Evidence map›Paper›PMID 39415662›Full record

ArticleJournal of clinical research in pediatric endocrinology2026

Unraveling a Genetic Puzzle: Could

Sirmen Kızılcan Çetin, Zeynep Şıklar, Zehra Aycan, Elif Özsu, Serdar Ceylaner, Merih Berberoğlu

Abstract readCase Reports
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 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

6 authors.

Sirmen Kızılcan ÇetinAnkara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, TürkiyeORCID 0000-0001-7397-3071
Zeynep ŞıklarAnkara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, TürkiyeORCID 0000-0003-0921-2694
Zehra AycanAnkara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, TürkiyeORCID 0000-0003-4584-2976
Elif ÖzsuAnkara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, TürkiyeORCID 0000-0002-3459-5781
Serdar CeylanerIntergen Genetic Diagnosis and Research Center, Department of Medical Genetics, Ankara, TürkiyeORCID 0000-0003-2786-1911
Merih BerberoğluAnkara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, TürkiyeORCID 0000-0003-3102-0242

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Noonan syndrome (NS) diagnosis may be challenging because of diverse clinical manifestations. This case report highlights a novel role for

Indexed as

Noonan SyndromeChildExome SequencingFemaleHumansMutationMAP3K7Noonan syndromeshort stature

Identifiers

PMID39415662
PMCPMC13197100

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.