ArticleGenes2023
Involvement of Mitochondrial Dysfunction in
Victoria A Bjerregaard, Amanda M Levy, Mille S Batz, Ravina Salehi, Mathis Hildonen, Trine B Hammer, Rikke S Møller, Claus Desler, Zeynep Tümer
Open access · goldAbstract read
In one paragraphArticle in Genes, 2023. 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
0.2field-weighted citation impact, top 44% of its field
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed, 1 citations in OpenAlex.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
9 authors at 3 institutions in 1 country.
Victoria A BjerregaardKennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, 2600 Glostrup, Denmark.
Amanda M LevyKennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, 2600 Glostrup, Denmark.ORCID 0000-0001-7863-4300 Mille S BatzKennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, 2600 Glostrup, Denmark.
Ravina SalehiKennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, 2600 Glostrup, Denmark.
Mathis HildonenKennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, 2600 Glostrup, Denmark.ORCID 0000-0002-2016-3670 Trine B HammerDanish Epilepsy Centre, Department of Epilepsy Genetics and Personalized Medicine, 4293 Dianalund, Denmark.
Rikke S MøllerDanish Epilepsy Centre, Department of Epilepsy Genetics and Personalized Medicine, 4293 Dianalund, Denmark.
Claus DeslerDepartment of Cellular and Molecular Medicine, Center for Healthy Aging, University of Copenhagen, 2200 Copenhagen, Denmark.
Zeynep TümerKennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, 2600 Glostrup, Denmark.ORCID 0000-0002-4777-5802 Copenhagen University Hospital · DKUniversity of Copenhagen · DKUniversity of Southern Denmark · DK
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
Rett SyndromeBrainForkhead Transcription FactorsGene Expression RegulationHumansMitochondriaNerve Tissue ProteinsForkhead Transcription FactorsFOXG1 protein, humanNerve Tissue ProteinsFOXG1 syndromemitochondrial dysfunctionmitochondrial homeostasismitochondrial morphologymitochondrial respiratory capacityneurodevelopmental disorders
Identifiers
PMID36833172
PMCPMC9957531
OpenAlexW4317106309
What OpenQuestion holds
Textmetadata
LicenceCC BY
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