Evidence map›Paper›PMID 35228874›Full record

ArticleClinical case reports2022

Genotype-phenotype correlation in IARS2-related diseases: A case report and review of literature.

Jariya Upadia, Yuwen Li, Nicolette Walano, Stephen Deputy, Kelly Gajewski, Hans C Andersson

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. A Pair of Compound HeterozygousGlobal medical genetics · 2024
    Article
  7. Article
  8. Article
  9. Frontiers in pediatrics · 2022
    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 2 institutions in 1 country.

Jariya UpadiaHayward Genetics Center Tulane University School of Medicine New Orleans Louisiana USA.ORCID https://orcid.org/0000-0002-7589-5991
Yuwen LiHayward Genetics Center Tulane University School of Medicine New Orleans Louisiana USA.
Nicolette WalanoHayward Genetics Center Tulane University School of Medicine New Orleans Louisiana USA.
Stephen DeputyDivision of Pediatric Neurology Department of Pediatrics Louisiana State University Health Sciences Center/Children's Hospital New Orleans Louisiana USA.
Kelly GajewskiDivision of Pediatric Cardiology Department of Pediatrics Louisiana State University Health Sciences Center/Children's Hospital New Orleans Louisiana USA.
Hans C AnderssonHayward Genetics Center Tulane University School of Medicine New Orleans Louisiana USA.
Tulane University · USChildren's Hospital of New Orleans · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Isoleucyl-tRNA synthetase 2

Indexed as

CAGSSSIARS2mitochondrial diseaseWest syndromeWPW

Identifiers

PMID35228874
PMCPMC8867157
OpenAlexW4213434658

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.