Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries - Talkowski, Michael E.; Rosenfeld, Jill A.; Blumenthal, Ian; Pillalamarri, Vamsee; Chiang, Colby; Heilbut, Adrian; Ernst, Carl; Hanscom, Carrie; Rossin, Elizabeth; Lindgren, Amelia M.; Pereira, Shahrin; Ruderfer, Douglas; et al. (Cell, 2012)
Keywords: alleles; Autism; Autistic Disorder - diagnosis; Autistic Disorder - genetics; Boundaries; Child; Child Development Disorders, Pervasive - diagnosis; Child Development Disorders, Pervasive - genetics; Chromosome Aberrations; Chromosome Breakage; Chromosome Deletion; Developmental stages; DNA Copy Number Variations; Foxp1 protein; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; loci; Mental disorders; Nervous System - growth & development; neurodevelopment; Neurodevelopmental disorders; patients; risk; Schizophrenia; Schizophrenia - genetics; Sequence Analysis, DNA; Signal Transduction