The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

This publication has 160 references indexed in Scilit:

• Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder
  Biological Psychiatry, 2008
• Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes
  Proceedings of the National Academy of Sciences, 2007
• Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: A potential model of autism spectrum disorder
  Behavioural Brain Research, 2007
• Gabrb3 gene deficient mice exhibit increased risk assessment behavior, hypotonia and expansion of the plexus of locus coeruleus dendrites
  Brain Research, 2006
• Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications
  Human Molecular Genetics, 2002
• De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
  Nature Genetics, 1997
• UBE3A/E6-AP mutations cause Angelman syndrome
  Nature Genetics, 1997
• Autism in Angelman syndrome: a population-based study
  Pediatric Neurology, 1996
• Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15
  Nature Genetics, 1995
• Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
  Nature Genetics, 1994