Publications | - CCMAR -
Found 7 results
Filters: Author is Regan, Regina  [Clear All Filters]
2014
Pinto D, Delaby E, Merico D, et al. 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
Hadley D, Wu Z-liang, Kao C, et al. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism. Nature Communications. 2014;5. doi:10.1038/ncomms5074
2012
Magalhaes TR, Casey JP, Conroy J, et al. 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
Casey JP, Magalhaes TR, Conroy JM, et al. 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
2011
Anney RJL, Kenny EM, O'Dushlaine C, et al. 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
2010
Pinto D, Pagnamenta AT, Klei L, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 2010;466(7304):368 - 372. doi:10.1038/nature09146
2009
Weiss LA, Arking DE, Daly MJ, et al. A genome-wide linkage and association scan reveals novel loci for autism. Nature. 2009;461(7265):802 - 808. doi:10.1038/nature08490