Evidence map›Paper›PMID 28824526›Full record

ArticleFrontiers in neurology2017

Glu20Ter Variant in

Roman V Deev, Sergei N Bardakov, Mikhail O Mavlikeev, Ivan A Yakovlev, Zoya R Umakhanova, Patimat G Akhmedova, Raisat M Magomedova, Irina A Chekmaryeva, Gimat D Dalgatov, Artur A Isaev

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy.Annals of clinical and translational neurology · 2024
    Article
  4. Article
  5. Effects of Copy Number Variations in the Plectin (Animals : an open access journal from MDPI · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. [Research advances in limb-girdle muscular dystrophy type 2Q].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2019
    Review
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

10 authors at 5 institutions in 1 country.

Roman V DeevHuman Stem Cells Institute, Moscow, Russia.
Sergei N BardakovDepartment of Neurology, S.M. Kirov Military Medical Academy, St. Petersburg, Russia.
Mikhail O MavlikeevInstitute of Fundamental Medicine and Biology, Kazan (Volga Region) Federal University, Kazan, Russia.
Ivan A YakovlevHuman Stem Cells Institute, Moscow, Russia.
Zoya R UmakhanovaDepartment of Neurology, Dagestan State Medical Academy, Makhachkala, Russia.
Patimat G AkhmedovaDepartment of Neurology, Dagestan State Medical Academy, Makhachkala, Russia.
Raisat M MagomedovaDepartment of Neurology, Dagestan State Medical Academy, Makhachkala, Russia.
Irina A ChekmaryevaLaboratory of Electron Microscopy, A.A. Vishnevsky Institute of Surgery, Moscow, Russia.
Gimat D DalgatovHuman Stem Cells Institute, Moscow, Russia.
Artur A IsaevHuman Stem Cells Institute, Moscow, Russia.
Dagestan State Medical Academy · RUHuman Stem Cells Institute PJSC (Russia) · RUKazan Federal University · RUInstitute of Surgery named after A. V. Vishnevskogo · RUS. M. Kirov Military Medical Academy · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plectinopathies are orphan diseases caused by

Indexed as

limb-girdle muscle dystrophy 2Qlung injurymuscular dystrophiesplectinplectinopathy

Identifiers

PMID28824526
PMCPMC5534468
OpenAlexW2741564483

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.