Evidence map›Paper›PMID 30870518›Full record

ArticlePloS one2019

Correction: Dectin-1 Polymorphism: A Genetic Disease Specifier in Autism Spectrum Disorders?

Meriem Bennabi, Richard Delorme, José Oliveira, Catherine Fortier, Mohamed Lajnef, Wahid Boukouaci, Jean-Paul Feugeas, François Marzais, Alexandru Gaman, Dominique Charron and 4 more

Abstract readPublished Erratum
In one paragraph

Article in PloS one, 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
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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Meriem Bennabi
Richard Delorme
José Oliveira
Catherine Fortier
Mohamed Lajnef
Wahid Boukouaci
Jean-Paul Feugeas
François Marzais
Alexandru Gaman
Dominique Charron
Bijan Ghaleh
Rajagopal Krishnamoorthy
Marion Leboyer
Ryad Tamouza

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.1371/journal.pone.0137339.].

Identifiers

PMID30870518
PMCPMC6417662

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.