Evidence map›Paper›PMID 22782518›Full record

ArticleGenetic epidemiology2012

Multivariate detection of gene-gene interactions.

Indika Rajapakse, Michael D Perlman, Paul J Martin, John A Hansen, Charles Kooperberg

Abstract read
In one paragraph

Article in Genetic epidemiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Statistical analysis for genome-wide association study.Journal of biomedical research · 2015
    Review
  7. Article
  8. Detecting epistasis in human complex traits.Nature reviews. Genetics · 2014
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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.

Indika RajapakseFred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.
Michael D Perlman
Paul J Martin
John A Hansen
Charles Kooperberg

Funding

Interdisciplinary Tranining in Cancer ResearchT32CA080416 · NCI · UNIVERSITY OF WASHINGTON · PI STODDARD, BARRY L. · 1998 to 2023
$9.7M
Use of Biomarkers in Diagnosis, Prognosis, Risk Prediction and Early Detection ofP01CA053996 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRENTICE, ROSS L · 1991 to 2015
$9.4M
STATISTICAL METHODS FOR CLINICAL STUDIESR01CA090998 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEBLANC, MICHAEL L. · 2001 to 2011
$2.2M
Adaptive Statistical Methods for Genetic Association StudiesR01HG006124 · NHGRI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 2011 to 2014
$1.4M
Quantitative models and methods for genetic organizationK25DK082791 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RAJAPAKSE, INDIKA · 2009 to 2013
$662k
CHARACTERIZATION OF HEPATIC GLUCOSE PRODUCTION IN SITUF32DK008279 · NIDDK · CORNELL UNIVERSITY ITHACA · PI CANFIELD, WESLEY K · 1988 to 1990
–
NCI NIH HHS P01 CA053996NCI NIH HHS P01 CA53996NCI NIH HHS R01 CA090998NCI NIH HHS R01 CA90998NCI NIH HHS T32 CA080416NCI NIH HHS T32 CA80416NHGRI NIH HHS R01 HG006124NHGRI NIH HHS R01 HG006164NIDDK NIH HHS K25 DK08279NIDDK NIH HHS K25 DK082791
6 · The paper itself

Abstract

Unraveling the nature of genetic interactions is crucial to obtaining a more complete picture of complex diseases. It is thought that gene-gene interactions play an important role in the etiology of cancer, cardiovascular, and immune-mediated disease. Interactions among genes are defined as phenotypic effects that differ from those observed for independent contributions of each gene, usually detected by univariate logistic regression methods. Using a multivariate extension of linkage disequilibrium (LD), we have developed a new method, based on distances between sample covariance matrices for groups of single nucleotide polymorphisms (SNPs), to test for interaction effects of two groups of genes associated with a disease phenotype. Since a disease-associated interacting locus will often be in LD with more than one marker in the region, a method that examines a set of markers in a region collectively can offer greater power than traditional methods. Our method effectively identifies interaction effects in simulated data, as well as in data on the genetic contributions to the risk for graft-versus-host disease following hematopoietic stem cell transplantation.

Indexed as

Epistasis, GeneticGenetic Predisposition to DiseaseLinkage DisequilibriumModels, GeneticPolymorphism, Single NucleotideCase-Control StudiesComputer SimulationGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansLogistic ModelsModels, StatisticalMultivariate Analysis

Identifiers

PMID22782518
PMCPMC3556521

What OpenQuestion holds

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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.