Found 7 results
Filters: Author is Pinto, Dalila [Clear All Filters]
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders. The American Journal of Human Genetics. 2014;94(5):677 - 694. doi:10.1016/j.ajhg.2014.03.018
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism. Nature Communications. 2014;5. doi:10.1038/ncomms5074
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. 2012;131(4):565 - 579. doi:10.1007/s00439-011-1094-6
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders. European Journal of Human Genetics. 2011;19(10):1082 - 1089. doi:10.1038/ejhg.2011.75
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. Journal of Neurodevelopmental Disorders. 2011;3(2):113 - 123. doi:10.1007/s11689-011-9072-9
Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 2010;466(7304):368 - 372. doi:10.1038/nature09146
A genome-wide linkage and association scan reveals novel loci for autism. Nature. 2009;461(7265):802 - 808. doi:10.1038/nature08490