Skip to main content

Spectrum: Autism Research News

Stephan Sanders on whole-exome sequencing

 /  28 November 2012
The Presenter
Presenter
Stephan J. Sanders
Assistant Specialist, University of California, San Francisco

Stephan Sanders uses genomics and bioinformatics to understand the complex etiology of autism.

Last week, as part of the new monthly SFARI Science Series of webinars, Stephan Sanders, a postdoctoral fellow in Matthew State’s lab at Yale University, discussed how whole-exome sequencing can identify autism risk genes. You can watch a complete replay of the session above.

We’ve created a special space on the SFARI Forum to discuss this presentation, where Sanders will be available to respond. Join the conversation here »

Press Policy
The Spectrum Webinar Series aims to facilitate the free exchange of ideas among autism researchers, including discussion of published and unpublished research, hypotheses and results. Members of the press may report information presented during a Spectrum webinar only if that material has already been published elsewhere or they have first obtained express written consent from the presenter.

About Webinars
Presentations by leading experts that showcase new findings, useful techniques and emerging topics in autism research. We invite questions before and during the presentations in the Comments section.