Evidence map›Paper›PMID 22497480›Full record

ArticleAnnals of human genetics2012

Similarity-based multimarker association tests for continuous traits.

Wan-Yu Lin, Hemant K Tiwari, Guimin Gao, Kui Zhang, John J Arcaroli, Edward Abraham, Nianjun Liu

Abstract readEvaluation Study
In one paragraph

Article in Annals of human genetics, 2012. 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

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

3 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Wan-Yu LinDepartment of Biostatistics, University of Alabama at Birmingham, USA.
Hemant K Tiwari
Guimin Gao
Kui Zhang
John J Arcaroli
Edward Abraham
Nianjun Liu

Funding

The molecular genetic analysis of human obesityR01DK052431 · NIDDK · ROCKEFELLER UNIVERSITY · PI CHUNG, WENDY K, LEIBEL, RUDOLPH L · 1996 to 2020
$11.6M
Urokinase, Neutrophil Activation and Acute Lung Injury.R01HL076206 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI LIU, GANG · 2005 to 2013
$2.8M
Genome Wide Haplotype Association AnalysisR01GM081488 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LIU, NIANJUN · 2008 to 2012
$1.3M
Haplotyping and QTL Mapping in Pedigrees with Missing DataR01GM073766 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI GAO, GUIMIN · 2007 to 2011
$1.3M
HMGB1 and neutrophil efferocytosis.R01GM087748 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ZMIJEWSKI, JAROSLAW WALDEMAR · 2009 to 2012
$1.2M
Haplotype Analysis in Linkage Disequilibrium MappingR01GM074913 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ZHANG, KUI · 2006 to 2010
$1.1M
NHLBI NIH HHS HL076206NHLBI NIH HHS R01 HL076206NIDDK NIH HHS DK52431NIDDK NIH HHS R01 DK052431NIGMS NIH HHS GM073766NIGMS NIH HHS GM074913NIGMS NIH HHS GM081488NIGMS NIH HHS GM087748NIGMS NIH HHS R01 GM073766NIGMS NIH HHS R01 GM074913NIGMS NIH HHS R01 GM081488NIGMS NIH HHS R01 GM087748
6 · The paper itself

Abstract

Testing multiple markers simultaneously not only can capture the linkage disequilibrium patterns but also can decrease the number of tests and thus alleviate the multiple-testing penalty. If a gene is associated with a phenotype, subjects with similar genotypes in this gene should also have similar phenotypes. Based on this concept, we have developed a general framework that is applicable to continuous traits. Two similarity-based tests (namely, SIMc and SIMp tests) were derived as special cases of the general framework. In our simulation study, we compared the power of the two tests with that of the single-marker analysis, a standard haplotype regression, and a popular and powerful kernel machine regression. Our SIMc test outperforms other tests when the average R(2) (a measure of linkage disequilibrium) between the causal variant and the surrounding markers is larger than 0.3 or when the causal allele is common (say, frequency = 0.3). Our SIMp test outperforms other tests when the causal variant was introduced at common haplotypes (the maximum frequency of risk haplotypes >0.4). We also applied our two tests to an adiposity data set to show their utility.

Indexed as

Genetic MarkersModels, StatisticalAdiposityComputersGenetic Association StudiesGenetic VariationGenotypeHaplotypesHumansLinkage DisequilibriumGenetic Markers

Identifiers

PMID22497480
PMCPMC3329946

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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.