Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders

Copy number variants (CNVs) at chromosome 16p13.11 have been associated with a range of neurodevelopmental disorders including autism, ADHD, intellectual disability and schizophrenia. Significant sex differences in prevalence, course and severity have been described for a number of these conditions...

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Veröffentlicht in:	PloS one 2013-04, Vol.8 (4), p.e61365
Hauptverfasser:	Tropeano, Maria, Ahn, Joo Wook, Dobson, Richard J B, Breen, Gerome, Rucker, James, Dixit, Abhishek, Pal, Deb K, McGuffin, Peter, Farmer, Anne, White, Peter S, Andrieux, Joris, Vassos, Evangelos, Ogilvie, Caroline Mackie, Curran, Sarah, Collier, David A
Format:	Artikel
Sprache:	eng
Schlagworte:	Association analysis Attention deficit hyperactivity disorder Autism Biology Bipolar disorder Brain research Child Chromosome 16 Chromosome Deletion Chromosome Duplication Chromosomes, Human, Pair 16 - genetics Cohort Studies Comparative analysis Comparative Genomic Hybridization Congenital diseases Copy number Cytogenetics Delay Developmental Disabilities - genetics Disorders DNA Copy Number Variations Enrichment Environmental factors Epilepsy Female Females Gender aspects Gender differences Genetic aspects Genomes Haplotypes Humans Intellectual disabilities Male Males Medicine Mental disorders Microencephaly Mutation Neurodevelopmental disorders Neurosciences Phenotype Psychiatry Reproduction (copying) Schizophrenia Sex Sex differences Speech
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