Evidence map›Paper›PMID 34385672›Full record

ArticleEuropean journal of human genetics : EJHG2021

Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases.

Birte Zurek, Kornelia Ellwanger, Lisenka E L M Vissers, Rebecca Schüle, Matthis Synofzik, Ana Töpf, Richarda M de Voer, Steven Laurie, Leslie Matalonga, Christian Gilissen and 20 more

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

Article in European journal of human genetics : EJHG, 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

30 authors.

Birte ZurekInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-8200-7542
Kornelia EllwangerInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0003-4845-5795
Lisenka E L M VissersDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0001-6470-5497
Rebecca SchüleDepartment of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany.
Matthis SynofzikDepartment of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-2280-7273
Ana TöpfJohn Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Richarda M de VoerDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0002-8222-0343
Steven LaurieCNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID http://orcid.org/0000-0003-3913-5829
Leslie MatalongaCNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Christian GilissenDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0003-1693-9699
Stephan OssowskiInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Peter A C 't HoenRadboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0003-4450-3112
Antonio VitobelloInserm-University of Burgundy-Franche Comté, Dijon, France.ORCID http://orcid.org/0000-0003-3717-8374
Julia M Schulze-HentrichInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Olaf RiessInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
Han G BrunnerDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Anthony J BrookesDepartment of Genetics and Genome Biology, University of Leicester, Leicester, UK.ORCID http://orcid.org/0000-0001-8686-0017
Ana RathINSERM, US14-Orphanet, Plateforme Maladies Rares, Paris, France.ORCID http://orcid.org/0000-0003-4308-6337
Gisèle BonneSorbonne Université, INSERM UMRS 974, Center of Research in Myology, Paris, France.ORCID http://orcid.org/0000-0002-2516-3258
Gulcin GumusEURORDIS-Rare Diseases Europe, Barcelona, Spain.
Alain VerloesGenetics Department, APHP-Robert Debré University Hospital, Université de Paris, Paris, France.ORCID http://orcid.org/0000-0003-4819-0264
Nicoline HoogerbruggeDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID http://orcid.org/0000-0003-2393-8141
Teresinha EvangelistaSorbonne Université, INSERM UMRS 974, Center of Research in Myology, Paris, France.
Tina HarmuthInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-4833-8057
Morris SwertzDepartment of Genetics, Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Dylan SpaldingEuropean Bioinformatics Institute, European Molecular Biology Laboratory, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID http://orcid.org/0000-0002-4285-2493
Alexander HoischenDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Sergi BeltranCNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.ORCID http://orcid.org/0000-0002-2810-3445
Holm GraessnerInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. holm.graessner@med.uni-tuebingen.de.ORCID http://orcid.org/0000-0001-9803-7183
Solve-RD consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34385672
PMCPMC8440583

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.