Found 6 results
Filtros: Autor is Conroy, Judith [Clear All Filters]
Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion. Epilepsia. 2016;57(1):e12 - e17. doi:10.1111/epi.13250
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
HGDP and HapMap analysis by Ancestry Mapper reveals local and global population relationships. PLoS One. 2012;7(11):e49438. doi:10.1371/journal.pone.0049438
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