Evidence map›Paper›PMID 40968361›Full record

ArticleOrphanet journal of rare diseases2025

Correction: Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics services.

Tasha Wainstein, Cyrus Boelman, Connie Ens, William T Gibson, Kevin Gregory-Evans, Olubayo U Kolawole, Sheila K Marshall, Kathryn Selby, Jehannine Austin, Alison M Elliott and 1 more

Abstract readPublished Erratum
In one paragraph

Article in Orphanet journal of rare diseases, 2025. 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

5 · Who and what money

Authors and funding

11 authors.

Tasha WainsteinDepartment of Medical Genetics, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada. tasha.wainstein@bcchr.ca.ORCID https://orcid.org/0000-0002-4890-9657
Cyrus BoelmanDivision of Neurology, Department of Pediatrics, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
Connie EnsPediatric Partnership Heart Program, Pediatric BC Inherited Arrhythmia Program, BC Children's Heart Centre, Vancouver, BC, Canada.
William T GibsonDepartment of Medical Genetics, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
Kevin Gregory-EvansDepartment of Medical Genetics, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
Olubayo U KolawoleDepartment of Ophthalmology and Visual Sciences, The University of British Columbia, Vancouver, BC, Canada.
Sheila K MarshallSchool of Social Work, University of British Columbia, Vancouver, BC, Canada.
Kathryn SelbyDivision of Neurology, Department of Pediatrics, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
Jehannine AustinDepartment of Medical Genetics, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
Alison M ElliottDepartment of Medical Genetics, Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
GenCOUNSEL Study

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID40968361
PMCPMC12447612

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.