Evidence map›Paper›PMID 17873875›Full record

ArticleNature genetics2007

Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes.

Harald H H Göring, Joanne E Curran, Matthew P Johnson, Thomas D Dyer, Jac Charlesworth, Shelley A Cole, Jeremy B M Jowett, Lawrence J Abraham, David L Rainwater, Anthony G Comuzzie and 7 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 316 papers, 15 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
316citing papers in PubMed, 15 pooled it
25.7field-weighted citation impact, top 1% 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

316 citing papers in PubMed, 15 syntheses or guidelines pooled it, 535 citations in OpenAlex.

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  15. CUBN is a gene locus for albuminuria.Journal of the American Society of Nephrology : JASN · 2011
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  18. Identification of genetic variants influencing the human plasma proteome.Proceedings of the National Academy of Sciences of the United States of America · 2013
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256 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 2 countries.

Harald H H GöringDepartment of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas 78245, USA. hgoring@sfbrgenetics.org
Joanne E Curran
Matthew P Johnson
Thomas D Dyer
Jac Charlesworth
Shelley A Cole
Jeremy B M Jowett
Lawrence J Abraham
David L Rainwater
Anthony G Comuzzie
Michael C Mahaney
Laura Almasy
Jean W MacCluer
Ahmed H Kissebah
Gregory R Collier
Eric K Moses
John Blangero
Texas Biomedical Research Institute · USCaulfield Hospital · AUDeakin University · AUMedical College of Wisconsin · USUniversity of Western Australia · AU

Funding

Quantitative Trait Locus Mapping in Human PedigreesR37MH059490 · NIMH · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI BLANGERO, JOHN · 2001 to 2010
$6.8M
QUANTITATIVE TRAIT LOCUS MAPPING IN HUMAN PEDIGREESR01MH059490 · NIMH · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI BLANGERO, JOHN · 1998 to 2000
$426k
MOLECULAR AND BIOCHEMICAL GENETICS LABORATORY RENOVATIONC06RR013556 · NCRR · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI SHADE, ROBERT E · 1998 to 1998
–
NCRR NIH HHS RR013556NHLBI NIH HHS HL045222NIMH NIH HHS MH059490
6 · The paper itself

Abstract

Quantitative differences in gene expression are thought to contribute to phenotypic differences between individuals. We generated genome-wide transcriptional profiles of lymphocyte samples from 1,240 participants in the San Antonio Family Heart Study. The expression levels of 85% of the 19,648 detected autosomal transcripts were significantly heritable. Linkage analysis uncovered >1,000 cis-regulated transcripts at a false discovery rate of 5% and showed that the expression quantitative trait loci with the most significant linkage evidence are often located at the structural locus of a given transcript. To highlight the usefulness of this much-enlarged map of cis-regulated transcripts for the discovery of genes that influence complex traits in humans, as an example we selected high-density lipoprotein cholesterol concentration as a phenotype of clinical importance, and identified the cis-regulated vanin 1 (VNN1) gene as harboring sequence variants that influence high-density lipoprotein cholesterol concentrations.

Indexed as

PhenotypeQuantitative Trait LociTranscription, GeneticAmidohydrolasesCardiovascular DiseasesCell Adhesion MoleculesCholesterol, HDLGene Expression ProfilingGenetic LinkageGenetic MarkersGenotypeGPI-Linked ProteinsHumansLymphocytesMexican AmericansPromoter Regions, GeneticAmidohydrolasesCell Adhesion MoleculesCholesterol, HDLGenetic MarkersGPI-Linked Proteinspantetheinase

Identifiers

PMID17873875
OpenAlexW2145090915

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.