Evidence map›Paper›PMID 32572046›Full record

ArticleScientific reports2020

Author Correction: Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cells.

Silvia Parisi, Elena V Polishchuk, Simona Allocca, Michela Ciano, Anna Musto, Maria Gallo, Lucia Perone, Giusy Ranucci, Raffaele Iorio, Roman S Polishchuk and 1 more

Open access · goldAbstract 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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Silvia ParisiDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy. silvia.parisi@unina.it.
Elena V PolishchukTelethon Institute of Genetics and Medicine, Pozzuoli, Italy.
Simona AlloccaDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
Michela CianoDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
Anna MustoDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
Maria GalloDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
Lucia PeroneTelethon Institute of Genetics and Medicine, Pozzuoli, Italy.
Giusy RanucciDepartment of Translational Medical Science, Section of Pediatric, University of Naples Federico II, Naples, Italy.
Raffaele IorioDepartment of Translational Medical Science, Section of Pediatric, University of Naples Federico II, Naples, Italy.
Roman S PolishchukTelethon Institute of Genetics and Medicine, Pozzuoli, Italy. polish@tigem.it.
Stefano BonattiDepartment of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy. bonatti@unina.it.ORCID http://orcid.org/0000-0002-7303-0644
University of Naples Federico II · ITTelethon Institute Of Genetics And Medicine · ITFederico II University Hospital · IT

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

PMID32572046
PMCPMC7308340
OpenAlexW3035790512

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.