Evidence map›Paper›PMID 30297699›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2019

Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations.

Kristof Van Schil, Sarah Naessens, Stijn Van de Sompele, Marjolein Carron, Alexander Aslanidis, Caroline Van Cauwenbergh, Anja K Mayer, Mattias Van Heetvelde, Miriam Bauwens, Hannah Verdin and 11 more

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

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 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. NovelInternational journal of molecular sciences · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Kristof Van SchilCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Sarah NaessensCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Stijn Van de SompeleCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Marjolein CarronCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Alexander AslanidisLaboratory for Experimental Immunology of the Eye, Department of Ophthalmology, University of Cologne, Cologne, Germany.
Caroline Van CauwenberghCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Anja K MayerMolecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tuebingen, Tuebingen, Germany.
Mattias Van HeetveldeCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Miriam BauwensCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Hannah VerdinCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Frauke CoppietersCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Michael E GreenbergDepartment of Neurobiology, Harvard Medical School, Boston, Massachusetts, USA.
Marty G YangDepartment of Neurobiology, Harvard Medical School, Boston, Massachusetts, USA.
Marcus KarlstetterLaboratory for Experimental Immunology of the Eye, Department of Ophthalmology, University of Cologne, Cologne, Germany.
Thomas LangmannLaboratory for Experimental Immunology of the Eye, Department of Ophthalmology, University of Cologne, Cologne, Germany.
Katleen De PreterCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Susanne KohlMolecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tuebingen, Tuebingen, Germany.
Timothy J CherryDepartment of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.
Bart P LeroyCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
CNV Study Group
Elfride De BaereCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium. Elfride.DeBaere@UGent.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The original version of this Article contained an error in the spelling of the author Anja K. Mayer, which was incorrectly given as Anja Kathrin Mayer. This has now been corrected in both the PDF and HTML versions of the Article.

Identifiers

PMID30297699
PMCPMC7609298

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.