Evidence map›Paper›PMID 38465286›Full record

ArticleFrontiers in cell and developmental biology2024

The genetic landscape of mitochondrial diseases in the next-generation sequencing era: a Portuguese cohort study.

C Nogueira, C Pereira, L Silva, Mateus Laranjeira, A Lopes, R Neiva, E Rodrigues, T Campos, E Martins, A Bandeira and 13 more

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
–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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
  3. Article
  4. Article
  5. Review
  6. Article
  7. 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

23 authors.

C Nogueira *Research & Development Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
C Pereira *Newborn Screening, Metabolism & Genetics Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
L SilvaResearch & Development Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
Mateus LaranjeiraResearch & Development Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
A LopesNewborn Screening, Metabolism & Genetics Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
R NeivaNewborn Screening, Metabolism & Genetics Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
E RodriguesInherited Metabolic Diseases Reference Centre, São João Hospital University Centre, Porto, Portugal.
T CamposInherited Metabolic Diseases Reference Centre, São João Hospital University Centre, Porto, Portugal.
E MartinsInherited Metabolic Diseases Reference Centre, Santo António Hospital University Centre, Porto, Portugal.
A BandeiraInherited Metabolic Diseases Reference Centre, Santo António Hospital University Centre, Porto, Portugal.
M CoelhoInherited Metabolic Diseases Reference Centre, Santo António Hospital University Centre, Porto, Portugal.
M MagalhãesNeurology Department, Santo António Hospital University Centre, Porto, Portugal.
J DamásioNeurology Department, Santo António Hospital University Centre, Porto, Portugal.
A GasparInherited Metabolic Diseases Reference Centre, Lisboa Norte Hospital University Centre, Lisboa, Portugal.
P JaneiroInherited Metabolic Diseases Reference Centre, Lisboa Norte Hospital University Centre, Lisboa, Portugal.
A Levy GomesNeurology Department, Lisboa Norte Hospital University Centre, Lisboa, Portugal.
A C FerreiraInherited Metabolic Diseases Reference Centre, Lisboa Central Hospital Centre, Lisboa, Portugal.
S JacintoInherited Metabolic Diseases Reference Centre, Lisboa Central Hospital Centre, Lisboa, Portugal.
J P VieiraInherited Metabolic Diseases Reference Centre, Lisboa Central Hospital Centre, Lisboa, Portugal.
L DiogoInherited Metabolic Diseases Reference Centre, Coimbra Hospital and University Centre, Coimbra, Portugal.
H SantosInherited Metabolic Diseases Reference Centre, Vila Nova de Gaia Hospital Centre, Vila Nova de Gaia, Portugal.
C MendonçaPediatric Department, Faro Hospital and University Centre, Faro, Portugal.
L VilarinhoResearch & Development Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

mitochondrial diseasesmitochondrial DNAnext-generation sequencingnuclear DNAnuclear genesoxidative phosphorylationrespiratory chain

Identifiers

PMID38465286
PMCPMC10920333

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.