Filters: Author is Sonnenblick, Lisa I [Clear All Filters]
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.. PLoS genetics. 5(6):e1000536.. 2009.
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.. Science translational medicine. 2(56):56ra80.. 2010.
Common genetic variants on 5p14.1 associate with autism spectrum disorders.. Nature. 459(7246):528-33.. 2009.