Experts
 Menu

Michael Gill

Institution

Trinity College Dublin

Contact

Subjects

Psychiatry

Details
Publications 187
As first author 45
As last author 61
Unique topics 830
Collaborations 102
Patents 1
Sources 10
Are you Michael Gill? Click here to provide feedback on your profile.
All
2015
2014
2013
2012
2011
2010
2009
2008
2007
Earlier
All
2015
2014
2013
2012
2011
2010
2009
2008
2007
Earlier

2015

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder.
2015

DNA methylation of the serotonin transporter gene (SLC6A4) is associated with brain function involved in processing emotional stimuli.
2015

Familiality and SNP heritability of age at onset and episodicity in major depressive disorder.
2015

Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment.
2015

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.
2015

Single-Nucleotide Polymorphism of the FKBP5 Gene and Childhood Maltreatment as Predictors of Structural Changes in Brain Areas Involved in Emotional Processing in Depression.
2014

Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients.
2014

An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.
2014

Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample.
2014

BDNF Val66Met genotype interacts with childhood adversity and influences the formation of hippocampal subfields.
2014

Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants.
2014

DNA methylation of the serotonin transporter gene in peripheral cells and stress-related changes in hippocampal volume: a study in depressed patients and healthy controls.
2014

Effects of MIR137 on fronto-amygdala functional connectivity.
2014

Evidence that duplications of 22q11.2 protect against schizophrenia.
2014

Expression of glucocorticoid inducible genes is associated with reductions in cornu ammonis and dentate gyrus volumes in patients with major depressive disorder.
2014

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
2014

Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a mendelian randomization analysis.
2014

Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study.
2014

Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants.
2014

Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT).
2014

No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset
2014

Relationship between obesity and the risk of clinically significant depression: Mendelian randomisation study.
2014

Repeated insulin-like growth factor 1 treatment in a patient with rett syndrome: a single case study.
2014

The phenotypic manifestations of rare CNVs in schizophrenia.
2014

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
2014

Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway.
2013

Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample.
2013

Attention network hypoconnectivity with default and affective network hyperconnectivity in adults diagnosed with attention-deficit/hyperactivity disorder in childhood.
2013

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
2013

Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene.
2013

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
2013

Development of Strategies for SNP Detection in RNA-Seq Data: Application to Lymphoblastoid Cell Lines and Evaluation Using 1000 Genomes Data.
2013

Effects of MIR137 on fronto-amygdala functional connectivity.
2013

Effects of ZNF804A on auditory P300 response in schizophrenia.
2013

Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style.
2013

Evidence that duplications of 22q11.2 protect against schizophrenia.
2013

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
2013

Methylphenidate improves some but not all measures of ATTENTION, as measured by the TEA-Ch in medication-naïve children with ADHD
2013

Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT).
2013

Neuropsychological Effects Of The CSMD1 Genome-Wide Associated Schizophrenia Risk Variant rs10503253.
2013

Social dysfunction in schizophrenia: An investigation of the GAF scale's sensitivity to deficits in social cognition.
2013

The miR-137 schizophrenia susceptibility variant rs1625579 does not predict variability in brain volume in a sample of schizophrenic patients and healthy individuals.
2013

The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis.
2012

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.
2012

Brain-derived neurotrophic factor Val66Met polymorphism and early life adversity affect hippocampal volume.
2012

Common variant at 16p11.2 conferring risk of psychosis
2012

Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data.
2012

Effect of genetic variant in BICC1 on functional and structural brain changes in depression.
2012

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
2012

Functional investigation of a schizophrenia GWAS signal at the CDC42 gene.
2012

Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia.
2012

Identification of common variants associated with human hippocampal and intracranial volumes
2012

Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
2012

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.
2012

Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis.
2012

Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137.
2012

Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253.
2012

Preserved cognitive function is associated with suicidal ideation and single suicide attempts in schizophrenia.
2012

Runs of homozygosity implicate autozygosity as a schizophrenia risk factor.
2012

Social cognition in bipolar disorder versus schizophrenia: comparability in mental state decoding deficits.
2012

The NOS1 variant rs6490121 is associated with variation in prefrontal function and gray matter density in healthy individuals
2012

The cognitive genetics of neuropsychiatric disorders.
2012

The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function.
2011

A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD).
2011

A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings.
2011

Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation.
2011

Association of serotonin and dopamine gene pathways with behavioural subphenotypes in dementia.
2011

Common Variants at ABCA7, MS4A6A/MS4A4E, EPHA1/CD33 and CD2AP are associated with Alzheimer's disease
2011

