Evidence map›Paper›PMID 25118027›Full record

ArticleEuropean journal of human genetics : EJHG2015

The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.

Christopher Geoffrey Woods, Mohamed Osman Eltahir Babiker, Iain Horrocks, John Tolmie, Ingo Kurth

Erratum issuedAbstract readLetter
In one paragraph

Article in European journal of human genetics : EJHG, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Peripheral temperature dysregulation associated with functionally altered NaPflugers Archiv : European journal of physiology · 2023
    Article
  5. Article
  6. Pathophysiology of Nociception and Rare Genetic Disorders with Increased Pain Threshold or Pain Insensitivity.Pathophysiology : the official journal of the International Society for Pathophysiology · 2022
    Review
  7. Genetic pain loss disorders.Nature reviews. Disease primers · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Differential Modulation of the Voltage-Gated NaFrontiers in molecular biosciences · 2021
    Article
  14. The development of somatosensory neurons: Insights into pain and itch.Current topics in developmental biology · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. Novel Compound HeterozygousFrontiers in genetics · 2020
    Article
  19. Article
  20. Voltage-gated sodium channels: (NaThe Journal of physiology · 2018
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Christopher Geoffrey WoodsDepartment of Medical Genetics, Cambridge Institute for Medical Research, Addenbrooke's Hospital, UK.
Mohamed Osman Eltahir BabikerFraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, Scotland, UK.
Iain HorrocksFraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, Scotland, UK.
John TolmieDepartment of Clinical Genetics, Southern General Hospital, Glasgow, Scotland, UK.
Ingo KurthInstitute of Human Genetics, Jena University Hospital, Jena, Germany.

Funding

Medical Research Council MR/J012742/1
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic VariationPhenotypeAllelesAmino Acid SubstitutionHumansMutationNAV1.9 Voltage-Gated Sodium ChannelPain Insensitivity, CongenitalNAV1.9 Voltage-Gated Sodium Channel

Identifiers

PMID25118027
PMCPMC4402639

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.