Evidence map›Paper›PMID 37663822›Full record

ArticleClinical case reports2023

Shivania Reddy, Russell Simmers, Arth Shah, Natario Couser

Abstract readCase Reports
In one paragraph

Article in Clinical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Strabismus in Genetic Syndromes: A Review.Clinical & experimental ophthalmology · 2025
    Review
  2. Clinical case reports · 2023
    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.

Shivania ReddyVirginia Commonwealth University School of Medicine Richmond Virginia USA.ORCID https://orcid.org/0009-0004-6855-6870
Russell SimmersVirginia Commonwealth University School of Medicine Richmond Virginia USA.
Arth ShahVirginia Commonwealth University School of Medicine Richmond Virginia USA.
Natario CouserDepartment of Human and Molecular Genetics Virginia Commonwealth University School of Medicine Richmond Virginia USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our case report and review contribute to the understanding of ocular manifestations in NPHP1 ciliopathies by reinforcing the relationship between pathogenic genetic variants and a wide array of ophthalmic abnormalities.

Indexed as

colobomaJoubert syndrome‐4juvenile nephronophthisis‐1NPHP1‐related ciliopathiesophthalmologysenior‐Loken Syndrome‐1

Identifiers

PMID37663822
PMCPMC10468586

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.