Evidence map›Paper›PMID 21734407›Full record

ArticleHuman heredity2011

A dimension reduction approach for modeling multi-locus interaction in case-control studies.

Saonli Basu, Wei Pan, William S Oetting

Abstract read
In one paragraph

Article in Human heredity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. [An improved association analysis pipeline for tumor susceptibility variant in haplotype amplification area].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    Article
  2. Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies.Computational and mathematical methods in medicine · 2017
    Article
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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

3 authors.

Saonli BasuDivision of Biostatistics, University of Minnesota, Minneapolis, USA. saonli @ umn.edu
Wei Pan
William S Oetting

Funding

Gene-set pathway analysis of GWAS data for T2DM and related quantitative traitsR21DK089351 · NIDDK · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2010 to 2011
$394k
NIDDK NIH HHS R21 DK089351NIDDK NIH HHS R21DK089351
6 · The paper itself

Abstract

Studying one locus or one single nucleotide polymorphism (SNP) at a time may not be sufficient to understand complex diseases because they are unlikely to result from the effect of only one SNP. Each SNP alone may have little or no effect on the risk of the disease, but together they may increase the risk substantially. Analyses focusing on individual SNPs ignore the possibility of interaction among SNPs. In this paper, we propose a parsimonious model to assess the joint effect of a group of SNPs in a case-control study. The model implements a data reduction strategy within a likelihood framework and uses a test to assess the statistical significance of the effect of the group of SNPs on the binary trait. The primary advantage of the proposed approach is that the dimension reduction technique produces a test statistic with degrees of freedom significantly lower than a multiple logistic regression with only main effects of the SNPs, and our parsimonious model can incorporate the possibility of interaction among the SNPs. Moreover, the proposed approach estimates the direction of association of each SNP with the disease and provides an estimate of the average effect of the group of SNPs positively and negatively associated with the disease in the given SNP set. We illustrate the proposed model on simulated and real data, and compare its performance with a few other existing approaches. Our proposed approach appeared to outperform the other approaches for independent SNPs in our simulation studies.

Indexed as

Case-Control StudiesModels, GeneticChromosome MappingComputer SimulationHumansLikelihood FunctionsLogistic ModelsPolymorphism, Single Nucleotide

Identifiers

PMID21734407
PMCPMC3136376

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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.