Genetic and Genomic Discovery in Autism: From SNPs, to Exomes and Genomes.

This panel will summarize the state-of-the-art in autism genetics and genomics. Updates on common variant association studies, whole exome sequencing, and whole genome sequencing will be presented, as well as novel approaches aimed at the integration of the different classes of variation into a unified model of genomic risk architecture.
Friday, May 3, 2019: 10:30 AM-12:30 PM
Room: 517A (Palais des congres de Montreal)
Panel Chairs:
J. Buxbaum and M. A. Pericak-Vance
10:30 AM
Common Risk Variants Identified in Autism Spectrum Disorder
J. Grove .. The iPSYCH-Broad/MGH Autism Working Group
See more of: Molecular Genetics