I. Craig

Robert Plomin, Jo Knight, Philip Asherson, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Neural mechanisms of anger regulation as a function of genetic risk for violence.

I. Craig, N. Volkow, N. Alia-Klein, 2009, Emotion.

DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: No evidence for association

P. Sham, I. Craig, J. Mill, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1)

Philip Asherson, I. Craig, J. Mill, 2005, BMC Genetics.

Engineering in Genomics [variable number tandem repeats as agents of functional regulation in the genome]

D. Collier, I. Craig, G. Breen, 2008, IEEE Engineering in Medicine and Biology Magazine.

Single-nucleotide polymorphism genotyping in DNA pools.

I. Craig, R. Plomin, L. Butcher, 2005, Methods in molecular biology.

The MAO-A genotype does not modulate resting brain metabolism in adults

I. Craig, N. Volkow, N. Alia-Klein, 2008, Psychiatry Research: Neuroimaging.

Antidepressant-dependent mRNA changes in mouse associated with hippocampal neurogenesis in a mouse model of depression

I. Craig, P. McGuffin, L. Schalkwyk, 2012, Pharmacogenetics and genomics.

The Genetics of Human Aggressive Behaviour

I. Craig, Kelly E. Halton, K. Halton, 2010 .

Language-impaired children: No sign of the FOXP2 mutation

I. Craig, R. Plomin, E. Meaburn, 2002, Neuroreport.

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

B. Franke, M. Gill, R. Anney, 2006, Molecular Psychiatry.

LANGUAGE DELAYS AND PHYSICAL AGGRESSION

A. Caspi, R. Poulton, T. Moffitt, 2003 .

Commentary on “A Role for the X Chromosome in Sex Differences in Variability in General Intelligence?” (Johnson et al., 2009)

I. Craig, R. Plomin, C. Haworth, 2009, Perspectives on psychological science : a journal of the Association for Psychological Science.

Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals†

M. Rietschel, M. Gill, N. Craddock, 2017, British Journal of Psychiatry.

MAOA, maltreatment, and gene–environment interaction predicting children's mental health: new evidence and a meta-analysis

A. Caspi, B. Williams, T. Moffitt, 2006, Molecular Psychiatry.

Moderation of breastfeeding effects on the IQ by genetic variation in fatty acid metabolism

A. Caspi, R. Poulton, T. Moffitt, 2007, Proceedings of the National Academy of Sciences.

Genome-wide Association for Major Depression Through Age at Onset Strati ﬁ cation: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

Blair H. Smith, N. Wray, I. Deary, 2016 .

Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contribution.

P. Muglia, M. Rietschel, M. Gill, 2014, Journal of affective disorders.

The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression

I. Craig, Z. Kutalik, S. Bergmann, 2013, Molecular Psychiatry.

The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression

A. Hofman, S. Cichon, M. Rietschel, 2011, Neuron.

Genome-wide association study of major recurrent depression in the U.K. population.

P. Muglia, N. Craddock, I. Craig, 2010, The American journal of psychiatry.

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

John P. Rice, M. Rietschel, M. Gill, 2015, Psychological Medicine.

University of Birmingham Familiality and SNP heritability of age at onset and episodicity in major depressive disorder

M. Rietschel, M. Gill, N. Craddock, 2015 .

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders

Dorret I. Boomsma, Gerome Breen, Nicholas G. Martin, 2014, Human Genetics.

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.

The Genetic Basis for Sex Differences in Human Behaviour: Role of the Sex Chromosomes

I. Craig, Emma Harper, C. Loat, 2004, Annals of human genetics.

The dopamine D4 receptor and the hyperactivity phenotype: a developmental-epidemiological study

K. Sugden, R. Poulton, T. Moffitt, 2002, Molecular Psychiatry.

Genetic Organization of the Serotonergic System

I. Craig, U. D'Souza, 2010 .

Depressive disorder moderates the effect of the FTO gene on body mass index

M. Rietschel, M. Gill, N. Craddock, 2012, Molecular Psychiatry.

Genetics of human aggressive behaviour

I. Craig, K. Halton, 2009, Human Genetics.

Functional genetic polymorphisms in serotonin and dopamine gene systems and their significance in behavioural disorders.

