Evidence map›Paper›PMID 31443485›Full record

ArticleGenes2019

Maternal Haplotypes in

Veronica Tisato, Paola Muggeo, Tracy Lupiano, Giovanna Longo, Maria Luisa Serino, Massimo Grassi, Ermanno Arcamone, Paola Secchiero, Giorgio Zauli, Nicola Santoro and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. "International journal of molecular sciences · 2019
    Review
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

11 authors at 1 institution in 1 country.

Veronica TisatoDepartment of Morphology, Surgery & Experimental Medicine and LTTA Centre, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0001-8448-066X
Paola MuggeoDepartment of Pediatric Oncology & Hematology, University Hospital Policlinico, 70124 Bari, Italy.
Tracy LupianoDepartment of Biomedical & Specialty Surgical Sciences, and Centre Haemostasis & Thrombosis, University of Ferrara, 44121 Ferrara, Italy.
Giovanna LongoDepartment of Biomedical & Specialty Surgical Sciences, and Centre Haemostasis & Thrombosis, University of Ferrara, 44121 Ferrara, Italy.
Maria Luisa SerinoDepartment of Biomedical & Specialty Surgical Sciences, and Centre Haemostasis & Thrombosis, University of Ferrara, 44121 Ferrara, Italy.
Massimo GrassiDepartment of Pediatric Oncology & Hematology, University Hospital Policlinico, 70124 Bari, Italy.
Ermanno ArcamoneDepartment of Pediatric Oncology & Hematology, University Hospital Policlinico, 70124 Bari, Italy.
Paola SecchieroDepartment of Morphology, Surgery & Experimental Medicine and LTTA Centre, University of Ferrara, 44121 Ferrara, Italy.
Giorgio ZauliDepartment of Morphology, Surgery & Experimental Medicine and LTTA Centre, University of Ferrara, 44121 Ferrara, Italy.
Nicola SantoroDepartment of Pediatric Oncology & Hematology, University Hospital Policlinico, 70124 Bari, Italy.
Donato GemmatiDepartment of Biomedical & Specialty Surgical Sciences, and Centre Haemostasis & Thrombosis, University of Ferrara, 44121 Ferrara, Italy. d.gemmati@unife.it.
University of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Childhood acute lymphoblastic leukemia (ALL) peaks around age 2-4, and in utero genetic epigenetic mother-fetus crosstalk might tune ALL onset during childhood life. Folate genes variably interact with vitamin status on ALL risk and prognosis. We investigated

Indexed as

Epigenesis, GeneticHaplotypesPolymorphism, Single NucleotideAdultAge of OnsetChildChild, PreschoolFemaleHomozygoteHumansMaleMethylenetetrahydrofolate Reductase (NADPH2)MothersPrecursor Cell Lymphoblastic Leukemia-LymphomaPromoter Regions, GeneticTetrahydrofolate DehydrogenaseMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanTetrahydrofolate DehydrogenaseALL onsetChildhood Acute Lymphoblastic LeukemiaDHFRepigeneticsfolatemother-fetus in utero crosstalkMTHFRMTXparent-origin effect (POE)polymorphism/gene variant

Identifiers

PMID31443485
PMCPMC6770441
OpenAlexW2969569698

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.