Human genetics: Fruits of exome sequencing for autism.

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. An integrative scoring approach for prioritization of rare autism spectrum disorder candidate variants from whole exome sequencing data.Scientific reports · 2025
   Article
2. Factors Affecting Family Compliance with Genetic Testing of Children Diagnosed with Autism Spectrum Disorder.Journal of autism and developmental disorders · 2021
   Article
3. Common genetic variants on 1p13.2 associate with risk of autism.Molecular psychiatry · 2014
   Article
4. Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder.PLoS genetics · 2014
   Article
5. The effect of paternal age on offspring intelligence and personality when controlling for paternal trait level.PloS one · 2014
   Article
6. Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects.Molecular autism · 2014
   Article
7. Hunting human disease genes: lessons from the past, challenges for the future.Human genetics · 2013
   Review

Corrections and comments

• Comment on
  Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism.2012
• Comment on
  De novo mutations revealed by whole-exome sequencing are strongly associated with autism.2012
• Comment on
  Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.2012
• Comment on
  Patterns and rates of exonic de novo mutations in autism spectrum disorders.2012
• Comment on
  De novo gene disruptions in children on the autistic spectrum.2012

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.