Evidence map›Paper›PMID 30607024›Full record

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

Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.

Stijn Van de Sompele, Claire Smith, Marianthi Karali, Marta Corton, Kristof Van Schil, Frank Peelman, Timothy Cherry, Toon Rosseel, Hannah Verdin, Julien Derolez and 17 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. 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

27 authors.

Stijn Van de SompeleCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Claire SmithSection of Ophthalmology and Neuroscience, School of Medicine, University of Leeds, St James's University Hospital, Leeds, UK.
Marianthi KaraliMedical Genetics, Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
Marta CortonGenetics Department, Instituto de Investigación Sanitaria-Fundación Jimenez Diaz University Hospital (IIS-FJD, UAM), Madrid, Spain.
Kristof Van SchilCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Frank PeelmanDepartment of Medical Protein Research, Faculty of Medicine and Health Sciences, Flanders Institute for Biotechnology (VIB), Ghent University, Ghent, Belgium.
Timothy CherryCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA, USA.
Toon RosseelCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Hannah VerdinCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Julien DerolezCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Thalia Van LaethemCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Kamron N KhanDepartment of Ophthalmology, St. James's University Hospital, Leeds, UK.
Martin McKibbinDepartment of Ophthalmology, St. James's University Hospital, Leeds, UK.
Carmel ToomesSection of Ophthalmology and Neuroscience, School of Medicine, University of Leeds, St James's University Hospital, Leeds, UK.
Manir AliSection of Ophthalmology and Neuroscience, School of Medicine, University of Leeds, St James's University Hospital, Leeds, UK.
Annalaura TorellaMedical Genetics, Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
Francesco TestaEye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
Belen JimenezDepartment of Ophthalmology, Fundación Jimenez Diaz University Hospital, Madrid, Spain.
Francesca SimonelliEye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy.
Julie De ZaeytijdDepartment of Ophthalmology, Ghent University and Ghent University Hospital, Ghent, Belgium.
Jenneke Van den EndeCenter for Medical Genetics, Antwerp University Hospital, Antwerp, Belgium.
Bart P LeroyCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Frauke CoppietersCenter for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
Carmen AyusoGenetics Department, Instituto de Investigación Sanitaria-Fundación Jimenez Diaz University Hospital (IIS-FJD, UAM), Madrid, Spain.
Chris F InglehearnSection of Ophthalmology and Neuroscience, School of Medicine, University of Leeds, St James's University Hospital, Leeds, UK.
Sandro BanfiMedical Genetics, Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy. banfi@tigem.it.
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 incorrect version of Fig. 3, which included two variants initially shown in black text in Fig. 3a that the authors removed from the final manuscript. The correct version of Fig. 3 without the two variants now appears in the PDF and HTML versions of the Article.

Identifiers

PMID30607024
PMCPMC6752296

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.