Evidence map›Paper›PMID 38002984›Full record

ArticleGenes2023

Epidemiology of

Tatyana A Vasilyeva, Andrey V Marakhonov, Anna A Voskresenskaya, Vitaly V Kadyshev, Natella V Sukhanova, Marina E Minzhenkova, Nadezhda V Shilova, Alla A Latyshova, Evgeny K Ginter, Sergey I Kutsev and 1 more

Open access · goldAbstract read
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. An Unusual Presentation of Novel Missense Variant inCurrent issues in molecular biology · 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

11 authors at 2 institutions in 1 country.

Tatyana A VasilyevaResearch Centre for Medical Genetics, 115522 Moscow, Russia.
Andrey V MarakhonovResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0002-0972-5118
Anna A VoskresenskayaFyodorov Eye Microsurgery Federal State Institution Cheboksary Branch, 428028 Cheboksary, Russia.ORCID 0000-0003-4213-4923
Vitaly V KadyshevResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0001-7765-3307
Natella V SukhanovaResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0003-4371-775X
Marina E MinzhenkovaResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0001-5458-0408
Nadezhda V ShilovaResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0002-0641-1084
Alla A LatyshovaRussian Research Institute of Health, 127254 Moscow, Russia.
Evgeny K GinterResearch Centre for Medical Genetics, 115522 Moscow, Russia.
Sergey I KutsevResearch Centre for Medical Genetics, 115522 Moscow, Russia.
Rena A ZinchenkoResearch Centre for Medical Genetics, 115522 Moscow, Russia.ORCID 0000-0003-3586-3458
Research Centre for Medical Genetics · RUIntersectoral Research and Technology Complex Eye Microsurgery · RU

Funding

Russian Science Foundation 22-25-00824
6 · The paper itself

Abstract

This study investigates the distribution of

Indexed as

AniridiaWAGR SyndromeChromosome DeletionHumansPAX6 Transcription FactorPrevalencePAX6 protein, humanPAX6 Transcription Factorcongenital aniridiagenetic epidemiologyPAX6prevalenceunexamined patientsWAGR syndrome

Identifiers

PMID38002984
PMCPMC10671545
OpenAlexW4388333643

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.