Evidence map›Paper›PMID 34282265›Full record

ArticleMolecular psychiatry2021

Correction: Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons.

Karen Runge, Rémi Mathieu, Stéphane Bugeon, Sahra Lafi, Corinne Beurrier, Surajit Sahu, Fabienne Schaller, Arthur Loubat, Leonard Herault, Stéphane Gaillard and 28 more

Registry-linked trialAbstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02450851 (Clinical and Genetic Evaluation of Patients With Undiagnosed Disorders Through the Undiagnosed Diseases Network), which is not on this 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.

NCT02450851 recruitingnot on this map

Clinical and Genetic Evaluation of Patients With Undiagnosed Disorders Through the Undiagnosed Diseases Network

TypeobservationalSponsorNational Human Genome Research Institute (NHGRI)Ran2015 to 2028Enrolled20,000ConditionsGenetic Disease
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

38 authors.

Karen Runge *INMED, INSERM, Aix-Marseille University, Marseille, France.
Rémi Mathieu *INMED, INSERM, Aix-Marseille University, Marseille, France.
Stéphane Bugeon *IBDM, Aix-Marseille University, CNRS, UMR, Marseille, France.
Sahra LafiINMED, INSERM, Aix-Marseille University, Marseille, France.
Corinne BeurrierIBDM, Aix-Marseille University, CNRS, UMR, Marseille, France.
Surajit SahuINMED, INSERM, Aix-Marseille University, Marseille, France.
Fabienne SchallerINMED, INSERM, Aix-Marseille University, Marseille, France.
Arthur LoubatINMED, INSERM, Aix-Marseille University, Marseille, France.
Leonard HeraultTAGC INSERM U1090, Aix-Marseille University, Marseille, France.
Stéphane GaillardPhenotype Expertise, 5 Boulevard du Maréchal Koenig, Marseille, France.
Emilie Pallesi-PocachardINMED, INSERM, Aix-Marseille University, Marseille, France.
Aurélie MontheilINMED, INSERM, Aix-Marseille University, Marseille, France.
Andreas BosioMiltenyi Biotec, Bergisch-Gladbach, Germany.
Jill A RosenfeldBaylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0001-5664-7987
Eva HudsonCook Children's Clinical Genetics, Fort Worth, TX, USA.
Kristin LindstromDivision of genetics and Metabolism, Phoenix Children's Hospital, Phoenix, AZ, USA.
Saadet Mercimek-AndrewsDepartment of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, Canada.
Lauren JeffriesPediatric Genomics Discovery Program, Department of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.
Arie van HaeringenDepartment of Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands.
Olivier VanakkerCenter for Medical Genetics, Department of Biomolecular Medicine, Ghent University and Ghent University Hospital, Ghent, Belgium.
Audrey Van HeckeDepartment of Neurology, Queen Fabiola Children's University Hospital, Brussels, Belgium.
Dina AmromDepartment of Neurology, Queen Fabiola Children's University Hospital, Brussels, Belgium.
Sebastien KüryCentre Hospitalier Universitaire de Nantes, Service de Génétique Médicale, Nantes, France.
Chana RatnerHackensack University Medical Center, Hackensack, NJ, USA.
Reena JethvaHackensack University Medical Center, Hackensack, NJ, USA.
Candace GambleCook Children's Clinical Genetics, Fort Worth, TX, USA.
Bernard JacqIBDM, Aix-Marseille University, CNRS, UMR, Marseille, France.
Laurent FasanoIBDM, Aix-Marseille University, CNRS, UMR, Marseille, France.
Gabriel SantpereDepartment of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-5909-8637
Belen Lorente-GaldosDepartment of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.
Nenad SestanDepartment of Neuroscience and Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0003-0966-9619
Antoinette GelotTrousseau Hospital, Paris, France.
Sylvie GiacuzzTrousseau Hospital, Paris, France.
Sandra GoebbelsMax-Planck-Institute of Experimental Medicine, Goettingen, Germany.
Alfonso RepresaINMED, INSERM, Aix-Marseille University, Marseille, France.
Carlos Cardoso *INMED, INSERM, Aix-Marseille University, Marseille, France.ORCID http://orcid.org/0000-0003-1914-9553
Harold Cremer *IBDM, Aix-Marseille University, CNRS, UMR, Marseille, France.
Antoine de ChevignyINMED, INSERM, Aix-Marseille University, Marseille, France. antoine.de-chevigny@inserm.fr.ORCID http://orcid.org/0000-0002-7413-0591

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34282265
PMCPMC8873008

What OpenQuestion holds

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Registered trials

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.