I. Craig, U. D'Souza, 2008, Progress in brain research.

The importance of stress and genetic variation in human aggression

I. Craig, 2007, BioEssays : news and reviews in molecular, cellular and developmental biology.

Functional polymorphisms in dopamine and serotonin pathway genes

I. Craig, U. D'Souza, Ian W Craig, 2006, Human mutation.

Gene–environment interaction analysis of serotonin system markers with adolescent depression

R Plomin, K. Sugden, I. Craig, 2004, Molecular Psychiatry.

Association analysis of MAOA and COMT with neuroticism assessed by peers

Robert Plomin, Thalia C Eley, I. Craig, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Allele association studies with SSR and SNP markers at known physical distances within a 1 Mb region embracing the ALDH2 locus in the Japanese, demonstrates linkage disequilibrium extending up to 400 kb.

P. Sham, I. Craig, D. Ball, 2000, Human molecular genetics.

Genotyping Pooled DNA on Microarrays: A Systematic Genome Screen of Thousands of SNPs in Large Samples to Detect QTLs for Complex Traits

I. Craig, R. Plomin, A. Al-Chalabi, 2004, Behavior genetics.

Brain Monoamine Oxidase A Activity Predicts Trait Aggression

Frank Telang, Jean Logan, Dardo Tomasi, 2008, The Journal of Neuroscience.

Evidence That Brain MAO A Activity Does Not Correspond to MAO A Genotype in Healthy Male Subjects

Nora D. Volkow, Frank Telang, Jean Logan, 2007, Biological Psychiatry.

Interaction between childhood maltreatment on immunogenetic risk in depression: Discovery and replication in clinical case-control samples

N. Craddock, I. Craig, G. Breen, 2018, Brain, Behavior, and Immunity.

Genome-wide association study of co-occurring anxiety in major depression

M. Rietschel, M. Gill, N. Craddock, 2013, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

A follow‐up case–control association study of tractable (druggable) genes in recurrent major depression

P. Muglia, N. Craddock, I. Craig, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Bipolar disorder susceptibility region on chromosome 3q29 not confirmed in a case–control association study

I. Craig, A. Farmer, P. McGuffin, 2011, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

NRG1 gene in recurrent major depression: No association in a large‐scale case–control association study

N. Craddock, I. Craig, P. McGuffin, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The current state of play on the molecular genetics of depression

I. Craig, P. McGuffin, P. McGuffin, 2012, Psychological Medicine.

A longitudinal study of epigenetic variation in twins

A. Caspi, R. Houts, B. Williams, 2010, Epigenetics.

Phenotypic association analyses with copy number variation in recurrent depressive disorder

Florian Holsboer, Gerome Breen, Marcella Rietschel, 2015 .

X Inactivation as a Source of Behavioural Differences in Monozygotic Female Twins

I. Craig, R. Plomin, M. Galsworthy, 2004, Twin Research.

X Inactivation as a Source of Behavioural Differences in Monozygotic Female Twins

I. Craig, R. Plomin, M. Galsworthy, 2004, Twin Research.

Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: Meta-analysis of data from genome-wide association studies

M. Rietschel, K. Tansey, I. Craig, 2018, European Neuropsychopharmacology.

The quest for quantitative trait loci associated with intelligence

I. Craig, R. Plomin, Joanna K. J. Kennedy, 2006 .

A Genome-Wide Association Study of Social and Non-Social Autistic-Like Traits in the General Population Using Pooled DNA, 500 K SNP Microarrays and Both Community and Diagnosed Autism Replication Samples

I. Craig, R. Plomin, L. Schalkwyk, 2009, Behavior genetics.

A Longitudinal Twin Study of Skewed X Chromosome-Inactivation

A. Caspi, R. Houts, B. Williams, 2011, PloS one.

SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children.

P. Sham, I. Craig, R. Plomin, 2005, Human molecular genetics.

Interaction between specific forms of childhood maltreatment and the serotonin transporter gene (5-HTT) in recurrent depressive disorder.

N. Craddock, I. Craig, A. Farmer, 2013, Journal of affective disorders.

Genome Wide Association Analysis of Copy Number Variation in Recurrent Depressive Disorder

D. Pinto, S. Scherer, P. Muglia, 2011, Molecular Psychiatry.

Stressful life events and the serotonin transporter gene (5-HTT) in recurrent clinical depression.

