Evidence map›Paper›PMID 25464374›Full record

ReviewCurrent opinion in neurobiology2015

Autism spectrum disorders: from genes to neurobiology.

A Jeremy Willsey, Matthew W State

Abstract readReview
In one paragraph

Review in Current opinion in neurobiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
–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

76 citing papers in PubMed.

  1. Review
  2. Review
  3. Convergence of autism proteins at the cilium.bioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Decoding the genetic landscape of autism: A comprehensive review.World journal of clinical pediatrics · 2024
    Article
  6. Reflections on the past two decades of Mind, Brain, and Education.Mind, brain and education : the official journal of the International Mind, Brain, and Education Society · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Neuronal oscillations: early biomarkers of psychiatric disease?Frontiers in behavioral neuroscience · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

16 more citing papers are in PubMed but not listed here.

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.

A Jeremy WillseyDepartment of Psychiatry, University of California, San Francisco, San Francisco, California 94158, United States; Institute for Human Genetics, University of California, San Francisco, San Francisco, California 94143, United States.
Matthew W StateDepartment of Psychiatry, University of California, San Francisco, San Francisco, California 94158, United States; Institute for Human Genetics, University of California, San Francisco, San Francisco, California 94143, United States. Electronic address: matthew.state@ucsf.edu.

Funding

Transcriptional and Epigenetic Signatures of Human Brain Development and AutismU01MH103339 · NIMH · YALE UNIVERSITY · PI SESTAN, NENAD, STATE, MATTHEW W. · 2014 to 2017
$6.5M
4/4 The Autism Sequencing Consortium: Autism gene discovery in the >20,000 exomes (supplement)U01MH100239 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STATE, MATTHEW W. · 2013 to 2015
$3.0M
Genomic Profiling and Functional Mutation Analysis in Autism Spectrum DisordersRC2MH089956 · NIMH · YALE UNIVERSITY · PI GIRALDEZ, ANTONIO J, STATE, MATTHEW W. · 2009 to 2010
$2.2M
Canadian Institutes of Health ResearchNIMH NIH HHS RC2 MH089956NIMH NIH HHS U01 MH100239NIMH NIH HHS U01 MH103339
6 · The paper itself

Abstract

Advances in genome-wide technology, coupled with the availability of large cohorts, are finally yielding a steady stream of autism spectrum disorder (ASD) genes carrying mutations of large effect. These findings represent important molecular clues, but at the same time present notable challenges to traditional strategies for moving from genes to neurobiology. A remarkable degree of genetic heterogeneity, the biological pleiotropy of ASD genes, and the tremendous complexity of the human brain are prompting the development of new strategies for translating genetic discoveries into therapeutic targets. Recent developments in systems biology approaches that 'contextualize' these genetic findings along spatial, temporal, and cellular axes of human brain development are beginning to bridge the gap between high-throughput gene discovery and testable pathophysiological hypotheses.

Indexed as

Genetic Predisposition to DiseaseNeurobiologyBrainChild Development Disorders, PervasiveHumans

Identifiers

PMID25464374
PMCPMC4586254

What OpenQuestion holds

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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.