Evidence map›Paper›PMID 32934367›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2021

Correction: Aminoacyl-tRNA synthetase deficiencies in search of common themes.

Sabine A Fuchs, Imre F Schene, Gautam Kok, Jurriaan M Jansen, Peter G J Nikkels, Koen L I van Gassen, Suzanne W J Terheggen-Lagro, Saskia N van der Crabben, Sanne E Hoeks, Laetitia E M Niers and 6 more

Abstract readPublished Erratum
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Correspondence on "Aminoacyl-tRNA synthetase deficiencies in search of common themes" by Fuchs et al.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Sabine A FuchsDepartment of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands. S.Fuchs@umcutrecht.nl.
Imre F Schene *Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Gautam Kok *Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Jurriaan M JansenDepartment of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Peter G J NikkelsDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Koen L I van GassenDepartment of Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
Suzanne W J Terheggen-LagroDepartment of Pediatric Pulmonology, Academic Medical Center Amsterdam, Amsterdam, The Netherlands.
Saskia N van der CrabbenDepartment of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
Sanne E HoeksDepartment of Neonatology, University Medical Center Utrecht, Utrecht, The Netherlands.
Laetitia E M NiersDepartment of Pediatrics, Maxima Medical Centre Veldhoven, Veldhoven, The Netherlands.
Nicole I WolfDepartment of Child Neurology, VU University Medical Center, Amsterdam, The Netherlands.
Maaike C de VriesNijmegen Centre for Mitochondrial Disorders at Department of Pediatrics, Radboud University Nijmegen Centre, Nijmegen, The Netherlands.
David A KoolenDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Roderick H J HouwenDivision of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Margot F MulderDepartment of Pediatrics, VU University Medical Center, Amsterdam, The Netherlands.
Peter M van HasseltDepartment of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID32934367
PMCPMC8586873

What OpenQuestion holds

Textmetadata
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.