G. Kirov

Panagiotis K. Papasaikas, G. Kirov, M. O’Donovan, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Thyroid disorders in lithium-treated patients.

G. Kirov, 1998, Journal of affective disorders.

De novo mutations in schizophrenia implicate synaptic networks

E. Banks, G. Kirov, M. Owen, 2014, Nature.

A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders.

R. Murray, Tao Li, D. Collier, 1996, Molecular psychiatry.

Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder.

G. Kirov, D. Grozeva, N. Craddock, 2005, Archives of general psychiatry.

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

C. Spencer, J. Marchini, D. Rujescu, 2008, Nature Genetics.

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

Manuel A. R. Ferreira, S. Gabriel, M. Daly, 2008, Nature Genetics.

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder

D. Clair, G. Kirov, D. Grozeva, 2011, Molecular Psychiatry.

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study

Marcos del Pozo Banos, G. Kirov, M. Owen, 2020, BJPsych Open.

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium

C. Spencer, K. Davis, P. Visscher, 2016, bioRxiv.

Analysis of copy number variations at 15 schizophrenia-associated loci

G. Kirov, M. Owen, M. O’Donovan, 2014, The British journal of psychiatry : the journal of mental science.

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

Melissa J. Green, Robert C. Thompson, Pamela B. Mahon, 2017, bioRxiv.

The Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK Biobank: Response to Lawn et al.

G. Kirov, M. Owen, J. Walters, 2019, The American journal of psychiatry.

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.

E. Banks, R. Handsaker, G. Kirov, 2012, American journal of human genetics.

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Ryan L. Collins, Beryl B. Cummings, Kristen M. Laricchia, 2020, Nature Communications.

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.

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Tariq Ahmad, Patrick F. Sullivan, Andres Metspalu, 2020, Nature Communications.

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Tariq Ahmad, Patrick F. Sullivan, Andres Metspalu, 2019, bioRxiv.

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

S Purcell, Pall I. Olason, H. Stefánsson, 2011, Molecular Psychiatry.

Genome-wide association study identifies five new schizophrenia loci

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

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

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

P3-196: A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

Sven Cichon, Carol Brayne, Rebecca Sims, 2008, Alzheimer's & Dementia.

Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

Janice M. Fullerton, D. Rujescu, S. Cichon, 2020, bioRxiv.

Copy number variation in bipolar disorder

G. Kirov, D. Grozeva, N. Craddock, 2015, Molecular Psychiatry.

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

M C O'Donovan, G. Kirov, D. Grozeva, 2009, Molecular Psychiatry.

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

V. Moskvina, P. McGuffin, D. Collier, 2009, British Journal of Psychiatry.

Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele

M J Owen, G. Kirov, N. Craddock, 2006, Molecular Psychiatry.

Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder.

Nick Craddock, Michael J Owen, Nadine Norton, 2006, Archives of general psychiatry.

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

M J Owen, A Preece, G. Kirov, 2004, Archives of general psychiatry.

No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder.

G. Kirov, N. Craddock, M. Owen, 2000, Bipolar disorders.

Identification of a potential Bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4

G. Kirov, N. Craddock, M. O’Donovan, 2005, Molecular Psychiatry.

Association analysis between dopamine receptor genes and bipolar affective disorder

R. Murray, Tao Li, D. Collier, 1999, Psychiatry Research.

No association between schizophrenia and polymorphisms in COMT in two large samples.

G. Kirov, M. Owen, S. MacGregor, 2005, The American journal of psychiatry.

Support for RGS4 as a susceptibility gene for schizophrenia

Michael C O'Donovan, Michael J Owen, Nadine Norton, 2004, Biological Psychiatry.

An InDel in Phospholipase-CB-1 is linked with euthyroid multinodular goiter 1 2 *

G. Kirov, M. Hamshere, H. Völzke, 2018 .

Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine

D. Collier, G. Kirov, M. Owen, 1998, Molecular Psychiatry.

The effect of LRRK2 loss-of-function variants in humans

Ryan L. Collins, Beryl B. Cummings, Kristen M. Laricchia, 2020, Nature Medicine.

Evaluating drug targets through human loss-of-function genetic variation

Ryan L. Collins, Beryl B. Cummings, Kristen M. Laricchia, 2019, Nature.

