Evidence map›Paper›PMID 42739309›Full record

ArticleDiagnostics (Basel, Switzerland)2026

Ahmet Kablan, Abdullah Sezer, Atakan Deniz, Elifcan Taşdelen, Firdevs Dinçsoy Bir, Abdulkerim Kolkıran, Melike Ataseven Kulalı, Kerem Teralı, Emregül Işık

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Diagnostics (Basel, Switzerland), 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

9 authors.

Ahmet KablanDepartment of Medical Genetics, Ankara Etlik City Hospital, Ankara 06170, Türkiye.ORCID 0000-0002-8966-2208
Abdullah SezerDepartment of Medical Genetics, Ankara Etlik City Hospital, Ankara 06170, Türkiye.ORCID 0000-0003-3886-3808
Atakan DenizDepartment of Medical Genetics, Ankara Etlik City Hospital, Ankara 06170, Türkiye.ORCID 0000-0003-4871-5374
Elifcan TaşdelenDepartment of Medical Genetics, Ankara Etlik City Hospital, Ankara 06170, Türkiye.ORCID 0000-0003-3917-9792
Firdevs Dinçsoy BirDepartment of Medical Genetics, Ankara Etlik City Hospital, Ankara 06170, Türkiye.ORCID 0009-0009-2187-1554
Abdulkerim KolkıranDepartment of Pediatric Genetics, Ankara Etlik City Hospital, Ankara 06170, Türkiye.ORCID 0000-0001-9316-9910
Melike Ataseven KulalıDepartment of Pediatric Genetics, Ankara Etlik City Hospital, Ankara 06170, Türkiye.ORCID 0000-0001-6377-6162
Kerem TeralıDepartment of Medical Biochemistry, Faculty of Medicine, Cyprus Health and Social Sciences University, Morphou 99750, Cyprus.ORCID 0000-0002-9964-6383
Emregül IşıkDepartment of Pediatric Endocrinology, Bilkent City Hospital, Ankara 06800, Türkiye.ORCID 0000-0003-0162-6745

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Helsmoortel–Van der Aa syndromenovel variantsreduced penetrance Turkish case series

Identifiers

PMID42739309
PMCPMC13565597

What OpenQuestion holds

Textmetadata
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.