Evidence map›Paper›PMID 35892614›Full record

ArticleChildren (Basel, Switzerland)2022

Development of an International Database for a Rare Genetic Disorder: The

Daniel Ta, Jenny Downs, Gareth Baynam, Andrew Wilson, Peter Richmond, Aron Schmidt, Amelia Decker, Helen Leonard

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Children (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Overexpression of mGluMolecular neurobiology · 2025
    Article
  3. 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 2 countries.

Daniel TaTelethon Kids Institute, University of Western Australia, Perth, WA 6009, Australia.ORCID 0000-0001-9875-0704
Jenny DownsTelethon Kids Institute, University of Western Australia, Perth, WA 6009, Australia.
Gareth BaynamTelethon Kids Institute, University of Western Australia, Perth, WA 6009, Australia.
Andrew WilsonTelethon Kids Institute, University of Western Australia, Perth, WA 6009, Australia.
Peter RichmondTelethon Kids Institute, University of Western Australia, Perth, WA 6009, Australia.
Aron SchmidtMECP2 Duplication Foundation, Tuscon, AZ 85724, USA.
Amelia DeckerMECP2 Duplication Foundation, Tuscon, AZ 85724, USA.
Helen LeonardTelethon Kids Institute, University of Western Australia, Perth, WA 6009, Australia.
The Kids Research Institute Australia · AUUniversity of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The natural history of

Indexed as

epilepsyintellectual disabilityMECP2 duplication syndromerare neurodevelopmental disorderrecurrent respiratory infections

Identifiers

PMID35892614
PMCPMC9332564
OpenAlexW4287838567

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.