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 …

Schizophrenia (SCZ) is a highly heritable neuropsychiatric disorder of complex genetic
etiology. Previous genome-wide surveys have revealed a greater burden of large, rare copy …

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 …

Importance At least 11 rare copy number variants (CNVs) have been shown to be major risk
factors for schizophrenia (SZ). These CNVs also increase the risk for other …

Schizophrenia is a complex disorder, caused by both genetic and environmental factors and
their interactions. Research on pathogenesis has traditionally focused on neurotransmitter …

We report a genome-wide assessment of single nucleotide polymorphisms (SNPs) and copy
number variants (CNVs) in schizophrenia. We investigated SNPs using 871 patients and …

Schizophrenia is an etiologically heterogeneous psychiatric disease, which exists in familial
and nonfamilial (sporadic) forms. Here, we examine the possibility that rare de novo copy …

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 …

Investigators have linked rare copy number variation (CNVs) to neuropsychiatric diseases,
such as schizophrenia. One hypothesis is that CNV events cause disease by affecting genes …

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 …