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Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data

PloS one, 2013-03, Vol.8 (3), p.e58815

2013

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Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disorders

Scientific reports, 2020-12, Vol.10 (1), p.22255-22255, Article 22255

2020

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Effects of MIR137 on fronto-amygdala functional connectivity

NeuroImage (Orlando, Fla.), 2014-04, Vol.90, p.189-195

2014

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Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology

PloS one, 2011-11, Vol.6 (11), p.e26488-e26488

2011

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Familial patterns and the origins of individual differences in synaesthesia

Cognition, 2008-02, Vol.106 (2), p.871-893

2008

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Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci

European journal of human genetics : EJHG, 2016-02, Vol.24 (2), p.291-297

2016

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Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample

Neurobiology of aging, 2014-06, Vol.35 (6), p.1510.e1-1510.e5

2014

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Corpus Callosum Microstructural Tract Integrity Relates to Longer Emotion Recognition Reaction Time in People with Schizophrenia

Brain sciences, 2022-09, Vol.12 (9), p.1208

2022

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Two patients walk into a clinic...a genomics perspective on the future of schizophrenia

BMC biology, 2011-11, Vol.9 (1), p.77-77, Article 77

Corvin, Aiden P

2011

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Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

Nature genetics, 2022-05, Vol.54 (5), p.541-547

2022

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Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression

Bipolar disorders, 2010-06, Vol.12 (4), p.440-445

2010

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Copy-number variants in neurodevelopmental disorders: promises and challenges

Trends in genetics, 2009-12, Vol.25 (12), p.536-544

2009

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Direct targets of MEF2C are enriched for genes associated with schizophrenia and cognitive function and are involved in neuron development and mitochondrial function

PLoS genetics, 2024-09, Vol.20 (9), p.e1011093

2024

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Dysbindin (DTNBP1) and the Biogenesis of Lysosome-Related Organelles Complex 1 (BLOC-1): Main and Epistatic Gene Effects Are Potential Contributors to Schizophrenia Susceptibility

Biological psychiatry (1969), 2008, Vol.63 (1), p.24-31

2008

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The Effect of the Neurogranin Schizophrenia Risk Variant rs12807809 on Brain Structure and Function

Twin research and human genetics, 2012-06, Vol.15 (3), p.296-303

2012

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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

Nature genetics, 2008-09, Vol.40 (9), p.1056-1058

2008

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Functional Genomics and Schizophrenia: Endophenotypes and Mutant Models

The Psychiatric clinics of North America, 2007-09, Vol.30 (3), p.365-399

2007

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Insulin-like growth factor 1 (IGF1) and its active peptide (1–3)IGF1 enhance the expression of synaptic markers in neuronal circuits through different cellular mechanisms

Neuroscience letters, 2012-06, Vol.520 (1), p.51-56

2012

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ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia

NeuroImage (Orlando, Fla.), 2011-02, Vol.54 (3), p.2132-2137

2011

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Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients

Schizophrenia research, 2014-08, Vol.157 (1), p.225-230

2014

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Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants

Neuroscience letters, 2014-06, Vol.574, p.6-10

2014

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Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2006-01, Vol.141B (1), p.96-101

2006

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No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset

Schizophrenia research, 2014-04, Vol.154 (1), p.79-82

2014

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Early Visual Processing Deficits in Dysbindin-Associated Schizophrenia

Biological psychiatry (1969), 2008-03, Vol.63 (5), p.484-489

2008

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The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals

NeuroImage (Orlando, Fla.), 2012-03, Vol.60 (1), p.614-622

2012

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Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data

Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disorders

Effects of MIR137 on fronto-amygdala functional connectivity

Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology

Familial patterns and the origins of individual differences in synaesthesia

Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci

Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample

Corpus Callosum Microstructural Tract Integrity Relates to Longer Emotion Recognition Reaction Time in People with Schizophrenia

Two patients walk into a clinic...a genomics perspective on the future of schizophrenia

Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression

Copy-number variants in neurodevelopmental disorders: promises and challenges

Direct targets of MEF2C are enriched for genes associated with schizophrenia and cognitive function and are involved in neuron development and mitochondrial function

Dysbindin (DTNBP1) and the Biogenesis of Lysosome-Related Organelles Complex 1 (BLOC-1): Main and Epistatic Gene Effects Are Potential Contributors to Schizophrenia Susceptibility

The Effect of the Neurogranin Schizophrenia Risk Variant rs12807809 on Brain Structure and Function

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

Functional Genomics and Schizophrenia: Endophenotypes and Mutant Models

Insulin-like growth factor 1 (IGF1) and its active peptide (1–3)IGF1 enhance the expression of synaptic markers in neuronal circuits through different cellular mechanisms

ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia

Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients

Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants

Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia

No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset

Early Visual Processing Deficits in Dysbindin-Associated Schizophrenia

The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals

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