Evidence map›Paper›PMID 37895004›Full record

ArticleInternational journal of molecular sciences2023

Hematologic Neoplasms Associated with Down Syndrome: Cellular and Molecular Heterogeneity of the Diseases.

Edoardo Peroni, Michele Gottardi, Lucia D'Antona, Maria Luigia Randi, Antonio Rosato, Giacomo Coltro

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

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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

6 authors at 4 institutions in 1 country.

Edoardo PeroniImmunology and Molecular Oncology Unit, Veneto Institute of Oncology, IOV-IRCCS, 35128 Padova, Italy.ORCID 0000-0002-2551-6295
Michele GottardiOnco Hematology, Department of Oncology, Veneto Institute of Oncology, IOV-IRCCS, 31033 Padua, Italy.ORCID 0000-0003-0704-6979
Lucia D'AntonaMedical Genetics Unit, Mater Domini University Hospital, 88100 Catanzaro, Italy.ORCID 0000-0002-8288-9784
Maria Luigia RandiFirst Medical Clinic, Department of Medicine-DIMED, University of Padova, 35128 Padova, Italy.ORCID 0000-0001-7945-1864
Antonio RosatoImmunology and Molecular Oncology Unit, Veneto Institute of Oncology, IOV-IRCCS, 35128 Padova, Italy.
Giacomo ColtroDepartment of Clinical and Experimental Medicine, University of Florence, 50134 Florence, Italy.ORCID 0000-0002-0816-5462
Istituto Oncologico Veneto · ITUniversity of Padua · ITAzienda Ospedaliero Universitario Mater Domini · ITUniversity of Florence · IT

Funding

Ministero della Salute Ricerca corrente
6 · The paper itself

Abstract

The molecular basis of Down syndrome (DS) predisposition to leukemia is not fully understood but involves various factors such as chromosomal abnormalities, oncogenic mutations, epigenetic alterations, and changes in selection dynamics. Myeloid leukemia associated with DS (ML-DS) is preceded by a preleukemic phase called transient abnormal myelopoiesis driven by

Indexed as

Down SyndromeHematologic NeoplasmsHumansJanus KinasesMutationSignal TransductionSTAT Transcription FactorsTumor MicroenvironmentJanus KinasesSTAT Transcription Factorsacute lymphoblastic leukemiaacute myeloid leukemiaDown syndromemulti-omics approachpersonalized medicinesingle-cell RNA sequencingtrisomy 21

Identifiers

PMID37895004
PMCPMC10607483
OpenAlexW4387737986

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.