Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Neuroimaging in developmental disorders.

Michael D Greicius1

  • 1Department of Neurology and Neurological Sciences, Stanford University School of Medicine, 401 Quarry Road, Stanford, CA 94305-5719, USA. greicius@stanford.edu

Current Opinion in Neurology
|March 20, 2003
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

APOE*4 risk-modifying genes and drug targets in Alzheimer's disease through cell-type-specific genomic analyses.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same author

An <i>APOE</i> *4-Informed Genomic Atlas of the X Chromosome in Alzheimer's Disease.

medRxiv : the preprint server for health sciences·2026
Same author

Proteomic Signatures of Protected <i>APOE</i>-ε4 Carriers Reveal Causal Pathways Associated with Delayed Alzheimer's Disease Onset.

medRxiv : the preprint server for health sciences·2026
Same author

Effects of α-synuclein pathology on synaptic dysfunction and clinical outcomes in normal aging.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same author

Population-scale burden analysis of rare damaging coding variants identifies novel risk genes for Alzheimer's disease and Parkinson's disease.

medRxiv : the preprint server for health sciences·2026
Same author

A quantitative trait locus for reduced microglial APOE expression associates with reduced cerebral amyloid angiopathy.

Nature genetics·2026
Same journal

Movement disorders and Parkinson's disease: collaborative and interdisciplinary research to advance understanding of neural circuit dysfunction, pathophysiology, and care: new horizons in technology, neuroimaging, neurophysiology, and genetics toward personalized medicine.

Current opinion in neurology·2026
Same journal

Editorial introduction.

Current opinion in neurology·2026
Same journal

Multimodal mapping of balance dysfunction in Parkinson's disease: a consensus roadmap for research and intervention.

Current opinion in neurology·2026
Same journal

Tourette syndrome: brain neurophysiology, circuit dysfunction, and neuromodulation across invasive and noninvasive approaches.

Current opinion in neurology·2026
Same journal

Dystonia: from phenotypes to genetics and therapeutic advances.

Current opinion in neurology·2026
Same journal

What can we learn from eye movements in movement disorders and Parkinson's disease?

Current opinion in neurology·2026
See all related articles

Neuroimaging studies reveal autistic individuals have larger brains, with accelerated infant growth. Research in fragile X syndrome indicates abnormal brain networks linked to behavior and protein expression.

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Medical Imaging

Background:

  • Developmental disorders like autism and fragile X syndrome present complex challenges.
  • Neuroimaging offers a non-invasive method to study brain development and function.

Purpose of the Study:

  • To review the role of neuroimaging in understanding autism and fragile X syndrome.
  • To highlight recent advancements and findings in the neuroimaging of these developmental disorders.

Main Methods:

  • Review of recent neuroimaging studies focusing on autism and fragile X syndrome.
  • Analysis of convergent findings and preliminary results from longitudinal and cross-sectional studies.

Main Results:

  • Consistent evidence shows larger brain volumes in individuals with autism, particularly evident from early childhood.

Related Experiment Videos

  • Accelerated brain growth in infancy, potentially followed by slowed growth in later childhood, is observed in autism.
  • Aberrant fronto-striatal and fronto-parietal networks are identified in fragile X syndrome, correlating with behavioral and molecular findings.
  • Conclusions:

    • Neuroimaging is a maturing, reliable in-vivo tool for studying developmental disorders.
    • Future research emphasizing larger, homogeneous groups and longitudinal designs will enhance the link between molecular biology and behavior.