Evidence map›Paper›PMID 34946954›Full record

ArticleGenes2021

Lower Fractions of

Ida Maria Westin, Andreas Viberg, Berit Byström, Irina Golovleva

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

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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 1 institution in 1 country.

Ida Maria WestinDepartment of Medical Biosciences, Medical and Clinical Genetics, University of Umeå, 901 85 Umeå, Sweden.
Andreas VibergDepartment of Clinical Sciences, Ophthalmology, University of Umeå, 901 85 Umeå, Sweden.
Berit ByströmDepartment of Clinical Sciences, Ophthalmology, University of Umeå, 901 85 Umeå, Sweden.
Irina GolovlevaDepartment of Medical Biosciences, Medical and Clinical Genetics, University of Umeå, 901 85 Umeå, Sweden.ORCID 0000-0001-8741-0616
Umeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fuchs' endothelial corneal dystrophy (FECD) is a bilateral disease of the cornea caused by gradual loss of corneal endothelial cells. Late-onset FECD is strongly associated with the CTG18.1 trinucleotide repeat expansion in the

Indexed as

AdultAgedAged, 80 and overAllelesCorneaEndothelial CellsEndothelium, CornealFemaleFuchs' Endothelial DystrophyGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedPolymorphism, GeneticTranscription Factor 4TCF4 protein, humanTranscription Factor 4Transcription Factorsalternative transcriptsddPCRFuchs corneal dystrophymRNA expressionTranscription Factor 4 (TCF4)

Identifiers

PMID34946954
PMCPMC8702116
OpenAlexW4200031761

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.