R. Stickgold and M. P. Walker, Memory consolidation and reconsolidation: what is the role of sleep?, Trends Neurosci, vol.28, pp.408-415, 2005.

M. J. Somerville, Severe expressive-language delay related to duplication of the Williams-Beuren locus, N Engl J Med, vol.353, pp.1694-1701, 2005.

L. A. Weiss, Association between microdeletion and microduplication at 16p11.2 and autism, N Engl J Med, vol.358, pp.667-675, 2008.

R. A. Kumar, Recurrent 16p11.2 microdeletions in autism, Hum Mol Genet, vol.17, pp.628-638, 2008.

S. E. Mccarthy, Microduplications of 16p11.2 are associated with schizophrenia, Nat Genet, vol.41, pp.1223-1227, 2009.

S. H. Elsea, G. , and S. , Smith-Magenis syndrome, Eur J Hum Genet, vol.16, pp.412-421, 2008.

L. Potocki, Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype, Am J Hum Genet, vol.80, pp.633-649, 2007.

L. Niklasson, Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome, Res Dev Disabil, vol.30, pp.763-773, 2009.

G. Cai, Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT, BMC Med Genomics, vol.1, p.82, 2008.
URL : https://hal.archives-ouvertes.fr/inserm-00375019

J. Gauthier, De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia, Proc Natl Acad Sci U S A, vol.107, pp.7863-7868

K. B. Garber, Fragile X syndrome, Eur J Hum Genet, vol.16, pp.666-672, 2008.

R. E. Amir, Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2, Nature Genetics, vol.23, pp.185-188, 1999.

M. Wiznitzer, Autism and tuberous sclerosis, J Child Neurol, vol.19, pp.675-679, 2004.

T. L. Rosser and R. J. Packer, Neurocognitive dysfunction in children with neurofibromatosis type 1, Curr Neurol Neurosci Rep, vol.3, pp.129-136, 2003.

M. G. Butler, Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations, J Med Genet, vol.42, pp.318-321, 2005.

I. Splawski, CACNA1H mutations in autism spectrum disorders, J Biol Chem, vol.281, pp.22085-22091, 2006.

J. Feng, High frequency of neurexin 1beta signal peptide structural variants in patients with autism, Neurosci Lett, vol.409, pp.10-13, 2006.

T. Fernandez, Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome, Am J Hum Genet, vol.82, pp.1-9, 2003.

J. I. Friedman, CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy, Mol Psychiatry, vol.13, pp.261-266, 2008.

D. Castermans, The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism, J Med Genet, vol.40, pp.352-356, 2003.

J. Gauthier, Novel de novo SHANK3 mutation in autistic patients, Am J Med Genet B Neuropsychiatr Genet, p.95, 2008.

S. Jamain, Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism, Nat Genet, vol.34, pp.27-29, 2003.
URL : https://hal.archives-ouvertes.fr/inserm-00124744

A. Piton, Mutations in the calcium-related gene IL1RAPL1 are, 2008.