Evidence map›Paper›PMID 29460449›Full record

ArticleGenetic epidemiology2018

Powerful and robust cross-phenotype association test for case-parent trios.

S Taylor Fischer, Yunxuan Jiang, K Alaine Broadaway, Karen N Conneely, Michael P Epstein

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

S Taylor FischerDepartment of Human Genetics and Center for Computational and Quantitative Genetics, Emory University, Atlanta, Georgia, United States of America.
Yunxuan JiangDepartment of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, United States of America.
K Alaine BroadawayDepartment of Human Genetics and Center for Computational and Quantitative Genetics, Emory University, Atlanta, Georgia, United States of America.
Karen N ConneelyDepartment of Human Genetics and Center for Computational and Quantitative Genetics, Emory University, Atlanta, Georgia, United States of America.
Michael P EpsteinDepartment of Human Genetics and Center for Computational and Quantitative Genetics, Emory University, Atlanta, Georgia, United States of America.ORCID 0000-0001-9647-9738

Funding

Statistical Tests for Mapping Genetic Determinants of Complex TraitsR01GM117946 · NIGMS · EMORY UNIVERSITY · PI EPSTEIN, MICHAEL PHILIP, GHOSH, DEBASHIS · 2016 to 2019
$1.2M
Enhanced Gene Identification in Complex Traits Using Kernel MachinesR01HG007508 · NHGRI · EMORY UNIVERSITY · PI EPSTEIN, MICHAEL PHILIP · 2013 to 2015
$1.0M
NHGRI NIH HHS R01 HG007508NIGMS NIH HHS R01 GM117946
6 · The paper itself

Abstract

There has been increasing interest in identifying genes within the human genome that influence multiple diverse phenotypes. In the presence of pleiotropy, joint testing of these phenotypes is not only biologically meaningful but also statistically more powerful than univariate analysis of each separate phenotype accounting for multiple testing. Although many cross-phenotype association tests exist, the majority of such methods assume samples composed of unrelated subjects and therefore are not applicable to family-based designs, including the valuable case-parent trio design. In this paper, we describe a robust gene-based association test of multiple phenotypes collected in a case-parent trio study. Our method is based on the kernel distance covariance (KDC) method, where we first construct a similarity matrix for multiple phenotypes and a similarity matrix for genetic variants in a gene; we then test the dependency between the two similarity matrices. The method is applicable to either common variants or rare variants in a gene, and resulting tests from the method are by design robust to confounding due to population stratification. We evaluated our method through simulation studies and observed that the method is substantially more powerful than standard univariate testing of each separate phenotype. We also applied our method to phenotypic and genotypic data collected in case-parent trios as part of the Genetics of Kidneys in Diabetes (GoKinD) study and identified a genome-wide significant gene demonstrating cross-phenotype effects that was not identified using standard univariate approaches.

Indexed as

Models, GeneticParentsGenetic VariationGenome, HumanGenome-Wide Association StudyHumansPhenotypeStatistics as Topiccase-parent trio designgenetic association testingpleiotropy

Identifiers

PMID29460449
PMCPMC6013339

What Socratic holds

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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 Socratic graph.