Evidence map›Paper›PMID 36460742›Full record

ArticleEuropean journal of human genetics : EJHG2023

Correction to: Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye.

Bertrand Chesneau, Véronique Ivashchenko, Christophe Habib, Véronique Gaston, Fréderic Escudié, Godelieve Morel, Yline Capri, Catherine Vincent-Delorme, Patrick Calvas, Nicolas Chassaing and 1 more

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

Article in European journal of human genetics : EJHG, 2023. 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

11 authors.

Bertrand ChesneauService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0001-9729-7346
Véronique IvashchenkoService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.
Christophe HabibService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0001-8746-7532
Véronique GastonService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0002-2323-7145
Fréderic EscudiéDépartement d'anatomopathologie, IUCT Oncopole, Toulouse, France.
Godelieve MorelService de Génétique Médicale, CHU de Rennes, Rennes, France.ORCID http://orcid.org/0000-0002-4132-6264
Yline CapriService de Génétique Médicale, Hôpital Robert Debré, APHP, Paris, France.
Catherine Vincent-DelormeService de Génétique Clinique, Hôpital Jeanne de Flandre, CHRU de Lille, Lille, France.
Patrick CalvasService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0002-7293-3382
Nicolas ChassaingService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.
Julie PlaisanciéService de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France. plaisancie.j@chu-toulouse.fr.ORCID http://orcid.org/0000-0001-7551-248X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID36460742
PMCPMC10172367

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.