Evidence map›Paper›PMID 25085501›Full record

ArticleBMC medical genomics2014

Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis.

Supinda Bunyavanich, Eric E Schadt, Blanca E Himes, Jessica Lasky-Su, Weiliang Qiu, Ross Lazarus, John P Ziniti, Ariella Cohain, Michael Linderman, Dara G Torgerson and 26 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Context-specific genetic effects inform endotypes and treatment in asthma.The Journal of allergy and clinical immunology · 2026
    Article
  4. Article
  5. Article
  6. Update on the genetics of allergic diseases.The Journal of allergy and clinical immunology · 2025
    Review
  7. Article
  8. Article
  9. Two-stage association study of mitochondrial DNA variants in allergic rhinitis.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2024
    Article
  10. New progress in pediatric allergic rhinitis.Frontiers in immunology · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Replication study of susceptibility variants associated with allergic rhinitis and allergy in Han Chinese.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2020
    Article
  20. 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

36 authors at 12 institutions in 5 countries.

Supinda Bunyavanich
Eric E Schadt
Blanca E Himes
Jessica Lasky-Su
Weiliang Qiu
Ross Lazarus
John P Ziniti
Ariella Cohain
Michael Linderman
Dara G Torgerson
Celeste S Eng
Maria Pino-Yanes
Badri Padhukasahasram
James J Yang
Rasika A Mathias
Terri H Beaty
Xingnan Li
Penelope Graves
Isabelle Romieu
Blanca del Rio Navarro
M Towhid Salam
Hita Vora
Dan L Nicolae
Carole Ober
Fernando D Martinez
Eugene R Bleecker
Deborah A Meyers
W James Gauderman
Frank Gilliland
Esteban G Burchard
Kathleen C Barnes
L Keoki Williams
Stephanie J London
Bin Zhang
Benjamin A Raby
Scott T Weiss
Brigham and Women's Hospital · USIcahn School of Medicine at Mount Sinai · USUniversity of California, San Francisco · USUniversity of Southern California · USHenry Ford Health System · USJohns Hopkins University · USWake Forest University · USUniversity of Arizona · USUniversity of Chicago · USCentre international de recherche sur le cancer · FRHospital Infantil de México Federico Gómez · MXNational Institutes of Health · US

