Evidence map›Paper›PMID 37351107›Full record

ArticleFrontiers in endocrinology2023

Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients.

Ivo P van de Peppel, Serwet Demirdas, Behiye Özcan

Abstract readComment
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Skeletal muscle disorders as risk factors for type 2 diabetes.Molecular and cellular endocrinology · 2025
    Review
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Ivo P van de PeppelDepartment of Clinical Genetics, Erasmus Medical Centre, Rotterdam, Netherlands.
Serwet DemirdasDepartment of Clinical Genetics, Erasmus Medical Centre, Rotterdam, Netherlands.
Behiye ÖzcanDepartment of Internal Medicine, Erasmus Medical Centre, Rotterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DeafnessDiabetes Mellitus, Type 2Mitochondrial DiseasesHumansMutationclinical geneticsdiabetes mellitusheteroplasmym.3243A>GMIDDmitochondrial disease

Identifiers

PMID37351107
PMCPMC10284591

What Socratic 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 Socratic graph.