Evidence map›Paper›PMID 41153437›Full record

ArticleGenes2025

Whole-Exome Sequencing of Discordant Monozygotic Twins for Congenital Scoliosis: A Family Case Study.

Diana Samarkhanova, Madina Seidualy, Ulykbek Kairov, Nurbek Nadirov, Maxat Zhabagin

Abstract readCase Reports
In one paragraph

Article in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Diana SamarkhanovaNational Center for Biotechnology, Astana 010000, Kazakhstan.ORCID 0000-0002-6558-6546
Madina SeidualyNational Center for Biotechnology, Astana 010000, Kazakhstan.
Ulykbek KairovCenter for Life Sciences, National Laboratory Astana, Nazarbayev University, Astana 010000, Kazakhstan.ORCID 0000-0001-8511-8064
Nurbek NadirovNational Center for Biotechnology, Astana 010000, Kazakhstan.
Maxat ZhabaginNational Center for Biotechnology, Astana 010000, Kazakhstan.ORCID 0000-0003-3414-0610

Funding

Ministry of Science and Higher Education of the Republic of Kazakhstan AP19579029
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Exome SequencingScoliosisTwins, MonozygoticHomeodomain ProteinsHumansMutationPedigreeHomeodomain Proteinscongenital scoliosisde novo variantsmonozygotic twinsvertebral malformationswhole-exome sequencing

Identifiers

PMID41153437
PMCPMC12562378

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.