Evidence map›Paper›PMID 32111011›Full record

ArticleGenes2020

Reversion to Normal of

Elisabetta Tabolacci, Roberta Pietrobono, Giulia Maneri, Laura Remondini, Veronica Nobile, Matteo Della Monica, Maria Grazia Pomponi, Maurizio Genuardi, Giovanni Neri, Pietro Chiurazzi

Open access · goldAbstract read
In one paragraph

Article in Genes, 2020. 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
1.6field-weighted citation impact, top 16% 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, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Mechanisms of theInternational journal of molecular sciences · 2022
    Review
  5. Article
  6. Review
  7. Characterization ofFrontiers in genetics · 2021
    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 3 institutions in 2 countries.

Elisabetta TabolacciFondazione Policlinico Universitario "A. Gemelli" IRCCS, Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, 00168 Roma, Italia.
Roberta PietrobonoFondazione Policlinico Universitario "A. Gemelli" IRCCS, Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, 00168 Roma, Italia.
Giulia ManeriFondazione Policlinico Universitario "A. Gemelli" IRCCS, Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, 00168 Roma, Italia.
Laura RemondiniFondazione Policlinico Universitario A. Gemelli IRCCS, UOC Genetica Medica, 00168 Roma, Italia.
Veronica NobileFondazione Policlinico Universitario "A. Gemelli" IRCCS, Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, 00168 Roma, Italia.
Matteo Della MonicaUOC Genetica Medica e di Laboratorio, Azienda Ospedaliera di Rilievo Nazionale "A. Cardarelli", 80100 Napoli, Italia.
Maria Grazia PomponiFondazione Policlinico Universitario A. Gemelli IRCCS, UOC Genetica Medica, 00168 Roma, Italia.
Maurizio GenuardiFondazione Policlinico Universitario "A. Gemelli" IRCCS, Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, 00168 Roma, Italia.
Giovanni NeriFondazione Policlinico Universitario "A. Gemelli" IRCCS, Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, 00168 Roma, Italia.
Pietro ChiurazziFondazione Policlinico Universitario "A. Gemelli" IRCCS, Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, 00168 Roma, Italia.
Università Cattolica del Sacro Cuore · ITAgostino Gemelli University Polyclinic · ITAzienda di Rilievo Nazionale ed Alta Specializzazione · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fragile X syndrome (FXS) is mostly due to the expansion and subsequent methylation of a polymorphic CGG repeat in the 5' UTR of the

Indexed as

5' Untranslated RegionsAdultAgedAllelesChildDNA MethylationFemaleFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeGene SilencingHeterozygoteHumansMaleMutationTrinucleotide Repeat Expansion5' Untranslated RegionsFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1CGG instabilityCGG reversionFMR1 genefragile X syndromegenetic test

Identifiers

PMID32111011
PMCPMC7140891
OpenAlexW3008199611

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.