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The Molecular Genetics of Autism Spectrum Disorders: Genomic Mechanisms, Neuroimmunopathology, and Clinical Implications
Author(s) -
Daniel J. Guerra
Publication year - 2011
Publication title -
autism research and treatment
Language(s) - English
Resource type - Journals
eISSN - 2090-1925
pISSN - 2090-1933
DOI - 10.1155/2011/398636
Subject(s) - autism , epigenetics , disease , neuroscience , mechanism (biology) , genomics , autism spectrum disorder , biology , genetics , computational biology , genome , human genetics , copy number variation , genetic architecture , bioinformatics , medicine , psychiatry , gene , philosophy , epistemology , pathology , phenotype
Autism spectrum disorders (ASDs) have become increasingly common in recent years. The discovery of single-nucleotide polymorphisms and accompanying copy number variations within the genome has increased our understanding of the architecture of the disease. These genetic and genomic alterations coupled with epigenetic phenomena have pointed to a neuroimmunopathological mechanism for ASD. Model animal studies, developmental biology, and affective neuroscience laid a foundation for dissecting the neural pathways impacted by these disease-generating mechanisms. The goal of current autism research is directed toward a systems biological approach to find the most basic genetic and environmental causes to this severe developmental disease. It is hoped that future genomic and neuroimmunological research will be directed toward finding the road toward prevention, treatment, and cure of ASD.

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