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12
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
Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study
Individual common variants exert weak effects on the risk for autism spectrum disorders
Increased risk of ADHD in families with ASD
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Towards a cognitive phenotype for autism: increased prevalence of executive dysfunction and superior spatial span amongst siblings of children with autism
Erratum: Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother
