Evidence map›Paper›PMID 18615621›Full record

ArticleGenetic epidemiology2009

A partial least-square approach for modeling gene-gene and gene-environment interactions when multiple markers are genotyped.

Tao Wang, Gloria Ho, Kenny Ye, Howard Strickler, Robert C Elston

Open access · greenAbstract read
In one paragraph

Article in Genetic epidemiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Gene-Environment Interaction: A Variable Selection Perspective.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
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  18. Gene-environment interactions in genome-wide association studies: current approaches and new directions.Journal of child psychology and psychiatry, and allied disciplines · 2013
    Review
  19. Article
  20. 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 at 3 institutions in 1 country.

Tao WangDivision of Biostatistics, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, USA. taowang@aecom.yu.edu
Gloria Ho
Kenny Ye
Howard Strickler
Robert C Elston
Yeshiva University · USAlbert Einstein College of Medicine · USCase Western Reserve University · US

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARK R CHANCE · 1987 to 2026
$142.3M
X-LINKED EXTENSION OF THE REVISED HASEMAN-ELSTON ALGORITHM FOR LINKAGE ANALYSISP41RR003655 · NCRR · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1987 to 2011
$11.5M
GENETIC ANALYSIS OF MULTIFACTORIAL TRAITSR37GM028356 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI ELSTON, ROBERT C. · 1998 to 2007
$2.9M
Polymorphisms of INS/IGF Signal Pathways &Female CancerR01CA102691 · NCI · YESHIVA UNIVERSITY · PI HO, GLORIA YUEN FUN · 2003 to 2006
$2.1M
Aspirin, Inflammation Markers, and Colorectal AdenomaR01CA108841 · NCI · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI HO, GLORIA YUEN FUN · 2004 to 2006
$626k
GENETIC ANALYSIS OF MULTIFACTORIAL TRAITSR01GM028356 · NIGMS · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1985 to 1997
–
NCI NIH HHS P30CAD43703NCI NIH HHS R01 CA102691NCI NIH HHS R01 CA108841NCRR NIH HHS P41 RR003655NCRR NIH HHS RR03655NIGMS NIH HHS GM28356NIGMS NIH HHS R01 GM028356NIGMS NIH HHS R37 GM028356
6 · The paper itself

Abstract

Genetic association studies achieve an unprecedented level of resolution in mapping disease genes by genotyping dense single nucleotype polymorphisms (SNPs) in a gene region. Meanwhile, these studies require new powerful statistical tools that can optimally handle a large amount of information provided by genotype data. A question that arises is how to model interactions between two genes. Simply modeling all possible interactions between the SNPs in two gene regions is not desirable because a greatly increased number of degrees of freedom can be involved in the test statistic. We introduce an approach to reduce the genotype dimension in modeling interactions. The genotype compression of this approach is built upon the information on both the trait and the cross-locus gametic disequilibrium between SNPs in two interacting genes, in such a way as to parsimoniously model the interactions without loss of useful information in the process of dimension reduction. As a result, it improves power to detect association in the presence of gene-gene interactions. This approach can be similarly applied for modeling gene-environment interactions. We compare this method with other approaches, the corresponding test without modeling any interaction, that based on a saturated interaction model, that based on principal component analysis, and that based on Tukey's one-degree-of-freedom model. Our simulations suggest that this new approach has superior power to that of the other methods. In an application to endometrial cancer case-control data from the Women's Health Initiative, this approach detected AKT1 and AKT2 as being significantly associated with endometrial cancer susceptibility by taking into account their interactions with body mass index.

Indexed as

Least-Squares AnalysisModels, GeneticCase-Control StudiesComputer SimulationEndometrial NeoplasmsEnvironmentEpistasis, GeneticFemaleGenetic MarkersGenotypeHumansModels, StatisticalMolecular EpidemiologyPolymorphism, Single NucleotideProto-Oncogene Proteins c-aktRisk FactorsAKT1 protein, humanAKT2 protein, humanGenetic MarkersProto-Oncogene Proteins c-akt

Identifiers

PMID18615621
PMCPMC2700837
OpenAlexW2141004317

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.