List of works - Michael Gill

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scientific article

Functional impact of global rare copy number variation in autism spectrum disorders

scientific article published on 15 July 2010

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

scientific article

Rare chromosomal deletions and duplications increase risk of schizophrenia

scientific article

Synaptic, transcriptional and chromatin genes disrupted in autism

scientific article

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

scientific article (publication date: May 2011)

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

Identification of common variants associated with human hippocampal and intracranial volumes

scientific article published on 15 April 2012

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

scientific article

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

scientific article

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

Microduplications of 16p11.2 are associated with schizophrenia

scientific article

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

scientific article

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

scientific article published on August 1, 2010

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

scientific journal article

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

scientific article

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

scientific article

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

scientific article

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

scientific article (publication date: 15 November 2010)

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal 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

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

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

Genome-wide association scan of attention deficit hyperactivity disorder

scientific article

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

scientific article published on February 2012

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

scientific article

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 28 February 2019

Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention.

scientific article

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

scientific article

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

scientific article published on February 2012

Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence

scientific article published in February 2010

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

scientific article published on February 1996

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders

scientific article published on 19 July 2008

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

Response variability in Attention Deficit Hyperactivity Disorder: Evidence for neuropsychological heterogeneity

article

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

scientific article

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

scientific article

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder

scientific article published on August 5, 2010

Genomewide Linkage Scan in Schizoaffective Disorder

scientific article published on 01 October 2005

A novel Alzheimer disease locus located near the gene encoding tau protein.

scientific article

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

scientific article published on 14 October 2011

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

scientific article

DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage

scientific article published in December 2008

List of works by Michael Gill

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Functional impact of global rare copy number variation in autism spectrum disorders

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

Rare chromosomal deletions and duplications increase risk of schizophrenia

Synaptic, transcriptional and chromatin genes disrupted in autism

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

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

Identification of common variants associated with human hippocampal and intracranial volumes

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

A genome-wide scan for common alleles affecting risk for autism

Microduplications of 16p11.2 are associated with schizophrenia

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

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

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

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

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

Individual common variants exert weak effects on the risk for autism spectrum disorders

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

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

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

Genome-wide association scan of attention deficit hyperactivity disorder

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

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

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention.

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders

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).

Response variability in Attention Deficit Hyperactivity Disorder: Evidence for neuropsychological heterogeneity

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

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

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder

Genomewide Linkage Scan in Schizoaffective Disorder

A novel Alzheimer disease locus located near the gene encoding tau protein.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

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

DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage