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Genetics

Saturday, 4 May 2013: 10:30-12:30
Chamber Hall (Kursaal Centre)
10:45
A Long Noncoding RNA, MSNP1AS, Contributes to ASD Risk
T. K. Kerin A. Ramanathan K. Rivas N. Grepo G. A. Coetzee D. B. Campbell
11:00
Whole-Exome and CNV Data for ASD Sex Bias
S. J. Sanders M. W. State
11:15
Identification of Common Epigenetic Alterations in Autism
A. P. Feinberg C. Ladd-Acosta N. Parikshak A. R. Runarsson K. D. Hansen R. Irizarry M. D. Fallin W. E. Kaufmann D. H. Geschwind
11:45
Whole Genome Sequencing in Autism Identifies Hotspots for De Novo Germline Mutation
J. J. Michaelson Y. Shi M. Gujral H. Zheng D. Malhotra T. E. Gadomski J. A. Estabillo C. Corsello N. Akshoomoff Y. Li L. M. Iakoucheva J. Wang J. Sebat
12:00
Simons VIP: Expanding the Characterization of the 16p11.2 Duplication Syndrome
A. V. Snow L. Green-Snyder R. Bernier R. P. Goin-Kochel F. K. Miller J. E. Olson K. Porche E. Hanson
See more of: Genetic Factors in ASD
See more of: Biological Mechanisms