Evidence map›Paper›PMID 32607130›Full record

ArticleMolecular cytogenetics2020

Identifying novel genetic alterations in pediatric acute lymphoblastic leukemia based on copy number analysis.

Jéssica Almeida Batista-Gomes, Fernando Augusto Rodrigues Mello, Edivaldo Herculano Corrêa de Oliveira, Michel Platini Caldas de Souza, Alayde Vieira Wanderley, Laudreisa da Costa Pantoja, Ney Pereira Carneiro Dos Santos, Bruna Cláudia Meireles Khayat, André Salim Khayat

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular cytogenetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 3 institutions in 1 country.

Jéssica Almeida Batista-GomesOncology Research Center, Federal University of Pará, Belém, Brazil.ORCID 0000-0002-2409-7041
Fernando Augusto Rodrigues MelloOncology Research Center, Federal University of Pará, Belém, Brazil.
Edivaldo Herculano Corrêa de OliveiraCell culture and Cytogenetic Laboratory, Evandro Chagas Institute, Ananindeua, Brazil.
Michel Platini Caldas de SouzaCell culture and Cytogenetic Laboratory, Evandro Chagas Institute, Ananindeua, Brazil.
Alayde Vieira WanderleyOctávio Lobo Children's Cancer Hospital, Belém, Brazil.
Laudreisa da Costa PantojaOctávio Lobo Children's Cancer Hospital, Belém, Brazil.
Ney Pereira Carneiro Dos SantosOncology Research Center, Federal University of Pará, Belém, Brazil.
Bruna Cláudia Meireles KhayatOncology Research Center, Federal University of Pará, Belém, Brazil.
André Salim KhayatOncology Research Center, Federal University of Pará, Belém, Brazil.
Universidade Federal do Pará · BRHospital Geral de Bonsucesso · BRInstituto Evandro Chagas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Copy number variations (CNVs) analysis may reveal molecular biomarkers and provide information on the pathogenesis of acute lymphoblastic leukemia (ALL). We investigated the gene copy number in childhood ALL by microarray and select three new recurrent CNVs to evaluate by real-time PCR assay:

Indexed as

ALL (acute lymphoblastic leukemia) childhood leukemiaCopy number variationsDMBT1KIAA0125PRDM16

Identifiers

PMID32607130
PMCPMC7320540
OpenAlexW3037403721

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.