Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia (Q28274064)

Andrew B Singleton

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Robert L Findling

Robert L Findling

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Judith L. Rapoport

Judith L Rapoport

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Stanley F Nelson

Stanley F Nelson

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author name string

Jon M McClellan

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Shane E McCarthy

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Sarah B Pierce

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Greg M Cooper

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Mary Kusenda

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Dheeraj Malhotra

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Abhishek Bhandari

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Sunday M Stray

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Caitlin F Rippey

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Patricia Roccanova

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Vlad Makarov

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B Lakshmi

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Linmarie Sikich

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Thomas Stromberg

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Barry Merriman

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Philip Butler

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Kristen Eckstrand

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Laila Noory

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Peter Gochman

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Robert Long

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Zugen Chen

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Carl Baker

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Paul S Meltzer

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Ming K Lee

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

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language of work or name

English

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publication date

25 April 2008

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published in

Science

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volume

320

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issue

5875

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page(s)

539-43

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cites work

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Disruption of the neuronal PAS3 gene in a family affected with schizophrenia

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Genetic variation in the 22q11 locus and susceptibility to schizophrenia

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Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

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Segmental duplications and copy-number variation in the human genome

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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Association between microdeletion and microduplication at 16p11.2 and autism

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Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

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The neuregulin receptor ErbB-4 interacts with PDZ-containing proteins at neuronal synapses

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Interactions among genes in the ErbB-Neuregulin signalling network are associated with increased susceptibility to schizophrenia

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Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence

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