Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs

Autism is a common heritable neurodevelopmental disorder with complex etiology. Several genome-wide linkage and association scans have been carried out to identify regions harboring genes related to autism or autism spectrum disorders, with mixed results. Given the overlap in autism features with ge...

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Veröffentlicht in:	PloS one 2010-09, Vol.5 (9), p.e12513
Hauptverfasser:	Fradin, Delphine, Cheslack-Postava, Keely, Ladd-Acosta, Christine, Newschaffer, Craig, Chakravarti, Aravinda, Arking, Dan E, Feinberg, Andrew, Fallin, M Daniele
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities Adolescent Adult Analysis Autism Autistic Disorder - genetics Biochemistry, Molecular Biology Child Chromosome Mapping Chromosomes Development and progression DNA methylation Empirical analysis Epidemiology Epigenetic inheritance Epigenetics Etiology Families & family life Female Genes Genetic abnormalities Genetic aspects Genetic Linkage Genetic Predisposition to Disease Genetic resources Genetics and Genomics/Complex Traits Genetics and Genomics/Epigenetics Genetics and Genomics/Gene Discovery Genetics and Genomics/Genetics of Disease Genome-Wide Association Study Genomes Genomic Imprinting Genomics Growth hormone Humans Imprinting Life Sciences Linkage analysis Male Medicine Mental disorders Mental health Middle Aged Neurodevelopmental disorders Pedigree Polymorphism, Single Nucleotide Proteins Public health Santé publique et épidémiologie Single-nucleotide polymorphism Statistical analysis Young Adult
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