Evidence map›Paper›PMID 36511482›Full record

ArticleJournal of clinical research in pediatric endocrinology2024

A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deletion Syndrome

Hümeyra Yaşar Köstek, Fatma Özgüç Çömlek, Hakan Gürkan, Emine Neşe Özkayın, Filiz Tütüncüler Kökenli

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 1 institution in 1 country.

Hümeyra Yaşar KöstekTrakya University Faculty of Medicine, Department of Pediatric Endocrinology, Edirne, TurkeyORCID 0000-0003-4268-3535
Fatma Özgüç ÇömlekTrakya University Faculty of Medicine, Department of Pediatric Endocrinology, Edirne, TurkeyORCID 0000-0002-2752-3480
Hakan GürkanTrakya University Faculty of Medicine, Department of Medical Genetics, Edirne, TurkeyORCID 0000-0002-8967-6124
Emine Neşe ÖzkayınTrakya University Faculty of Medicine, Department of Pediatric Nephrology, Edirne, TurkeyORCID 0000-0002-8480-2267
Filiz Tütüncüler KökenliTrakya University Faculty of Medicine, Department of Pediatric Endocrinology, Edirne, TurkeyORCID 0000-0003-3710-288X
Trakya University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maturity onset diabetes of the young (MODY) is characterized by noninsulin-dependent diabetes diagnosed before the age of 25 years with an autosomal dominant inheritance. Rare mutations in the hepatocyte nuclear factor-1-beta (

Indexed as

Chromosome DeletionChromosomes, Human, Pair 17Diabetes Mellitus, Type 2Hepatocyte Nuclear Factor 1-betaChildFemaleHumansHepatocyte Nuclear Factor 1-betaHNF1B protein, human17q12 deletiondiabetes mellitushypomagnesemiaMODY5

Identifiers

PMID36511482
PMCPMC11590729
OpenAlexW4311293031

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.