B. Abrahams and D. Geschwind, Advances in autism genetics: on the threshold of a new neurobiology, Nature Reviews Genetics, vol.9, issue.5, pp.341-355, 2008.
DOI : 10.1038/nrg2346

M. Alarcon, B. Abrahams, J. Stone, J. Duvall, J. Perederiy et al., Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene, The American Journal of Human Genetics, vol.82, issue.1, pp.150-159, 2008.
DOI : 10.1016/j.ajhg.2007.09.005

D. Arking, D. Cutler, C. Brune, T. Teslovich, K. West et al., A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism, The American Journal of Human Genetics, vol.82, issue.1, pp.160-164, 2008.
DOI : 10.1016/j.ajhg.2007.09.015

S. Baieli, L. Pavone, C. Meli, A. Fiumara, and M. Coleman, Autism and phenylketonuria, Journal of Autism and Developmental Disorders, vol.33, issue.2, pp.201-204, 2003.
DOI : 10.1023/A:1022999712639

G. Baird, E. Simonoff, A. Pickles, S. Chandler, T. Loucas et al., Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP), The Lancet, vol.368, issue.9531, pp.210-215, 2006.
DOI : 10.1016/S0140-6736(06)69041-7

B. Bakkaloglu, O. Roak, B. Louvi, A. Gupta, A. Abelson et al., Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders, The American Journal of Human Genetics, vol.82, issue.1, pp.165-173, 2008.
DOI : 10.1016/j.ajhg.2007.09.017

C. Bartlett, N. Gharani, J. Millonig, and L. Brzustowicz, Three autism candidate genes: a synthesis of human genetic analysis with other disciplines, International Journal of Developmental Neuroscience, vol.23, issue.2-3, pp.221-234, 2005.
DOI : 10.1016/j.ijdevneu.2004.10.004

J. Berg, N. Brunetti-pierri, S. Peters, S. Kang, C. Fong et al., Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11, 2007.

E. Bonora, K. Beyer, J. Lamb, J. Parr, S. Klauck et al., Analysis of reelin as a candidate gene for autism, Molecular Psychiatry, vol.8, issue.10, pp.885-892, 2003.
DOI : 10.1038/sj.mp.4001310

E. Bonora, J. Lamb, G. Barnby, N. Sykes, T. Moberly et al., Mutation screening and association analysis of six candidate genes for autism on chromosome 7q, European Journal of Human Genetics, vol.13, issue.2, pp.198-207, 2005.
DOI : 10.1038/sj.ejhg.5201315

C. Brune, E. Korvatska, K. Allen-brady, E. Cook, . Jr et al., Heterogeneous association between engrailed-2 and autism in the CPEA network, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol.40, issue.128, pp.187-193, 2008.
DOI : 10.1002/ajmg.b.30585

M. Bucan, B. Abrahams, K. Wang, J. Glessner, E. Herman et al., Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes, PLoS Genetics, vol.4, issue.6, p.1000536, 2009.
DOI : 10.1371/journal.pgen.1000536.s007

M. Butler, M. Dasouki, X. Zhou, Z. Talebizadeh, M. Brown et al., Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations, Journal of Medical Genetics, vol.42, issue.4, pp.318-321, 2005.
DOI : 10.1136/jmg.2004.024646

D. Campbell, T. Buie, H. Winter, M. Bauman, J. Sutcliffe et al., Distinct Genetic Risk Based on Association of MET in Families With Co-occurring Autism and Gastrointestinal Conditions, PEDIATRICS, vol.123, issue.3, pp.1018-1024, 2009.
DOI : 10.1542/peds.2008-0819

D. Campbell, D. Oronzio, R. Garbett, K. Ebert, P. Mirnics et al., Disruption of cerebral cortex MET signaling in autism spectrum disorder, Annals of Neurology, vol.61, issue.3, pp.243-250, 2007.
DOI : 10.1002/ana.21180

P. Levitt, A genetic variant that disrupts MET transcription is associated with autism, Proc Natl Acad Sci, vol.103, pp.16834-16839, 2006.

