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Lista de obras de Aiden Corvin

A NOS1 variant implicated in cognitive performance influences evoked neural responses during a high density EEG study of early visual perception

artículo científico publicado en 2011

A comprehensive family-based replication study of schizophrenia genes

artículo científico publicado en 2013

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A dysbindin risk haplotype associated with less severe manic-type symptoms in psychosis

article by Aiden Corvin et al published January 2008 in Neuroscience Letters

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

artículo científico publicado en 2013

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

artículo científico publicado en 2010

A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809.

artículo científico publicado en 2010

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.

scientific article published on 09 April 2013

Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation

artículo científico publicado en 2011

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

artículo científico publicado en 2014

An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis

artículo científico publicado en 2014

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

artículo científico publicado en 2008

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of shared heritability in common disorders of the brain

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

artículo científico publicado en 2013

Are deficits in executive sub-processes simply reflecting more general cognitive decline in schizophrenia?

artículo científico publicado en 2006

Are relational style and neuropsychological performance predictors of social attributions in chronic schizophrenia?

artículo científico publicado en 2008

Are the cognitive deficits associated with impaired insight in schizophrenia specific to executive task performance?

artículo científico publicado en 2005

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 01 May 2019

BDNF Val66Met polymorphism is associated with aggressive behavior in schizophrenia

artículo científico publicado en 2010

Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16.

artículo científico publicado en 2007

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

artículo científico publicado en 2014

Childhood trauma, parental bonding, and social cognition in patients with schizophrenia and healthy adults

artículo científico publicado en 2020

Chitinase-3-like 1 (CHI3L1) gene and schizophrenia: genetic association and a potential functional mechanism

artículo científico publicado en 2008

Clinical symptomatology and the psychosis risk gene ZNF804A.

artículo científico publicado en 2010

Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory

artículo científico publicado en 2017

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

artículo científico publicado en 2008

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

artículo científico publicado en 2012

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

artículo científico publicado en 2013

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

artículo científico publicado en 2010

Computerised working-memory focused cognitive remediation therapy for psychosis--A preliminary study

artículo científico publicado en 2015

Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus

artículo científico publicado en 2004

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.

artículo científico publicado en 2012

Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene

artículo científico publicado en 2013

Copy-number variants in neurodevelopmental disorders: promises and challenges

artículo científico publicado en 2009

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

artículo científico publicado en 2020

Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium

article

D-amino acid oxidase (DAO) genotype and mood symptomatology in schizophrenia

artículo científico publicado en 2007

DAOA ARG30LYS and verbal memory function in schizophrenia

artículo científico publicado en 2007

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

artículo científico publicado en 2014

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

artículo científico publicado en 2013

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

artículo científico publicado en 2010

Do antisaccade deficits in schizophrenia provide evidence of a specific inhibitory function?

artículo científico publicado en 2006

Does the ability to sustain attention underlie symptom severity in schizophrenia?

artículo científico publicado en 2008

Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets.

artículo científico publicado en 2013

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

artículo científico publicado en 2011

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

artículo científico publicado en 2011

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

article

Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia

artículo científico publicado en 2023

Early visual processing deficits in dysbindin-associated schizophrenia

artículo científico publicado en 2007

Effects of MIR137 on fronto-amygdala functional connectivity

artículo científico publicado en 2013

Effects of ZNF804A on auditory P300 response in schizophrenia

scientific article published on 14 January 2014

Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style

artículo científico publicado en 2013

Erratum: Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function and bipolar disorder susceptibility

scholarly article published in Molecular Psychiatry

Erratum: Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

scholarly article published in Molecular Psychiatry

Erratum: Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22

article

Erratum: Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium.

artículo científico publicado en 2015

Evaluating historical candidate genes for schizophrenia

artículo científico publicado en 2015

Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples

artículo científico publicado en 2006

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

artículo científico publicado en 2010

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha

artículo científico publicado en 2009

Evidence that duplications of 22q11.2 protect against schizophrenia

artículo científico publicado en 2013

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

artículo científico publicado en 2006

Evidence that specific executive functions predict symptom variance among schizophrenia patients with a predominantly negative symptom profile

article

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders

artículo científico publicado en 2013

Familial patterns and the origins of individual differences in synaesthesia

artículo científico publicado en 2007

Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

artículo científico publicado en 2010

Functional genomics and schizophrenia: endophenotypes and mutant models.

artículo científico publicado en 2007

Functional investigation of a schizophrenia GWAS signal at the CDC42 gene

artículo científico publicado en 2012

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

artículo científico publicado en 2010

GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

article

GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium

artículo científico publicado en 2017

GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.

artículo científico publicado en 2017

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

artículo científico publicado en 2019

Genes predict village of origin in rural Europe

artículo científico publicado en 2010

Genetic classification of populations using supervised learning

artículo científico publicado en 2011

Genetic differences between five European populations

artículo científico

Genetic modifiers and subtypes in schizophrenia: investigations of age at onset, severity, sex and family history

artículo científico publicado en 2014

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

artículo científico publicado en 2011

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

artículo científico publicado en 2013

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

article

Genome-wide association studies: a primer

artículo científico publicado en 2009

Genome-wide association studies: findings at the major histocompatibility complex locus in psychosis

artículo científico

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

artículo científico publicado en 2012

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

artículo científico publicado en 2009

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

artículo científico publicado en 2015

Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms

artículo científico publicado en 2015

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

artículo científico publicado en 2014

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

artículo científico publicado en 2012

Genomewide Linkage Scan in Schizoaffective Disorder

artículo científico publicado en 2005

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

Greater number of older siblings is associated with decreased theory of mind ability in psychosis