N. Craddock, I. Craig, L. Jones, 2012, Journal of affective disorders.

Copy number variants and therapeutic response to antidepressant medication in major depressive disorder

T. Peters, M. Rietschel, K. Tansey, 2014, The Pharmacogenomics Journal.

Methyl‐CpG‐binding protein 2 polymorphisms and vulnerability to autism

P. Bolton, D. Geschwind, D. Geschwind, 2008, Genes, brain, and behavior.

The serotonin transporter gene as a QTL for ADHD

P. Sham, I. Craig, S. Purcell, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings.

I. Craig, S. Purcell, D. Ball, 2000, Twin research : the official journal of the International Society for Twin Studies.

Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms

I. Craig, R. Plomin, L. Schalkwyk, 2005, Molecular Psychiatry.

Functional effects of a tandem duplication polymorphism in the 5′flanking region of the DRD4 gene

I. Craig, P. McGuffin, J. Mill, 2004, Biological Psychiatry.

Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP)

M. Rietschel, I. Craig, G. Breen, 2018, Translational Psychiatry.

Investigating the Relationship Between FMR1 Allele Length and Cognitive Ability in Children: A Subtle Effect of the Normal Allele Range on the Normal Ability Range?

I. Craig, R. Plomin, G. Craig, 2006, Annals of human genetics.

Pharmacoproteomic investigation into antidepressant response in two mouse inbred strains

I. Craig, P. McGuffin, L. Schalkwyk, 2012, Proteomics.

Imprinting, Inactivation and the Behavioural Genetics of the X Chromosome

I. Craig, 2011 .

Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes

I. Craig, J. Mill, L. Schalkwyk, 2004, European Journal of Human Genetics.

P2RX7: A bipolar and unipolar disorder candidate susceptibility gene?

G. Kirov, D. Grozeva, N. Craddock, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Polygenic interactions with environmental adversity in the aetiology of major depressive disorder

J. Potash, N. Craddock, M. Owen, 2015, Psychological Medicine.

Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain

I. Craig, J. Mill, R. Pidsley, 2014, Epigenetics.

Genes within the serotonergic system are differentially expressed in human brain

K. Sugden, I. Craig, A. Tichopád, 2009, BMC Neuroscience.

Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays

R Plomin, I. Craig, R. Plomin, 2008, Genes, brain, and behavior.

A Genome-Wide Scan of 1842 DNA Markers for Allelic Associations with General Cognitive Ability: A Five-Stage Design Using DNA Pooling and Extreme Selected Groups

I. Craig, P. McGuffin, S. Purcell, 2001, Behavior genetics.

A novel expression based approach for assessing the inactivation status of human X-linked genes

I. Craig, D. Benjamin, I. V. Bakel, 2000, European Journal of Human Genetics.

A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample.

R. Murray, D. Collier, I. Craig, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Candidate Genes Expression Profile Associated with Antidepressants Response in the GENDEP Study: Differentiating between Baseline ‘Predictors' and Longitudinal ‘Targets'

I. Craig, G. Breen, A. Farmer, 2012, Neuropsychopharmacology.

Candidate Genes Expression Profile Associated with Antidepressants Response in the GENDEP Study: Differentiating between Baseline ‘Predictors’ and Longitudinal ‘Targets’

I. Craig, G. Breen, A. Farmer, 2013, Neuropsychopharmacology.

Assessing Individual Differences in Genome-Wide Gene Expression in Human Whole Blood: Reliability Over Four Hours and Stability Over 10 Months

I. Craig, R. Plomin, L. Schalkwyk, 2009, Twin Research and Human Genetics.

Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol‐O‐methyltransferase (COMT) gene

A. Caspi, B. Williams, T. Moffitt, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression

David A Collier, D. Collier, I. Craig, 2006, BMC Medical Genetics.

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

M. Rietschel, M. Gill, N. Craddock, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project

M. Rietschel, I. Craig, G. Breen, 2010, The Pharmacogenomics Journal.

Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression

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

Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders

N. Wray, H. Stefánsson, S. Cichon, 2015, Neuron.

Exploring the role of drug-metabolising enzymes in antidepressant side effects

M. Rietschel, K. Tansey, I. Craig, 2015, Psychopharmacology.

Genetic Predictors of Response to Serotonergic and Noradrenergic Antidepressants in Major Depressive Disorder: A Genome-Wide Analysis of Individual-Level Data and a Meta-Analysis

T. Peters, M. Rietschel, K. Tansey, 2012, PLoS medicine.

Variation in GNB3 predicts response and adverse reactions to antidepressants

M. Rietschel, I. Craig, A. Elkin, 2011, Journal of psychopharmacology.

Moderation of antidepressant response by the serotonin transporter gene

M. Rietschel, I. Craig, A. Farmer, 2009, British Journal of Psychiatry.

Interaction between serotonin transporter gene variants and life events predicts response to antidepressants in the GENDEP project

M. Rietschel, I. Craig, A. Farmer, 2011, The Pharmacogenomics Journal.

Tumor necrosis factor and its targets in the inflammatory cytokine pathway are identified as putative transcriptomic biomarkers for escitalopram response

A. Danese, K. Tansey, I. Craig, 2013, European Neuropsychopharmacology.

Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.

