Funded Projects
SFARI Funded Publications
Inherited and de novo genetic risk for autism impacts shared networks.
Ruzzo E.K., Pérez-Cano L., Jung J.Y., Wang L.K., Kashef-Haghighi D., Hartl C., Singh C., Xu J., Hoekstra J.N., Leventhal O., Leppä V.M., Gandal M., Paskov K., Stockham N., Polioudakis D., Lowe J.K., Prober D.A., Geschwind D., Wall D.
Outgroup machine learning approach identifies single nucleotide variants in noncoding DNA associated with autism spectrum disorder.
Varma M., Paskov K.M., Jung J.Y., Sierra Chrisman B., Stockham N.T., Washington P.Y., Wall D.
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.
Kosmicki J.A., Samocha K.E., Howrigan D.P., Sanders S., Slowikowski K., Lek M., Karczewski K.J., Cutler D.J., Devlin B., Roeder K., Buxbaum J., Neale B.M., MacArthur D.G., Wall D., Robinson E., Daly M.