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

artículo científico publicado en 2011

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex.

artículo científico publicado en 2016

Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1).

artículo científico publicado en 2004

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identification of loci associated with schizophrenia by genome-wide association and follow-up

artículo científico publicado en 2008

Implication of a rare deletion at distal 16p11.2 in schizophrenia

artículo científico publicado en 2013

Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment

artículo científico publicado en 2015

Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects

artículo científico publicado en 2009

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

artículo científico publicado en 2012

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

artículo científico publicado en 2011

Interstitial deletion of chromosome 21q and schizophrenia susceptibility

artículo científico publicado en 2005

Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPs

artículo científico publicado en 2005

Is "clinical" insight the same as "cognitive" insight in schizophrenia?

artículo científico publicado en 2009

Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets

artículo científico publicado en 2017

MIR137HG risk variant rs1625579 genotype is related to corpus callosum volume in schizophrenia

artículo científico publicado en 2015

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Mental state decoding v. mental state reasoning as a mediator between cognitive and social function in psychosis

artículo científico publicado en 2008

Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT).

artículo científico publicado en 2013

Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility

artículo científico publicado en 2010

Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137.

artículo científico publicado en 2012

Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31

article

Mosaic copy number variation in schizophrenia

artículo científico publicado en 2013

Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018)

artículo científico publicado en 2018

Multiplex target enrichment using DNA indexing for ultra-high throughput SNP detection

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Nanotechnologies for the study of the central nervous system

artículo científico

Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253.

artículo científico publicado en 2013

Neurocognition and suicidal behaviour in an Irish population with major psychotic disorders

artículo científico publicado en 2006

Neuronal cell adhesion genes: Key players in risk for schizophrenia, bipolar disorder and other neurodevelopmental brain disorders?

artículo científico publicado en 2010

Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253.

artículo científico publicado en 2013

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

artículo científico publicado en 2015

Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study

article

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

artículo científico publicado en 2014

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

Parental age, birth order and neurodevelopmental disorders

artículo científico publicado en 2015

Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways

artículo científico publicado en 2019

Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia

artículo científico publicado en 2013

Population structure and genome-wide patterns of variation in Ireland and Britain

artículo científico publicado en 2010

Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

artículo científico publicado en 2019

Positive symptoms associate with cortical thinning in the superior temporal gyrus via the ENIGMA Schizophrenia consortium.

artículo científico publicado en 2017

Prefrontal cortical thinning links to negative symptoms in schizophrenia via the ENIGMA consortium.

artículo científico publicado en 2017

Preserved cognitive function is associated with suicidal ideation and single suicide attempts in schizophrenia

artículo científico publicado en 2012

Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia

artículo científico publicado en 2011

Psychiatric genetics in the post-genome age.

artículo científico publicado en 2003

Psychiatric genetics: what's new in 2015?

artículo científico publicado en 2016

Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia

artículo científico publicado en 2010

Rare chromosomal deletions and duplications increase risk of schizophrenia

artículo científico publicado en 2008

Reduced occipital and prefrontal brain volumes in dysbindin-associated schizophrenia

artículo científico publicado en 2010

Replicated genetic evidence supports a role for HOMER2 in schizophrenia

artículo científico publicado en 2009

Schizophrenia at a Genetics Crossroads: Where to Now? ⬇️

artículo científico publicado el 21 de marzo de 2013

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

artículo científico publicado en 2022

Social cognition in bipolar disorder versus schizophrenia: comparability in mental state decoding deficits

artículo científico publicado en 2012

Social dysfunction in schizophrenia: an investigation of the GAF scale's sensitivity to deficits in social cognition

artículo científico publicado en 2013

Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.

artículo científico publicado en 2005

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

artículo científico publicado en 2018

Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium

artículo científico publicado en 2016

The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project

artículo científico publicado en 2017

The Letter-Number Sequencing Test and its association with potential to work among people with psychotic illness

artículo científico publicado en 2009

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

artículo científico publicado en 2011

The Psychosis Susceptibility Gene ZNF804A: Associations, Functions, and Phenotypes ⬇️

artículo científico publicado el 5 de agosto de 2010

The SNP ratio test: pathway analysis of genome-wide association datasets

article

The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report

article by P Bennett et al published February 2002 in Molecular Psychiatry

The cognitive genetics of neuropsychiatric disorders

artículo científico publicado en 2012

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

artículo científico publicado en 2014

The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function.

artículo científico publicado en 2012

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

The miR-137 schizophrenia susceptibility variant rs1625579 does not predict variability in brain volume in a sample of schizophrenic patients and healthy individuals

artículo científico publicado en 2014

The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis

artículo científico publicado en 2013

The phenotypic manifestations of rare CNVs in schizophrenia

artículo científico publicado en 2014

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder

artículo científico publicado en 2014

The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up

artículo científico publicado en 2013

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

artículo científico publicado el 11 de noviembre de 2011

Unlocking the treasure trove: from genes to schizophrenia biology

artículo científico

Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway

artículo científico publicado en 2014

Variance in facial recognition performance associated with BDNF in schizophrenia

artículo científico publicado en 2007

Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: a preliminary study

artículo científico publicado en 2006

What have the genomics ever done for the psychoses?

scientific article published on 12 October 2009

Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group.

artículo científico publicado en 2017

ZNF804A and social cognition in patients with schizophrenia and healthy controls

artículo científico publicado en 2011

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

artículo científico publicado en 2010

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