Evidence map›Paper›PMID 19797905›Full record

ArticleHuman heredity2010

Allelic based gene-gene interaction in case-control studies.

Jeesun Jung, Yiqiang Zhao

Abstract read
In one paragraph

Article in Human heredity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Jeesun JungDepartment of Medical and Molecular Genetics, School of Medicine, Indiana University, Indianapolis, IN, USA. jeejung@iupui.edu
Yiqiang Zhao

Funding

Effects of Somatic Growth and Sodium Retention on Blood PressureR01HL095086 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI PRATT, JOHN HOWARD, TU, WANZHU · 2009 to 2012
$1.5M
NHLBI NIH HHS R01 HL095086NHLBI NIH HHS R01 HL095086-01
6 · The paper itself

Abstract

In case-control studies identifying disease susceptibility loci, it has been shown that the interaction caused by multiple single nucleotide polymorphisms (SNPs) within a gene as well as by SNPs at unlinked genes plays an important role in influencing risk of a disease. A novel statistical approach is proposed to detect gene-gene interactions at the allelic level contributing to a disease trait. With a new allelic score inferred from the observed genotypes at two or more unlinked SNPs, we derive a score test from logistic regression and test for association of the allelic scores with a disease trait. Furthermore, F and likelihood ratio tests are derived from Cochran-Armitage regression. By testing for the association, the interaction can be assessed both in cases where the SNP association can be detected and cannot be detected as a main effect in single SNP approach. The analytical power and type I error rates over 6 two-way interaction models are investigated based on the non-centrality parameter approximation of the score test. Simulation studies demonstrate that (1) the power of the score test is asymptotically equivalent to that of the test statistics by the Cochran-Armitage method and (2) the allelic based method provides higher power than two genotypic based methods.

Indexed as

AllelesEpistasis, GeneticPolymorphism, Single NucleotideAlgorithmsBrain-Derived Neurotrophic FactorCase-Control StudiesGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansLogistic ModelsMajor Depressive DisorderModels, GeneticReceptor, Serotonin, 5-HT2ABrain-Derived Neurotrophic FactorReceptor, Serotonin, 5-HT2A

Identifiers

PMID19797905
PMCPMC2880732

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.