Genetics of epilepsy: epilepsy research foundation workshop report.

J. H. Cross, Michael R. Johnson, I. Scheffer, 2007, Epileptic disorders : international epilepsy journal with videotape.

A comprehensive family-based replication study of schizophrenia genes.

D. Rujescu, S. Djurovic, O. Andreassen, 2013, JAMA psychiatry.

Electroconvulsive therapy for depression: 80 years of progress

G. Kirov, P. Sienaert, D. McLoughlin, 2021, The British Journal of Psychiatry.

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

D. Conrad, C. Barnes, M. Hurles, 2014, Biological Psychiatry.

Characterization of Single Gene Copy Number Variants in Schizophrenia

G. Kirov, M. Owen, P. Sullivan, 2019, Biological Psychiatry.

Characterization of Single Gene Copy Number Variants in Schizophrenia

G. Kirov, M. Owen, P. Sullivan, 2019, Biological Psychiatry.

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes 1 2 Primary

John P. Rice, Melissa J. Green, Robert C. Thompson, 2018 .

Genome‐wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type

G. Kirov, D. Grozeva, N. Craddock, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A new form of familial multi-nodular goitre with progression to differentiated thyroid cancer.

G. Kirov, J. Gregory, E. D. Williams, 2006, Endocrine-related cancer.

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders

H. Stefánsson, D. Rujescu, A. Ingason, 2016, PLoS genetics.

Characterisation of age and polarity at onset in bipolar disorder

Till F. M. Andlauer, S. Cichon, S. Djurovic, 2021, The British Journal of Psychiatry.

5-HT2A receptor and bipolar affective disorder: association studies in affected patients

M. Rietschel, M. Nöthen, D. Collier, 1997, Neuroscience Letters.

Genome Wide Linkage Analysis of 972 Bipolar Pedigrees Using Single Nucleotide Polymorphisms

Daniel L. Koller, G. Kirov, D. Grozeva, 2011, Molecular Psychiatry.

Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.

G. Kirov, M. Owen, M. O’Donovan, 2002, American journal of medical genetics.

Effects of chronic lithium treatment on renal function.

G. Kirov, J. Tredget, A. Kirov, 2010, Journal of affective disorders.

Quick recovery of orientation after magnetic seizure therapy for major depressive disorder

Klaus P. Ebmeier, G. Kirov, M. Husain, 2008, British Journal of Psychiatry.

Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

G. Kirov, M. Owen, M. O’Donovan, 2020, Nature Communications.

Possible parent‐of‐origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder

D. Collier, G. Kirov, N. Craddock, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Linkage analysis between bipolar affective disorder and markers on chromosome X

R. Murray, G. Kirov, M. Gill, 1998, Psychiatric genetics.

Ethnic differences in the presentation of bipolar affective disorder

G. Kirov, R. Murray, 1999, European Psychiatry.

SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype

G. Kirov, M. Owen, M. Samuel, 2014, Journal of Neurology.

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

Minna Männikkö, David Curtis, Peter Holmans, 2016, Nature Neuroscience.

Contents Vol. 1, 2015

Caroline A. Montojo, G. Lynch, G. Kirov, 2015, Molecular Neuropsychiatry.

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

M. Daly, H. Stefánsson, D. Rujescu, 2016, Molecular Psychiatry.

Observations on switching patients with schizophrenia to risperidone treatment

R. Murray, G. Kirov, R. Seth, 1997, Acta psychiatrica Scandinavica.

Religious Faith after Psychotic Illness

G. Kirov, A. David, R. Kemp, 1998, Psychopathology.

Apolipoprotein E: Depressive illness, depressive symptoms, and Alzheimer's disease

D. Collier, G. Kirov, S. Lovestone, 1998, Biological Psychiatry.

Cost-effectiveness evaluation of compliance therapy for people with psychosis

G. Kirov, M. Knapp, J. Beecham, 1998, British Journal of Psychiatry.

A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

Sven Cichon, Rebecca Sims, Michael J Owen, 2008, BMC Medical Genomics.

A network of dopaminergic gene variations implicated as risk factors for schizophrenia.

Michael E Talkowski, Bernie Devlin, Michael J Owen, 2008, Human molecular genetics.