P. Muglia, M. Rietschel, T. Schulze, 2010, The American journal of psychiatry.

Genetic predictors of response to antidepressants in the GENDEP project

Thomas G Schulze, Marcella Rietschel, Erik Roj Larsen, 2009, The Pharmacogenomics Journal.

Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

N. Wray, Zhongming Zhao, P. Sham, 2012, European Journal of Human Genetics.

Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder.

N. Craddock, M. Owen, I. Craig, 2009, Human molecular genetics.

oderation of the Effect of Adolescent-Onset Cannabis se on Adult Psychosis by a Functional Polymorphism n the Catechol-O-Methyltransferase Gene: ongitudinal Evidence of a Gene X Environment nteraction

H. Harrington, R. Poulton, T. Moffitt, 2005 .

Quantitative trait loci for IQ and other complex traits: single‐nucleotide polymorphism genotyping using pooled DNA and microarrays

I. Craig, R. Plomin, I. Craig, 2006, Genes, brain, and behavior.

Genotyping DNA pools on microarrays: Tackling the QTL problem of large samples and large numbers of SNPs

Robert Plomin, Ammar Al-Chalabi, I. Craig, 2005, BMC Genomics.

Validation of single nucleotide polymorphism quantification in pooled DNA samples with SNaPIT™

P. Sham, I. Craig, E. Taylor, 2002, Molecular biotechnology.

Genetics, environment and cognitive abilities: review and work in progress towards a genome scan for quantitative trait locus associations using DNA pooling.

I. Craig, R. Plomin, I. Craig, 2001, The British journal of psychiatry. Supplement.

Chasing behaviour genes into the next millennium.

I. Craig, R. Plomin, J. McClay, 2000, Trends in Biotechnology.

DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children.

I. Craig, P. McGuffin, D. Ball, 1999, Human molecular genetics.

Psychiatry and the ‘new genetics’: hunting for genes for behaviour and drug response

I. Craig, P. McGuffin, K. Aitchison, 2005, British Journal of Psychiatry.

Quantitative Trait Locus Analysis of Candidate Gene Alleles Associated With Attention Deficit Hyperactivity Disorder ( ADHD ) in Five Genes : DRD 4 , DAT 1 , DRD 5 , SNAP-25 , and 5 HT 1 B

P. Sham, I. Craig, R. Plomin, 2005 .

The Bipolar Association Case–Control Study (BACCS) and meta‐analysis: No association with the 5,10‐Methylenetetrahydrofolate reductase gene and bipolar disorder

P. Muglia, N. Craddock, M. Owen, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.

Stephan Ripke, Steven P. Hamilton, Florian Holsboer, 2013, The American journal of psychiatry.

Integrative mouse and human mRNA studies using WGCNA nominates novel candidate genes involved in the pathogenesis of major depressive disorder.

Peter McGuffin, Rudolf Uher, Frans Sluyter, 2013, Pharmacogenomics.

ATP-binding cassette sub-family F member 1 (ABCF1) is identified as a putative therapeutic target of escitalopram in the inflammatory cytokine pathway

K. Tansey, I. Craig, G. Breen, 2013, Journal of psychopharmacology.

Convergent Animal and Human Evidence Suggests a Role of PPM1A Gene in Response to Antidepressants

M. Rietschel, I. Craig, A. Farmer, 2011, Biological Psychiatry.

No association with the 5,10‐methylenetetrahydrofolate reductase gene and major depressive disorder: Results of the depression case control (DeCC) study and a meta‐analysis

N. Craddock, M. Owen, I. Craig, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression.

N. Craddock, M. Owen, I. Craig, 2013, Journal of psychiatric research.

Stressful life events and the brain-derived neurotrophic factor gene in bipolar disorder.

