Evidence map›Paper›PMID 36217027›Full record

ArticleJournal of human genetics2023

A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family.

Ilyas Ahmad, Ayaz Khan, Hafiza Noor Ul Ayan, Birgit Budde, Janine Altmüller, Asad Aslam Korejo, Gudrun Nürnberg, Holger Thiele, Muhmmad Tariq, Peter Nürnberg and 1 more

Open access · hybridAbstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of human genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Ilyas AhmadInstitute for Cardiogenetics, University of Lübeck, Lübeck, Germany. ilyas.ahmad@uni-luebeck.de.ORCID 0000-0003-4845-9227
Ayaz KhanNational Institute for Biotechnology and Genetic Engineering College, Pakistan Institute of Engineering and Applied Sciences (NIBGE-C, PIEAS), Faisalabad, 38000, Pakistan.
Hafiza Noor Ul AyanInstitute for Cardiogenetics, University of Lübeck, Lübeck, Germany.
Birgit BuddeCologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931, Cologne, Germany.
Janine AltmüllerCologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931, Cologne, Germany.
Asad Aslam KorejoNational Institute of Cardiovascular Disease, Karachi, 75510, Pakistan.
Gudrun NürnbergCologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931, Cologne, Germany.
Holger ThieleCologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931, Cologne, Germany.
Muhmmad TariqNational Institute for Biotechnology and Genetic Engineering College, Pakistan Institute of Engineering and Applied Sciences (NIBGE-C, PIEAS), Faisalabad, 38000, Pakistan.ORCID 0000-0002-5334-403X
Peter NürnbergCologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931, Cologne, Germany.
Jeanette ErdmannInstitute for Cardiogenetics, University of Lübeck, Lübeck, Germany.
University of Cologne · DENational Institute for Biotechnology and Genetic Engineering · PKGerman Centre for Cardiovascular Research · DENational Institute of Cardiovascular Diseases · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MAP Kinase Kinase KinasesMyopathies, Structural, CongenitalHumansMuscle, SkeletalMutationPakistanMAP3K20 protein, humanMAP Kinase Kinase Kinases

Identifiers

PMID36217027
PMCPMC9873553
OpenAlexW4304140090

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.