Evidence map›Paper›PMID 42074581›Full record

ArticleGenes2026

Similarities and Differences of Multiple Epiphyseal Dysplasias: Genetic Features and Natural Course in 22 Patients.

Hasan Emir Taner, Dilek Uludağ Alkaya, Ayşe Kalyoncu Uçar, Ali Şeker, Tuncay Centel, Timur Yıldırım, Nilay Güneş, Beyhan Tüysüz

Abstract read
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In one paragraph

Article in Genes, 2026. 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

8 authors.

Hasan Emir TanerDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, 34098 Istanbul, Turkey.
Dilek Uludağ AlkayaDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, 34098 Istanbul, Turkey.ORCID 0000-0002-0495-6152
Ayşe Kalyoncu UçarDepartment of Radiology, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, 34098 Istanbul, Turkey.ORCID 0000-0001-8433-1883
Ali ŞekerDepartment of Orthopedics and Traumatology, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, 34098 Istanbul, Turkey.ORCID 0000-0003-1259-6668
Tuncay CentelIndependent Researcher, 34158 Istanbul, Turkey.ORCID 0009-0003-8527-2004
Timur YıldırımIndependent Researcher, 34158 Istanbul, Turkey.
Nilay GüneşDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, 34098 Istanbul, Turkey.ORCID 0000-0002-7787-3630
Beyhan TüysüzDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, 34098 Istanbul, Turkey.ORCID 0000-0002-9620-5021

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

OsteochondrodysplasiasAdolescentCartilage Oligomeric Matrix ProteinChildChild, PreschoolCollagen Type IXExome SequencingFemaleHumansMaleMatrilin ProteinsMutationPhenotypeSulfate TransportersCartilage Oligomeric Matrix ProteinCOL9A2 protein, humanCOL9A3 protein, humanCollagen Type IXMATN3 protein, humanMatrilin ProteinsSLC26A2 protein, humanSulfate TransportersTSP5 protein, humanCANT1COL9A2COL9A3COMPMATN3multiple epiphyseal dysplasiaphenotype variabilitySLC26A2

Identifiers

PMID42074581
PMCPMC13115595

What OpenQuestion holds

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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.