Evidence map›Paper›PMID 37455927›Full record

ArticleFrontiers in endocrinology2023

Investigating the role of ASCC1 in the causation of bone fragility.

Barbara Voraberger, Johannes A Mayr, Nadja Fratzl-Zelman, Stéphane Blouin, Suma Uday, Robert Kopajtich, Marijke Koedam, Helena Hödlmayr, Saskia B Wortmann, Bernhard Csillag and 4 more

Open access · goldAbstract read
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 25% 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, 6 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

14 authors at 8 institutions in 4 countries.

Barbara VorabergerDepartment of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria.
Johannes A MayrUniversity Children's Hospital Salzburg, Paracelsus Medical University Salzburg, Salzburg, Austria.
Nadja Fratzl-ZelmanLudwig Boltzmann Institute of Osteology at the Hanusch Hospital of OEGK and AUVA Trauma Center Meidling, 1st Medical Department, Hanusch Hospital, Vienna, Austria.
Stéphane BlouinLudwig Boltzmann Institute of Osteology at the Hanusch Hospital of OEGK and AUVA Trauma Center Meidling, 1st Medical Department, Hanusch Hospital, Vienna, Austria.
Suma UdayDepartment of Endocrinology and Diabetes, Birmingham Women's and Children's NHS Foundation Trust, Institute of Metabolism and Systems Research, University of Birmingham Edgbaston, Birmingham, United Kingdom.
Robert KopajtichInstitute of Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany.
Marijke KoedamLaboratory for Calcium and Bone Metabolism, Department of Internal Medicine, Erasmus MC, Erasmus University Medical Center, Rotterdam, Netherlands.
Helena HödlmayrDepartment of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria.
Saskia B WortmannUniversity Children's Hospital Salzburg, Paracelsus Medical University Salzburg, Salzburg, Austria.
Bernhard CsillagDepartment of Neonatology, Kepler University Hospital, Linz, Austria.
Holger ProkischInstitute of Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany.
Bram C J van der EerdenLaboratory for Calcium and Bone Metabolism, Department of Internal Medicine, Erasmus MC, Erasmus University Medical Center, Rotterdam, Netherlands.
Ahmed El-GazzarDepartment of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria.
Wolfgang HöglerDepartment of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria.
Johannes Kepler University of Linz · ATErasmus MC · NLHanusch Hospital · ATHelmholtz Zentrum München · DEBirmingham Women’s and Children’s NHS Foundation Trust · GBKepler Universitätsklinikum · ATParacelsus Medical University · ATRadboud University Nijmegen · NL

Funding

Austrian Science Fund FWF I 4695
6 · The paper itself

Abstract

Bi-allelic variants in

Indexed as

AdipogenesisProteinsCarrier ProteinsCell DifferentiationFemaleHomozygoteHumansInfantSequence DeletionASCC1 protein, humanCarrier ProteinsProteinsadipogenesisASCC1bone fragilitymesenchymal stromal cellmuscular atrophyosteoblastogenesisosteoporosisSMABF2

Identifiers

PMID37455927
PMCPMC10348481
OpenAlexW4382787558

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.