Questionable pathogenicity of FOXG1 duplication.

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.

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.

Who cites it

7 citing papers in PubMed.

1. International journal of molecular sciences · 2019
   Review
2. Regulatory variants of FOXG1 in the context of its topological domain organisation.European journal of human genetics : EJHG · 2018
   Article
3. Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite.BMC medical genetics · 2014
   Article
4. Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12.European journal of human genetics : EJHG · 2013
   Article
5. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.European journal of human genetics : EJHG · 2013
   Article
6. Do regulatory regions matter in FOXG1 duplications?European journal of human genetics : EJHG · 2013
   Article
7. 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.European journal of human genetics : EJHG · 2012
   Article

Corrections and comments

• Commented on by
  Do regulatory regions matter in FOXG1 duplications?2013
• Comment on
  Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.2011

Authors and funding

4 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as