publication venue for
- A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees. 10:20. 2018
- Developmental phenotype in Phelan-McDermid (22q13.3 deletion) syndrome: a systematic and prospective study in 34 children. 8:16. 2016
- Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation. 8:36. 2016
- Wnt signaling networks in autism spectrum disorder and intellectual disability. 8:45. 2016
- Behavioral, cognitive, and adaptive development in infants with autism spectrum disorder in the first 2 years of life. 7:24. 2015
- A molecular genetic study of autism and related phenotypes in extended pedigrees. 5:30. 2013
- Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. 3:113-123. 2011