“Individual common variants exert weak effects on the risk for autism spectrum disorders.”, Hum Mol Genet, vol. 21, no. 21, pp. 4781-92, 2012.
, “A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.”, Hum Genet, vol. 131, no. 4, pp. 565-79, 2012.
, “Functional impact of global rare copy number variation in autism spectrum disorders.”, Nature, vol. 466, no. 7304, pp. 368-72, 2010.
, “A genome-wide scan for common alleles affecting risk for autism.”, Hum Mol Genet, vol. 19, no. 20, pp. 4072-82, 2010.
, “The modified checklist for autism in toddlers: a follow-up study investigating the early detection of autism spectrum disorders.”, J Autism Dev Disord, vol. 38, no. 5, pp. 827-39, 2008.
, “Screening for autism in older and younger toddlers with the Modified Checklist for Autism in Toddlers.”, Autism, vol. 12, no. 5, pp. 513-35, 2008.
, “The structure of intelligence in children and adults with high functioning autism.”, Neuropsychology, vol. 22, no. 3, pp. 301-312, 2008.
, “Three diagnostic approaches to Asperger syndrome: implications for research.”, J Autism Dev Disord, vol. 35, no. 2, pp. 221-34, 2005.
,