Case–control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population

Yusuke Nakamura, Naoyuki Kamatani, Michiaki Kubo, 2009, Journal of Human Genetics.

Schizophrenia two‐hit hypothesis in velo‐cardio facial syndrome

Michael J Owen, George Kirov, G. Kirov, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Edinburgh Explorer Quick recovery of orientation after magnetic seizure therapy for major depressive disorder

Klaus P. Ebmeier, G. Kirov, M. Husain, 2018 .

Quick recovery of orientation after 100 Hz magnetic seizure therapy ( MST ) for major depressive disorder

Klaus P. Ebmeier, G. Kirov, M. Husain, 2009 .

Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia

G. Kirov, M. Owen, M. O’Donovan, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Disappearance of gender differences in age at onset in schizophrenics with a familial loading.

G. Kirov, P. Jones, R. Murray, 1994, Acta psychiatrica Scandinavica.

Erratum: Common alleles contribute to schizophrenia in CNV carriers

G. Kirov, K. Tansey, S. Mccarroll, 2015, Molecular psychiatry.

Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13.

G. Kirov, M. Gill, N. Craddock, 2005, Archives of general psychiatry.

The Effects of Etomidate on Seizure Duration and Electrical Stimulus Dose in Seizure-resistant Patients During Electroconvulsive Therapy

G. Kirov, N. Khalid, M. Atkins, 2006, The journal of ECT.

A cross-sectional and a prospective study of thyroid disorders in lithium-treated patients.

G. Kirov, M. Owen, J. Lazarus, 2005, Journal of affective disorders.

Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder

R. Murray, D. Collier, G. Kirov, 1998, Molecular Psychiatry.

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects

Michael J. Owen, Valentina Escott-Price, George Kirov, 2017, Biological Psychiatry.

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

M. Nöthen, G. Kirov, W. Peitsch, 2011, European Journal of Human Genetics.

Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples

D. Collier, D. Clair, G. Kirov, 2006, Biological Psychiatry.

Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

Hunna J. Watson, Ryan L. Collins, Dan J Stein, 2019, bioRxiv.

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.

Sex-biased reduction in reproductive success drives selective constraint on human genes

M. Hurles, G. Kirov, K. Samocha, 2020 .

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

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.

Common alleles contribute to schizophrenia in CNV carriers

G. Kirov, M. Owen, M. O’Donovan, 2015, Molecular Psychiatry.

Reduced burden of very large and rare CNVs in bipolar affective disorder.

D. Conrad, C. Barnes, M. Hurles, 2013, Bipolar disorders.

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

D. Conrad, C. Barnes, M. Hurles, 2012, Schizophrenia Research.

A genome-wide association study in 574 schizophrenia trios using DNA pooling

M C O'Donovan, M J Owen, S Cichon, 2009, Molecular Psychiatry.

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.

G. Kirov, D. Grozeva, N. Craddock, 2009, Human molecular genetics.

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.

Fikret Erdogan, Reinhard Ullmann, Wei Chen, 2007, Human molecular genetics.

Analysis of neurogranin (NRGN) in schizophrenia

G. Kirov, M. Owen, H. Williams, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Linkage studies in bipolar affective disorder with markers on chromosome 21.

R. Murray, D. Collier, G. Kirov, 1996, Journal of affective disorders.

The molecular genetics of schizophrenia: progress so far.

G. Kirov, R. Murray, 1997, Molecular medicine today.

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

D. Rujescu, S. Cichon, A. Ingason, 2011, Molecular Psychiatry.

Linkage disequilibrium mapping of bipolar affective disorder at 12q23‐q24 provides evidence for association at CUX2 and FLJ32356

G. Kirov, N. Craddock, M. Owen, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease.

G. Kirov, N. Craddock, M. Owen, 2005, The American journal of psychiatry.

Molecular pathology in neuropsychiatric disorders

G. Kirov, E. Rees, 2020 .

The contribution of rare variants to risk of 1 schizophrenia in individuals with and without 2 intellectual disability

Elvira Bramon, David Curtis, Mandy Johnstone, 2017 .

The genetics of the mood disorder spectrum: genome-wide association analyses of over 185,000 cases and 439,000 controls

Melissa J. Green, Robert C. Thompson, Pamela B. Mahon, 2018, bioRxiv.

