Evidence map›Paper›PMID 35456463›Full record

ArticleGenes2022

A Novel Splice-Site Deletion in the

Samar S Hassan, Mohamed Abdullah, Katarina Trebusak Podkrajsek, Salwa Musa, Areej Ibrahim, Omer Babiker, Jernej Kovac, Tadej Battelino, Magdalena Avbelj Stefanija

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

Article in Genes, 2022. 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
0.4field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

9 authors at 5 institutions in 2 countries.

Samar S HassanDepartment of Pediatric Endocrinology and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum 11114, Sudan.
Mohamed AbdullahDepartment of Pediatric Endocrinology and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum 11114, Sudan.
Katarina Trebusak PodkrajsekClinical Institute of Special Laboratory Diagnostics, University Children's Hospital, Ljubljana University Medical Centre, 1000 Ljubljana, Slovenia.ORCID 0000-0002-0154-3547
Salwa MusaDepartment of Pediatric Endocrinology and Diabetes, Gaafar Ibn Auf Pediatric Tertiary Hospital, Khartoum 11114, Sudan.
Areej IbrahimSudan Childhood Diabetes Center, Khartoum 11111, Sudan.
Omer BabikerSudan Childhood Diabetes Center, Khartoum 11111, Sudan.
Jernej KovacClinical Institute of Special Laboratory Diagnostics, University Children's Hospital, Ljubljana University Medical Centre, 1000 Ljubljana, Slovenia.ORCID 0000-0003-3080-4838
Tadej BattelinoFaculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0002-0273-4732
Magdalena Avbelj StefanijaFaculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0002-0836-5114
Sudan Childhood Diabetes Association · SDUniversity of Ljubljana · SIAl-Neelain University · SDLjubljana University Medical Centre · SIUniversity of Khartoum · SD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic variants within the gene encoding the pituitary-specific transcription factor, POU class 1 homeobox 1 (

Indexed as

Genes, HomeoboxHypopituitarismFemaleHumansMutationPedigreeTranscription Factor Pit-1Transcription FactorsPOU1F1 protein, humanTranscription Factor Pit-1Transcription Factorscombined pituitary hormone deficiencyDyke–Davidoff–Masson syndromehypopituitarismmeningitisPOU1F1 gene

Identifiers

PMID35456463
PMCPMC9032872
OpenAlexW4224288605

What OpenQuestion 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 OpenQuestion graph.