Evidence map›Paper›PMID 35743313›Full record

ArticleInternational journal of molecular sciences2022

Novel

Katarina Stingl, Britta Baumann, Pietro De Angeli, Ajoy Vincent, Elise Héon, Monique Cordonnier, Elfriede De Baere, Salmo Raskin, Mario Teruo Sato, Naoye Shiokawa and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 45% 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, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
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

12 authors at 5 institutions in 4 countries.

Katarina StinglCentre for Ophthalmology, University Eye Hospital, University of Tübingen, 72076 Tübingen, Germany.ORCID 0000-0002-8132-911X
Britta BaumannInstitute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, 72076 Tübingen, Germany.
Pietro De AngeliInstitute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, 72076 Tübingen, Germany.ORCID 0000-0002-8993-551X
Ajoy VincentDepartment of Ophthalmology and Vision Sciences, The Hospital for Sick Children and University of Toronto, Toronto, ON M5G 1X8, Canada.ORCID 0000-0001-6446-3846
Elise HéonDepartment of Ophthalmology and Vision Sciences, The Hospital for Sick Children and University of Toronto, Toronto, ON M5G 1X8, Canada.
Monique CordonnierDepartment of Ophthalmology, Hôpital Erasme, Cliniques Universitaires de Bruxelles, Université Libre de Bruxelles, 1070 Bruxelles, Belgium.
Elfriede De BaereCenter for Medical Genetics, Ghent University Hospital, Department of Biomolecular Medicine, Ghent University, 9000 Ghent, Belgium.ORCID 0000-0002-5609-6895
Salmo RaskinLaboratório Genetika, Curitiba 80730-180, Brazil.
Mario Teruo SatoDepartment of Ophthalmology & Otorhinolaryngology, Federal University of Paraná, Curitiba 80060-900, Brazil.
Naoye ShiokawaRetina and Vitreo Consulting Eye Clinic, Curitiba 80530-010, Brazil.
Susanne KohlInstitute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, 72076 Tübingen, Germany.ORCID 0000-0002-6438-6331
Bernd WissingerInstitute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, 72076 Tübingen, Germany.ORCID 0000-0001-8964-5953
STZ eyetrial · DERetina Clinic · BRUniversity of Toronto · CAGhent University Hospital · BEUniversité Libre de Bruxelles · BE

Funding

Deutsche Forschungsgemeinschaft Wi1189/12-1
6 · The paper itself

Abstract

Certain combinations of common variants in exon 3 of

Indexed as

Color Vision DefectsExonsHaplotypesHEK293 CellsHumansRetinal Cone Photoreceptor CellsRod Opsinslong-wavelength opsinmiddle-wavelength opsinRod OpsinsBlue Cone MonochromacyBornholm Eye Diseasecone photoreceptor LWS and MWS opsin genesexonic splicing defecthaplotypeminigene assay

Identifiers

PMID35743313
PMCPMC9224739
OpenAlexW4283263304

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.