Evidence map›Paper›PMID 31064398›Full record

ArticleGenome biology2019

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.

Warren A Cheung, Xiaojian Shao, Andréanne Morin, Valérie Siroux, Tony Kwan, Bing Ge, Dylan Aïssi, Lu Chen, Louella Vasquez, Fiona Allum and 23 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Genome biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors.

Warren A CheungDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Xiaojian ShaoDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Andréanne MorinDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Valérie SirouxTeam of Environmental Epidemiology Applied to Reproduction and Respiratory Health, Inserm U1209, CNRS, University Grenoble Alpes, Institute for Advanced Biosciences, Grenoble, France.
Tony KwanDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Bing GeDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Dylan AïssiTeam of Environmental Epidemiology Applied to Reproduction and Respiratory Health, Inserm U1209, CNRS, University Grenoble Alpes, Institute for Advanced Biosciences, Grenoble, France.
Lu ChenDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK.
Louella VasquezDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK.
Fiona AllumDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Frédéric GuénardInstitute of Nutrition and Functional Foods (INAF), Laval University, Québec, QC, G1V 0A6, Canada.
Emmanuelle BouzigonGenetic Variation and Human Diseases Unit, UMR-946, INSERM, Université Paris Diderot, Université Sorbonne Paris Cité, Paris, France.
Marie-Michelle SimonMcGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada.
Elodie BoulierMcGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada.
Adriana RedensekMcGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada.
Stephen WattDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK.
Avik DattaEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK.
Laura ClarkeEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK.
Paul FlicekEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK.
Daniel MeadDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK.
Dirk S PaulUCL Cancer Institute, University College London, 72 Huntley Street, London, WC1E 6BT, UK.
Stephan BeckUCL Cancer Institute, University College London, 72 Huntley Street, London, WC1E 6BT, UK.
Guillaume BourqueDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
Mark LathropDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada.
André TchernofQuébec Heart and Lung Institute, Laval University, Québec, QC, G1V 4G5, Canada.
Marie-Claude VohlInstitute of Nutrition and Functional Foods (INAF), Laval University, Québec, QC, G1V 0A6, Canada.
Florence DemenaisGenetic Variation and Human Diseases Unit, UMR-946, INSERM, Université Paris Diderot, Université Sorbonne Paris Cité, Paris, France.
Isabelle PinTeam of Environmental Epidemiology Applied to Reproduction and Respiratory Health, Inserm U1209, CNRS, University Grenoble Alpes, Institute for Advanced Biosciences, Grenoble, France.
Kate DownesDepartment of Haematology, University of Cambridge, Cambridge Biomedical Campus, Long Road, Cambridge, CB2 0PT, UK.
Hendrick G StunnenbergFaculty of Science, Department of Molecular Biology, Radboud University, Nijmegen, 6525GA, The Netherlands.
Nicole SoranzoDepartment of Human Genetics, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1HH, UK.
Tomi PastinenDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada. tomi.pastinen@gmail.com.
Elin GrundbergDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada. elin.grundberg@mcgill.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Following publication of the original article [1], the authors reported an error in Additional file 1.

Identifiers

PMID31064398
PMCPMC6503438

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.