Evidence map›Paper›PMID 22760990›Full record

ArticleGenetic epidemiology2012

A likelihood ratio-based Mann-Whitney approach finds novel replicable joint gene action for type 2 diabetes.

Qing Lu, Changshuai Wei, Chengyin Ye, Ming Li, Robert C Elston

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Evolutionary footprint of epistasis.PLoS computational biology · 2018
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Detecting epistasis in human complex traits.Nature reviews. Genetics · 2014
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. 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.

Qing LuDepartment of Epidemiology and Biostatistics, Michigan State University, East Lansing, Michigan, USA.
Changshuai Wei
Chengyin Ye
Ming Li
Robert C Elston

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024989 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI DAVIS, PAMELA B · 2007 to 2011
$53.7M
Geisinger eGenonic Medicine (GeM) ProgramU01HG006382 · NHGRI · GEISINGER CLINIC · PI CAREY, DAVID J., WILLIAMS, MARC S. · 2011 to 2014
$4.3M
High-dimensional Statistical Genetic Approach for Family-based Orofacial CleftsR03DE022379 · NIDCR · MICHIGAN STATE UNIVERSITY · PI LU, QING · 2012 to 2013
$441k
Role of Mitochondrial CYP2E1 in Chemical Exposure-Driven NeurodegenerationF32ES027306 · NIEHS · DUKE UNIVERSITY · PI HARTMAN, JESSICA HELENE · 2016 to 2018
$171k
NHGRI NIH HHS 1U01HG006382NHGRI NIH HHS U01 HG006382NHGRI NIH HHS U01HG006382NIDCR NIH HHS R03 DE022379NIDCR NIH HHS R03DE022379NIEHS NIH HHS 27306C0004Wellcome Trust
6 · The paper itself

Abstract

The potential importance of the joint action of genes, whether modeled with or without a statistical interaction term, has long been recognized. However, identifying such action has been a great challenge, especially when millions of genetic markers are involved. We propose a likelihood ratio-based Mann-Whitney test to search for joint gene action either among candidate genes or genome-wide. It extends the traditional univariate Mann-Whitney test to assess the joint association of genotypes at multiple loci with disease, allowing for high-order statistical interactions. Because only one overall significance test is conducted for the entire analysis, it avoids the issue of multiple testing. Moreover, the approach adopts a computationally efficient algorithm, making a genome-wide search feasible in a reasonable amount of time on a high performance personal computer. We evaluated the approach using both theoretical and real data. By applying the approach to 40 type 2 diabetes (T2D) susceptibility single-nucleotide polymorphisms (SNPs), we identified a four-locus model strongly associated with T2D in the Wellcome Trust (WT) study (permutation P-value < 0.001), and replicated the same finding in the Nurses' Health Study/Health Professionals Follow-Up Study (NHS/HPFS) (P-value = 3.03×10-11). We also conducted a genome-wide search on 385,598 SNPs in the WT study. The analysis took approximately 55 hr on a personal computer, identifying the same first two loci, but overall a different set of four SNPs, jointly associated with T2D (P-value = 1.29×10-5). The nominal significance of this same association reached 4.01×10-6 in the NHS/HPFS.

Indexed as

Genetic MarkersGenetic Predisposition to DiseasePolymorphism, Single NucleotideAlgorithmsDiabetes Mellitus, Type 2Genome-Wide Association StudyHumansLikelihood FunctionsModels, GeneticModels, StatisticalGenetic Markers

Identifiers

PMID22760990
PMCPMC3634342

What OpenQuestion holds

Textmetadata
LicenceTDM
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.