S. Chakrabarti and E. Fombonne, Pervasive Developmental Disorders in Preschool Children: Confirmation of High Prevalence, American Journal of Psychiatry, vol.162, issue.6, pp.1133-1141, 2005.
DOI : 10.1176/appi.ajp.162.6.1133

S. Chess, P. Fernandez, and S. Korn, Behavioral consequences of congenital rubella, The Journal of Pediatrics, vol.93, issue.4, pp.699-703, 1978.
DOI : 10.1016/S0022-3476(78)80921-4

I. Cusco, A. Medrano, B. Gener, M. Vilardell, F. Gallastegui et al., Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder, Human Molecular Genetics, vol.18, issue.10, pp.1795-1804, 2009.
DOI : 10.1093/hmg/ddp092

C. Depienne, D. Moreno-de-luca, D. Heron, D. Bouteiller, A. Gennetier et al., Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders, Biological Psychiatry, vol.66, issue.4, 2009.
DOI : 10.1016/j.biopsych.2009.01.025
URL : https://hal.archives-ouvertes.fr/inserm-00369261

B. Devlin, P. Bennett, G. Dawson, D. Figlewicz, E. Grigorenko et al., Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network, American Journal of Medical Genetics, vol.7, issue.1, pp.46-50, 2004.
DOI : 10.1002/ajmg.b.20125

Z. Donaldson and L. Young, Oxytocin, Vasopressin, and the Neurogenetics of Sociality, Science, vol.322, issue.5903, pp.900-904, 2008.
DOI : 10.1126/science.1158668

C. Durand, C. Betancur, T. Boeckers, J. Bockmann, P. Chaste et al., Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders, Nature Genetics, vol.28, issue.1, pp.25-27, 2007.
DOI : 10.1038/ng1933
URL : https://hal.archives-ouvertes.fr/inserm-00126175

J. Duvall, A. Lu, R. Cantor, R. Todd, J. Constantino et al., A Quantitative Trait Locus Analysis of Social Responsiveness in Multiplex Autism Families, American Journal of Psychiatry, vol.164, issue.4, pp.656-662, 2007.
DOI : 10.1176/ajp.2007.164.4.656

S. Fatemi, T. Reutiman, T. Folsom, and P. Thuras, GABAA Receptor Downregulation in Brains of Subjects with Autism, Journal of Autism and Developmental Disorders, vol.113, issue.2, pp.223-230, 2009.
DOI : 10.1007/s10803-008-0646-7

L. Feuk, A. Carson, and S. Scherer, Structural variation in the human genome, Nature Reviews Genetics, vol.37, issue.2, pp.85-97, 2006.
DOI : 10.1038/nrg1767

S. Fisher, F. Vargha-khadem, K. Watkins, A. Monaco, and M. Pembrey, Localisation of a gene implicated in a severe speech and language disorder, Nature Genetics, vol.58, issue.2, pp.168-170, 1998.
DOI : 10.1126/science.274.5287.540

E. Fombonne, The Prevalence of Autism, JAMA, vol.289, issue.1, pp.87-89, 2003.
DOI : 10.1001/jama.289.1.87

C. Freitag, The genetics of autistic disorders and its clinical relevance: a review of the literature, Molecular Psychiatry, vol.28, issue.1, pp.2-22, 2007.
DOI : 10.1086/321292

J. Gauthier, D. Spiegelman, A. Piton, R. Lafreniere, S. Laurent et al., Novel de novo SHANK3 mutation in autistic patients, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol.40, issue.8, pp.421-424, 2009.
DOI : 10.1002/ajmg.b.30822

J. Glessner, K. Wang, G. Cai, O. Korvatska, C. Kim et al., Autism genome-wide copy number variation reveals ubiquitin and neuronal genes, Nature, vol.8, issue.7246, 2009.
DOI : 10.1038/nature07953
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925224

X. Gong, R. Delorme, F. Fauchereau, C. Durand, P. Chaste et al., An investigation of ribosomal protein L10 gene in autism spectrum disorders, BMC Medical Genetics, vol.434, issue.6, p.7, 2009.
DOI : 10.1038/nature03479
URL : https://hal.archives-ouvertes.fr/inserm-00374531

