In one paragraphArticle in bioRxiv : the preprint server for biology, 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
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.
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
19 authors.
Marnie L MaddockMolecular Horizons, School of Medical and Indigenous Health Sciences, Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, New South Wales, Australia.ORCID 0000-0001-6393-4837 Sara MielletMolecular Horizons, School of Medical and Indigenous Health Sciences, Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, New South Wales, Australia.ORCID 0000-0003-1400-9711 Anjila DongolMolecular Horizons, School of Medical and Indigenous Health Sciences, Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, New South Wales, Australia.ORCID 0000-0003-3355-6585 Amy J HulmeMolecular Horizons, School of Medical and Indigenous Health Sciences, Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, New South Wales, Australia.ORCID 0000-0001-7700-3486 Chloe K KennedyMolecular Horizons, School of Medical and Indigenous Health Sciences, Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, New South Wales, Australia.ORCID 0009-0004-3795-8391 Rocio K Finol-UrdanetaMolecular Horizons, School of Medical and Indigenous Health Sciences, Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, New South Wales, Australia.ORCID 0000-0003-2157-4532 Alberto Nettel-AguirreSchool of Social Sciences, University of Wollongong, Wollongong, New South Wales, Australia.
Martin B DelatyckiBruce Lefroy Centre, Murdoch Children's Research Institute, Victoria, Australia.
Joel M GottesfeldScripps Research Institute, La Jolla, California, USA.
Massimo PandolfoDepartment of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.
Sanjay I BidichandaniDepartment of Pediatrics, University of Oklahoma College of Medicine, Oklahoma City, Oklahoma, USA.ORCID 0000-0001-6191-6475 Jill S NapieralaDepartment of Neurology, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0002-5141-0822 Marek NapieralaDepartment of Neurology, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0002-9987-0641 Mirella DottoriMolecular Horizons, School of Medical and Indigenous Health Sciences, Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, New South Wales, Australia.ORCID 0000-0003-0598-4195 Funding
RNA-induced transcriptional gene silencing in Friedreich ataxiaR01NS072418 · NINDS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI BIDICHANDANI, SANJAY I · 2010 to 2014
$1.2MNINDS NIH HHS R01 NS072418
6 · The paper itselfAbstract
Friedreich ataxia (FRDA) is a progressive multisystem neurodegenerative disease mostly caused by a homozygous GAA repeat expansion in the
Indexed as
BiomarkersCardiomyocytesCell-type specificityFriedreich ataxiaMeta-analysisNeurodegenerative diseaseRNA sequencingSelective vulnerabilitySensory neuronsTranscriptomic atlas
Identifiers
PMID41890103
PMCPMC13015369
What OpenQuestion holds
Textmetadata
LicenceCC BY-ND
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