Evidence map›Paper›PMID 34257424›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2021

Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities.

Virginie Carmignac, Cyril Mignot, Emmanuelle Blanchard, Paul Kuentz, Marie-Hélène Aubriot-Lorton, Victoria E R Parker, Arthur Sorlin, Sylvie Fraitag, Jean-Benoît Courcet, Yannis Duffourd and 34 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, 2021. 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. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

44 authors.

Virginie CarmignacINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France. virginie.carmignac@chu-dijon.fr.
Cyril MignotNeuropaediatrics and Development Pathology Department, Trousseau Hospital, AP-HP, Paris, France.
Emmanuelle BlanchardPlateforme IBiSA de Microscopie Electronique, Anatomie et cytologie pathologique, Université et CHRU de Tours, Tours, France.
Paul KuentzINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Marie-Hélène Aubriot-LortonPathology department, Dijon-Burgundy University Hospital, Dijon, France.
Victoria E R ParkerThe University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK.
Arthur SorlinINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Sylvie FraitagService d'Anatomie et Cytologie Pathologique, Necker-Enfants Malades Hospital, Paris, France.
Jean-Benoît CourcetINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Yannis DuffourdINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Diana RodriguezGenetics Department and Reference Center for rare causes of Intellectual Disability, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
Rachel G KnoxThe University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK.
Satyamaanasa PolubothuPaediatric Dermatology, Great Ormond St Hospital for Children NHS Foundation Trust, London, UK.
Anne BolandNational Genotyping Center, Genomic Institute, CEA, Evry, France.
Robert OlasoNational Genotyping Center, Genomic Institute, CEA, Evry, France.
Marc DelepineNational Genotyping Center, Genomic Institute, CEA, Evry, France.
Véronique DarmencyPediatrics and Medical Genetics Department, Dijon-Bourgogne University Hospital, Dijon, France.
Melissa RiachiUCL GOS Institute of Child Health, London, UK.
Chloé QuelinClinical Genetics department, Rennes University Hospital, Rennes, France.
Paul RollierClinical Genetics department, Rennes University Hospital, Rennes, France.
Louise GoujonClinical Genetics department, Rennes University Hospital, Rennes, France.
Sarah GrottoGenetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
Yline CapriGenetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.
Marie-Line JacquemontMedical Genetics Unit, CHU La Réunion, Saint-Pierre, France.
Sylvie OdentClinical Genetics department, Rennes University Hospital, Rennes, France.
Daniel AmramClinical Genetics Department, Créteil Hospital, Créteil, France.
Martin ChevarinINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Catherine Vincent-DelormeMedical Genetic Department, Jeanne de Flandre Hospital, Lille, France.
Benoît CatteauDermatology department, Lille University Hospital, Lille, France.
Laurent GuibaudPediatric and Fetal Imaging Department, Hospices Civils de Lyon, Bron, France.
Alexis ArzimanoglouDepartment of Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology, University Hospitals of Lyon (HCL), Lyon, France.
Malika KeddarCytogenetics Department, Dijon University Hospital, Dijon, France.
Catherine SarretMedical genetics department, Pôle Femme et Enfant, Clermont-Ferrand University Hospital-Hôpital d'Estaing, Clermont-Ferrand, France.
Patrick CallierINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Didier BessisDermatology Department, Montpellier University Hospital, Montpellier, France.
David GenevièveMedical Genetics Department, Montpellier University Hospital, Montpellier, France.
Jean-François DeleuzeNational Genotyping Center, Genomic Institute, CEA, Evry, France.
Christel ThauvinINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Robert K SempleThe University of Cambridge Metabolic Research Laboratories, Institute of Metabolic Science, Cambridge, UK.
Christophe PhilippeINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Jean-Baptiste RivièreINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Veronica A KinslerPaediatric Dermatology, Great Ormond St Hospital for Children NHS Foundation Trust, London, UK.
Laurence FaivreINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.
Pierre VabresINSERM UMR1231, Bourgogne Franche-Comté University, Dijon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34257424
PMCPMC8414795

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.