R. Hagerman, E. Berry-kravis, W. Kaufmann, M. Ono, N. Tartaglia et al., Advances in the Treatment of Fragile X Syndrome, PEDIATRICS, vol.123, issue.1, pp.378-390, 2009.
DOI : 10.1542/peds.2008-0317

C. Henrichsen, E. Chaignat, and A. Reymond, Copy number variants, diseases and gene expression, Human Molecular Genetics, vol.18, issue.R1, pp.1-8, 2009.
DOI : 10.1093/hmg/ddp011

G. Herman, E. Butter, B. Enrile, M. Pastore, T. Prior et al., Increasing knowledge of PTEN germline mutations: two additional patients with autism and macrocephaly, Am J Med Genet A, vol.143, pp.589-593, 2007.

D. Hessl, F. Tassone, L. Cordeiro, K. Koldewyn, C. Mccormick et al., Brief Report: Aggression and Stereotypic Behavior in Males with Fragile X Syndrome???Moderating Secondary Genes in a ???Single Gene??? Disorder, Journal of Autism and Developmental Disorders, vol.48, issue.1, pp.184-189, 2008.
DOI : 10.1007/s10803-007-0365-5

C. Huang and S. Santangelo, Autism and serotonin transporter gene polymorphisms: A systematic review and meta-analysis, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol.2, issue.2, pp.903-913, 2008.
DOI : 10.1002/ajmg.b.30720

H. Hutcheson, L. Olson, Y. Bradford, S. Folstein, S. Santangelo et al., Examination of NRCAM, LRRN3, KIAA0716, and LAMB1as autism candidate genes, BMC Medical Genetics, vol.29, issue.1, p.12, 2004.
DOI : 10.1038/ng1001-217

A. Iafrate, L. Feuk, M. Rivera, M. Listewnik, P. Donahoe et al., Detection of large-scale variation in the human genome, Nature Genetics, vol.10, issue.9, pp.949-951, 2004.
DOI : 10.1038/ng1307

S. Jacob, C. Brune, C. Carter, B. Leventhal, C. Lord et al., Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism, Neuroscience Letters, vol.417, issue.1, pp.6-9, 2007.
DOI : 10.1016/j.neulet.2007.02.001

M. Jacquemont, D. Sanlaville, R. Redon, R. O. Cormier-daire, V. Lyonnet et al., Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders, Journal of Medical Genetics, vol.43, issue.11, pp.843-849, 2006.
DOI : 10.1136/jmg.2006.043166

S. Jamain, H. Quach, L. Quintana-murci, C. Betancur, P. A. Gillberg et al., Y chromosome haplogroups in autistic subjects, Molecular Psychiatry, vol.7, issue.2, pp.217-219, 2002.
DOI : 10.1038/sj.mp.4000968
URL : https://hal.archives-ouvertes.fr/inserm-00124377

S. Klauck, B. Felder, A. Kolb-kokocinski, C. Schuster, A. Chiocchetti et al., Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism, Molecular Psychiatry, vol.10, issue.12, pp.1073-1084, 2006.
DOI : 10.1038/sj.mp.4001883

M. Krebs, C. Betancur, S. Leroy, M. Bourdel, C. Gillberg et al., Absence of association between a polymorphic GGC repeat in the 5??? untranslated region of the reelin gene and autism, Molecular Psychiatry, vol.7, issue.7, pp.801-804, 2002.
DOI : 10.1038/sj.mp.4001071
URL : https://hal.archives-ouvertes.fr/inserm-00124376

R. Kumar, S. Karamohamed, J. Sudi, D. Conrad, C. Brune et al., Recurrent 16p11.2 microdeletions in autism, Human Molecular Genetics, vol.17, issue.4, pp.628-638, 2008.
DOI : 10.1093/hmg/ddm376

E. Lerer, S. Levi, S. Salomon, A. Darvasi, N. Yirmiya et al., Association between the oxytocin receptor (OXTR) gene, 2007.

