Evidence map›Paper›PMID 32296074›Full record

ArticleScientific reports2020

Author Correction: Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1.

Tyler B Johnson, Keegan Mechels, Ruthellen H Anderson, Jacob T Cain, David A Sturdevant, Stephen Braddock, Hailey Pinz, Mark A Wilson, Megan Landsverk, Kyle J Roux and 1 more

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

Article in Scientific reports, 2020. 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

11 authors.

Tyler B JohnsonPediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID http://orcid.org/0000-0002-6431-942X
Keegan MechelsPediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
Ruthellen H AndersonPediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
Jacob T CainPediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.ORCID http://orcid.org/0000-0003-0230-9979
David A SturdevantPediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA.
Stephen BraddockDivision of Medical Genetics, Department of Pediatrics, Saint Louis University School of Medicine, Saint Louis, Missouri, USA.
Hailey PinzDivision of Medical Genetics, Department of Pediatrics, Saint Louis University School of Medicine, Saint Louis, Missouri, USA.
Mark A WilsonDepartment of Biochemistry and Redox Biology Center, University of Nebraska, Lincoln, Nebraska, USA.
Megan LandsverkDepartment of Pediatrics, Sanford School of Medicine at the University of South Dakota, Sioux Falls, South Dakota, USA.
Kyle J RouxPediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. kyle.roux@sanfordhealth.org.
Jill M WeimerPediatric and Rare Disease Group, Sanford Research, Sioux Falls, South Dakota, USA. jill.weimer@sanfordhealth.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Identifiers

PMID32296074
PMCPMC7160118

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.