Evidence map›Paper›PMID 37107692›Full record

ArticleGenes2023

Functional Analysis of a Novel, Non-Canonical

Samuel Koller, Tim Beltraminelli, Jordi Maggi, Agnès Wlodarczyk, Silke Feil, Luzy Baehr, Christina Gerth-Kahlert, Moreno Menghini, Wolfgang Berger

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors at 2 institutions in 1 country.

Samuel KollerInstitute of Medical Molecular Genetics, University of Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0003-0965-0539
Tim BeltraminelliDepartment of Ophthalmology, Institute of Clinical Neurosciences of Southern Switzerland, Ente Ospedaliero Cantonale (EOC), 6962 Lugano, Switzerland.ORCID 0000-0002-1183-8736
Jordi MaggiInstitute of Medical Molecular Genetics, University of Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0002-9906-8739
Agnès WlodarczykInstitute of Medical Molecular Genetics, University of Zurich, 8952 Schlieren, Switzerland.
Silke FeilInstitute of Medical Molecular Genetics, University of Zurich, 8952 Schlieren, Switzerland.
Luzy BaehrInstitute of Medical Molecular Genetics, University of Zurich, 8952 Schlieren, Switzerland.
Christina Gerth-KahlertDepartment of Ophthalmology, University Hospital, University of Zurich, 8091 Zurich, Switzerland.ORCID 0000-0001-6298-615X
Moreno MenghiniDepartment of Ophthalmology, Institute of Clinical Neurosciences of Southern Switzerland, Ente Ospedaliero Cantonale (EOC), 6962 Lugano, Switzerland.
Wolfgang BergerInstitute of Medical Molecular Genetics, University of Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0002-0370-3815
University of Zurich · CHEnte Ospedaliero Cantonale · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked retinitis pigmentosa (XLRP) caused by mutations in the

Indexed as

Eye ProteinsRetinitis PigmentosaDNA, ComplementaryHumansMutationRetinaDNA, ComplementaryEye ProteinsRPGR protein, humanminigenenon-canonical splice variantretinitis pigmentosaRPGR

Identifiers

PMID37107692
PMCPMC10137330
OpenAlexW4366278977

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.