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The impact of genotype calling errors on family-based studies
Common genetic variants, acting additively, are a major source of risk for autism
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Between a ROC and a hard place: decision making and making decisions about using the SCQ.
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
A functional common polymorphism in a Sp1 recognition site of the epidermal growth factor receptor gene promoter.
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome
Combining information from multiple sources in the diagnosis of autism spectrum disorders
