Evidence map›Paper›PMID 29601641›Full record

ArticleGenetic epidemiology2018

Testing cross-phenotype effects of rare variants in longitudinal studies of complex traits.

Pratyaydipta Rudra, K Alaine Broadaway, Erin B Ware, Min A Jhun, Lawrence F Bielak, Wei Zhao, Jennifer A Smith, Patricia A Peyser, Sharon L R Kardia, Michael P Epstein and 1 more

Open access · bronzeAbstract 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 25% of its field
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, 7 citations in OpenAlex.

  1. Article
  2. A Kernel-based Test of Independence for Cluster-correlated Data.Advances in neural information processing systems · 2021
    Article
  3. 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

11 authors at 3 institutions in 2 countries.

Pratyaydipta RudraDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, Colorado, United States of America.ORCID 0000-0002-1089-7283
K Alaine BroadawayDepartment of Human Genetics, Emory University, Atlanta, Georgia, United States of America.
Erin B WareDepartment of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
Min A JhunDepartment of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
Lawrence F BielakDepartment of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
Wei ZhaoDepartment of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
Jennifer A SmithDepartment of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
Patricia A PeyserDepartment of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
Sharon L R KardiaDepartment of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
Michael P EpsteinDepartment of Human Genetics, Emory University, Atlanta, Georgia, United States of America.
Debashis GhoshDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, Colorado, United States of America.
University of Michigan · USColorado School of Public Health · USEmory University · US

Funding

Genome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2M
Genetic and Trauma-Related Risk Factors for PTSDR01MH071537 · NIMH · EMORY UNIVERSITY · PI RESSLER, KERRY J. · 2005 to 2014
$8.5M
GENETIC DETERMINANTS OF HIGH BP IN THREE RACIAL GROUPSU01HL054457 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KARDIA, SHARON L · 2000 to 2004
$2.8M
Genetic Mechanisms of Arteriosclerosis in Hypertensive SibshipsR01HL119443 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KARDIA, SHARON L · 2014 to 2017
$2.1M
Segmental chromosome sharing in affected relatives with Juvenile ArthritisR01AR060893 · NIAMS · EMORY UNIVERSITY · PI PRAHALAD, SAMPATH · 2011 to 2014
$1.5M
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
Genetic and Trauma-Related Risk Factors for PTSD: From GWAS to FunctionR56MH071537 · NIMH · EMORY UNIVERSITY · PI RESSLER, KERRY J. · 2015 to 2015
$148k
GENETIC DETERMINANTS OF HIGH BP IN THREE RACIAL GROUPSU10HL054457 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SING, CHARLES F · 1995 to 1999
–
NHGRI NIH HHS R01 HG007508NHLBI NIH HHS R01 HL086694NHLBI NIH HHS R01 HL119443NHLBI NIH HHS U01 HL054457NHLBI NIH HHS U10 HL054457NIAMS NIH HHS R01 AR060893NIGMS NIH HHS R01 GM117946NIMH NIH HHS R01 MH071537NIMH NIH HHS R56 MH071537
6 · The paper itself

Abstract

Many gene mapping studies of complex traits have identified genes or variants that influence multiple phenotypes. With the advent of next-generation sequencing technology, there has been substantial interest in identifying rare variants in genes that possess cross-phenotype effects. In the presence of such effects, modeling both the phenotypes and rare variants collectively using multivariate models can achieve higher statistical power compared to univariate methods that either model each phenotype separately or perform separate tests for each variant. Several studies collect phenotypic data over time and using such longitudinal data can further increase the power to detect genetic associations. Although rare-variant approaches exist for testing cross-phenotype effects at a single time point, there is no analogous method for performing such analyses using longitudinal outcomes. In order to fill this important gap, we propose an extension of Gene Association with Multiple Traits (GAMuT) test, a method for cross-phenotype analysis of rare variants using a framework based on the distance covariance. The approach allows for both binary and continuous phenotypes and can also adjust for covariates. Our simple adjustment to the GAMuT test allows it to handle longitudinal data and to gain power by exploiting temporal correlation. The approach is computationally efficient and applicable on a genome-wide scale due to the use of a closed-form test whose significance can be evaluated analytically. We use simulated data to demonstrate that our method has favorable power over competing approaches and also apply our approach to exome chip data from the Genetic Epidemiology Network of Arteriopathy.

Indexed as

Genetic VariationQuantitative Trait, HeritableComputer SimulationDatabases, GeneticExomeGenome-Wide Association StudyHumansLongitudinal StudiesModels, GeneticPhenotypecomplex human traitsgene mappinglongitudinal datapleiotropyrare variant

Identifiers

PMID29601641
PMCPMC5980726
OpenAlexW2794446911

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

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.