Evidence map›Paper›PMID 25885490›Full record

ArticleGenetic epidemiology2015

Kernel Approach for Modeling Interaction Effects in Genetic Association Studies of Complex Quantitative Traits.

K Alaine Broadaway, Richard Duncan, Karen N Conneely, Lynn M Almli, Bekh Bradley, Kerry J Ressler, Michael P Epstein

Abstract 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

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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

7 authors.

K Alaine BroadawayDepartment of Human Genetics, Emory University, Atlanta, Georgia, United States of America.
Richard DuncanDepartment of Human Genetics, Emory University, Atlanta, Georgia, United States of America.
Karen N ConneelyDepartment of Human Genetics, Emory University, Atlanta, Georgia, United States of America.
Lynn M AlmliDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, Georgia, United States of America.
Bekh BradleyDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, Georgia, United States of America.
Kerry J ResslerDepartment of Psychiatry and Behavioral Sciences, Emory University, Atlanta, Georgia, United States of America.
Michael P EpsteinDepartment of Human Genetics, Emory University, Atlanta, Georgia, United States of America.

Funding

Genetic and Trauma-Related Risk Factors for PTSDR01MH071537 · NIMH · EMORY UNIVERSITY · PI RESSLER, KERRY J. · 2005 to 2014
$8.5M
Mechanisms of Intergenerational Impact of Maternal TraumaR01HD071982 · NICHD · EMORY UNIVERSITY · PI BRADLEY, BEKH · 2013 to 2017
$2.1M
Segmental chromosome sharing in affected relatives with Juvenile ArthritisR01AR060893 · NIAMS · EMORY UNIVERSITY · PI PRAHALAD, SAMPATH · 2011 to 2014
$1.5M
Enhanced Gene Identification in Complex Traits Using Kernel MachinesR01HG007508 · NHGRI · EMORY UNIVERSITY · PI EPSTEIN, MICHAEL PHILIP · 2013 to 2015
$1.0M
NHGRI NIH HHS NIH R01-HG007508NHGRI NIH HHS R01 HG007508NIAMS NIH HHS R01 AR060893NIAMS NIH HHS R01-AR060893NICHD NIH HHS R01 HD071982NIMH NIH HHS R01 MH071537NIMH NIH HHS R01-MH071537
6 · The paper itself

Abstract

The etiology of complex traits likely involves the effects of genetic and environmental factors, along with complicated interaction effects between them. Consequently, there has been interest in applying genetic association tests of complex traits that account for potential modification of the genetic effect in the presence of an environmental factor. One can perform such an analysis using a joint test of gene and gene-environment interaction. An optimal joint test would be one that remains powerful under a variety of models ranging from those of strong gene-environment interaction effect to those of little or no gene-environment interaction effect. To fill this demand, we have extended a kernel machine based approach for association mapping of multiple SNPs to consider joint tests of gene and gene-environment interaction. The kernel-based approach for joint testing is promising, because it incorporates linkage disequilibrium information from multiple SNPs simultaneously in analysis and permits flexible modeling of interaction effects. Using simulated data, we show that our kernel machine approach typically outperforms the traditional joint test under strong gene-environment interaction models and further outperforms the traditional main-effect association test under models of weak or no gene-environment interaction effects. We illustrate our test using genome-wide association data from the Grady Trauma Project, a cohort of highly traumatized, at-risk individuals, which has previously been investigated for interaction effects.

Indexed as

Gene-Environment InteractionGenome, HumanModels, GeneticSoftwareChromosome MappingComputer SimulationGenetic Association StudiesHumansLinkage DisequilibriumPhenotypePolymorphism, Single NucleotideQuantitative Trait LociStress Disorders, Post-Traumaticgene-environment interactiongene mappingGWASquantitative human traits

Identifiers

PMID25885490
PMCPMC4469530

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Registered trials

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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.