YING · 2009 to 2011
$1.1M
Flexible Statistical Methods for Complex Survival Data in Biomedical StudiesR01CA140632 · NCI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI LU, WENBIN · 2010 to 2013
$795k
NCI NIH HHS P01 CA142538NCI NIH HHS P01CA142538NCI NIH HHS R01 CA140632NHGRI NIH HHS U01 HG005160NIGMS NIH HHS 5T32GM081057NIGMS NIH HHS T32 GM081057NIMH NIH HHS R01 MH084022NINDS NIH HHS R01 NS034447NINDS NIH HHS R01 NS34447
6 · The paper itself

Abstract

Kernel machine (KM) models are a powerful tool for exploring associations between sets of genetic variants and complex traits. Although most KM methods use a single kernel function to assess the marginal effect of a variable set, KM analyses involving multiple kernels have become increasingly popular. Multikernel analysis allows researchers to study more complex problems, such as assessing gene-gene or gene-environment interactions, incorporating variance-component based methods for population substructure into rare-variant association testing, and assessing the conditional effects of a variable set adjusting for other variable sets. The KM framework is robust, powerful, and provides efficient dimension reduction for multifactor analyses, but requires the estimation of high dimensional nuisance parameters. Traditional estimation techniques, including regularization and the "expectation-maximization (EM)" algorithm, have a large computational cost and are not scalable to large sample sizes needed for rare variant analysis. Therefore, under the context of gene-environment interaction, we propose a computationally efficient and statistically rigorous "fastKM" algorithm for multikernel analysis that is based on a low-rank approximation to the nuisance effect kernel matrices. Our algorithm is applicable to various trait types (e.g., continuous, binary, and survival traits) and can be implemented using any existing single-kernel analysis software. Through extensive simulation studies, we show that our algorithm has similar performance to an EM-based KM approach for quantitative traits while running much faster. We also apply our method to the Vitamin Intervention for Stroke Prevention (VISP) clinical trial, examining gene-by-vitamin effects on recurrent stroke risk and gene-by-age effects on change in homocysteine level.

Indexed as

AlgorithmsGene-Environment InteractionGenetic VariationHomocysteineHumansModels, GeneticQuantitative Trait LociRegression AnalysisRisk FactorsSoftwareStrokeVitaminsHomocysteineVitaminsexon level association testgene-environment interactiongene-gene interactionskernel machine regressionmultiple-kernel analysis

Identifiers

PMID26139508
PMCPMC4544636
OpenAlexW1793038698

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.