Funded Projects
SFARI Funded Publications
Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder.
Borges-Monroy R., Chu C., Dias C., Choi J., Lee S., Gao Y., Shin T., Park P., Walsh C., Lee E.A.
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Rodin R.E., Dou Y., Kwon M., Sherman M.A., D'Gama A.M., Doan R., Rento L.M., Girskis K.M., Bohrson C.L., Kim S.N., Nadig A., Luquette L.J., Gulhan D.C., Brain Somatic Mosaicism Network, Park P., Walsh C.
Large mosaic copy number variations confer autism risk.
Sherman M.A., Rodin R.E., Genovese G., Dias C., Barton A.R., Mukamel R.E., Berger B., Park P., Walsh C., Loh P.-R