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Detection of Clinically Relevant Variants in Autism Spectrum Disorder
(
6/12/2013
)
82
minutes
Conference:
M.I.N.D. Institute Lecture Series on Neurodevelopmental Disorders
Host:
UC Davis MIND Institute
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description:
Autism Spectrum Disorder (ASD) demonstrates high heritability, familial clustering and ~4:1 male to female bias, yet the causes are only partially understood, due to extensive clinical and genetic heterogeneity. Whole genome sequencing (WGS) promises added value to identify novel ASD risk genes, as well as new mutations in known loci, but an assessment of its full utility in an ASD group has not been performed.
more on this subject:
The MET Receptor Tyrosine Kinase and Autism Risk
FGF Signaling and Neocortical Patterning
Automatically Mapping the Language Learning Environment of Young Children with Autism: Implications for Assessment and Intervention
see all from Neuroscience and Neurobiology >
conference links:
Lecture series information
more from this conference:
The MET Receptor Tyrosine Kinase and Autism Risk
FGF Signaling and Neocortical Patterning
Automatically Mapping the Language Learning Environment of Young Children with Autism: Implications for Assessment and Intervention
Neural Signatures of Atypical Brain Development in Autism
see all from this conference >