Autistic disturbances of affective contact, Nerv. Child, vol.2, pp.217-250, 1943. ,
Die ???Autistischen Psychopathen??? im Kindesalter, Archiv f??r Psychiatrie und Nervenkrankheiten, vol.117, issue.1, pp.76-137, 1944. ,
DOI : 10.1007/978-3-662-36651-6
The ESSENCE in child psychiatry: Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations, Research in Developmental Disabilities, vol.31, issue.6, pp.31-1543, 2010. ,
DOI : 10.1016/j.ridd.2010.06.002
The Genetic Landscapes of Autism Spectrum Disorders, Annual Review of Genomics and Human Genetics, vol.14, issue.1, pp.191-213, 2013. ,
DOI : 10.1146/annurev-genom-091212-153431
URL : https://hal.archives-ouvertes.fr/pasteur-01470293
From the genetic architecture to synaptic plasticity in autism spectrum disorder, Nature Reviews Neuroscience, vol.511, issue.9, pp.551-563, 2015. ,
DOI : 10.1016/j.cell.2004.09.011
URL : https://hal.archives-ouvertes.fr/hal-01576592
Autism spectrum disorders and autistic traits: A decade of new twin studies, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol.1, issue.3, pp.156-255, 2011. ,
DOI : 10.1007/BF01557347
The Familial Risk of Autism, JAMA, vol.311, issue.17, pp.1770-1777, 2014. ,
DOI : 10.1001/jama.2014.4144
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders, The American Journal of Human Genetics, vol.94, issue.5, pp.94-677, 2014. ,
DOI : 10.1016/j.ajhg.2014.03.018
URL : https://hal.archives-ouvertes.fr/inserm-00986225
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism, Nature Genetics, vol.34, issue.1, pp.27-29, 2003. ,
DOI : 10.1038/ng1136
URL : https://hal.archives-ouvertes.fr/inserm-00124744
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders, Nature Genetics, vol.28, issue.1, pp.39-64, 2007. ,
DOI : 10.1038/ng1933
URL : https://hal.archives-ouvertes.fr/inserm-00126175
The contribution of de novo coding mutations to autism spectrum disorder, Nature, vol.43, issue.7526, pp.216-221, 2014. ,
DOI : 10.1038/ng.902
Excess of rare, inherited truncating mutations in autism, Nature Genetics, vol.40, issue.6, pp.47-582, 2015. ,
DOI : 10.18637/jss.v040.i12
Most genetic risk for autism resides with common variation, Nature Genetics, vol.460, issue.8, pp.881-885, 2014. ,
DOI : 10.1016/j.cell.2013.10.020
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137411
Changing perceptions: The power of autism, Nature, vol.39, issue.7371, pp.33-35, 2011. ,
DOI : 10.1017/S0021963098002601