Evidence map›Paper›PMID 36833191›Full record

ArticleGenes2023

Case Report: Rare

Laura N Eadie, Jacqueline A Rehn, James Breen, Michael P Osborn, Sophie Jessop, Charlotte E J Downes, Susan L Heatley, Barbara J McClure, David T Yeung, Tamas Revesz and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article 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 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, 2 citations in OpenAlex.

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

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 itself

Abstract

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
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.