Evidence map›Paper›PMID 37239361›Full record

ArticleGenes2023

The

Vera G Pshennikova, Fedor M Teryutin, Alexandra M Cherdonova, Tuyara V Borisova, Aisen V Solovyev, Georgii P Romanov, Igor V Morozov, Alexander A Bondar, Olga L Posukh, Sardana A Fedorova 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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 3 institutions in 1 country.

Vera G PshennikovaLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yaroslavskogo 6/3, 677019 Yakutsk, Russia.ORCID 0000-0001-6866-9462
Fedor M TeryutinLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yaroslavskogo 6/3, 677019 Yakutsk, Russia.
Alexandra M CherdonovaLaboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.
Tuyara V BorisovaLaboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.
Aisen V SolovyevLaboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.
Georgii P RomanovLaboratory of Molecular Biology, Institute of Natural Sciences, M.K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.ORCID 0000-0002-2936-5818
Igor V MorozovNovosibirsk State University, 630090 Novosibirsk, Russia.ORCID 0000-0002-0307-4203
Alexander A BondarInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russia.ORCID 0000-0001-9181-0487
Olga L PosukhNovosibirsk State University, 630090 Novosibirsk, Russia.ORCID 0000-0003-1352-3591
Sardana A FedorovaLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yaroslavskogo 6/3, 677019 Yakutsk, Russia.ORCID 0000-0002-6952-3868
Nikolay A BarashkovLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yaroslavskogo 6/3, 677019 Yakutsk, Russia.ORCID 0000-0002-6984-7934
North-Eastern Federal University · RUNovosibirsk State University · RUInstitute of Chemical Biology and Fundamental Medicine · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The

Indexed as

Connexin 26Hearing LossHearing Loss, SensorineuralHumansMutationRussiaConnexin 26GJB2 protein, humanBaikal Lake regionconnexin 26 (Cx26)genotype-phenotype analysisGJB2 genehaplotype analysishearing impairmentRussiaSiberia

Identifiers

PMID37239361
PMCPMC10218609
OpenAlexW4367315066

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.