J. Li, L. Nguyen, C. Gleason, L. Lotspeich, D. Spiker et al., Lack of evidence for an association between WNT2 and RELN polymorphisms and autism, American Journal of Medical Genetics, vol.105, issue.1, pp.51-57, 2004.
DOI : 10.1002/ajmg.b.20122

D. Lugtenberg, T. Kleefstra, A. Oudakker, W. Nillesen, H. Yntema et al., Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy, European Journal of Human Genetics, vol.9, issue.4, pp.444-453, 2009.
DOI : 10.1002/humu.9482

D. Ma, D. Salyakina, J. Jaworski, I. Konidari, P. Whitehead et al., A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1, Annals of Human Genetics, vol.358, issue.3, pp.263-273, 2009.
DOI : 10.1111/j.1469-1809.2009.00523.x

D. Ma, M. Cuccaro, J. Jaworski, C. Haynes, D. Stephan et al., Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14, Molecular Psychiatry, vol.10, issue.4, pp.376-384, 2007.
DOI : 10.1038/sj.mp.4001927

T. Manolio, F. Collins, N. Cox, D. Goldstein, L. Hindorff et al., Finding the missing heritability of complex diseases, Nature, vol.41, issue.7265, pp.747-753, 2009.
DOI : 10.1038/nature08494

C. Marshall, A. Noor, J. Vincent, A. Lionel, L. Feuk et al., Structural Variation of Chromosomes in Autism Spectrum Disorder, The American Journal of Human Genetics, vol.82, issue.2, pp.477-488, 2008.
DOI : 10.1016/j.ajhg.2007.12.009

M. Mccarthy, G. Abecasis, L. Cardon, D. Goldstein, J. Little et al., Genome-wide association studies for complex traits: consensus, uncertainty and challenges, Nature Reviews Genetics, vol.3, issue.5, pp.356-369, 2008.
DOI : 10.1038/nrg2344

W. Mcmahon, B. Baty, and J. Botkin, Genetic counseling and ethical issues for autism, American Journal of Medical Genetics Part C: Seminars in Medical Genetics, vol.8, issue.1, pp.52-57, 2006.
DOI : 10.1002/ajmg.c.30082

H. Mefford, A. Sharp, C. Baker, A. Itsara, Z. Jiang et al., Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes, New England Journal of Medicine, vol.359, issue.16, pp.1685-1699, 2008.
DOI : 10.1056/NEJMoa0805384

R. Moessner, C. Marshall, J. Sutcliffe, J. Skaug, D. Pinto et al., Contribution of SHANK3 Mutations to Autism Spectrum Disorder, The American Journal of Human Genetics, vol.81, issue.6, pp.1289-1297, 2007.
DOI : 10.1086/522590

D. Page, O. Kuti, C. Prestia, and M. Sur, cooperatively influences brain size and social behavior, Proceedings of the National Academy of Sciences, vol.106, issue.6, pp.1989-1994, 2009.
DOI : 10.1073/pnas.0804428106

A. Persico, D. Agruma, L. Maiorano, N. Totaro, A. Militerni et al., Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder, Molecular Psychiatry, vol.6, issue.2, pp.150-159, 2001.
DOI : 10.1038/sj.mp.4000850

K. Reddy, Cytogenetic abnormalities and fragile-x syndrome in Autism Spectrum Disorder, BMC Medical Genetics, vol.27, issue.2, pp.3-19, 2005.
DOI : 10.1023/A:1022155201662

G. Schellenberg, G. Dawson, Y. Sung, A. Estes, J. Munson et al., Evidence for multiple loci from a genome scan of autism kindreds, Molecular Psychiatry, vol.54, issue.11, pp.1049-1060, 2006.
DOI : 10.1002/(SICI)1098-2272(1997)14:6<719::AID-GEPI28>3.0.CO;2-S

J. Sebat, B. Lakshmi, D. Malhotra, J. Troge, C. Lese-martin et al., Strong Association of De Novo Copy Number Mutations with Autism, Science, vol.316, issue.5823, pp.445-449, 2007.
DOI : 10.1126/science.1138659

