Evidence map›Paper›PMID 42266416›Full record

ArticleJIMD reports2026

Expanding the

Alberte Aspaas Lundquist, Sumit Parikh, Thomas van Overeem Hansen, Flemming Wibrand, Elsebet Østergaard

Abstract read
In one paragraph

Article in JIMD reports, 2026. 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.

Alberte Aspaas LundquistDepartment of Clinical Genetics, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.ORCID https://orcid.org/0000-0002-8574-9824
Sumit ParikhDepartment of Child Neurology Cleveland Clinic Children's Hospital Cleveland Ohio USA.ORCID https://orcid.org/0000-0003-3712-8959
Thomas van Overeem HansenDepartment of Clinical Genetics, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.ORCID https://orcid.org/0000-0003-4635-2653
Flemming WibrandDepartment of Clinical Genetics, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.ORCID https://orcid.org/0000-0001-9742-8115
Elsebet ØstergaardDepartment of Clinical Genetics, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.ORCID https://orcid.org/0000-0002-8047-063X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

combined oxidative phosphorylation deficiency 32genotype–phenotype correlationhypomorphic splice variantleigh syndrome spectrummitochondrial diseaseMRPS34

Identifiers

PMID42266416
PMCPMC13243876

What OpenQuestion holds

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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.