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

Melissa J. Green, Robert C. Thompson, Pamela B. Mahon, 2017, bioRxiv.

De novo mutation in schizophrenia.

G. Kirov, M. Owen, M. O’Donovan, 2012, Schizophrenia bulletin.

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.

S. Scherer, G. Kirov, D. Merico, 2013, Human molecular genetics.

Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

D. Geschwind, J. Suvisaari, E. Bramon, 2016, bioRxiv.

The Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK Biobank.

G. Kirov, M. Owen, J. Walters, 2019, The American journal of psychiatry.

What a psychiatrist needs to know about copy number variants

G. Kirov, E. Rees, J. Walters, 2015 .

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

G. Kirov, M. Owen, M. O’Donovan, 2015, Neuron.

Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample

G. Kirov, M. Owen, H. Williams, 2012, Schizophrenia Research.

The role of copy number variation in schizophrenia

George Kirov, G. Kirov, 2010, Expert review of neurotherapeutics.

Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis

G. Kirov, M. Gill, M. Owen, 2019, Biological Psychiatry.

Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1)

Ivan Nikolov, Stuart MacGregor, Michael J. Owen, 2005, Biological Psychiatry.

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

G. Kirov, M. Gill, N. Craddock, 2002, Molecular Psychiatry.

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk

G. Kirov, M. Owen, P. Holmans, 2012, Human molecular genetics.

De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia

G. Kirov, M. Owen, M. O’Donovan, 2019, Nature Neuroscience.

Clinical indicators of treatment-resistant psychosis

G. Kirov, M. Owen, M. O’Donovan, 2019, The British Journal of Psychiatry.

Association of Rare Copy Number Variants With Risk of Depression

G. Kirov, M. Owen, M. O’Donovan, 2019, JAMA psychiatry.

Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank

G. Kirov, X. Caseras, E. Rees, 2018, bioRxiv.

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.

D. Collier, G. Kirov, M. Owen, 2016, JAMA psychiatry.

The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay

G. Kirov, M. Owen, M. O’Donovan, 2014, Biological Psychiatry.

De Novo Rates and Selection of Schizophrenia-Associated Copy Number Variants

G. Kirov, M. Owen, M. O’Donovan, 2011, Biological Psychiatry.

Neurexin 1 (NRXN1) deletions in schizophrenia.

D. Rujescu, A. Ingason, D. Collier, 2009, Schizophrenia bulletin.

Implication of a rare deletion at distal 16p11.2 in schizophrenia.

J. Sebat, D. Malhotra, Annette Lee, 2013, JAMA psychiatry.

A rare deletion at distal 16 p 11 . 2 is implicated in schizophrenia

Degenhardt, Dheeraj, Franziska, 2013 .

A functional polymorphism in the promoter of monoamine oxidase A gene and bipolar affective disorder.

G. Kirov, N. Craddock, M. Owen, 1999, The international journal of neuropsychopharmacology.

Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits

G. Kirov, M. Owen, M. O’Donovan, 2019, JAMA psychiatry.

Genetic association study of psychotic experiences in UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, bioRxiv.

Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

D. Rujescu, O. Andreassen, R. Ophoff, 2017, bioRxiv.

Genetic Differences between Five European Populations

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

Add-on topiramate reduces weight in overweight patients with affective disorders: a clinical case series

G. Kirov, J. Tredget, 2005, BMC psychiatry.

Screening the human protocadherin 8 (PCDH8) gene in schizophrenia

G. Kirov, N. Norton, H. Williams, 2002, Genes, brain, and behavior.

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

M C O'Donovan, M J Owen, T G Schulze, 2009, Molecular Psychiatry.

Population structure and genome-wide patterns of variation in Ireland and Britain

G. Kirov, M. Gill, V. Moskvina, 2010, European Journal of Human Genetics.

Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder

G. Kirov, S. Oldfield, S. Lightman, 2001, Molecular Psychiatry.

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

M C O'Donovan, M J Owen, P M Visscher, 2012, Molecular Psychiatry.

