Evidence map›Paper›PMID 33077719›Full record

ArticleNature communications2020

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology.

Sahar Elouej, Karim Harhouri, Morgane Le Mao, Genevieve Baujat, Sheela Nampoothiri, Hϋlya Kayserili, Nihal Al Menabawy, Laila Selim, Arianne Llamos Paneque, Christian Kubisch and 20 more

Open access · goldAbstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Nature communications, 2020. 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, top 84% of its field
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, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 13 institutions in 7 countries.

Sahar ElouejAix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
Karim HarhouriAix Marseille Univ, INSERM, MMG, U1251, Marseille, France.ORCID http://orcid.org/0000-0003-2904-5221
Morgane Le MaoMitoLab, Mitochondrial Medicine Research Centre, Institut MITOVASC, CNRS UMR 6015, INSERM U1083, Université d'Angers, CHU d'Angers, Angers, France.
Genevieve BaujatDepartment of Medical Genetics, INSERM UMR 1163, Paris Descartes-Sorbonne Paris Cité University, IMAGINE Institute, Necker Enfants Malades Hospital, Paris, France.
Sheela NampoothiriDepartment of Pediatric Genetics, Amrita Institute of Medical Sciences & Research Centre, AIMS Ponekkara PO Cochin, Kerala, India.
Hϋlya KayseriliMedical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey.ORCID http://orcid.org/0000-0003-0376-499X
Nihal Al MenabawyNeurology and Metabolic Division, Cairo University Children Hospital, Cairo, Egypt.ORCID http://orcid.org/0000-0001-9177-2505
Laila SelimNeurology and Metabolic Division, Cairo University Children Hospital, Cairo, Egypt.
Arianne Llamos PanequeMedical Genetics Service Specialties Hospital FF AA No.1, Quito, Ecuador.
Christian KubischInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Davor LesselInstitute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID http://orcid.org/0000-0003-4496-244X
Robert RubinsztajnPole of Anesthesiology and Reanimation, , Necker Enfants Malades Hospital, Paris, France.
Chayki ChararDepartment of Genetics, Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
Catherine BartoliAix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
Coraline AiraultAix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
Jean-François DeleuzeCentre National de Recherche en Génomique Humaine (CNRGH) and Centre d'Etude du Polymorphisme Humain (CEPH), Institut de Biologie François Jacob, CEA, Université Paris-Saclay and Fondation Jean Dausset, Paris, France.ORCID http://orcid.org/0000-0002-5358-4463
Agnes RötigINSERM UMR1163, Institut Imagine, Paris, France.ORCID http://orcid.org/0000-0003-0589-0703
Peter BauerCENTOGENE AG, Rostock, Germany.
Catarina PereiraCENTOGENE AG, Rostock, Germany.
Abigail LohInstitute of Medical Biology, A*STAR, Singapore, Singapore.
Nathalie Escande-BeillardMedical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey.ORCID http://orcid.org/0000-0002-7706-1608
Antoine MuchirSorbonne Université, INSERM, Institute of Myology, Center of Research in Myology, Paris, France.ORCID http://orcid.org/0000-0002-4780-9275
Lisa MartinoCeleScreen SAS, Paris, France.
Yosef GruenbaumDepartment of Genetics, Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
Song-Hua LeeCeleScreen SAS, Paris, France.ORCID http://orcid.org/0000-0002-6998-3426
Philippe ManivetCeleScreen SAS, Paris, France.ORCID http://orcid.org/0000-0003-2510-6357
Guy LenaersMitoLab, Mitochondrial Medicine Research Centre, Institut MITOVASC, CNRS UMR 6015, INSERM U1083, Université d'Angers, CHU d'Angers, Angers, France.
Bruno ReversadeMedical Genetics Department, Koç University, School of Medicine (KUSoM), Istanbul, Turkey.ORCID http://orcid.org/0000-0002-4070-7997
Nicolas LévyAix Marseille Univ, INSERM, MMG, U1251, Marseille, France.
Annachiara De Sandre-GiovannoliAix Marseille Univ, INSERM, MMG, U1251, Marseille, France. annachiara.desandre-giovannoli@univ-amu.fr.ORCID http://orcid.org/0000-0002-2324-2462
Inserm · FRAgency for Science, Technology and Research · SGCairo University · EGCelescreen (France) · FRCentogene (Germany) · DECentre National de la Recherche Scientifique · FRHebrew University of Jerusalem · ILUniversität Hamburg · DEAmrita Institute of Medical Sciences and Research Centre · INCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRDélégation Paris 5 · FRKoç University · TRMedical Genetics Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Identifiers

PMID33077719
PMCPMC7572408
OpenAlexW3093077820

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.