Evidence map›Paper›PMID 29682782›Full record

ArticleGenetic epidemiology2018

A hierarchical clustering method for dimension reduction in joint analysis of multiple phenotypes.

Xiaoyu Liang, Qiuying Sha, Yeonwoo Rho, Shuanglin Zhang

Abstract read
In one paragraph

Article in Genetic epidemiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. The Use of AI for Phenotype-Genotype Mapping.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
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  12. Natural compounds attenuate heavy metal-induced PC12 cell damage.The Journal of international medical research · 2020
    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

4 authors.

Xiaoyu LiangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.
Qiuying ShaDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.
Yeonwoo RhoDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.
Shuanglin ZhangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan, United States of America.ORCID 0000-0002-9478-1199

Funding

Genetic Epidemiology of COPDU01HL089897 · NHLBI · NATIONAL JEWISH HEALTH · PI CRAPO, JAMES D · 2007 to 2021
$56.9M
Genetic Epidemiology of COPDU01HL089856 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SILVERMAN, EDWIN K · 2007 to 2021
$20.7M
Statistical Methods for Rare Variant Association StudiesR15HG008209 · NHGRI · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI SHA, QIUYING · 2016 to 2016
$437k
NHGRI NIH HHS R15 HG008209NHLBI NIH HHS U01 HL089856NHLBI NIH HHS U01 HL089897
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have become a very effective research tool to identify genetic variants of underlying various complex diseases. In spite of the success of GWAS in identifying thousands of reproducible associations between genetic variants and complex disease, in general, the association between genetic variants and a single phenotype is usually weak. It is increasingly recognized that joint analysis of multiple phenotypes can be potentially more powerful than the univariate analysis, and can shed new light on underlying biological mechanisms of complex diseases. In this paper, we develop a novel variable reduction method using hierarchical clustering method (HCM) for joint analysis of multiple phenotypes in association studies. The proposed method involves two steps. The first step applies a dimension reduction technique by using a representative phenotype for each cluster of phenotypes. Then, existing methods are used in the second step to test the association between genetic variants and the representative phenotypes rather than the individual phenotypes. We perform extensive simulation studies to compare the powers of multivariate analysis of variance (MANOVA), joint model of multiple phenotypes (MultiPhen), and trait-based association test that uses extended simes procedure (TATES) using HCM with those of without using HCM. Our simulation studies show that using HCM is more powerful than without using HCM in most scenarios. We also illustrate the usefulness of using HCM by analyzing a whole-genome genotyping data from a lung function study.

Indexed as

Cluster AnalysisComputer SimulationGenome-Wide Association StudyHumansModels, GeneticMultifactor Dimensionality ReductionPhenotypePulmonary Disease, Chronic Obstructiveassociation studydimension reductionhierarchical clusteringmultiple phenotypes

Identifiers

PMID29682782
PMCPMC5980772

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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.