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

G. Kirov, M. Owen, M. O’Donovan, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Finding schizophrenia genes.

G. Kirov, M. Owen, M. O’Donovan, 2005, The Journal of clinical investigation.

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

G. Kirov, M. Owen, M. O’Donovan, 2003, British Journal of Psychiatry.

Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

G. Kirov, N. Williams, N. Norton, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Background Velo-cardio-facial syndrome (VCFS) is associatedwith interstitial deletions of chromosome 22q11.About 30% of patientswithVCFS

G. Kirov, M. Owen, M. O’Donovan, 2003 .

Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach

G. Kirov, M. Owen, M. Hamshere, 2002, Molecular Psychiatry.

De novo point mutations and copy number variants in discordant monozygotic twins reveals disease-susceptibility genes

Tomas W. Fitzgerald, R. Murray, G. Kirov, 2019 .

Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5

G. Kirov, N. Craddock, M. Owen, 1999, Molecular Psychiatry.

Linkage studies of bipolar disorder with chromosome 18 markers.

R. Murray, D. Collier, G. Kirov, 1999, American journal of medical genetics.

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

G. Kirov, M. Owen, P. Holmans, 2016, BMC Medical Genetics.

Copy number variation and neuropsychiatric illness

G. Kirov, E. Rees, 2021, Current opinion in genetics & development.

The rate of de novo CNVs in healthy controls

G. Kirov, M. Owen, M. O’Donovan, 2019, bioRxiv.

Effects of pathogenic CNVs on biochemical markers: a study on the UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, bioRxiv.

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2018, Journal of Medical Genetics.

Sequence analysis of 17 NRXN1 deletions

D. Rujescu, A. Ingason, T. Hansen, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

De novo CNVs in bipolar affective disorder and schizophrenia

Peter Holmans, Steven McCarroll, Michael J. Owen, 2014, Human molecular genetics.

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha

D. Rujescu, G. Kirov, D. Grozeva, 2010, Molecular Psychiatry.

A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder

G. Kirov, M. Owen, A. Thapar, 2019, Translational Psychiatry.

Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes

G. Kirov, M. Owen, P. Holmans, 2019, bioRxiv.

Analyses of de novo and common alleles implicate rare missense variants in SLC6A1 in schizophrenia

G. Kirov, M. Owen, P. Holmans, 2019 .

Gender differences in CNV burden do not confound schizophrenia CNV associations

G. Kirov, M. Owen, P. Holmans, 2016, Scientific Reports.

Copy number variation in schizophrenia in Sweden

M C O'Donovan, S Purcell, G. Kirov, 2014, Molecular Psychiatry.

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

D. Rujescu, S. Cichon, I. Giegling, 2021, Biological Psychiatry.

Complement genes contribute sex-biased vulnerability in diverse illnesses

Simon C. Potter, Christopher W. Whelan, M. Pirinen, 2020, Nature.

Exome Aggregation Consortium

Adam Kiezun, Sergio Islas-Andrade, Pierre Fontanillas, 2016 .

Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank

G. Kirov, K. Murphy, X. Caseras, 2020, The British Journal of Psychiatry.

Contribution of de novo and inherited rare CNVs to very preterm birth

G. Kirov, M. O’Donovan, A. Thapar, 2020, Journal of Medical Genetics.

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, The British Journal of Psychiatry.

S0033291718000454jra 2499..2504

G. Kirov, M. Owen, Danny J. Smith, 2019 .

Title: Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort

G. Kirov, M. Owen, M. O’Donovan, 2018 .

Association of copy number variation across the genome with neuropsychiatric traits in the general population

Tom R. Gaunt, G. Kirov, M. Owen, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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.

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

Thomas W. Mühleisen, N. Wray, D. Rujescu, 2017, Translational Psychiatry.

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

P. Visscher, N. Wray, M. Daly, 2015, International journal of epidemiology.

Genetic association of FMRP targets with psychiatric disorders

G. Kirov, M. Owen, M. O’Donovan, 2020, bioRxiv.

Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation

G. Kirov, M. Owen, H. Williams, 2016, Psychiatric genetics.

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

G. Kirov, M. Gill, M. Owen, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia

K. Davis, G. Kirov, N. Craddock, 2006, Proceedings of the National Academy of Sciences.

Support for Neuregulin 1 as a Susceptibility Gene for Bipolar Disorder and Schizophrenia

G. Kirov, D. Grozeva, M. Owen, 2008, Biological Psychiatry.

The serotonin transporter is a potential susceptibility factor for bipolar affective disorder.

