Evidence map›Paper›PMID 39030555›Full record

ArticleOrphanet journal of rare diseases2024

Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification.

Raymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, Fleur S van Dijk, David O Sillence

Abstract readLetterComment
PubMed Full text at PMC Publisher
In one paragraph

Article in Orphanet journal of rare diseases, 2024. 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

5 authors.

Raymond DalgleishDepartment of Genetics and Genome Biology, University of Leicester, Leicester, UK. raymond.dalgleish@leicester.ac.uk.ORCID 0000-0001-7667-187X
Dimitra MichaDepartment of Human Genetics, Amsterdam Reproduction and Development, Amsterdam Movement Sciences, Amsterdam UMC, Amsterdam, The Netherlands.ORCID 0000-0001-7890-4411
Andrea Superti-FurgaUniversity of Lausanne and Genetica AG, Lausanne, Switzerland.ORCID 0000-0002-3543-7531
Fleur S van DijkNorth West Thames Regional Genetics Service, London North West University Health Care NHS Trust, Harrow, UK.ORCID 0000-0001-6341-169X
David O SillenceGenomic Medicine and Paediatrics & Adolescent Health, Sydney University Clinical School, Children's Hospital, Westmead, NSW, Australia.ORCID 0000-0002-5638-2998

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A paper published in Orphanet Journal of Rare Diseases proposes a new classification of osteogenesis imperfecta (OI) based upon underlying pathological mechanisms. The proposed numbering of OI types conflicts with the currently used numbering and is likely to lead to confusion. In addition, classification of OI according to underlying pathogenic mechanisms is not novel.

Indexed as

Osteogenesis ImperfectaHumansClassificationNosologyOsteogenesis imperfecta

Identifiers

PMID39030555
PMCPMC11264877

What OpenQuestion holds

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Registered trials

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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.