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“Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population.”, Am J Psychiatry, vol. 167, no. 11, pp. 1364-72, 2010.
, “Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.”, Nature, vol. 459, no. 7246, pp. 569-73, 2009.
, “Common genetic variants on 5p14.1 associate with autism spectrum disorders.”, Nature, vol. 459, no. 7246, pp. 528-33, 2009.
, “Common variation contributes to the genetic architecture of social communication traits.”, Mol Autism, vol. 4, no. 1, p. 34, 2013.
, “Functional impact of global rare copy number variation in autism spectrum disorders.”, Nature, vol. 466, no. 7304, pp. 368-72, 2010.
, “Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.”, PLoS Genet, vol. 5, no. 6, p. e1000536, 2009.
, “A genome-wide scan for common alleles affecting risk for autism.”, Hum Mol Genet, vol. 19, no. 20, pp. 4072-82, 2010.
, “Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.”, Mol Autism, vol. 5, no. 1, p. 5, 2014.
, “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.
, “Rare genomic deletions and duplications and their role in neurodevelopmental disorders.”, Curr Top Behav Neurosci, vol. 12, pp. 345-60, 2012.
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