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
0.6field-weighted citation impact, top 33% of its field
1 · What the graph read from itWhat 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, 2 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
12 authors at 6 institutions in 1 country.
Laura N EadieBlood Cancer Program, Precision Cancer Medicine Theme, South Australian Health & Medical Research Institute, Adelaide, SA 5000, Australia.ORCID 0000-0003-1912-7602 Jacqueline A RehnBlood Cancer Program, Precision Cancer Medicine Theme, South Australian Health & Medical Research Institute, Adelaide, SA 5000, Australia.ORCID 0000-0001-5043-6943 James BreenFaculty of Health and Medical Sciences, University of Adelaide, Adelaide, SA 5000, Australia.
Michael P OsbornFaculty of Health and Medical Sciences, University of Adelaide, Adelaide, SA 5000, Australia.ORCID 0000-0002-1288-9930 Sophie JessopAustralian & New Zealand Children's Haematology/Oncology Group, Clayton, VIC 3168, Australia.ORCID 0000-0001-6403-0186 Charlotte E J DownesBlood Cancer Program, Precision Cancer Medicine Theme, South Australian Health & Medical Research Institute, Adelaide, SA 5000, Australia.ORCID 0000-0001-7458-836X Susan L HeatleyBlood Cancer Program, Precision Cancer Medicine Theme, South Australian Health & Medical Research Institute, Adelaide, SA 5000, Australia.ORCID 0000-0001-7497-6477 Barbara J McClureBlood Cancer Program, Precision Cancer Medicine Theme, South Australian Health & Medical Research Institute, Adelaide, SA 5000, Australia.
David T YeungBlood Cancer Program, Precision Cancer Medicine Theme, South Australian Health & Medical Research Institute, Adelaide, SA 5000, Australia.
Tamas ReveszFaculty of Health and Medical Sciences, University of Adelaide, Adelaide, SA 5000, Australia.
Benjamin SaxonFaculty of Health and Medical Sciences, University of Adelaide, Adelaide, SA 5000, Australia.ORCID 0000-0003-1598-5343 Deborah L WhiteBlood Cancer Program, Precision Cancer Medicine Theme, South Australian Health & Medical Research Institute, Adelaide, SA 5000, Australia.ORCID 0000-0003-4844-333X South Australian Health and Medical Research Institute · AUANZCHOG · AURoyal Adelaide Hospital · AUWomen's and Children's Hospital · AUAustralian Centre for Plant Functional Genomics · AUAustralian Red Cross Lifeblood · AU
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
Chromosomal rearrangements involving the
Indexed as
F-Box ProteinsPrecursor Cell Lymphoblastic Leukemia-LymphomaChromosome AberrationsGene FusionGenomicsHumansIkaros Transcription FactorInfantInfant, NewbornJumonji Domain-Containing Histone DemethylasesTranscription FactorsF-Box ProteinsIkaros Transcription FactorIKZF1 protein, humanJumonji Domain-Containing Histone DemethylasesKDM2A protein, humanTranscription Factorscase reportchromosomal abnormalitiescongenital acute lymphoblastic leukemiafusion geneIKZF1 translocationinfant ALLKMT2A-rearranged ALLmRNA-sequencing
Identifiers
PMID36833191
PMCPMC9956107
OpenAlexW4317503101
What OpenQuestion holds
Textmetadata
LicenceCC BY
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