Evidence map›Paper›PMID 23512279›Full record

ArticleGenetic epidemiology2013

A nonparametric test to detect quantitative trait loci where the phenotypic distribution differs by genotypes.

Hugues Aschard, Noah Zaitlen, Rulla M Tamimi, Sara Lindström, Peter Kraft

Abstract read
In one paragraph

Article in Genetic epidemiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 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

5 authors.

Hugues AschardDepartment of Epidemiology, Harvard School of Public Health, Boston, MA 02115, USA. haschard@hsph.harvard.edu
Noah Zaitlen
Rulla M Tamimi
Sara Lindström
Peter Kraft

Funding

Statistical MethodsP01CA087969 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI TWOROGER, SHELLEY S · 2000 to 2019
$77.8M
GRADUATE TRAINING IN BIOSTATISTICST32ES007142 · NIEHS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI Brent Andrew Coull · 1985 to 2026
$11.9M
Epidemiologic StudiesU19CA148065 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI AHSAN, HABIBUL, BRUGGE, JOAN SIEFERT · 2010 to 2014
$10.6M
COHORT STUDY OF GENETIC SUSCEPTIBILITY TO BREAST CANCERR01CA065725 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI HUNTER, DAVID JOHN · 1996 to 2010
$4.5M
Whole Genome Association Study of Mammographic DensityR01CA131332 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI TAMIMI, RULLA M · 2009 to 2012
$1.9M
Evaluating the Clinical Validity of Novel Gene-Environment Risk ProfilesR21DK084529 · NIDDK · HARVARD SCHOOL OF PUBLIC HEALTH · PI KRAFT, PETER · 2009 to 2010
$409k
Methods to Identify Genetic Markers That Interact with Multiple Environmental ExpR21CA165920 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI KRAFT, PETER · 2012 to 2013
$346k
NCI NIH HHS CA131332NCI NIH HHS P01 CA087969NCI NIH HHS P01CA87969NCI NIH HHS R01 CA065725NCI NIH HHS R01 CA131332NCI NIH HHS R21 CA165920NCI NIH HHS R21CA165920NCI NIH HHS U19 CA148065NCI NIH HHS U19 CA148065-01NIDDK NIH HHS R21 DK084529NIDDK NIH HHS R21DK084529NIEHS NIH HHS T32 ES007142
6 · The paper itself

Abstract

Searching for genetic variants involved in gene-gene and gene-environment interactions in large-scale data raises multiple methodological issues. Many existing methods have focused on the problem of dimensionality, trying to explore the largest number of combinations between risk factors while considering simple interaction models. Despite evidence demonstrating the efficacy of these methods in simulated data, their application in real data has been unsuccessful so far. The classical test of a linear marginal genetic effect has been widely used for agnostic genome-wide association studies, with the underlying idea that most variants involved in interactions might display marginal effect on the phenotypic mean. Although this approach may allow for the identification of genetic variants involved in interactions in many scenarios, the linear marginal effects of some causal alleles on the phenotypic mean might not be always detectable at genome-wide significance level. We introduce in this study a general association test for quantitative trait loci that compare the distributions of phenotypic values by genotypic classes as opposed to most standard tests that compare phenotypic means by genotypic classes. Using simulations we show that in presence of interactions, this approach can be more powerful than the standard test of the linear marginal effect, with a gain of power increasing with increasing interaction effect and decreasing frequencies of the interacting exposures. We demonstrate the potential utility of our method on real data by analyzing mammographic density genome-wide data from the Nurses' Health Study.

Indexed as

Genome-Wide Association StudyQuantitative Trait LociComputer SimulationFemaleGenotypeHumansLinear ModelsMammographyPhenotypeQuantitative Trait, HeritableSoftware

Identifiers

PMID23512279
PMCPMC4088942

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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.