Evidence map›Paper›PMID 20170901›Full record

ArticleAmerican journal of human genetics2010

Systems genetics analysis of gene-by-environment interactions in human cells.

Casey E Romanoski, Sangderk Lee, Michelle J Kim, Leslie Ingram-Drake, Christopher L Plaisier, Roumyana Yordanova, Charles Tilford, Bo Guan, Aiqing He, Peter S Gargalovic and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 2 pooled it
5.1field-weighted citation impact, top 4% 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

81 citing papers in PubMed, 2 syntheses or guidelines pooled it, 115 citations in OpenAlex.

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21 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 3 countries.

Casey E RomanoskiDepartment of Human Genetics, University of California, Los Angeles, CA, 90095, USA. casey.romanoski@ucla.edu
Sangderk Lee
Michelle J Kim
Leslie Ingram-Drake
Christopher L Plaisier
Roumyana Yordanova
Charles Tilford
Bo Guan
Aiqing He
Peter S Gargalovic
Todd G Kirchgessner
Judith A Berliner
Aldons J Lusis
Bristol-Myers Squibb (Germany) · DEUniversity of California, Los Angeles · USInstitute for Systems Biology · US

Funding

ULTRASTRUCTURE OF THE INTIMA IN EARLY LESION FORMATIONP01HL030568 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FOGELMAN, ALAN M · 1985 to 2019
$55.2M
Training Grant in Genomic Analysis and InterpretationT32HG002536 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Valerie A Arboleda, Harold Pimentel · 2002 to 2026
$8.6M
Vascular Biology Training GrantT32HL069766 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2002 to 2022
$7.4M
NHGRI NIH HHS T32 HG002536NHLBI NIH HHS HL069766NHLBI NIH HHS P01 HL030568NHLBI NIH HHS P01-HL030568NHLBI NIH HHS T32 HL069766
6 · The paper itself

Abstract

Gene by environment (GxE) interactions are clearly important in many human diseases, but they have proven to be difficult to study on a molecular level. We report genetic analysis of thousands of transcript abundance traits in human primary endothelial cell (EC) lines in response to proinflammatory oxidized phospholipids implicated in cardiovascular disease. Of the 59 most regulated transcripts, approximately one-third showed evidence of GxE interactions. The interactions resulted primarily from effects of distal-, trans-acting loci, but a striking example of a local-GxE interaction was also observed for FGD6. Some of the distal interactions were validated by siRNA knockdown experiments, including a locus involved in the regulation of multiple transcripts involved in the ER stress pathway. Our findings add to the understanding of the overall architecture of complex human traits and are consistent with the possibility that GxE interactions are responsible, in part, for the failure of association studies to more fully explain common disease variation.

Indexed as

Gene Expression RegulationCell LineEndothelial CellsEnvironmentFemaleGenetic VariationGenome-Wide Association StudyHumansMaleModels, GeneticOligonucleotide Array Sequence AnalysisPhosphatidylcholinesPolymorphism, Single NucleotideQuantitative Trait LociRNA, Small InterferingSystems Biologyoxidized-L-alpha-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholinePhosphatidylcholinesRNA, Small Interfering

Identifiers

PMID20170901
PMCPMC2833388
OpenAlexW2083380010

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.