Evidence map›Paper›PMID 37790699›Full record

ArticleFrontiers in genetics2023

Phenotype reversion as "natural gene therapy" in Fanconi anemia by a gene conversion event.

Ilaria Persico, Ilaria Fiscarelli, Alessandra Pelle, Michela Faleschini, Barbara Pasini, Anna Savoia, Roberta Bottega

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

7 authors at 5 institutions in 2 countries.

Ilaria Persico *Genomic Instability DNA Repair Syndromes Group, Joint Research Unit in Genomic Medicine UAB-IR Sant Pau, Sant Pau Biomedical Research Institute (IIB Sant Pau), Barcelona, Spain.
Ilaria Fiscarelli *Dipartimento di Scienze Mediche, Università degli Studi di Torino, Torino, Italy.
Alessandra PelleSC Genetica Medica U, AOU Città della Salute e della Scienza di Torino, Torino, Italy.
Michela FaleschiniInstitute for Maternal and Child Health-IRCCS "Burlo Garofolo", Trieste, Italy.
Barbara PasiniDipartimento di Scienze Mediche, Università degli Studi di Torino, Torino, Italy.
Anna SavoiaDepartment of Engineering for Innovation Medicine, University of Verona, Verona, Italy.
Roberta BottegaInstitute for Maternal and Child Health-IRCCS "Burlo Garofolo", Trieste, Italy.
IRCCS Materno Infantile Burlo Garofolo · ITUniversity of Turin · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITHospital de Sant Pau · ESUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic mosaicism appears as a recurrent phenomenon among patients suffering from Fanconi anemia (FA), but its direct prognostic significance mostly remains an open question. The clinical picture of FA mosaic subjects could indeed vary from just mild features to severe hematologic failure. Here, we illustrate the case of a proband whose FA familiarity, modest signs (absence of hematological anomalies and fertility issues), and chromosome fragility test transition to negative overtime were suggestive of somatic mosaicism. In line with this hypothesis, genetic testing on patient's peripheral blood and buccal swab reported the presence of the only

Indexed as

Fanconi anemiagene conversionmosaicismnatural gene therapyphenotype reversion

Identifiers

PMID37790699
PMCPMC10544911
OpenAlexW4386850044

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.