Evidence map›Paper›PMID 38149214›Full record

ReviewMolecular genetics and metabolism reports2024

The mutation spectrum and ethnic distribution of Wilson disease, a review.

Zahra Beyzaei, Arman Mehrzadeh, Niko Hashemi, Bita Geramizadeh

Open access · goldAbstract readReview
In one paragraph

Review in Molecular genetics and metabolism reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Age-associated clinical characteristics andFrontiers in genetics · 2026
    Article
  5. Review
  6. Article
  7. Liver diseases: epidemiology, causes, trends and predictions.Signal transduction and targeted therapy · 2025
    Review
  8. Effect of primary copper metabolism disturbance on elemental, protein, and lipid composition of the organs in Jackson toxic milk mouse.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2025
    Article
  9. Spectrum and classification ofSaudi medical journal · 2025
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Clinical and Molecular Analysis ofSultan Qaboos University medical journal · 2025
    Article
  16. Article
  17. Review
  18. 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

4 authors at 1 institution in 1 country.

Zahra BeyzaeiTransplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Arman MehrzadehSchool of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Niko HashemiSchool of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Bita GeramizadehTransplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Shiraz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wilson's disease is a complicated medical condition caused by the accumulation of copper, mostly in the liver and brain. The genetic basis of Wilson's disease is attributed to the presence of pathogenic variants in the

Indexed as

ATP7BEthnicsGenotypeMutation spectrumVariantsWilson

Identifiers

PMID38149214
PMCPMC10750106
OpenAlexW4389412595

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.