The genetics of obsessive compulsive disorder: A review of the evidence, American Journal of Medical Genetics Part C: Seminars in Medical Genetics, vol.119, issue.2, pp.133-139, 2008. ,
DOI : 10.1002/ajmg.c.30168
Tourette syndrome in a pedigree with a 7 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3, Am J Hum Genet, vol.18, issue.59, pp.999-1005, 1996. ,
Multiple childhood behavioral disorders (Tourette Syndrome, multiple tics, ADD and OCD) presenting in a family with a balanced chromosome translocation (t1;8)(q21.1;q22.1), Psychiatric Genetics, vol.9, issue.3, pp.149-151, 1999. ,
DOI : 10.1097/00041444-199909000-00007
De novo balanced translocation (2;10)(q24;q22) associated with mental retardation, Annales de G??n??tique, vol.46, issue.4, pp.471-473, 2003. ,
DOI : 10.1016/S0003-3995(03)00019-4
Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder, Genomics, vol.82, issue.1, pp.1-9, 2003. ,
DOI : 10.1016/S0888-7543(03)00097-1
Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22, American Journal of Medical Genetics, vol.82, issue.1, pp.37-39, 2004. ,
DOI : 10.1002/ajmg.a.30066
Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype, Proceedings of the National Academy of Sciences, vol.100, issue.8, pp.4684-4689, 2003. ,
DOI : 10.1073/pnas.0730775100
A Population-Based Study of the 22q11.2 Deletion: Phenotype, Incidence, and Contribution to Major Birth Defects in the Population, PEDIATRICS, vol.112, issue.1, pp.101-107, 2003. ,
DOI : 10.1542/peds.112.1.101
Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden, Archives of Disease in Childhood, vol.89, issue.2, pp.148-151, 2004. ,
DOI : 10.1136/adc.2003.026880
Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes, The Lancet, vol.370, issue.9596, pp.1443-1452, 2007. ,
DOI : 10.1016/S0140-6736(07)61601-8
Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome, Developmental Disabilities Research Reviews, vol.29, issue.1, pp.59-68, 2008. ,
DOI : 10.1002/ddrr.9
Obsessivecompulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome, Am J Med Genet B Neuropsychiatr Genet, vol.126, pp.99-105, 2004. ,
DOI : 10.1002/ajmg.b.20124
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?, Am J Psychiatry, vol.153, pp.1541-1547, 1996. ,
Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk, Biological Psychiatry, vol.51, issue.4, pp.312-318, 2002. ,
DOI : 10.1016/S0006-3223(01)01231-8
Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives, The Journal of Nervous and Mental Disease, vol.182, issue.8, pp.476-478, 1994. ,
DOI : 10.1097/00005053-199408000-00010
The met158 allele of catechol-O-methyltransferase (COMT) is associated with obsessive-compulsive disorder in men: case???control study and meta-analysis, Molecular Psychiatry, vol.11, issue.6, pp.556-561, 2007. ,
DOI : 10.1038/sj.mp.4001951
Prader???Willi syndrome: clinical genetics, cytogenetics and molecular biology, Expert Reviews in Molecular Medicine, vol.7, issue.14, pp.1-20, 2005. ,
DOI : 10.1017/S1462399405009531
Obsessions and Compulsions in Prader-Willi Syndrome, Journal of Child Psychology and Psychiatry, vol.177, issue.8, pp.995-1002, 1996. ,
DOI : 10.1002/ajmg.1320280415
Emergence of Compulsive Behavior and Tantrums in Children with Prader-Willi Syndrome, American Journal on Mental Retardation, vol.106, issue.1, pp.39-51, 2001. ,
DOI : 10.1352/0895-8017(2001)106<0039:EOCBAT>2.0.CO;2
Prader--Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey, The British Journal of Psychiatry, vol.180, issue.4, pp.358-362, 2002. ,
DOI : 10.1192/bjp.180.4.358
Rituals and compulsivity in Prader-Willi syndrome: profile and stability, Journal of Intellectual Disability Research, vol.38, issue.6, pp.428-438, 2003. ,
DOI : 10.1023/A:1005231912747
MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams???Beuren syndrome regions, European Journal of Medical Genetics, vol.50, issue.1, pp.33-42, 2007. ,
DOI : 10.1016/j.ejmg.2006.10.002
Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification, American Journal of Medical Genetics Part A, vol.76, issue.24, pp.2924-2930, 2007. ,
DOI : 10.1002/ajmg.a.32101
Diagnostic Interview for Genetic Studies, Archives of General Psychiatry, vol.51, issue.11, pp.849-859, 1994. ,
DOI : 10.1001/archpsyc.1994.03950110009002
Retrospective Assessment of Prepubertal Major Depression with the Kiddie-SADS-E, Journal of the American Academy of Child Psychiatry, vol.21, issue.4, pp.392-397, 1982. ,
DOI : 10.1016/S0002-7138(09)60944-4
MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q, Human Mutation, vol.77, issue.8, pp.814-821, 2006. ,
DOI : 10.1002/humu.20330
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 Medical Genomics, vol.12, issue.11, p.50, 2008. ,
DOI : 10.1038/sj.mp.4002069
URL : https://hal.archives-ouvertes.fr/inserm-00375019
Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders, Biological Psychiatry, vol.66, issue.4, pp.349-359, 2009. ,
DOI : 10.1016/j.biopsych.2009.01.025
URL : https://hal.archives-ouvertes.fr/inserm-00369261
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation, Neurology, vol.68, issue.10, pp.743-750, 2007. ,
DOI : 10.1212/01.wnl.0000256367.70365.e0
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication, Am J Hum Genet, vol.60, pp.928-934, 1997. ,
The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders, American Journal of Medical Genetics, vol.5, issue.8 ,
DOI : 10.1002/ajmg.1551
Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients, The American Journal of Human Genetics, vol.73, issue.5, pp.1027-1040, 2003. ,
DOI : 10.1086/378818
A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome, Clinical Genetics, vol.9, issue.4, pp.400-404, 2004. ,
DOI : 10.1111/j.0009-9163.2004.0212.x
The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies, American Journal of Medical Genetics Part A, vol.76, issue.14, pp.1608-1613, 2006. ,
DOI : 10.1002/ajmg.a.31227
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes, Genetics in Medicine, vol.168, issue.4, pp.267-277, 2008. ,
DOI : 10.1097/GIM.0b013e31816b64c2
Clinical variability of the 22q11.2 duplication syndrome, European Journal of Medical Genetics, vol.51, issue.6, pp.501-510, 2008. ,
DOI : 10.1016/j.ejmg.2008.07.005
The Promise and Challenge of Obsessive-Compulsive Disorder Research, Biological Psychiatry, vol.61, issue.3, pp.263-265, 2007. ,
DOI : 10.1016/j.biopsych.2006.12.012
Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Nat Genet, vol.39, pp.319-328, 2007. ,
Large recurrent microdeletions associated with schizophrenia, Nature, vol.1, issue.7210, pp.232-236, 2008. ,
DOI : 10.1038/nature07229
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687075
Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia, Science, vol.320, issue.5875, pp.539-543, 2008. ,
DOI : 10.1126/science.1155174
Strong association of de novo copy number mutations with sporadic schizophrenia, Nature Genetics, vol.182, issue.7, pp.880-885, 2008. ,
DOI : 10.1126/science.1155174
Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder BMC Medical Genetics, p.100, 2010. ,
URL : https://hal.archives-ouvertes.fr/inserm-00520828