Evidence map›Paper›PMID 33015249›Full record

ArticleBone reports2020

Clinical phenotype of adult offspring carriers of the p.Pro392Leu mutation within the

Mariam Dessay, François Jobin Gervais, David Simonyan, Andréanne Samson, Guylaine Gleeton, Edith Gagnon, Caroline Albert, Jacques P Brown, Laëtitia Michou

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

Article in Bone reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Update on the pathogenesis and genetics of Paget's disease of bone.Frontiers in cell and developmental biology · 2022
    Review
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 2 institutions in 1 country.

Mariam DessayCHU de Québec-Université Laval Research Centre, Quebec, Quebec, Canada.
François Jobin GervaisCHU de Québec-Université Laval Research Centre, Quebec, Quebec, Canada.
David SimonyanCHU de Québec-Université Laval Research Centre, Quebec, Quebec, Canada.
Andréanne SamsonCHU de Québec-Université Laval Research Centre, Quebec, Quebec, Canada.
Guylaine GleetonCHU de Québec-Université Laval Research Centre, Quebec, Quebec, Canada.
Edith GagnonCHU de Québec-Université Laval Research Centre, Quebec, Quebec, Canada.
Caroline AlbertDepartment of Biochemistry, CHUM, Montreal, QC, Canada.
Jacques P BrownCHU de Québec-Université Laval Research Centre, Quebec, Quebec, Canada.
Laëtitia MichouCHU de Québec-Université Laval Research Centre, Quebec, Quebec, Canada.
Université Laval · CACentre Hospitalier de l’Université de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paget's disease of bone (PDB) is a common chronic bone disorder. In the French-Canadian population, the p.Pro392Leu mutation within the

Indexed as

Bone scanClinical phenotypePaget's disease of bonep.Pro392Leu mutationSQSTM1 gene

Identifiers

PMID33015249
PMCPMC7522747
OpenAlexW3087212636

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.