R. Murray, Tao Li, D. Collier, 1996, Neuroreport.

Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder

T. G. Bruun, D. Collier, G. Kirov, 1999, Molecular Psychiatry.

Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping

G. Kirov, M. Owen, M. O’Donovan, 2008, BMC psychiatry.

IGF1, growth pathway polymorphisms and schizophrenia: A pooling study

G. Kirov, M. O’Donovan, D. Gunnell, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment

G. Kirov, M. Owen, I. Nikolov, 2005, The Pharmacogenomics Journal.

Genetic variation in the seven‐pass transmembrane cadherin CELSR1: lack of association with schizophrenia

G. Kirov, M. Owen, I. Nikolov, 2003, Psychiatric genetics.

Association analysis of the HOPA12bp polymorphism in schizophrenia and manic depressive illness

G. Kirov, M. Owen, I. Nikolov, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies

G. Kirov, M. Owen, I. Nikolov, 2002, Psychiatric genetics.

Dopamine transporter gene (DAT1) VNTR polymorphism in major psychiatric disorders: family‐based association study in the Bulgarian population

G. Kirov, I. Nikolov, D. Toncheva, 2002, Acta psychiatrica Scandinavica.

Pooled genotyping of microsatellite markers in parent-offspring trios.

G. Kirov, N. Craddock, M. Owen, 2000, Genome research.

Bipolar disorder and the serotonin transporter gene: a family-based association study

G. Kirov, N. Craddock, M. Owen, 1999, Psychological Medicine.

Evidence that duplications of 22q11.2 protect against schizophrenia

G. Kirov, M. Gill, N. Craddock, 2013, Molecular Psychiatry.

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

Bradley P. Coe, M. Pirinen, C. Spencer, 2014, Human molecular genetics.

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

G. Kirov, M. Gill, M. Owen, 2013, Human molecular genetics.

Mosaic copy number variation in schizophrenia

D. Clair, G. Kirov, M. Owen, 2013, European Journal of Human Genetics.

Phenotypic variations on the theme of CNVs

G. Kirov, M. Owen, M. O’Donovan, 2008, Nature Genetics.

pathogenesis of schizophrenia

G. Kirov, N. Craddock, M. Owen, 2009 .

Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

G. Kirov, M. Gill, M. Owen, 2018, bioRxiv.

Targeted Sequencing of 10 , 198 Schizophrenia Samples

G. Kirov, A. Corvin, A. Pocklington, 2022 .

Polygenic dissection of the bipolar phenotype

G. Kirov, D. Grozeva, N. Craddock, 2011, British Journal of Psychiatry.

Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia

G. Kirov, M. Gill, M. Owen, 2020, Biological Psychiatry.

Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder

G. Kirov, N. Craddock, M. Owen, 2006, British Journal of Psychiatry.

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

P. Donnelly, D. Collier, D. Clair, 2008, Molecular Psychiatry.

The Bipolar Affective Disorder Dimension Scale (BADDS) – a dimensional scale for rating lifetime psychopathology in Bipolar spectrum disorders

G. Kirov, N. Craddock, L. Jones, 2004, BMC psychiatry.

Schizophrenia copy number variants and associative learning

G. Kirov, L. Wilkinson, A. Pocklington, 2016, Molecular Psychiatry.

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness.

H. Stefánsson, D. Rujescu, S. Cichon, 2011, The American journal of psychiatry.

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.

G. Kirov, D. Grozeva, N. Craddock, 2010, Archives of general psychiatry.

Strong evidence that GNB1L is associated with schizophrenia.

D. Rujescu, I. Giegling, G. Kirov, 2008, Human molecular genetics.

No Association Between the Putative Functional ZDHHC8 Single Nucleotide Polymorphism rs175174 and Schizophrenia in Large European Samples

S. Cichon, M. Rietschel, M. Nöthen, 2005, Biological Psychiatry.

Association between PRODH and schizophrenia is not confirmed

G. Kirov, M. Owen, I. Nikolov, 2003, Molecular Psychiatry.

Creativity and mental disorder.

