Evidence map›Paper›PMID 40227798›Full record

ArticleCancers2025

Low WT1 Expression Identifies a Subset of Acute Myeloid Leukemia with a Distinct Genotype.

Michela Rondoni, Giovanni Marconi, Annalisa Nicoletti, Barbara Giannini, Elisa Zuffa, Maria Benedetta Giannini, Annamaria Mianulli, Marianna Norata, Federica Monaco, Irene Zaccheo and 6 more

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. c-Medical sciences (Basel, Switzerland) · 2026
    Review
  2. Article
  3. Review
  4. 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

16 authors.

Michela RondoniUO Ematologia, Ospedale S. Maria delle Croci, Via Randi 5, 48121 Ravenna, Italy.ORCID 0000-0003-1870-5554
Giovanni MarconiUO Ematologia, Ospedale S. Maria delle Croci, Via Randi 5, 48121 Ravenna, Italy.
Annalisa NicolettiU.O. Genetica Medica, AUSL della Romagna, Piazzale della Liberazione 60, 47522 Pievesestina di Cesena, Italy.
Barbara GianniniU.O. Genetica Medica, AUSL della Romagna, Piazzale della Liberazione 60, 47522 Pievesestina di Cesena, Italy.
Elisa ZuffaU.O. Genetica Medica, AUSL della Romagna, Piazzale della Liberazione 60, 47522 Pievesestina di Cesena, Italy.
Maria Benedetta GianniniIRCSS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori"-IRST S.r.l., 47014 Meldola, Italy.
Annamaria MianulliUO Ematologia, Ospedale Infermi, Viale Luigi Settembrini 2, 47923 Rimini, Italy.
Marianna NorataIRCSS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori"-IRST S.r.l., 47014 Meldola, Italy.
Federica MonacoUO Ematologia, Ospedale Infermi, Viale Luigi Settembrini 2, 47923 Rimini, Italy.
Irene ZaccheoIRCSS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori"-IRST S.r.l., 47014 Meldola, Italy.
Serena RocchiUO Ematologia, Ospedale S. Maria delle Croci, Via Randi 5, 48121 Ravenna, Italy.ORCID 0000-0002-2731-7898
Beatrice Anna ZannettiUO Ematologia, Ospedale S. Maria delle Croci, Via Randi 5, 48121 Ravenna, Italy.
Adele SantoniDipartimento Scienze Mediche, Chirurgiche e Neuroscienze, University of Siena, 53100 Siena, Italy.ORCID 0009-0006-9848-645X
Claudio GrazianoU.O. Genetica Medica, AUSL della Romagna, Piazzale della Liberazione 60, 47522 Pievesestina di Cesena, Italy.ORCID 0000-0003-3875-6869
Monica BocchiaDipartimento Scienze Mediche, Chirurgiche e Neuroscienze, University of Siena, 53100 Siena, Italy.
Francesco LanzaUO Ematologia, Ospedale S. Maria delle Croci, Via Randi 5, 48121 Ravenna, Italy.ORCID 0000-0002-5189-7167

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AMLCHIP mutationslow WT1 expressionmarrow dysplasiameasurable residual diseasenext-generation sequencingprognosisWT1

Identifiers

PMID40227798
PMCPMC11988028

What OpenQuestion holds

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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.