Evidence map›Paper›PMID 34966298›Full record

ArticleFrontiers in psychiatry2021

Experiences of the Molecular Diagnosis of Fragile X Syndrome in Ecuador.

Juan Pozo-Palacios, Arianne Llamos-Paneque, Christian Rivas, Emily Onofre, Andrea López-Cáceres, Jenniffer Villareal

Open access · goldAbstract read
In one paragraph

Article in Frontiers in psychiatry, 2021. 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
0.2field-weighted citation impact, top 37% 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, 2 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 4 institutions in 2 countries.

Juan Pozo-PalaciosFacultad de Ciencias Médicas, Escuela de Medicina, Universidad de Cuenca, Cuenca, Ecuador.
Arianne Llamos-PanequeMedical Genetic Services, Hospital de las Fuerzas Armadas, Quito, Ecuador.
Christian RivasMedical Genetic Services, Hospital de las Fuerzas Armadas, Quito, Ecuador.
Emily OnofreMedical Genetic Services, Hospital de las Fuerzas Armadas, Quito, Ecuador.
Andrea López-CáceresNeurodesarrollo Quito, Quito, Ecuador.
Jenniffer VillarealNeurodesarrollo Quito, Quito, Ecuador.
Escuela Politécnica del Ejército · ECFundación Santa Fe de Bogotá · COUniversidad Internacional del Ecuador · ECUniversity of Cuenca · EC

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fragile X syndrome (FXS) is the most common cause of hereditary intellectual disability and the second most common cause of intellectual disability of genetic etiology. This complex neurodevelopmental disorder is caused by an alteration in the CGG trinucleotide expansion in fragile X mental retardation gene 1 (

Indexed as

dynamic mutation diseasesFMR1fragile X syndromeintellectual disabilitiesrepetitions

Identifiers

PMID34966298
PMCPMC8710471
OpenAlexW4200389221

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.