Evidence map›Paper›PMID 34449556›Full record

ArticleCurrent issues in molecular biology2021

Disease Progression in

Manca Tekavčič Pompe, Nika Vrabič, Marija Volk, Andrej Meglič, Martina Jarc-Vidmar, Borut Peterlin, Marko Hawlina, Ana Fakin

Open access · goldAbstract read
In one paragraph

Article in Current issues in molecular biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. CNGA3-Related Achromatopsia: A 10-Year Follow-Up.Journal of vitreoretinal diseases · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. An early onset cone dystrophy due to CEP290 mutation: a case report.Documenta ophthalmologica. Advances in ophthalmology · 2023
    Article
  7. Article
  8. 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 1 institution in 1 country.

Manca Tekavčič PompeEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0003-3730-0229
Nika VrabičEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Marija VolkClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Andrej MegličEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Martina Jarc-VidmarEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Borut PeterlinClinical Institute of Genomic Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Marko HawlinaEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Ana FakinEye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Ljubljana University Medical Centre · SI

Funding

ARRS J3-1750 1750
6 · The paper itself

Abstract

Achromatopsia has been proposed to be a morphologically predominately stable retinopathy with rare reports of progression of structural changes in the macula. A five-grade system of optical coherence tomography (OCT) features has been used for the classification of structural macular changes. However, their association with age remains questionable. We characterized the Slovenian cohort of 12 patients with pathogenic variants in

Indexed as

MutationAdolescentAdultAgedAge FactorsChildChild, PreschoolCohort StudiesColor Vision DefectsCyclic Nucleotide-Gated Cation ChannelsDisease ProgressionFemaleGenetic Predisposition to DiseaseHumansInfantLongitudinal StudiesCNGA3 protein, humanCNGB3 protein, humanCyclic Nucleotide-Gated Cation ChannelsachromatopsiaautofluorescenceCNGA3CNGB3color visioncone-dystrophydegenerationdisease stageelectroretinographyERGFAFfoveal hypoplasianystagmusOCToptical coherence tomographyprogression

Identifiers

PMID34449556
PMCPMC8929018
OpenAlexW3193636175

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.