Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia

(2009) Pei-Lung Chen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Dorsal telencephalon-specificRA-GEF-1knockout mice develop heterotopic cortical mass and commissural fiber defect

(2009) Shymaa E. Bilasy et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

On the frequency of copy number variants

(2008) Iuliana Ionita-Laza et al.   BIOINFORMATICS

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE

Large recurrent microdeletions associated with schizophrenia

(2008) Hreinn Stefansson et al.   NATURE

Genotype, haplotype and copy-number variation in worldwide human populations

(2008) Mattias Jakobsson et al.   NATURE

Psychiatric genetics gets a boost

(2008) Brion S Maher et al.   NATURE GENETICS

Strong association of de novo copy number mutations with sporadic schizophrenia

(2008) Bin Xu et al.   NATURE GENETICS

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

(2008) T. Walsh et al.   SCIENCE