J. Sebat, B. Lakshmi, J. Troge, A. J. Young, J. Lundin et al., Large-Scale Copy Number Polymorphism in the Human Genome, Science, vol.305, issue.5683, pp.525-528, 2004.
DOI : 10.1126/science.1098918

F. Serajee and A. Huq, Association of Y Chromosome Haplotypes With Autism, Journal of Child Neurology, vol.146, issue.12, 2009.
DOI : 10.1177/0883073809333530

F. Serajee, H. Zhong, M. Huq, and A. , Association of Reelin gene polymorphisms with autism, Genomics, vol.87, issue.1, pp.75-83, 2006.
DOI : 10.1016/j.ygeno.2005.09.008

W. Shen, A. Balajee, J. Wang, H. Wu, C. Eng et al., Essential Role for Nuclear PTEN in Maintaining Chromosomal Integrity, Cell, vol.128, issue.1, pp.157-170, 2007.
DOI : 10.1016/j.cell.2006.11.042

D. Sikora, K. Pettit-kekel, J. Penfield, L. Merkens, and R. Steiner, The near universal presence of autism spectrum disorders in children with Smith???Lemli???Opitz syndrome, American Journal of Medical Genetics Part A, vol.289, issue.14, pp.1511-1518, 2006.
DOI : 10.1002/ajmg.a.31294

J. Silverman, J. Buxbaum, N. Ramoz, J. Schmeidler, A. Reichenberg et al., Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol.141, issue.3, pp.408-410, 2008.
DOI : 10.1002/ajmg.b.30614

E. Simonoff, Genetic counseling in autism and pervasive developmental disorders, Journal of Autism and Developmental Disorders, vol.28, issue.5, pp.447-456, 1998.
DOI : 10.1023/A:1026060623511

D. Skaar, Y. Shao, J. Haines, J. Stenger, J. Jaworski et al., Analysis of the RELN gene as a genetic risk factor for autism, Molecular Psychiatry, vol.49, issue.6, pp.563-571, 2005.
DOI : 10.1002/gepi.10295

A. Skol, L. Scott, G. Abecasis, and M. Boehnke, Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies, Nature Genetics, vol.28, issue.2, pp.209-213, 2006.
DOI : 10.1038/ng1706

A. Monaco, MET and autism susceptibility: family and case-control studies, Eur J Hum Genet, vol.17, pp.749-758, 2009.

B. Stiles, Phosphatase and tensin homologue deleted on chromosome 10: Extending its PTENtacles, The International Journal of Biochemistry & Cell Biology, vol.41, issue.4, pp.757-761, 2009.
DOI : 10.1016/j.biocel.2008.09.022

N. Sykes, C. Toma, N. Wilson, E. Volpi, I. Sousa et al., Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection, European Journal of Human Genetics, vol.30, issue.10, 2009.
DOI : 10.1002/ajmg.b.30287

P. Szatmari, A. Paterson, L. Zwaigenbaum, W. Roberts, J. Brian et al., Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Nature Genetics, vol.57, issue.3, pp.319-328, 2007.
DOI : 10.1086/503920
URL : https://hal.archives-ouvertes.fr/inserm-00937094

T. Trikalinos, A. Karvouni, E. Zintzaras, T. Ylisaukko-oja, L. Peltonen et al., A heterogeneity-based genome search meta-analysis for autism-spectrum disorders, Molecular Psychiatry, vol.96, issue.1, pp.29-36, 2006.
DOI : 10.1038/sj.mp.4001750

B. Van-der-zwaag, L. Franke, M. Poot, R. Hochstenbach, H. Spierenburg et al., Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism, PLoS ONE, vol.86, issue.5, pp.5324-771634, 2008.
DOI : 10.1371/journal.pone.0005324.s005

E. Varga, M. Pastore, T. Prior, G. Herman, and K. Mcbride, The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly, Genetics in Medicine, vol.44, issue.2, pp.111-117, 2009.
DOI : 10.1097/GIM.0b013e31818fd762

