Evidence map›Paper›PMID 31164657›Full record

ArticleScientific reports2019

Publisher Correction: In silico discovery of a FOXM1 driven embryonal signaling pathway in therapy resistant neuroblastoma tumors.

Suzanne Vanhauwaert, Bieke Decaesteker, Sara De Brouwer, Carina Leonelli, Kaat Durinck, Pieter Mestdagh, Jo Vandesompele, Karen Sermon, Geertrui Denecker, Christophe Van Neste and 2 more

Open access · goldAbstract readPublished Erratum
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 92% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Suzanne VanhauwaertCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.
Bieke DecaestekerCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0003-2264-781X
Sara De BrouwerCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.
Carina LeonelliCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.
Kaat DurinckCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.
Pieter MestdaghCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.
Jo VandesompeleCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.
Karen SermonResearch Group Reproduction and Genetics, Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel, Laarbeeklaan 103, 1090, Brussels, Belgium.
Geertrui DeneckerCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0002-2515-2911
Christophe Van NesteCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0002-5958-5731
Frank SpelemanCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0002-6628-8559
Katleen De PreterCenter for Medical Genetics (CMGG), Ghent University, Ghent, Belgium. Katleen.depreter@ugent.be.
Ghent University Hospital · BEVrije Universiteit Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.

Identifiers

PMID31164657
PMCPMC6547841
OpenAlexW2949005240

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.