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.
2011

Epistasis between neurochemical gene polymorphisms and risk for ADHD
2011

Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data.
2011

Fine mapping of ZNF804A and genomime-wide significant evidence for it's involvement in Schizophrenia and bipolar disorder.
2011

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia.
2011

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for Autism.
2011

Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders.
2011

Genetic Classification of Populations using Supervised Learning.
2011

Genome-wide association study identifies five new schizophrenia loci.
2011

Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression
2011

Geonome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms
2011

Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings.
2011

Mutation of Semaphorin-6A Disrupts Limbic and Cortical Connectivity and Models Neurodevelopmental Psychopathology
2011

The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals.
2011

The Role of Variation at AßPP, PSEN1, PSEN2, and MAPT in Late Onset Alzheimer's Disease.
2011

The impact of study design and diagnostic approach in a larege multi-centre ADHD study. Part 1: ADHD Symptom patterns.
2011

The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ
2011

fMRI activation during response inhibition and error processing: the role of the DAT1 gene in typically developing adolescents and those diagnosed with ADHD
2010

A NOS1 variant implicated in cognitive performance influences evoked neural responses during a high density EEG study of early visual perception.
2010

A genomewide scan for common alleles affecting risk for autism.
2010

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.
2010

Clinical symptomatology and the psychosis risk gene, ZNF804A
2010

Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression.
2010

Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD
2010

Functional assessment of a promoter polymorphism in S100B, a putative risk variant for bipolar disorder.
2010

Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism.
2010

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.
2010

Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility.
2010

Multiplex Target Enrichment Using DNA Indexing for Ultra-High Throughput SNP Detection.
2010

Predictability and construct validity of oppositional defiant disorder in children and adolescents with ADHD combined type.
2010

Predictability of oppositional defiant disorder and symptom dimensions in children and adolescents with ADHD combined type
2010

What have the genomics ever done for the psychoses?
2010

ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia
2009

A genome-wide linkage and association scan reveals novel loci for autism.
2009

ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype.
2009

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.
2009

Detecting subtle facial emotion recognition deficits in high-functioning Autism using dynamic stimuli of varying intensities.
2009

Dopaminergic genotype influences spatial bias in healthy adults.
2009

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.
2009

Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
2009

Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects.
2009

Is 'Clinical' insight the same as 'Cognitive' insight in schizophrenia?
2009

Microduplications of 16p11.2 are associated with schizophrenia
2009

Noradrenergic genotype predicts lapses in sustained attention
2009

Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies.
2009

Reduced occipital and prefrontal brain volumes in dysbindin-associated schizophrenia.
2009

Replicated genetic evidence supports a role for HOMER2 in schizophrenia.
2009

Replication of an Association of a Promoter Polymorphism of the Dopamine Transporter Gene and Attention Deficit Hyperactivity Disorder
2009

Right-sided spatial difficulties in ADHD demonstrated in continuous movement control.
2009

The SNP ratio test: pathway analysis of genome-wide association datasets.
2009

What have the genomics ever done for the psychoses?
2009

fMRI activation during response inhibition and error processing: the role of the DAT1 gene in typically developing adolescents and those diagnosed with ADHD.
2008

Absence of the 7-repeat variant of the DRD4 VNTR is associated with drifting sustained attention in children with ADHD but not in controls.
2008

An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases
2008

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
2008

Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.
2008

Dissociation in response to methylphenidate on response variability in a group of medication naïve children with ADHD
2008

Does the ability to sustain attention underlie symptom severity in schizophrenia?
2008

Early Visual Processing Deficits in Dysbindin-Associated Schizophrenia,
2008

Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32.
2008

Impaired conflict resolution and alerting in children with ADHD: evidence from the Attention Network Task (ANT).
2008

Mental state decoding v. mental state reasoning as a mediator between cognitive and social function in psychosis
2008

Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies.
2008

Noradrenergic genotype predicts lapses in sustained attention.
2008

Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) program.
2008

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
2007

A dysbindin risk haplotype associated with less severe manic-type symptoms in psychosis.
2007

An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases.
2007

Are relational style and neuropsychological performance predictors of social attributions in chronic schizophrenia?
2007

Bipolar affective puerperal psychosis- genome-wide significant evidence for linkage to chromosome 16.
2007

Chitinase-3-like 1 (CHI3L1) gene and schizophrenia: genetic association and a potential functional mechanism.
2007

D-amino acid oxidase (DAO) genotype and mood symptomatology in schizophrenia.
2007

Dissociation in performance of children with ADHD and autism on a task of sustained attention
2007

Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention.
2007

Dissociation in response to methylphenidate on response variability in a group of medication naïve children with ADHD.
2007

Early visual processing deficits in dysbindin-associated schizophrenia.
2007

Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample.
2007

Functional genomics and schizophrenia: endophenotypes and mutant models.
2007

Gene-environment interplay in attention-deficit hyperactivity disorder and the importance of a develomental perspective
2007

Response variability in Attention Deficit Hyperactivity Disorder: evidence for neuropsychological heterogeneity
2007

Spatial attentional bias as a marker of genetic risk, symptom severity and stimulant response in ADHD.
2006

A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence.
2006

Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention.
2006

Do antisaccade deficits in schizophrenia provide evidence of a specific inhibitory function?
2006

Neurocognition and suicidal behaviour in an Irish population with major psychotic disorders.
2006

The cognitive genetics of attention deficit hyperactivity disorder (ADHD): sustained attention as a candidate phenotype.
2006

Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: a preliminary study.
2005

Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children.
2005

Association between dopamine transporter (DAT1)genotype, left sided inattention, and an enhanced response to methylphenidate in attention deficit hyperactivity disorder
2005

Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q
2005

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31
2005

DRD4 gene variants and sustained attention in attention deficit hyperactivity disorder (ADHD): effects of associated alleles at the VNTR and -521 SNP.
2005

Preferential Transmission of Paternal Alleles at Risk Genes in Attention Deficit/Hyperactivity Disorder
2005

Response variability in attention deficit hyperactivity disorder: evidence for neuropsychological heterogeneity.
2005

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.
2005

Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD.
2005

Whole genome linkage scan of recurrent depressive disorder from the depression network study
2004

Dissecting the attention deficit hyperactivity disorder (ADHD) phenotype: sustained attention, response variability and spatial attentional asymmetries in relation to dopamine transporter (DAT1) genotype.
2004

Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPs.
2004

Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined Subtypes
2004

Phenotype studies of the DRD4 gene polymorphisms in ADHD: association with oppositional defiant disorder and positive family history.
2004

The Depression Network (DeNT) Study: Methodology and Sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetics study
2004

The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.
2003

Association of the 480 bp DAT1 allele with methylphenidate response in a sample of Irish children with ADHD.
2003

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder
2003

Psychiatric Genetics in the post genome age
2002

Dopaminergic system genes in ADHD: toward a biological hypothesis
2002

Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis.
2002

Serotonergic System and Attention Deficit Hyperactivity Disorder (ADHD): a potential susceptibility locus at the 5-HT1B receptor gene in 270 Trios from a multi-center sample
2002

Sibling pairs with affective disorders: resemblance of demographic and clinical features.
2002

Synaptosomal-Associated Protein 25 (SNAP-25) and Attention Deficit Hyperactivity Disorder (ADHD): Evidence of linkage and Association in the Irish Population.
2002

The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report
2001

Cigarette smoking and psychotic symptoms in bipolar affective disorder
2001

Dementia in people with Down's syndrome.
2001

Dopa decarboxylase gene polymorphisms and attention deficit hyperactivity disorder (ADHD): no evidence for association in the Irish population
2001

Synaptosomal-associated protein 25 (SNAP-25) and attention deficit hyperactivity disorder (ADHD): evidence of linkage and association in the Irish population.
2000

Lack of gender effect on familial schizophrenia. A Brazilian study.
1999

Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children.
1999

Presenilin 1 and alpha-1-antichymotrypsin polymorphisms in Down syndrome: no effect on the presence of dementia.

These are the 10 unique sources for Michael Gill's 187 publications. A single publication may appear in multiple sources. Click on a name or publication count to see the publications for a particular source.

Source #
Ireland -> National University of Ireland Galway 3
Ireland -> National University of Ireland Galway -> PubMed 3
Ireland -> Royal College of Surgeons in Ireland 4
Ireland -> Royal College of Surgeons in Ireland -> PubMed 2
Ireland -> Trinity College Dublin 179
Ireland -> Trinity College Dublin -> PubMed 84
Ireland -> University College Cork 1
Ireland -> University College Cork -> PubMed 1
Ireland -> University College Dublin 4
Ireland -> University College Dublin -> PubMed 1
14-Jun-2006

A test method for ADHD response
+

  1. Further insights

    Clicking through these tabs will give you a wealth of further insights into this expert through their commonly used topics, the evolution of their expertise, their collaborators and their publications.

  2. Details

    Here is a quick breakdown of this expert's publication history

  3. Contact

    If this is the expert you have been looking for, simply click here to make contact.