Evidence map›Paper›PMID 30082726›Full record

ArticleNature communications2018

Genome-wide identification of directed gene networks using large-scale population genomics data.

René Luijk, Koen F Dekkers, Maarten van Iterson, Wibowo Arindrarto, Annique Claringbould, Paul Hop, Dorret I Boomsma, Cornelia M van Duijn, Marleen M J van Greevenbroek, Jan H Veldink and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Causal effects of gestational hypertension on women's health: A Mendelian randomization analysis.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Making Genetic Testing More Clinically Valuable.Integrative medicine (Encinitas, Calif.) · 2018
    Article
  17. 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

20 authors at 7 institutions in 1 country.

René LuijkMolecular Epidemiology Section, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands.
Koen F DekkersMolecular Epidemiology Section, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands.
Maarten van ItersonMolecular Epidemiology Section, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands.
Wibowo ArindrartoSequence Analysis Support Core, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands.ORCID http://orcid.org/0000-0003-0499-0948
Annique ClaringbouldDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, 9713 AV, The Netherlands.
Paul HopMolecular Epidemiology Section, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands.
Dorret I BoomsmaDepartment of Biological Psychology, VU University Amsterdam, Neuroscience Campus Amsterdam, Amsterdam, 1081 TB, The Netherlands.
Cornelia M van DuijnGenetic Epidemiology Unit, Department of Epidemiology, ErasmusMC, Rotterdam, 3015 GE, The Netherlands.
Marleen M J van GreevenbroekDepartment of Internal Medicine, Maastricht University Medical Center, Maastricht, 6211 LK, The Netherlands.
Jan H VeldinkDepartment of Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, 3584 CG, The Netherlands.
Cisca WijmengaDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, 9713 AV, The Netherlands.
Lude FrankeDepartment of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, 9713 AV, The Netherlands.ORCID http://orcid.org/0000-0002-5159-8802
Peter A C 't HoenDepartment of Human Genetics, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands.ORCID http://orcid.org/0000-0003-4450-3112
Rick JansenDepartment of Psychiatry, VU University Medical Center, Neuroscience Campus Amsterdam, Amsterdam, 1081 HV, The Netherlands.ORCID http://orcid.org/0000-0002-3333-6737
Joyce van MeursDepartment of Internal Medicine, ErasmusMC, Rotterdam, 3015 CE, The Netherlands.
Hailiang MeiSequence Analysis Support Core, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands.
P Eline SlagboomMolecular Epidemiology Section, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands.
Bastiaan T HeijmansMolecular Epidemiology Section, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands. b.t.heijmans@lumc.nl.ORCID http://orcid.org/0000-0001-5918-0534
Erik W van ZwetMedical Statistics Section, Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, Zuid-Holland, 2333 ZC, The Netherlands. e.w.van_zwet@lumc.nl.
BIOS (Biobank-based Integrative Omics Study) Consortium
Leiden University Medical Center · NLUniversity Medical Center Groningen · NLErasmus MC · NLAmsterdam Neuroscience · NLMaastricht University · NLSURFsara (Netherlands) · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identification of causal drivers behind regulatory gene networks is crucial in understanding gene function. Here, we develop a method for the large-scale inference of gene-gene interactions in observational population genomics data that are both directed (using local genetic instruments as causal anchors, akin to Mendelian Randomization) and specific (by controlling for linkage disequilibrium and pleiotropy). Analysis of genotype and whole-blood RNA-sequencing data from 3072 individuals identified 49 genes as drivers of downstream transcriptional changes (Wald P < 7 × 10

Indexed as

Gene Regulatory NetworksGenetics, PopulationMetagenomicsCohort StudiesEndopeptidasesEpistasis, GeneticGene ExpressionGene Expression ProfilingGene Expression RegulationGenotypeHumansLinkage DisequilibriumMinor Histocompatibility AntigensPhenotypeProto-Oncogene Proteins c-bcl-2Sequence Analysis, RNABCL2-related protein A1EndopeptidasesMinor Histocompatibility AntigensProto-Oncogene Proteins c-bcl-2SENP7 protein, humanTranscription Factors

Identifiers

PMID30082726
PMCPMC6079029
OpenAlexW2771948419

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.