Funding

Translational Research Support CoreP30ES007048 · NIEHS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Joseph Leo Wiemels · 1996 to 2026
$46.4M
Understanding Asthma EndotypesU19AI077439 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI David J Erle · 2008 to 2026
$41.1M
THE PHARMACOGENETICS OF ASTHMA TREATMENTU01HL065899 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI TANTISIRA, KELAN G, WEISS, SCOTT T · 2000 to 2014
$38.5M
Urban Air Pollution and Children's Respiratory HealthP01ES011627 · NIEHS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI AVOL, EDWARD · 2002 to 2011
$30.2M
PEDIATRIC ASTHMA NETWORK DATA COORDINATING CENTERU10HL064313 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MAUGER, DAVID T. · 1999 to 2008
$18.3M
The Genetic Epidemiology of Asthma in Costa RicaR37HL066289 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI WEISS, SCOTT T · 2007 to 2015
$14.6M
Statistical GeneticsP01HL083069 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI WEISS, SCOTT T · 2007 to 2011
$12.2M
CHILDHOOD ASTHMA: EARLY PREVENTION AND PHARMACOGENETICSU10HL064307 · NHLBI · UNIVERSITY OF ARIZONA · PI MARTINEZ, FERNANDO D · 1999 to 2008
$9.0M
The Asthma BioRepository for Integrative Genomics ResearchRC2HL101543 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI RABY, BENJAMIN ALEXANDER, WEISS, SCOTT T · 2009 to 2010
$8.3M
Genome Wide Association for Asthma and Lung FunctionR01HL087665 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MEYERS, DEBORAH A. · 2007 to 2009
$7.7M
Sex-Specific Genetic Architecture of Asthma-Associated Quantitative TraitsR01HL085197 · NHLBI · UNIVERSITY OF CHICAGO · PI OBER, CAROLE · 2007 to 2015
$7.6M
The EVE Asthma Genetics Consortium: Building Upon GWASRC2HL101651 · NHLBI · UNIVERSITY OF CHICAGO · PI NICOLAE, DAN LIVIU, OBER, CAROLE · 2009 to 2010
$7.4M
Intramural NIH HHSNHLBI NIH HHS HL061768NHLBI NIH HHS HL064307NHLBI NIH HHS HL064313NHLBI NIH HHS HL066289NHLBI NIH HHS HL069167NHLBI NIH HHS HL072414NHLBI NIH HHS HL075419NHLBI NIH HHS HL076647NHLBI NIH HHS HL078885NHLBI NIH HHS HL079055NHLBI NIH HHS HL083069NHLBI NIH HHS HL085197NHLBI NIH HHS HL087665NHLBI NIH HHS HL087680NHLBI NIH HHS HL087699NHLBI NIH HHS HL088133NHLBI NIH HHS HL101543NHLBI NIH HHS HL101651NHLBI NIH HHS HL49596NHLBI NIH HHS HL65899NHLBI NIH HHS R00 HL105663NHLBI NIH HHS R01 HL086601NHLBI NIH HHS R37 HL066289NHLBI NIH HHS U01 HL065899NIAID NIH HHS AI061774NIAID NIH HHS AI070503NIAID NIH HHS AI077439NIAID NIH HHS AI079139NIAID NIH HHS K08 AI093538NIAID NIH HHS K08AI093538NIDDK NIH HHS DK064695NIEHS NIH HHS ES007048NIEHS NIH HHS ES009581NIEHS NIH HHS ES011627NIEHS NIH HHS ES015794NIEHS NIH HHS ES020801NIEHS NIH HHS ES022719NIEHS NIH HHS P01ES011627NIEHS NIH HHS P30 ES007048NIEHS NIH HHS P30ES007048NIEHS NIH HHS Z01 ES049019ORD VA RD831861World Health Organization 001
6 · The paper itself

Abstract

backgroundAllergic rhinitis is a common disease whose genetic basis is incompletely explained. We report an integrated genomic analysis of allergic rhinitis.

methodsWe performed genome wide association studies (GWAS) of allergic rhinitis in 5633 ethnically diverse North American subjects. Next, we profiled gene expression in disease-relevant tissue (peripheral blood CD4+ lymphocytes) collected from subjects who had been genotyped. We then integrated the GWAS and gene expression data using expression single nucleotide (eSNP), coexpression network, and pathway approaches to identify the biologic relevance of our GWAS.

resultsGWAS revealed ethnicity-specific findings, with 4 genome-wide significant loci among Latinos and 1 genome-wide significant locus in the GWAS meta-analysis across ethnic groups. To identify biologic context for these results, we constructed a coexpression network to define modules of genes with similar patterns of CD4+ gene expression (coexpression modules) that could serve as constructs of broader gene expression. 6 of the 22 GWAS loci with P-value ≤ 1x10-6 tagged one particular coexpression module (4.0-fold enrichment, P-value 0.0029), and this module also had the greatest enrichment (3.4-fold enrichment, P-value 2.6 × 10-24) for allergic rhinitis-associated eSNPs (genetic variants associated with both gene expression and allergic rhinitis). The integrated GWAS, coexpression network, and eSNP results therefore supported this coexpression module as an allergic rhinitis module. Pathway analysis revealed that the module was enriched for mitochondrial pathways (8.6-fold enrichment, P-value 4.5 × 10-72).

conclusionsOur results highlight mitochondrial pathways as a target for further investigation of allergic rhinitis mechanism and treatment. Our integrated approach can be applied to provide biologic context for GWAS of other diseases.

Indexed as

Gene Regulatory NetworksGenome-Wide Association StudyPolymorphism, Single NucleotideAdolescentAdultAgedAged, 80 and overCD4-Positive T-LymphocytesChildChild, PreschoolFemaleGenetic LociGenomicsGenotypeHumansMale

Identifiers

PMID25085501
PMCPMC4127082
OpenAlexW2119942549

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.