Evidence map›Paper›PMID 23239965›Full record

ArticlePloS one2012

Structural, genetic, and functional signatures of disordered neuro-immunological development in autism spectrum disorder.

Vishal Saxena, Shweta Ramdas, Courtney Rothrock Ochoa, David Wallace, Pradeep Bhide, Isaac Kohane

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. The Microbiota Shapes Central Nervous System Myelination in Early Life.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. An Investigation ofPsychiatry investigation · 2018
    Article
  8. Article
  9. A starring role for microglia in brain sex differences.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2015
    Review
  10. Article
  11. 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

6 authors.

Vishal SaxenaDepartment of Neurology, Massachusetts General Hospital, Charlestown, Massachusetts, United States of America. vishal@mit.edu
Shweta Ramdas
Courtney Rothrock Ochoa
David Wallace
Pradeep Bhide
Isaac Kohane

Funding

Modeling the temporal succession of phenotypes & environnnental cuesP50MH094267 · NIMH · UNIVERSITY OF CHICAGO · PI RZHETSKY, ANDREY · 2011 to 2015
$10.2M
NIMH NIH HHS P50 MH094267NIMH NIH HHS P50MH94267
6 · The paper itself

Abstract

backgroundNumerous linkage studies have been performed in pedigrees of Autism Spectrum Disorders, and these studies point to diverse loci and etiologies of autism in different pedigrees. The underlying pattern may be identified by an integrative approach, especially since ASD is a complex disorder manifested through many loci.

methodAutism spectrum disorder (ASD) was studied through two different and independent genome-scale measurement modalities. We analyzed the results of copy number variation in autism and triangulated these with linkage studies.

resultsConsistently across both genome-scale measurements, the same two molecular themes emerged: immune/chemokine pathways and developmental pathways.

conclusionLinkage studies in aggregate do indeed share a thematic consistency, one which structural analyses recapitulate with high significance. These results also show for the first time that genomic profiling of pathways using a recombination distance metric can capture pathways that are consistent with those obtained from copy number variations (CNV).

Indexed as

Genetic Predisposition to DiseaseChildChild Development Disorders, PervasiveDevelopmental DisabilitiesDNA Copy Number VariationsGenetic LinkageGenome-Wide Association StudyHumansMetabolic Networks and PathwaysPolymorphism, Single Nucleotide

Identifiers

PMID23239965
PMCPMC3514226

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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.