Reducing indel calling errors in whole genome and exome sequencing data.
Research Articles
Developmental regression among children with autism spectrum disorders: Onset, duration, and effects on functional outcomes.
Rare-variant extensions of the transmission disequilibrium test: Application to autism exome sequence data.
The contribution of de novo coding mutations to autism spectrum disorder.
Differences in the right inferior longitudinal fasciculus but no general disruption of white matter tracts in children with autism spectrum disorder.
Psychotropic medication use among children with autism spectrum disorders within the Simons Simplex Collection: Are core features of autism spectrum disorder related?
Accurate de novo and transmitted indel detection in exome-capture data using microassembly.
A multi-rater study on being teased among children/adolescents with autism spectrum disorder (ASD) and their typically developing siblings.
Recurrent de novo mutations implicate novel genes underlying simplex autism risk.
Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.
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