Evidence map›Paper›PMID 33004807›Full record

ArticleNature communications2020

Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.

Paige B Martin, Yu Kigoshi-Tansho, Roger B Sher, Gianina Ravenscroft, Jennifer E Stauffer, Rajesh Kumar, Ryo Yonashiro, Tina Müller, Christopher Griffith, William Allen and 18 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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 15 institutions in 7 countries.

Paige B Martin *The Jackson Laboratory, Bar Harbor, ME, USA.
Yu Kigoshi-Tansho *Center for Molecular Biology of Heidelberg University (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany.
Roger B SherDepartment of Neurobiology & Behavior, Stony Brook University, Stony Brook, NY, USA.
Gianina RavenscroftHarry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, WA, Australia.
Jennifer E StaufferThe Jackson Laboratory, Bar Harbor, ME, USA.
Rajesh KumarCenter for Molecular Biology of Heidelberg University (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany.
Ryo YonashiroDepartment of Molecular Medicine, Scripps Research, Jupiter, FL, USA.
Tina MüllerDepartment of Molecular Medicine, Scripps Research, Jupiter, FL, USA.
Christopher GriffithCollege of Medicine Pediatrics, University of South Florida, Tampa, FL, USA.
William AllenMission Fullerton Genetics Center, Mission Health, Asheville, NC, USA.
Davut PehlivanDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Tamar HarelDepartment of Genetic and Metabolic Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Martin ZenkerInstitute of Human Genetics, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.ORCID http://orcid.org/0000-0003-1618-9269
Denise HowtingHarry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, WA, Australia.
Denny SchanzeInstitute of Human Genetics, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.ORCID http://orcid.org/0000-0003-2748-9929
Eissa A FaqeihDepartment of Genetics, King Fahad Medical City, Riyadh, Saudi Arabia.
Naif A M AlmontashiriThe Center for Genetics and Inherited Diseases, Taibah University, Almadinah Almunwarah, Saudi Arabia.ORCID http://orcid.org/0000-0003-3607-395X
Reza MaroofianNeurogenetics Laboratory, UCL Queen Square Institute of Neurology, London, UK.
Henry HouldenNeurogenetics Laboratory, UCL Queen Square Institute of Neurology, London, UK.ORCID http://orcid.org/0000-0002-2866-7777
Neda MazaheriDepartment of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Hamid GalehdariDepartment of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Ganka DouglasGeneDx, Inc, Gaithsberg, MD, USA.ORCID http://orcid.org/0000-0003-4113-6505
Jennifer E PoseyDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Monique RyanDepartment of Neurology, The Royal Children's Hospital, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0001-6397-1910
James R LupskiDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Nigel G LaingHarry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, WA, Australia.
Claudio A P JoazeiroCenter for Molecular Biology of Heidelberg University (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany. c.joazeiro@zmbh.uni-heidelberg.de.
Gregory A CoxThe Jackson Laboratory, Bar Harbor, ME, USA. Greg.Cox@jax.org.
Baylor College of Medicine · USJackson Laboratory · USScripps Research Institute · USThe University of Western Australia · AUHeidelberg University · DENational Hospital for Neurology and Neurosurgery · GBOtto-von-Guericke-Universität Magdeburg · DEShahid Chamran University of Ahvaz · IRHadassah Medical Center · ILKing Fahd Medical City · SAMission Health · USRoyal Children's Hospital · AUStony Brook University · USTaibah University · SAUniversity of South Florida · US

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

PMID33004807
PMCPMC7529740
OpenAlexW3091404388

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.