Evidence map›Paper›PMID 26479245›Full record

ArticlePloS one2015

Association Tests of Multiple Phenotypes: ATeMP.

Xiaobo Guo, Yixi Li, Xiaohu Ding, Mingguang He, Xueqin Wang, Heping Zhang

Abstract read
In one paragraph

Article in PloS one, 2015. 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

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

6 citing papers in PubMed.

  1. Article
  2. Comparison ofFrontiers in genetics · 2019
    Article
  3. Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits.Computational and mathematical methods in medicine · 2018
    Article
  4. Review
  5. Article
  6. 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

6 authors.

Xiaobo GuoDepartment of Statistical Science, School of Mathematics & Computational Science, Sun Yat-Sen University, Guangzhou, GD 510275, China; SYSU-CMU Shunde International Joint Research Institute, Shunde, GD 528300, China; Southern China Research Center of Statistical Science, Sun Yat-Sen University, Guangzhou, GD 510275, China.
Yixi LiPeking University HSBC Business School, Shenzhen, GD 518055, China.
Xiaohu DingState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou, GD 510080, China.
Mingguang HeState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou, GD 510080, China.
Xueqin WangDepartment of Statistical Science, School of Mathematics & Computational Science, Sun Yat-Sen University, Guangzhou, GD 510275, China; SYSU-CMU Shunde International Joint Research Institute, Shunde, GD 528300, China; Southern China Research Center of Statistical Science, Sun Yat-Sen University, Guangzhou, GD 510275, China; Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, GD 510080, China.
Heping ZhangDepartment of Statistical Science, School of Mathematics & Computational Science, Sun Yat-Sen University, Guangzhou, GD 510275, China; Department of Biostatistics, Yale University School of Public Health, New Haven, CT 06520, United States of America; Southern China Research Center of Statistical Science, Sun Yat-Sen University, Guangzhou, GD 510275, China.

Funding

Statistical Methods in Genetic Studies of Substance UseR01DA016750 · NIDA · YALE UNIVERSITY · PI ZHANG, HEPING · 2004 to 2016
$3.3M
NIDA NIH HHS R01 DA016750
6 · The paper itself

Abstract

Joint analysis of multiple phenotypes has gained growing attention in genome-wide association studies (GWASs), especially for the analysis of multiple intermediate phenotypes which measure the same underlying complex human disorder. One of the multivariate methods, MultiPhen (O' Reilly et al. 2012), employs the proportional odds model to regress a genotype on multiple phenotypes, hence ignoring the phenotypic distributions. Despite the flexibilities of MultiPhen, the properties and performance of MultiPhen are not well understood, especially when the phenotypic distributions are non-normal. In fact, it is well known in the statistical literature that the estimation is attenuated when the explanatory variables contain measurement errors. In this study, we first established an equivalence relationship between MultiPhen and the generalized Kendall tau association test, shedding light on why MultiPhen can perform well for joint association analysis of multiple phenotypes. Through the equivalence, we show that MultiPhen may lose power when the phenotypes are non-normal. To maintain the power, we propose two solutions (ATeMP-rn and ATeMP-or) to improve MultiPhen, and demonstrate their effectiveness through extensive simulation studies and a real case study from the Guangzhou Twin Eye Study.

Indexed as

Computer SimulationModels, TheoreticalComputational BiologyGenome-Wide Association StudyGenotypeHumansPhenotype

Identifiers

PMID26479245
PMCPMC4610695

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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.