Evidence map›Paper›PMID 33752678›Full record

ArticleOrphanet journal of rare diseases2021

Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome.

Antonio Atalaia, Rachel Thompson, Alberto Corvo, Leigh Carmody, Davide Piscia, Leslie Matalonga, Alfons Macaya, Angela Lochmuller, Bertrand Fontaine, Birte Zurek and 22 more

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

Article in Orphanet journal of rare diseases, 2021. 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

32 authors.

Antonio AtalaiaSorbonne Universite - Inserm UMRS 974, Center of Research in Myology, Institut de Myologie, G.H. Pitié-Salpêtrière Paris, 47, boulevard de l'Hopital, 75 651, Paris Cedex 13, France. antonio.marques-atalaia@inserm.fr.ORCID https://orcid.org/0000-0002-9345-0953
Rachel ThompsonChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Canada.
Alberto CorvoCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Leigh CarmodyThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Davide PisciaCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Leslie MatalongaCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Alfons MacayaPaediatric Neurology, Vall D'Hebron University Hospital and VHIR (Euro-NMD, ERN-RND), 08035, Barcelona, Spain.
Angela LochmullerDepartment of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Bertrand FontaineSorbonne Universite - Inserm UMRS 974, Center of Research in Myology, Institut de Myologie, G.H. Pitié-Salpêtrière Paris, 47, boulevard de l'Hopital, 75 651, Paris Cedex 13, France.
Birte ZurekInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany.
Carles Hernandez-FerrerCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Carola ReinhardInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany.
David Gómez-AndrésPaediatric Neurology, Vall D'Hebron University Hospital and VHIR (Euro-NMD, ERN-RND), 08035, Barcelona, Spain.
Jean-François DesaphyDepartment of Biomedical Sciences and Human Oncology, School of Medicine, University of Bari Aldo Moro, Bari, Italy.
Katherine SchonDepartment of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Katja LohmannInstitute of Neurogenetics, University of Lübeck, 23538, Lübeck, Germany.
Matthew J JenningsDepartment of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Matthis SynofzikDepartment of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research and Center of Neurology, University of Tübingen, Tübingen, Germany.
Olaf RiessInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany.
Rabah Ben YaouSorbonne Universite - Inserm UMRS 974, Center of Research in Myology, Institut de Myologie, G.H. Pitié-Salpêtrière Paris, 47, boulevard de l'Hopital, 75 651, Paris Cedex 13, France.
Teresinha EvangelistaUnité de Morphologie Neuromusculaire, Institut de Myologie, GHU Pitié-Salpêtrière, Paris, France.
Thiloka RatnaikeDepartment of Paediatrics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, England.
Virginie Bros-FacerEURORDIS - Rare Diseases Europe, Paris, France.
Gulcin GumusEURORDIS - Rare Diseases Europe, Paris, France.
Rita HorvathDepartment of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge Biomedical Campus, Cambridge, UK.
Patrick ChinneryDepartment of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge and MRC Mitochondrial Biology Unit, Cambridge Biomedical Campus, Cambridge, UK.
Steven LaurieCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Holm GraessnerInstitute of Medical Genetics and Applied Genomics, University of Tuebingen, Tübingen, Germany.
Peter RobinsonThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Hanns LochmullerChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Canada.
Sergi BeltranCNAG-CRG, Centre for Genomic Regulation (CRG), Barcelona Institute of Science and Technology (BIST), Barcelona, Spain.
Gisèle BonneSorbonne Universite - Inserm UMRS 974, Center of Research in Myology, Institut de Myologie, G.H. Pitié-Salpêtrière Paris, 47, boulevard de l'Hopital, 75 651, Paris Cedex 13, France.

Funding

Medical Research Council G1000848Medical Research Council MR/N010035/1Medical Research Council MR/N025431/1Medical Research Council MR/N025431/2Medical Research Council MR/V009346/1
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID33752678
PMCPMC7986249

What OpenQuestion holds

Textmetadata
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Registered trials

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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.