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Edwin H Cook
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researcher
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Works
10
The impact of genotype calling errors on family-based studies
scientific article published on 22 June 2016
Common genetic variants, acting additively, are a major source of risk for autism
scientific article
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
scientific article
Between a ROC and a hard place: decision making and making decisions about using the SCQ.
scientific article published in September 2007
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
scientific article
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
scientific article
A functional common polymorphism in a Sp1 recognition site of the epidermal growth factor receptor gene promoter.
scientific article
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
scientific article
Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome
scientific article published on 6 May 2016
Combining information from multiple sources in the diagnosis of autism spectrum disorders
scientific article published in September 2006
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