Evidence map›Paper›PMID 21121902›Full record

ArticleAnnals of human genetics2011

Detecting epistatic SNPs associated with complex diseases via a Bayesian classification tree search method.

Min Chen, Judy Cho, Hongyu Zhao

Abstract read
In one paragraph

Article in Annals of human genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Comments on Fifty Years of Classification and Regression Trees.International statistical review = Revue internationale de statistique · 2014
    Article
  3. 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

3 authors.

Min ChenDepartment of Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, USA.
Judy Cho
Hongyu Zhao

Funding

YALE UNIVERSITY CLINICAL AND TRANSLATIONAL SCIENCE AWARD PROGRAMUL1RR024139 · NCRR · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2006 to 2011
$56.8M
Inflammatory Bowel Disease Genetics Consortium Data Coordinating CenterU01DK062429 · NIDDK · YALE UNIVERSITY · PI CHO, JUDY H. · 2002 to 2016
$16.8M
Yale University Inflammatory Bowel Disease Genetics Research CenterU01DK062422 · NIDDK · YALE UNIVERSITY · PI Ling-shiang Chuang · 2002 to 2026
$10.8M
STATISTICAL METHODS TO MAP GENES FOR COMPLEX TRAITSR01GM059507 · NIGMS · YALE UNIVERSITY · PI ZHAO, HONGYU · 1999 to 2013
$3.6M
Mapping Chromosome 3q Inflammatory Bowel Disease GenesR01DK072373 · NIDDK · YALE UNIVERSITY · PI CHO, JUDY H. · 2006 to 2008
$845k
NCRR NIH HHS UL1 RR024139NIDDK NIH HHS 1R01DK072373NIDDK NIH HHS R01 DK072373NIDDK NIH HHS U01 DK062422NIDDK NIH HHS U01 DK062429NIGMS NIH HHS GM 59507NIGMS NIH HHS R01 GM059507
6 · The paper itself

Abstract

Complex phenotypes are known to be associated with interactions among genetic factors. A growing body of evidence suggests that gene-gene interactions contribute to many common human diseases. Identifying potential interactions of multiple polymorphisms thus may be important to understand the biology and biochemical processes of the disease etiology. However, despite the great success of genome-wide association studies that mostly focus on single locus analysis, it is challenging to detect these interactions, especially when the marginal effects of the susceptible loci are weak and/or they involve several genetic factors. Here we describe a Bayesian classification tree model to detect such interactions in case-control association studies. We show that this method has the potential to uncover interactions involving polymorphisms showing weak to moderate marginal effects as well as multi-factorial interactions involving more than two loci.

Indexed as

Bayes TheoremEpistasis, GeneticGenetic Predisposition to DiseasePolymorphism, Single NucleotideCrohn DiseaseDiseaseHumans

Identifiers

PMID21121902
PMCPMC3178841

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Registered trials

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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.