Reply: ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.

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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

Corrections and comments

• Comment on
  Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.2014
• Comment on
  ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.2016

Authors and funding

4 authors at 3 institutions in 2 countries.

Funding

Abstract

PubMed holds no abstract for this paper.

Indexed as