Evidence map›Paper›PMID 29713264›Full record

ReviewFrontiers in molecular neuroscience2018

Modeling Fragile X Syndrome in

Małgorzata Drozd, Barbara Bardoni, Maria Capovilla

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in molecular neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Decoding Nucleotide Repeat Expansion Diseases: Novel Insights fromInternational journal of molecular sciences · 2024
    Review
  7. Article
  8. Review
  9. Article
  10. Mouse models of fragile X-related disorders.Disease models & mechanisms · 2023
    Review
  11. Genes · 2022
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. The international exchange of Drosophila melanogaster strains.Revue scientifique et technique (International Office of Epizootics) · 2022
    Article
  17. Article
  18. Impaired Functional Connectivity Underlies Fragile X Syndrome.International journal of molecular sciences · 2022
    Article
  19. Fragile X Syndrome: From Molecular Aspect to Clinical Treatment.International journal of molecular sciences · 2022
    Review
  20. 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

3 authors at 2 institutions in 1 country.

Małgorzata DrozdUniversité Côte d'Azur, CNRS, IPMC, Valbonne, France.
Barbara BardoniCNRS LIA (Neogenex), Valbonne, France.
Maria CapovillaUniversité Côte d'Azur, CNRS, IPMC, Valbonne, France.
Institut de Pharmacologie Moléculaire et Cellulaire · FRUniversité Côte d'Azur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intellectual disability (ID) and autism are hallmarks of Fragile X Syndrome (FXS), a hereditary neurodevelopmental disorder. The gene responsible for FXS is Fragile X Mental Retardation gene 1 (

Indexed as

behaviordFRM1DrosophilaFMR1Fragile X Mental Retardation ProteinFragile X Syndromemushroom bodiesneuromuscular junction

Identifiers

PMID29713264
PMCPMC5911982
OpenAlexW2800628225

What Socratic 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 Socratic graph.