Evidence map›Paper›PMID 26558264›Full record

ArticleBioMed research international2015

Corrigendum to "Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing".

Helle Høyer, Geir J Braathen, Øyvind L Busk, Øystein L Holla, Marit Svendsen, Hilde T Hilmarsen, Linda Strand, Camilla F Skjelbred, Michael B Russell

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

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 93% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Helle HøyerSection of Medical Genetics, Department of Laboratory Medicine, Telemark Hospital, 3710 Skien, Norway ; Head and Neck Research Group, Research Centre, Akershus University Hospital, Lørenskog, Norway ; Campus Akershus University Hospital, University of Oslo, Nordbyhagen, Norway.
Geir J BraathenSection of Medical Genetics, Department of Laboratory Medicine, Telemark Hospital, 3710 Skien, Norway ; Head and Neck Research Group, Research Centre, Akershus University Hospital, Lørenskog, Norway ; Campus Akershus University Hospital, University of Oslo, Nordbyhagen, Norway.
Øyvind L BuskSection of Medical Genetics, Department of Laboratory Medicine, Telemark Hospital, 3710 Skien, Norway.
Øystein L HollaSection of Medical Genetics, Department of Laboratory Medicine, Telemark Hospital, 3710 Skien, Norway.
Marit SvendsenSection of Medical Genetics, Department of Laboratory Medicine, Telemark Hospital, 3710 Skien, Norway.
Hilde T HilmarsenSection of Medical Genetics, Department of Laboratory Medicine, Telemark Hospital, 3710 Skien, Norway.
Linda StrandSection of Medical Genetics, Department of Laboratory Medicine, Telemark Hospital, 3710 Skien, Norway.
Camilla F SkjelbredSection of Medical Genetics, Department of Laboratory Medicine, Telemark Hospital, 3710 Skien, Norway.
Michael B RussellHead and Neck Research Group, Research Centre, Akershus University Hospital, Lørenskog, Norway ; Campus Akershus University Hospital, University of Oslo, Nordbyhagen, Norway.
Telemark Hospital · NOAkershus University Hospital · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID26558264
PMCPMC4617881
OpenAlexW2157552482

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.