Evidence map›Paper›PMID 29314255›Full record

ArticleGenetic epidemiology2018

Inference on phenotype-specific effects of genes using multivariate kernel machine regression.

Arnab Maity, Jing Zhao, Patrick F Sullivan, Jung-Ying Tzeng

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. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Arnab MaityDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.ORCID 0000-0002-3364-8933
Jing ZhaoBioinformatics Research Center, North Carolina State University, Raleigh, North Carolina, United States of America.
Patrick F SullivanDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Jung-Ying TzengDepartment of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
1/7 Psychiatric Genomics Consortium: Finding actionable variationU01MH109528 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULLIVAN, PATRICK F · 2016 to 2020
$2.5M
Statistical Methods for Analysis of High-Dimensional Gene and Environment DataR00ES017744 · NIEHS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI MAITY, ARNAB · 2011 to 2013
$663k
NCI NIH HHS P01 CA142538NIEHS NIH HHS R00 ES017744NIMH NIH HHS U01 MH109528
6 · The paper itself

Abstract

We consider the problem of assessing the joint effect of a set of genetic markers on multiple, possibly correlated phenotypes of interest. We develop a kernel machine based multivariate regression framework, where the joint effect of the marker set on each of the phenotypes is modeled using prespecified kernel functions with unknown variance components. Unlike most existing methods that mainly focus on the global association between the marker set and the phenotype set, we develop estimation and testing procedures to study phenotype-specific associations. Specifically, we develop an estimation method based on the penalized likelihood approach to estimate phenotype-specific effects and their corresponding standard errors while accounting for possible correlation among the phenotypes. We develop testing procedures for the association of the marker set with any subset of phenotypes using a score-based variance components testing method. We assess the performance of our proposed methodology via a simulation study and demonstrate the utility of the proposed method using the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) data.

Indexed as

Computer SimulationLikelihood FunctionsModels, GeneticPhenotypeAge FactorsAntipsychotic AgentsGenetic MarkersHumansSex FactorsAntipsychotic AgentsGenetic Markerskernel machinemixed modelsmultivariate regressionrestricted maximum likelihoodvariance components

Identifiers

PMID29314255
PMCPMC5768462

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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.