G. Kirov, Geoffrey Miller, 2012, The British journal of psychiatry : the journal of mental science.

Non-random mating, parent-of-origin, and maternal–fetal incompatibility effects in schizophrenia

G. Kirov, M. Owen, P. Sullivan, 2013, Schizophrenia Research.

Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, Molecular Psychiatry.

Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.

S. Cichon, M. Rietschel, M. Nöthen, 2009, Bipolar disorders.

Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation

G. Kirov, D. Grozeva, N. Craddock, 2006, Molecular Psychiatry.

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.

Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene

Yusuke Nakamura, Naoyuki Kamatani, Michiaki Kubo, 2013, Psychiatric genetics.

No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci

G. Kirov, M. Owen, M. O’Donovan, 2015, PloS one.

The role of rare copy number variants in depression

G. Kirov, M. Owen, M. O’Donovan, 2018, bioRxiv.

An InDel in Phospholipase-C-B-1 Is Linked with Euthyroid Multinodular Goiter.

G. Kirov, M. Hamshere, H. Völzke, 2018, Thyroid : official journal of the American Thyroid Association.

SGCE mutations cause psychiatric disorders: clinical and genetic characterization.

G. Kirov, M. Owen, Danny J. Smith, 2013, Brain : a journal of neurology.

Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls

Eric S. Lander, Margot Albus, Michael J. Owen, 2001, Nature Genetics.

Do obstetric complications cause the earlier age at onset in male than female schizophrenics?

Peter B. Jones, R. Murray, G. Kirov, 1996, Schizophrenia Research.

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

G. Kirov, M. Gill, N. Craddock, 2002, Psychological Medicine.

DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls

G. Kirov, D. Grozeva, N. Craddock, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Randomised controlled trial of compliance therapy

G. Kirov, P. Hayward, A. David, 1998, British Journal of Psychiatry.

Variation at the DAOA / G 30 Locus Influences Susceptibility to Major Mood Episodes but Not Psychosis in Schizophrenia and Bipolar Disorder

G. Kirov, D. Grozeva, N. Craddock, 2006 .

Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

Ivan Nikolov, Michael C O'Donovan, Michael J Owen, 2004, Biological Psychiatry.

Genome‐wide association study on bipolar disorder in the Bulgarian population

G. Kirov, M. Owen, Y. Kamatani, 2011, Genes, brain, and behavior.

Tryptophan hydroxylase gene and manic-depressive illness.

G. Kirov, N. Craddock, M. Owen, 1999, Archives of general psychiatry.

Direct analysis of the genes encoding G proteins GαT2, Gαo, GαZ in ADHD

G. Kirov, M. Owen, A. Thapar, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome‐wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

Stephan Ripke, Andrew McQuillin, Hugh Gurling, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric 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.

Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

Michael Owen, Michael O'Donovan, Nadine Norton, 2000, Human Genetics.

Variation in the protocadherin γ A gene cluster

G. Kirov, M. Owen, I. Nikolov, 2003 .

Family aggregation of high myopia: estimation of the sibling recurrence risk ratio.

G. Kirov, M. Owen, J. Guggenheim, 2004, Investigative ophthalmology & visual science.

Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population.

G. Kirov, M. Owen, Yusuke Nakamura, 2009, Journal of affective disorders.

Linkage analysis of the genetic loci for high myopia on 18p, 12q, and 17q in 51 U.K. families.

G. Kirov, M. Owen, C. Haley, 2004, Investigative ophthalmology & visual science.

Meta-analysis of studies on genetic variation in 5-HT2A receptors and clozapine response

M. J. Arranz, R. W. Kerwin, D. Collier, 1998, Schizophrenia Research.

Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis

G. Kirov, M. Owen, D. Wimpory, 2007, Molecular Psychiatry.

Copy Number Variation in Schizophrenia in the Japanese Population

G. Kirov, M. Owen, M. O’Donovan, 2010, Biological Psychiatry.

Neurexin 1 ( NRXN 1 ) Deletions in Schizophrenia

D. Rujescu, A. Ingason, G. Kirov, 2009 .

Supplementary Material 1) Samples P 2 2) Genotyping and Cnv Calling in the Bulgarian Samples P 5

H. Stefánsson, K. Stefánsson, G. Kirov, 2022 .

De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes

Tomas W. Fitzgerald, R. Murray, G. Kirov, 2019, European Journal of Human Genetics.

