Cited by 514Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

The neurobiology of autism

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Pardo, Carlos A., Eberhart, Charles G.·2007·Brain Pathology

Abstract

Improving clinical tests are allowing us to more precisely classify autism spectrum disorders and diagnose them at earlier ages. This raises the possibility of earlier and potentially more effective therapeutic interventions. To fully capitalize on this opportunity, however, will require better understanding of the neurobiological changes underlying this devastating group of developmental disorders. It is becoming clear that the normal trajectory of neurodevelopment is altered in autism, with aberrations in brain growth, neuronal patterning and cortical connectivity. Changes to the structure and function of synapses and dendrites have also been strongly implicated in the pathology of autism by morphological, genetic and animal modeling studies. Finally, environmental factors are likely to interact with the underlying genetic profile, and foster the clinical heterogeneity seen in autism spectrum disorders. In this review we attempt to link the molecular pathways altered in autism to the neurodevelopmental and clinical changes that characterize the disease. We focus on signaling molecules such as neurotrophin, Reelin, PTEN and hepatocyte growth factor, neurotransmitters such as serotonin and glutamate, and synaptic proteins such as neurexin, SHANK and neuroligin. We also discuss evidence implicating oxidative stress, neuroglial activation and neuroimmunity in autism.

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Crossref · 10.1111/j.1750-3639.2007.00102.x

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  • Recent imaging studies in autism have shown that the most abnormal aspect of brain development in this disorder is often the time course and trajectory rather than the final product.

    “This is particularly relevant since recent imaging studies in autism have shown that the most abnormal aspect of brain development in this disorder is often the time course and trajectory rather the final product (2, 39).”

    From A Meta-Analysis of the Corpus Callosum in Autism (2009) · cites this paper as [39]

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References 234 · Cited by 514

Authors
Pardo, C. A., & Eberhart, C. G.
Affiliations
Johns Hopkins University (US)
Corresponding author
Pardo, Carlos A.
Venue
Brain Pathology
Publisher
Wiley
Published
2007-10
Volume
17
Issue
4
Pages
434-447
ISSN
  • 1015-6305 (ISSN-L)
  • 1750-3639
OpenAlex
W1998944144
Cited by
514
References
234
Citations by year
2026: 5 · 2025: 12 · 2024: 8 · 2023: 15 · 2022: 5 · 2021: 19 · 2020: 8 · 2019: 21 · 2018: 9 · 2017: 18 · 2016: 23 · 2015: 28 · 2014: 33 · 2013: 43 · 2012: 51
FWCI
3.63
Type
journal article
Language
en
Open access
Locations
  • Brain Pathology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institute on Drug Abuse (K08DA16160, K08DA016160)
  • National Institute of Neurological Disorders and Stroke (R01NS055089)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords
autism spectrum disorder, brain development, brain growth, neuronal patterning, cortical connectivity, dendrites, neurotrophins, reelin, PTEN, hepatocyte growth factor, serotonin, glutamate, synaptic proteins, neurexin, shank, neuroligins, oxidative stress, neuroimmunity, genetic heterogeneity, environmental factors
MeSH terms
Reelin Protein, Autistic Disorder, Brain, Female, Humans, Nervous System Malformations, Neural Pathways, Pregnancy, Prenatal Exposure Delayed Effects, Signal Transduction, Gene Expression Regulation, Developmental, Genetic Predisposition to Disease

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