P. Muglia, I. Craig, A. Farmer, 2010, Journal of affective disorders.

Pharmacogenetics of antidepressant response: A polygenic approach

T. Peters, M. Rietschel, T. Schulze, 2016, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Dissecting the Genetic Heterogeneity of Depression Through Age at Onset

John P. Rice, P. Muglia, M. Rietschel, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic Predictors of Increase in Suicidal Ideation During Antidepressant Treatment in the GENDEP Project

M. Rietschel, T. Schulze, I. Craig, 2009, Neuropsychopharmacology.

Transcriptomics and the mechanisms of antidepressant efficacy

M. Rietschel, K. Tansey, I. Craig, 2016, European Neuropsychopharmacology.

AVPR1A and SLC6A4 Polymorphisms in Choral Singers and Non-Musicians: A Gene Association Study

I. Craig, C. Lewis, Gavin Craig, 2012, PloS one.

Association of the dystrobrevin binding protein 1 gene (DTNBP1) in a bipolar case–control study (BACCS)

P. Muglia, I. Craig, A. Farmer, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

GENESiS : creating a composi te index of the vulnerabi l i ty to anxiety and depression in a communi ty-based sample of sibl ings

I. Craig, R. Plomin, P. Sham, 2007 .

A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds.

P. Sham, I. Craig, R. Plomin, 2005, Journal of child psychology and psychiatry, and allied disciplines.

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.

The genetics of affective disorder and suicide

I. Craig, P. McGuffin, C. Lewis, 2010, European Psychiatry.

A Genome Wide Association Study of Mathematical Ability Reveals an Association at Chromosome 3q29, a Locus Associated with Autism and Learning Difficulties: A Preliminary Study

Simon E. Fisher, Leena Peltonen, Simon Baron-Cohen, 2014, PloS one.

Genetic differences in cytochrome P450 enzymes and antidepressant treatment response

M. Rietschel, K. Tansey, I. Craig, 2014, Journal of psychopharmacology.

A genome-wide significant linkage for severe depression on chromosome 3: the depression network study.

P. Muglia, M. Rietschel, M. Gill, 2011, The American journal of psychiatry.

Association analysis of monoamine genes with measures of depression and anxiety in a selected community sample of siblings

K. Sugden, I. Craig, S. Purcell, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic Polymorphisms in Stress Response

I. Craig, 2007 .

Behavioral genetics in the postgenomic era

Robert Plomin, John C. DeFries, Peter McGuffin, 2003 .

Association of the serotonin transporter gene, neuroticism and smoking behaviours

D. Collier, P. Sham, I. Craig, 2008, Journal of Human Genetics.

Genome-wide association for major depression through age at onset stratificationGenomic analysis of age at onset in depression

Naomi, Blair H. Smith, I. Deary, 2016 .

Prediction of heterogeneity in intelligence and adult prognosis by genetic polymorphisms in the dopamine system among children with attention-deficit/hyperactivity disorder: evidence from 2 birth cohorts.

A. Caspi, B. Williams, R. Poulton, 2006, Archives of general psychiatry.

Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children

I. Craig, R. Plomin, L. Schalkwyk, 2008, Molecular Psychiatry.

Estimating the heritability of reporting stressful life events captured by common genetic variants

John P. Rice, P. Muglia, M. Rietschel, 2012, Psychological Medicine.

DNA pooling and dense marker maps: a systematic search for genes for cognitive ability.

I. Craig, P. McGuffin, D. Ball, 1999, Neuroreport.

Differential methylation of the X‐chromosome is a possible source of discordance for bipolar disorder female monozygotic twins

I. Craig, P. McGuffin, W. Nolen, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Rapid Publication Expression of the Dopamine Transporter Gene is Regulated by the 3 0 UTR VNTR : Evidence From Brain and Lymphocytes Using Quantitative RT-PCR

I. Craig, J. Mill, P. Asherson, 2002 .

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

Matti Pirinen, Peter Donnelly, Robert Plomin, 2014, Nature Communications.

A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays

Claire L. Simpson, P. Sham, I. Craig, 2005, Nucleic acids research.

Title A central resource for accurate allele frequency estimation frompooled DNA genotyped on DNA microarrays

P. Sham, I. Craig, J. Powell, 2005 .

THE SEARCHFORGENES INFLUENCINGBEHAVIOUR

I. Craig, P. McGuffin, K. Aitchison, 2004 .

The role of monoamine oxidase A, MAOA, in the aetiology of antisocial behaviour: the importance of gene-environment interactions.

I. Craig, 2005, Novartis Foundation symposium.