Evidence map›Paper›PMID 21937981›Full record

ReviewNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2012

Networking in autism: leveraging genetic, biomarker and model system findings in the search for new treatments.

Jeremy Veenstra-VanderWeele, Randy D Blakely

Abstract readReview
In one paragraph

Review in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 2 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

58 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Contribution of the serotonergic system to developmental brain abnormalities in autism spectrum disorder.Autism research : official journal of the International Society for Autism Research · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Drug development for Autism Spectrum Disorder (ASD): Progress, challenges, and future directions.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2021
    Review
  11. Review
  12. Article
  13. 5-Hydroxytryptamine, Glutamate, and ATP: Much More Than Neurotransmitters.Frontiers in cell and developmental biology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Saliva MicroRNA Differentiates Children With Autism From Peers With Typical and Atypical Development.Journal of the American Academy of Child and Adolescent Psychiatry · 2020
    Article
  19. Review
  20. 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

2 authors.

Jeremy Veenstra-VanderWeeleDepartment of Psychiatry, Vanderbilt University School of Medicine, Nashville, TN 37232-8548, USA.
Randy D Blakely

Funding

Project 6 Interactions of Serotonin and Circadian Signaling NetworksP50MH078028 · NIMH · VANDERBILT UNIVERSITY · PI MCDONALD, MICHAEL A · 2007 to 2011
$9.8M
Regulation of Serotonin TransportersR01MH094527 · NIMH · VANDERBILT UNIVERSITY · PI BLAKELY, RANDY D. · 2011 to 2021
$4.4M
Neurobiological Signatures of Social Dysfunction and Repetitive BehaviorR01MH094604 · NIMH · VANDERBILT UNIVERSITY · PI VEENSTRA-VANDERWEELE, JEREMY · 2011 to 2015
$2.0M
Transgenic Mouse Model to Address Heterogeneity in Autism Spectrum DisordersR01HD065278 · NICHD · VANDERBILT UNIVERSITY · PI BLAKELY, RANDY D. · 2009 to 2010
$923k
Murine Genetic Models of AutismK08MH081066 · NIMH · VANDERBILT UNIVERSITY · PI VEENSTRA-VANDERWEELE, JEREMY · 2007 to 2011
$832k
NICHD NIH HHS HD065278NICHD NIH HHS R01 HD065278NIMH NIH HHS K08 MH081066NIMH NIH HHS MH078028NIMH NIH HHS MH081066NIMH NIH HHS MH094527NIMH NIH HHS MH094604NIMH NIH HHS P50 MH078028NIMH NIH HHS R01 MH094527NIMH NIH HHS R01 MH094604
6 · The paper itself

Abstract

Autism Spectrum Disorder (ASD) is a common neurodevelopmental disorder affecting approximately 1% of children. ASD is defined by core symptoms in two domains: negative symptoms of impairment in social and communication function, and positive symptoms of restricted and repetitive behaviors. Available treatments are inadequate for treating both core symptoms and associated conditions. Twin studies indicate that ASD susceptibility has a large heritable component. Genetic studies have identified promising leads, with converging insights emerging from single-gene disorders that bear ASD features, with particular interest in mammalian target of rapamycin (mTOR)-linked synaptic plasticity mechanisms. Mouse models of these disorders are revealing not only opportunities to model behavioral perturbations across species, but also evidence of postnatal rescue of brain and behavioral phenotypes. An intense search for ASD biomarkers has consistently pointed to elevated platelet serotonin (5-HT) levels and a surge in brain growth in the first 2 years of life. Following a review of the diversity of ASD phenotypes and its genetic origins and biomarkers, we discuss opportunities for translation of these findings into novel ASD treatments, focusing on mTor- and 5-HT-signaling pathways, and their possible intersection. Paralleling the progress made in understanding the root causes of rare genetic syndromes that affect cognitive development, we anticipate progress in models systems using bona fide ASD-associated molecular changes that have the potential to accelerate the development of ASD diagnostics and therapeutics.

Indexed as

Autistic DisorderDisease Models, AnimalMiceAnimalsBiomarkersGenetic Predisposition to DiseaseHumansPsychotropic DrugsSignal TransductionBiomarkersPsychotropic Drugs

Identifiers

PMID21937981
PMCPMC3238072

What OpenQuestion holds

Textmetadata
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.