Evidence map›Paper›PMID 37090830›Full record

ArticleJournal of pediatric genetics2023

Variant in

Juan Jose Nieto-Barcelo, Noelia Gonzalez Montes, Isabel Gonzalo Alonso, Francisco Martinez, Maria Jose Aparisi, Marina Martinez-Matilla, Ana Victoria Marco Hernandez, Miguel Tomás Vila

Open access · greenAbstract readCase Reports
In one paragraph

Article in Journal of pediatric genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

8 authors at 2 institutions in 1 country.

Juan Jose Nieto-BarceloHospital Universitari i Politecnic La Fe, Valencia, Spain.
Noelia Gonzalez MontesPediatrics Unit, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Isabel Gonzalo AlonsoPediatrics Unit, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Francisco MartinezGenetics Unit, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Maria Jose AparisiGenomics Unit, Health Research Institute Hospital La Fe (IIS La Fe), Valencia, Spain.
Marina Martinez-MatillaGenomics Unit, Health Research Institute Hospital La Fe (IIS La Fe), Valencia, Spain.
Ana Victoria Marco HernandezGenomics Unit, Health Research Institute Hospital La Fe (IIS La Fe), Valencia, Spain.
Miguel Tomás VilaNeuropediatrics Unit, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Hospital Universitari i Politècnic La Fe · ESInstituto de Investigación Sanitaria La Fe · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in

Indexed as

CACNA1Ggenetic modifierneonatal epilepsySCN2A

Identifiers

PMID37090830
PMCPMC10118702
OpenAlexW3131886988

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.