Evidence map›Paper›PMID 37834872›Full record

ReviewJournal of clinical medicine2023

Updates on Emerging Interventions for Autosomal Recessive

Liang Wang, Serena M Shah, Simran Mangwani-Mordani, Ninel Z Gregori

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Genotype frequency of Stargardt disease in Labrador Retrievers in Japan.The Journal of veterinary medical science · 2026
    Article
  3. Article
  4. Review
  5. Dysregulated DNA Methylation inInternational journal of molecular sciences · 2025
    Article
  6. Review
  7. Review
  8. Review
  9. Therapeutic Applications of Aptamers.International journal of molecular sciences · 2024
    Review
  10. 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 2 institutions in 1 country.

Liang WangUniversity of Miami Miller School of Medicine, Miami, FL 33136, USA.ORCID 0000-0002-8761-0770
Serena M ShahUniversity of Miami Miller School of Medicine, Miami, FL 33136, USA.ORCID 0000-0002-0981-7792
Simran Mangwani-MordaniDepartment of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USA.ORCID 0000-0002-9417-3353
Ninel Z GregoriDepartment of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
University of Miami · USUnited States Department of Veterans Affairs · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal recessive Stargardt disease (STGD1) is an inherited retinal degenerative disease associated with a mutated ATP-binding cassette, subfamily A, member 4 (

Indexed as

ABCA4adeno-associated viral vectorsdeuterated vitamin Aemixustatgene therapyhuman embryonic stem cellsStargardt diseasestem cell therapyvisual cycle modulators

Identifiers

PMID37834872
PMCPMC10573680
OpenAlexW4387119462

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.