Evidence map›Paper›PMID 29422661›Full record

ArticleEuropean journal of human genetics : EJHG2018

Understanding the role of the chromosome 15q25.1 in COPD through epigenetics and transcriptomics.

Ivana Nedeljkovic, Elena Carnero-Montoro, Lies Lahousse, Diana A van der Plaat, Kim de Jong, Judith M Vonk, Cleo C van Diemen, Alen Faiz, Maarten van den Berge, Ma'en Obeidat and 11 more

Open access · greenAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Different Associations Between theFrontiers in genetics · 2020
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. The etiologic origins for chronic obstructive pulmonary disease.International journal of chronic obstructive pulmonary disease · 2019
    Review
  14. Applying Functional Genomics to Chronic Obstructive Pulmonary Disease.Annals of the American Thoracic Society · 2018
    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

21 authors at 9 institutions in 5 countries.

Ivana NedeljkovicDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-0370-1473
Elena Carnero-MontoroDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Lies LahousseDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Diana A van der PlaatDepartment of Epidemiology University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Kim de JongDepartment of Epidemiology University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Judith M VonkDepartment of Epidemiology University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Cleo C van DiemenDepartment of Epidemiology University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Alen FaizGroningen Research Institute for Asthma and COPD (GRIAC), University of Groningen, Groningen, The Netherlands.
Maarten van den BergeDepartment of Pulmonology University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Ma'en ObeidatCentre for Heart Lung Innovation, University of British Columbia, Vancouver, BC, Canada.
Yohan BosséDepartment of Molecular Medicine, Laval University, Institut universitaire de cardiologie et de pneumologie de Québec, Quebec, QC, Canada.ORCID http://orcid.org/0000-0002-3067-3711
David C NickleGenetics and Pharmacogenomics (GpGx), Merck Research Laboratories, Seattle, WA, USA.
Bios Consortium
Andre G UitterlindenDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Joyce J B van MeursDepartment of Internal Medicine, Erasmus Medical Centre, Rotterdam, The Netherlands.
Bruno C H StrickerDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Guy G BrusselleDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Dirkje S PostmaGroningen Research Institute for Asthma and COPD (GRIAC), University of Groningen, Groningen, The Netherlands.
H Marike BoezenDepartment of Epidemiology University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Cornelia M van DuijnDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Najaf AminDepartment of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands. n.amin@erasmusmc.nl.
University Medical Center Groningen · NLErasmus University Rotterdam · NLGhent University Hospital · BEUniversity of Groningen · NLErasmus MC · NLInstitut universitaire de cardiologie et de pneumologie de Québec · CAMerck & Co., Inc., Rahway, NJ, USA (United States) · USPfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research · ESUniversity of British Columbia · CA

Funding

CIHR MOP − 123369
6 · The paper itself

Abstract

Chronic obstructive pulmonary disease (COPD) is a major health burden in adults and cigarette smoking is considered the most important environmental risk factor of COPD. Chromosome 15q25.1 locus is associated with both COPD and smoking. Our study aims at understanding the mechanism underlying the association of chromosome 15q25.1 with COPD through epigenetic and transcriptional variation in a population-based setting. To assess if COPD-associated variants in 15q25.1 are methylation quantitative trait loci, epigenome-wide association analysis of four genetic variants, previously associated with COPD (P < 5 × 10

Indexed as

AgedChromosomes, Human, Pair 15Cigarette SmokingDNA MethylationFemaleGene Expression RegulationGenetic Association StudiesGenetic Predisposition to DiseaseHumansIron Regulatory Protein 2MaleMiddle AgedProteasome Endopeptidase ComplexPulmonary Disease, Chronic ObstructiveQuantitative Trait LociReceptors, NicotinicIron Regulatory Protein 2Proteasome Endopeptidase ComplexPSMA4 protein, humanReceptors, Nicotinic

Identifiers

PMID29422661
PMCPMC5945654
OpenAlexW2786797148

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.