| scholarly article | Q13442814 |
| P50 | author | Christopher Gillberg | Q1788006 |
| Marion Leboyer | Q28444907 | ||
| Maria Råstam | Q4976287 | ||
| Alain Verloes | Q64955175 | ||
| Delphine Héron | Q113000981 | ||
| Sandra Chantot-Bastaraud | Q114410121 | ||
| Jean-Pierre Siffroi | Q122853076 | ||
| Catalina Betancur | Q30668370 | ||
| Richard Delorme | Q58121713 | ||
| P2093 | author name string | Gudrun Nygren | |
| Pauline Chaste | |||
| Christel Depienne | |||
| Maria Johansson | |||
| Daniel Moreno-De-Luca | |||
| Alexis Brice | |||
| Eric Leguern | |||
| Lydie Burglen | |||
| Delphine Bouteiller | |||
| Oriane Trouillard | |||
| Baya Benyahia | |||
| Svenny Kopp | |||
| Aurélie Gennetier | |||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | autism | Q38404 |
| autism spectrum disorder | Q1436063 | ||
| P304 | page(s) | 349-359 | |
| P577 | publication date | 2009-03-17 | |
| P1433 | published in | Biological Psychiatry | Q4914961 |
| P1476 | title | Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders | |
| P478 | volume | 66 |
| Q48224906 | 15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes |
| Q35159036 | A genomic point-of-view on environmental factors influencing the human brain methylome |
| Q33597870 | A key role for an impaired detoxification mechanism in the etiology and severity of autism spectrum disorders |
| Q34722075 | A single-tube quantitative high-resolution melting curve method for parent-of-origin determination of 15q duplications |
| Q37782049 | A three-step workflow procedure for the interpretation of array-based comparative genome hybridization results in patients with idiopathic mental retardation and congenital anomalies |
| Q34391238 | Altered serotonin, dopamine and norepinepherine levels in 15q duplication and Angelman syndrome mouse models |
| Q28115364 | Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE |
| Q57828426 | Array-based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation |
| Q35762766 | Autism spectrum disorder and epilepsy: Disorders with a shared biology |
| Q38104700 | Autism spectrum disorders: the quest for genetic syndromes |
| Q26864726 | Channelopathy pathogenesis in autism spectrum disorders |
| Q37739718 | Chromosomal microarray analysis in clinical evaluation of neurodevelopmental disorders-reporting a novel deletion of SETDB1 and illustration of counseling challenge |
| Q33792567 | Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern |
| Q57737823 | Clinical and genetic study of a family with a paternally inherited 15q11-q13 duplication |
| Q42693517 | Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy |
| Q40816230 | Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism |
| Q55098524 | Common Ribs of Inhibitory Synaptic Dysfunction in the Umbrella of Neurodevelopmental Disorders. |
| Q33812099 | Communication, interventions, and scientific advances in autism: a commentary |
| Q35257406 | Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder |
| Q36393300 | Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature |
| Q35591685 | Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function |
| Q33778683 | Decreased exploratory activity in a mouse model of 15q duplication syndrome; implications for disturbance of serotonin signaling |
| Q34249436 | Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk? |
| Q37754018 | Evolving role of MeCP2 in Rett syndrome and autism |
| Q38900958 | Genetic Studies in Autism |
| Q34162345 | Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders |
| Q38216145 | Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era. |
| Q38088742 | Genetic risk in autism: new associations and clinical testing |
| Q24627520 | Genetics of autistic disorders: review and clinical implications |
| Q92904373 | Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue |
| Q36249309 | Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders |
| Q36876026 | Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome |
| Q35779834 | Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples |
| Q34257185 | Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy |
| Q43063737 | Lack of association between MAGEL2 and schizophrenia and mood disorders in the Japanese population |
| Q24597588 | Linkage and candidate gene studies of autism spectrum disorders in European populations |
| Q37624868 | MLPA analysis in a cohort of patients with autism |
| Q39003471 | Model mice for 15q11-13 duplication syndrome exhibit late-onset obesity and altered lipid metabolism. |
| Q89477342 | New Horizons for Molecular Genetics Diagnostic and Research in Autism Spectrum Disorder |
| Q34294538 | Overview of mouse models of autism spectrum disorders |
| Q51826464 | Prader-Willi syndrome. |
| Q37397662 | Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders |
| Q38462559 | Recent advances in the genetics of autism spectrum disorder |
| Q33611367 | Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder |
| Q36154515 | Significant neuronal soma volume deficit in the limbic system in subjects with 15q11.2-q13 duplications |
| Q30009298 | Synaptic proteins and receptors defects in autism spectrum disorders |
| Q48513662 | Syndromic autism spectrum disorders: moving from a clinically defined to a molecularly defined approach |
| Q42414524 | The autism-related gene SNRPN regulates cortical and spine development via controlling nuclear receptor Nr4a1. |
| Q38152705 | The contribution of epigenetics to understanding genetic factors in autism |
| Q36931989 | The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility |
| Q37449290 | The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature |
| Q36169407 | The molecular genetics of autism spectrum disorders: genomic mechanisms, neuroimmunopathology, and clinical implications |
| Q35680716 | The neurobiology of mouse models syntenic to human chromosome 15q. |
| Q41809824 | Three supernumerary marker chromosomes in a patient with developmental delay, mental retardation, and dysmorphic features |
| Q30572502 | Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts |
Search more.