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Works
10
Analysis of shared heritability in common disorders of the brain
Functional impact of global rare copy number variation in autism spectrum disorders
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Introduction
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
Synaptic Disorders
Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting
