Michael Gill

Michael Gill, M. Gill, J. Waddington, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.

Susanne Walitza, Aribert Rothenberger, Stephan Ripke, 2010, Journal of the American Academy of Child and Adolescent Psychiatry.

Is “clinical” insight the same as “cognitive” insight in schizophrenia?

Michael Gill, Sandra Barry, Nicola McGlade, 2009, Journal of the International Neuropsychological Society.

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

Michael Gill, Derek W. Morris, John L. Waddington, 2005, Schizophrenia Research.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

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

Mao Sheng Yang, Michael Gill, M. Gill, 2007, International Journal of Developmental Neuroscience.

Genetic Differences between Five European Populations

Naomi R. Wray, Michele T. Pato, Peter Holmans, 2010, Human Heredity.

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

Aribert Rothenberger, Herbert Roeyers, Tobias Banaschewski, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

Richard Reilly, Hugh Garavan, Michael Gill, 2006, Journal of the International Neuropsychological Society.

Attention Deficit/Hyperactivity Disorder-Derived Coding Variation in the Dopamine Transporter Disrupts Microdomain Targeting and Trafficking Regulation

Michael Gill, Erica Bowton, Randy D Blakely, 2012, The Journal of Neuroscience.

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

Michael Gill, Katherine A. Johnson, Katherine A Johnson, 2008, Journal of child psychology and psychiatry, and allied disciplines.

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

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

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

Michael Gill, Katherine A. Johnson, Thomas Frodl, 2013, JAMA psychiatry.

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

Aribert Rothenberger, Christoph Lange, Herbert Roeyers, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia.

Michael Gill, Hans-Jürgen Möller, Pierandrea Muglia, 2010, Archives of general psychiatry.

Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease

Seth Love, Brian Lawlor, Martin Rossor, 2010, PloS one.

Genome‐wide association scan of attention deficit hyperactivity disorder

Genome-wide Association Study of Alzheimer’s disease with Psychotic Symptoms

Brian Lawlor, Oscar L. Lopez, David Craig, 2011, Molecular Psychiatry.

Fine mapping of ZNF 804 A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

Ivan Nikolov, Brien Riley, Peter Holmans, 2011 .

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

Michael Fitzgerald, Deirdre O'Donnell, Michael Gill, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

Sven Bergmann, Florian Holsboer, Bertram Müller-Myhsok, 2015, BMC Medicine.

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

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

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

Ian H. Robertson, Michael Gill, Mark A. Bellgrove, 2005, Neuropsychologia.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

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

Michael Gill, James Sutcliffe, Richard J L Anney, 2011, European Journal of Human Genetics.

The hierarchical factor model of ADHD: invariant across age and national groupings?

Aribert Rothenberger, Herbert Roeyers, Tobias Banaschewski, 2012, Journal of child psychology and psychiatry, and allied disciplines.

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

Michael Gill, Hans-Jürgen Möller, Pierandrea Muglia, 2009, Archives of general psychiatry.

Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan

Genome-wide association study identifies five new schizophrenia loci

Anders D. Børglum, Peter Donnelly, Jianxin Shi, 2011, Nature Genetics.

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

Michael Gill, Katherine A. Johnson, Simon P Kelly, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Reduced Occipital and Prefrontal Brain Volumes in Dysbindin-Associated Schizophrenia

Carlo Caltagirone, Andrea Cherubini, Michael Gill, 2010, Neuropsychopharmacology.

Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression

Bertram Müller-Myhsok, Gerome Breen, Michael Gill, 2011, PloS one.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

A Review of Neuropsychological and Neuroimaging Research in Autistic Spectrum Disorders: Attention, Inhibition and Cognitive Flexibility.

Hugh Garavan, Michael Gill, Katherine A. Johnson, 2008 .

Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder

Michael Gill, M. Gill, D. Coghill, 2009, Neuroscience Letters.

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

John J. Foxe, Michael Gill, Aiden Corvin, 2012, Human brain mapping.

Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes.

Jan K Buitelaar, Florence Levy, Michael Gill, 2004, American journal of human genetics.

No linkage or linkage disequilibrium between brain-derived neurotrophic factor (BDNF) dinucleotide repeat polymorphism and schizophrenia in Irish families

Michael Gill, Dermot Walsh, Kenneth S Kendler, 1998, Psychiatry Research.

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

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

No evidence for an association of affective disorders with high- or low-activity allele of catechol-o-methyltransferase gene

Robin M. Murray, Michael Gill, David A. Collier, 1997, Biological Psychiatry.

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

Patrick F. Sullivan, Brien Riley, Giulio Genovese, 2013, Human molecular genetics.

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

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3

Susanne Walitza, Herbert Roeyers, Peter Holmans, 2012, The American journal of psychiatry.