J. Vincent, S. Horike, S. Choufani, A. Paterson, W. Roberts et al., An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster, Journal of Medical Genetics, vol.43, issue.5, pp.429-434, 2006.
DOI : 10.1136/jmg.2005.039693

F. Volkmar, C. Lord, A. Bailey, R. Schultz, and A. Klin, Autism and pervasive developmental disorders, Journal of Child Psychology and Psychiatry, vol.37, issue.12, pp.135-170, 2004.
DOI : 10.1037//0033-2909.124.3.283

J. Vorstman, M. Morcus, S. Duijff, P. Klaassen, H. Boer et al., The 22q11.2 Deletion in Children, Journal of the American Academy of Child & Adolescent Psychiatry, vol.45, issue.9, pp.1104-1113, 2006.
DOI : 10.1097/01.chi.0000228131.56956.c1

J. Vorstman, W. Staal, E. Van-daalen, H. Van-engeland, P. Hochstenbach et al., Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism, Molecular Psychiatry, vol.38, issue.1, pp.18-19, 2006.
DOI : 10.1038/sj.mp.4001757

K. Wang, H. Zhang, D. Ma, M. Bucan, J. Glessner et al., Common genetic variants on 5p14.1 associate with autism spectrum disorders, Nature, vol.17, issue.7246, 2009.
DOI : 10.1038/nature07999

L. Wang, M. Jia, W. Yue, F. Tang, M. Qu et al., Association of the ENGRAILED 2 (EN2) gene with autism in Chinese Han population, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol.40, issue.4, pp.434-438, 2008.
DOI : 10.1002/ajmg.b.30623

L. Weiss, D. Arking, M. Daly, and A. Chakravarti, A genome-wide linkage and association scan reveals novel loci for autism, Nature, vol.25, issue.7265, pp.802-808, 2009.
DOI : 10.1038/nature08490

L. Weiss, Y. Shen, J. Korn, D. Arking, D. Miller et al., Association between Microdeletion and Microduplication at 16p11.2 and Autism, New England Journal of Medicine, vol.358, issue.7, pp.667-675, 2008.
DOI : 10.1056/NEJMoa075974

G. Williams, J. King, M. Cunningham, M. Stephan, B. Kerr et al., Fetal valproate syndrome and autism: additional evidence of an association, Developmental Medicine & Child Neurology, vol.39, issue.3, pp.202-206, 2001.
DOI : 10.1111/j.1469-8749.2001.tb00188.x

S. Wu, M. Jia, Y. Ruan, J. Liu, Y. Guo et al., Positive Association of the Oxytocin Receptor Gene (OXTR) with Autism in the Chinese Han Population, Biological Psychiatry, vol.58, issue.1, pp.74-77, 2005.
DOI : 10.1016/j.biopsych.2005.03.013

P. Yang, F. Lung, Y. Jong, H. Hsieh, C. Liang et al., Association of the Homeobox Transcription Factor Gene ENGRAILED 2 with Autistic Disorder in Chinese Children, Neuropsychobiology, vol.57, issue.1-2, pp.3-8, 2008.
DOI : 10.1159/000123115

T. Ylisaukko-oja, K. Rehnstrom, M. Auranen, R. Vanhala, R. Alen et al., Analysis of four neuroligin genes as candidates for autism, European Journal of Human Genetics, vol.63, issue.12, 2005.
DOI : 10.1073/pnas.0405939101

H. Zhang, X. Liu, C. Zhang, E. Mundo, F. Macciardi et al., Reelin gene alleles and susceptibility to autism spectrum disorders, Molecular Psychiatry, vol.7, issue.9, pp.1012-1017, 2002.
DOI : 10.1038/sj.mp.4001124

X. Zhao, A. Leotta, V. Kustanovich, C. Lajonchere, D. Geschwind et al., A unified genetic theory for sporadic and inherited autism, Proceedings of the National Academy of Sciences, vol.104, issue.31, pp.12831-12836, 2007.
DOI : 10.1073/pnas.0705803104