List of works - Aiden Corvin

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

scientific article

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

scientific article

Rare chromosomal deletions and duplications increase risk of schizophrenia

scientific article

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

scientific article published in October 2013

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

scientific article

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

scientific article

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

scientific article

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

scientific article

Identification of common variants associated with human hippocampal and intracranial volumes

scientific article published on 15 April 2012

Common genetic variants influence human subcortical brain structures

scientific article

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

scientific article

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

scientific article

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

scientific article

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 06 April 2010

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

scientific article published on December 2011

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

scientific article

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

scientific article

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

scientific article

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

scientific article

Evaluating historical candidate genes for schizophrenia

scientific article

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

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

scientific article

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

article

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

article

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

scientific article published on 17 December 2013

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

scientific article

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

scientific article

Genomewide Linkage Scan in Schizoaffective Disorder

scientific article published on 01 October 2005

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

scientific article published on 18 August 2015

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

scientific article (publication date: 3 October 2016)

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

scientific article

A comprehensive family-based replication study of schizophrenia genes

scientific article

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

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

scientific article published on 15 October 2013

Copy-number variants in neurodevelopmental disorders: promises and challenges

scientific article

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

scientific article

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

scientific article published on 17 January 2017

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

article

Evidence that duplications of 22q11.2 protect against schizophrenia

scientific article

Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia

scientific article

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

scientific article published on 22 August 2006

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

scientific article published in February 2004

Familial patterns and the origins of individual differences in synaesthesia

scientific article published on 27 June 2007

List of works by Aiden Corvin

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

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

Rare chromosomal deletions and duplications increase risk of schizophrenia

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

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

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

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

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

Identification of common variants associated with human hippocampal and intracranial volumes

Common genetic variants influence human subcortical brain structures

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

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

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

Analysis of shared heritability in common disorders of the brain

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

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

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

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

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

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

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

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

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

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

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

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

Evaluating historical candidate genes for schizophrenia

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

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

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

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

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

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

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

Genomewide Linkage Scan in Schizoaffective Disorder

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

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

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

A comprehensive family-based replication study of schizophrenia genes

Novel genetic loci associated with hippocampal volume

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

Copy-number variants in neurodevelopmental disorders: promises and challenges

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

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

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

Evidence that duplications of 22q11.2 protect against schizophrenia

Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia

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

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

Familial patterns and the origins of individual differences in synaesthesia