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Neuroanatomical Phenotypes Are Consistent With Autism‐Like Behavioral Phenotypes in the 15q11‐13 Duplication Mouse Model

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Is There A Connection Between Autism, Prader‐Willi Syndrome, Catatonia, And GABA?

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Characterization of an Autism-Associated Segmental Maternal Heterodisomy of the Chromosome 15q11–13 Region

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Transmission disequilibrium testing of the chromosome 15q11‐q13 region in autism

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Animal Models of Psychiatric Disorders That Reflect Human Copy Number Variation

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Phenotypic spectrum of 20 novel patients with molecularly defined supernumerary marker chromosomes 15 and a review of the literature

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Significant transcriptional changes in 15q duplication but not Angelman syndrome deletion stem cell-derived neurons

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Face and gaze processing in Prader‐Willi syndrome

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Molecular genetics of autism spectrum disorders

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Clinical and genetic study of a family with a paternally inherited 15q11–q13 duplication

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Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures

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The neurobiology of mouse models syntenic to human chromosome 15q

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Genome-Wide SNP Array Analysis in Patients with Features of Sotos Syndrome

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The role of ubiquitin ligase E3A in polarized contact guidance and rescue strategies in UBE3A-deficient hippocampal neurons

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Significant neuronal soma volume deficit in the limbic system in subjects with 15q11.2-q13 duplications

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Monogenic and chromosomal causes of isolated speech and language impairment

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Brief Report: Visual-Spatial Deficit in a 16-year-old Girl with Maternally Derived Duplication of Proximal 15q

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Structural Chromosome Rearrangements

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QOL in caregivers of Japanese patients with Prader–Willi syndrome with reference to age and genotype

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The genetic overlap of attention deficit hyperactivity disorder and autistic spectrum disorder

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Publisher's note

Tordjman, S., Cohen, D., Coulon, N., Anderson, G. M., Botbol, M., Canitano, R., & Roubertoux, P. L. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.030 · Cited by 19

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Early Origin and Evolution of the Angelman Syndrome Ubiquitin Ligase Gene Ube3a

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Sensory Over-responsivity and Aberrant Plasticity in Cerebellar Cortex in a Mouse Model of Syndromic Autism

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Model mice for 15q11–13 duplication syndrome exhibit late-onset obesity and altered lipid metabolism

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A longitudinal follow‐up study of autistic symptoms in children and adults with duplications of 15q11‐13

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A patient with Prader–Willi syndrome and a supernumerary marker chromosome r(15)(q11.1‐13p11.1)pat and maternal heterodisomy

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Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy

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Developmental Encephalopathies

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Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders

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Estimate of the prevalence of chromosome 15q11‐q13 duplications

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A quantitative polymerase chain reaction method for determining copy number within the Prader–Willi/Angelman syndrome critical region

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Electro-clinical features in epileptic children with chromosome 15q duplication syndrome

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Cryptic duplication and deletion of 9q34.3 → qter in a family with a t(9;22)(q34.3;p11.2)

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Planning studies of etiology

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Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features

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Infantile spasms and 15q11.2q13.1 chromosome duplication in two successive generations

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Parental-reported pain insensitivity in Dup15q

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Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: A cytogenetic pitfall

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Variant Chromosomes and Abnormalities of No Phenotypic Consequence

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Relationship Between Sensory Processing and Autism Spectrum Disorder-Like Behaviors in Prader-Willi Syndrome

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The Autistic Spectrum Disorders (ASD): From the Clinics to the Molecular Analysis

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Epigenetic Dysregulation of 15q11-13 GABAA Receptor Genes in Autism

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Diagnostic Utility of Chromosomal Microarray Analysis in a Turkish Pediatric Cohort: Insights from 1,022 Patients with Neurodevelopmental Disorders and Congenital Anomalies

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MLPA analysis in a cohort of patients with autism

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Genetic Studies of Prader-Willi Patients Provide Evidence for Conservation of Genomic Architecture in Proximal Chromosome 15q

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Gametogenesis and Conception, Pregnancy Loss and Infertility

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Robertsonian Translocations

Gardner, R. J. M., Sutherland, G. R., & Shaffer, L. G. (2011) · Oxford University Press eBooks · doi:10.1093/med/9780195375336.003.0007 · Cited by 3

Synaptic protein mutations in autism

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Parental Sex Chromosome Aneuploidy

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Prenatal Diagnostic Procedures

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Elements of Medical Cytogenetics

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Sex Chromosome Translocations

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Chromosome Heteromorphism (Summaries)

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inv dup(15) and inv dup(22)

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Genetics of Autism

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Construction of a Genetic Classifier for ASD Using Gene Pathway Analysis

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Inversions

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Chromosome Instability Syndromes

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Autosomal ring chromosomes

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Deriving and Using a Risk Figure

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The Origins and Consequences of Chromosome Pathology

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Structural rearrangements

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Socio-sexual functioning in autism spectrum disorders

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Preimplantation Genetic Diagnosis

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Complete Penetrance but Different Phenotypes in a Korean Family with Maternal Interstitial Duplication at 15q11.2-q13.1: A Case Report

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