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Michael C O’Donovan
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Abstract
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Unresolved referenced work
1991
Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies
10.1001/archpsyc.60.12.1187 · 2003
De novo mutations in human genetic disease
10.1038/nrg3241 · 2012
Rate of de novo mutations and the importance of father's age to disease risk
10.1038/nature11396 · 2012
A comprehensive assessment of parental age and psychiatric disorders
10.1001/jamapsychiatry.2013.4081 · 2014
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
10.1038/mp.2011.154 · 2012
High frequencies of de novo CNVs in bipolar disorder and schizophrenia
10.1016/j.neuron.2011.11.007 · 2011
Strong association of de novo copy number mutations with sporadic schizophrenia
10.1038/ng.162 · 2008
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams Syndrome region, are strongly associated with autism
10.1016/j.neuron.2011.05.002 · 2011
De novo rates and selection of schizophrenia-associated copy number variants
10.1016/j.biopsych.2011.07.011 · 2011
De novo mutations in schizophrenia implicate synaptic networks
10.1038/nature12929 · 2014
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
10.1038/mp.2014.29 · 2014
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia
10.1038/ng.2446 · 2012
Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network
10.1016/j.cell.2013.06.049 · 2013
Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene
10.1016/j.neuron.2014.04.043 · 2014
De Novo gene disruptions in children on the autistic spectrum
10.1016/j.neuron.2012.04.009 · 2012
Rare chromosomal deletions and duplications increase risk of schizophrenia
10.1038/nature07239 · 2008
Support for the involvement of large CNVs in the pathogenesis of schizophrenia
10.1093/hmg/ddp043 · 2009
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
10.1093/hmg/ddt540 · 2014
Copy number variation in schizophrenia in Sweden
10.1038/mp.2014.40 · 2014
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
10.1073/pnas.92.17.7612 · 1995
High rates of schizophrenia in adults with velo-cardio-facial syndrome
10.1001/archpsyc.56.10.940 · 1999
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis
10.1093/hmg/ddu025 · 2014
Analysis of copy number variations at 15 schizophrenia-associated loci
10.1192/bjp.bp.113.131052 · 2014
Explaining additional genetic variation in complex traits
10.1016/j.tig.2014.02.003 · 2014
Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits
10.1016/s0168-9525(98)01555-8 · 1998
Neuroligins and neurexins link synaptic function to cognitive disease
10.1038/nature07456 · 2008
The penetrance of copy number variations for schizophrenia and developmental delay
10.1016/j.biopsych.2013.07.022 · 2014
CNVs: Harbingers of a rare variant revolution in psychiatric genetics
10.1016/j.cell.2012.02.039 · 2012
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
10.1038/nature07953 · 2009
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
10.1093/brain/awp262 · 2010
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
10.1038/ng.292 · 2009
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
10.1016/s0140-6736(10)61109-9 · 2010
Phenotypic heterogeneity of genomic disorders and rare copy-number variants
10.1056/nejmoa1200395 · 2012
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
10.1097/gim.0b013e31822c79f9 · 2011
Phenotypic variability and genetic susceptibility to genomic disorders
10.1093/hmg/ddq366 · 2010
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
10.1038/nature10406 · 2011
Evidence that duplications of 22q11.2 protect against schizophrenia
10.1038/mp.2013.156 · 2014
CNVs conferring risk of autism or schizophrenia affect cognition in controls
10.1038/nature12818 · 2014
Deep resequencing and association analysis of schizophrenia candidate genes
10.1038/mp.2012.28 · 2013
Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice
10.1186/gm546 · doi-reference
Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)
10.1038/mp.2013.166 · doi-reference
Identification of loci associated with schizophrenia by genome-wide association and follow-up
10.1038/ng.201 · doi-reference
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
10.1016/s0140-6736(12)62129-1 · doi-reference
Genome-wide association studies: findings at the major histocompatibility complex locus in psychosis
10.1016/j.biopsych.2013.09.018 · doi-reference
A framework for interpreting genome-wide association studies of psychiatric disorders
10.1038/mp.2008.126 · doi-reference
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
10.1038/ng.2711 · doi-reference
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
10.1038/ng.1108 · doi-reference
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
10.1038/nature08185 · doi-reference
Biological insights from 108 schizophrenia-associated genetic loci
10.1038/nature13595 · doi-reference
Genome-wide association study identifies five new schizophrenia loci
10.1038/ng.940 · doi-reference
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
10.1038/ng.2742 · doi-reference
A polygenic burden of rare disruptive mutations in schizophrenia
10.1038/nature12975 · doi-reference
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia
10.1016/j.ajhg.2012.06.018 · doi-reference