A small number of rare, recurrent genomic copy number variants (CNVs) are known to
substantially increase susceptibility to schizophrenia. As a consequence of the low fecundity …

Objective Structural variations of DNA, such as copy number variations (CNVs), are
recognized to contribute both to normal genomic variability and to risk for human diseases …

Schizophrenia is a major psychiatric disease with strong evidence of genetic risk factors.
Recent studies based on genome-wide study of copy number variations (CNVs) have …

Large and rare copy number variants (CNVs) at several loci have been shown to increase
risk for schizophrenia. Aiming to discover novel susceptibility CNV loci, we analyzed 6882 …

Copy number variants (CNVs) have been strongly implicated in the genetic etiology of
schizophrenia (SCZ). However, genome-wide investigation of the contribution of CNV to risk …

BACKGROUND: At least 10 large and rare recurrent DNA copy number variants (CNVs)
have been identified as risk factors for schizophrenia and other neurodevelopmental …

Context Recent studies suggest that copy number variation in the human genome is
extensive and may play an important role in susceptibility to disease, including …

Schizophrenia is a psychiatric disorder with onset in late adolescence and unclear etiology
characterized by both positive and negative symptoms, as well as cognitive deficits. To …

Copy number variants (CNVs) are risk factors in neurodevelopmental disorders, including
autism, epilepsy, intellectual disability (ID) and schizophrenia. Childhood onset …

Genome-wide screenings for copy number variations (CNVs) in patients with schizophrenia
have demonstrated the presence of several CNVs that increase the risk of developing the …