Evidence map›Paper›PMID 36828588›Full record

ArticleGenome research2023

The aberrant epigenome of

Varsha Poondi Krishnan, Barbara Morone, Shir Toubiana, Monika Krzak, Salvatore Fioriniello, Floriana Della Ragione, Maria Strazzullo, Claudia Angelini, Sara Selig, Maria R Matarazzo

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 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
–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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
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  6. Article
  7. ICF1-Syndrome-AssociatedBiomolecules · 2023
    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

10 authors at 5 institutions in 3 countries.

Varsha Poondi KrishnanInstitute of Genetics and Biophysics Adriano Buzzati Traverso, (IGB-ABT) CNR, Naples 80131, Italy.ORCID 0000-0002-4002-0511
Barbara MoroneInstitute of Genetics and Biophysics Adriano Buzzati Traverso, (IGB-ABT) CNR, Naples 80131, Italy.
Shir ToubianaDepartment of Genetics and Developmental Biology, Rappaport Faculty of Medicine and Research Institute, Technion, Haifa 31096, Israel.ORCID 0000-0003-3001-5281
Monika KrzakInstitute for Applied Computing (IAC) "Mauro Picone", CNR, Naples 80131 Italy.
Salvatore FiorinielloInstitute of Genetics and Biophysics Adriano Buzzati Traverso, (IGB-ABT) CNR, Naples 80131, Italy.
Floriana Della RagioneInstitute of Genetics and Biophysics Adriano Buzzati Traverso, (IGB-ABT) CNR, Naples 80131, Italy.
Maria StrazzulloInstitute of Genetics and Biophysics Adriano Buzzati Traverso, (IGB-ABT) CNR, Naples 80131, Italy; maria.matarazzo@igb.cnr.it claudia.angelini@cnr.it seligs@technion.ac.il.
Claudia AngeliniInstitute for Applied Computing (IAC) "Mauro Picone", CNR, Naples 80131 Italy; maria.matarazzo@igb.cnr.it claudia.angelini@cnr.it seligs@technion.ac.il.ORCID 0000-0001-8350-8464
Sara SeligDepartment of Genetics and Developmental Biology, Rappaport Faculty of Medicine and Research Institute, Technion, Haifa 31096, Israel; maria.matarazzo@igb.cnr.it claudia.angelini@cnr.it seligs@technion.ac.il.ORCID 0000-0001-5759-9948
Maria R MatarazzoInstitute of Genetics and Biophysics Adriano Buzzati Traverso, (IGB-ABT) CNR, Naples 80131, Italy.ORCID 0000-0002-8192-4322
Institute of Genetics and Biophysics · ITIstituto per le Applicazioni del Calcolo Mauro Picone · ITIstituto Neurologico Mediterraneo · ITRappaport Family Institute for Research in the Medical Sciences · ILTechnion – Israel Institute of Technology · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bi-allelic hypomorphic mutations in

Indexed as

Induced Pluripotent Stem CellsDNA (Cytosine-5-)-MethyltransferasesDNA MethylationEpigenetic MemoryEpigenomeHistonesDNA (Cytosine-5-)-Methyltransferaseshistone H3 trimethyl Lys4Histones

Identifiers

PMID36828588
PMCPMC10069469
OpenAlexW4321791415

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.