Evidence map›Paper›PMID 31231543›Full record

ArticleNPJ genomic medicine2019

Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.

Mark A Corbett, Clare L van Eyk, Dani L Webber, Stephen J Bent, Morgan Newman, Kelly Harper, Jesia G Berry, Dimitar N Azmanov, Karen J Woodward, Alison E Gardner and 4 more

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

Article in NPJ genomic medicine, 2019. 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. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Mark A Corbett1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.ORCID 0000-0001-9298-3072
Clare L van Eyk1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.ORCID 0000-0003-0345-9944
Dani L Webber1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
Stephen J BentData61, Commonwealth Scientific and Industrial Research Organisation, Ecosciences Precinct, Dutton Park, Brisbane, QLD 4102 Australia.
Morgan Newman3School of Biological Sciences, University of Adelaide, Adelaide, South Australia 5005 Australia.
Kelly Harper1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
Jesia G Berry1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
Dimitar N Azmanov4Department of Diagnostic Genomics, Queen Elizabeth II Medical Centre, PathWest, Nedlands, WA 6009 Australia.
Karen J Woodward4Department of Diagnostic Genomics, Queen Elizabeth II Medical Centre, PathWest, Nedlands, WA 6009 Australia.
Alison E Gardner1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
Jennie Slee6Genetic Services of Western Australia, King Edward Memorial Hospital, Subiaco, WA 6008 Australia.
Luís A Pérez-Jurado7Genetics Unit, Universitat Pompeu Fabra, Barcelona, 08003 Spain.ORCID 0000-0002-1988-3005
Alastair H MacLennan1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
Jozef Gecz1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.1038/s41525-018-0073-4.].

Indexed as

Gene expressionNeurodevelopmental disordersNext-generation sequencingStructural variation

Identifiers

PMID31231543
PMCPMC6544631

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.