Publicações | Page 17 | - CCMAR -
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Filtros: Autor is Conroy, Judith  [Clear All Filters]
2016
Allen NM, Conroy J, Shahwan A, et al. Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion. Epilepsia. 2016;57(1):e12 - e17. doi:10.1111/epi.13250
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
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