The heritability of high myopia: a reanalysis of Goldschmidt's data

G. Kirov, J. Guggenheim, S. Hodson, 2000, Journal of medical genetics.

Allelic functional variation of serotonin transporter expression is a susceptibility factor for late onset Alzheimer's disease

G. Kirov, P. Sham, K. Lesch, 1997, Neuroreport.

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility

G. Kirov, M. Owen, V. Moskvina, 2006, Schizophrenia Research.

Bulgarian psychiatry: development, ideas, achievements

G. Kirov, A. Beveridge, K. Kirov, 1993 .

Authors' reply

G. Kirov, M. Atkins, 2016, British Journal of Psychiatry.

An international collaborative family-based whole-genome linkage scan for high-grade myopia.

G. Kirov, M. Owen, Yi-Ju Li, 2009, Investigative ophthalmology & visual science.

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 .

Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

M. Daly, H. Stefánsson, D. Rujescu, 2016, Molecular Psychiatry.

Relative Suppression of Magical Thinking: A Transcranial Magnetic Stimulation Study

H. Ellis, G. Kirov, P. Halligan, 2007, Cortex.

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

S. Cichon, M. Rietschel, M. Nöthen, 2004, Nature Genetics.

No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene

G. Kirov, N. Craddock, M. Leboyer, 1997, British Journal of Psychiatry.

Age-at-onset in bipolar-I disorder: mixture analysis of 1369 cases identifies three distinct clinical sub-groups.

G. Kirov, N. Craddock, S. Caesar, 2009, Journal of affective disorders.

Magnesium, schizophrenia and manic-depressive disease.

G. Kirov, K. Tsachev, 1990, Neuropsychobiology.

International Consortium on the Genetics of Electroconvulsive Therapy and Severe Depressive Disorders (Gen-ECT-ic)

G. Kirov, N. Craddock, P. Sullivan, 2019, European Archives of Psychiatry and Clinical Neuroscience.

The Effectiveness of Electroconvulsive Therapy in Treatment-Resistant Depression: A Naturalistic Study

G. Kirov, N. Khalid, M. Giles, 2008, The journal of ECT.

COVID-19 and mortality risk in patients with psychiatric disorders

G. Kirov, E. Baker, 2021, medRxiv.

Improving insight and compliance: Predictions and consequences

B. Everitt, G. Kirov, A. David, 1998, Schizophrenia Research.

Effect of lithium on the thyroid and endocrine glands

G. Kirov, J. Lazarus, B. Harris, 2006 .

Variation in the protocadherin gamma A gene cluster.

G. Kirov, M. Owen, I. Nikolov, 2003, Genomics.

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

J. Danesh, M. Daly, M. Hurles, 2016, bioRxiv.

Biological Insights From 108 Schizophrenia-Associated Genetic Loci

C. Spencer, K. Davis, P. Visscher, 2014, Nature.

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

N. Wray, D. Geschwind, H. Stefánsson, 2019, Nature Genetics.

A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

S. Cichon, G. Kirov, M. Owen, 2008 .

A family-based study of common polygenic variation and risk of schizophrenia

G. Kirov, M. Owen, S. Purcell, 2011, Molecular Psychiatry.

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

D. Rujescu, I. Giegling, G. Kirov, 2011, Molecular Psychiatry.

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case–control sample

M C O'Donovan, M J Owen, S Purcell, 2013, Molecular Psychiatry.

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

G. Kirov, M. Gill, N. Craddock, 2006, Molecular Psychiatry.

Whole Genome Association Study in a Homogenous Population in Shandong Peninsula of China Reveals JARID2 as a Susceptibility Gene for Schizophrenia

G. Kirov, M. Owen, N. Williams, 2009, Journal of biomedicine & biotechnology.

Schizophrenia genetic variants are not associated with intelligence

A F Terwisscha van Scheltinga, S C Bakker, N E M van Haren, 2013, Psychological Medicine.

Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia

H. Stefánsson, D. Rujescu, A. Jonasdottir, 2016, Molecular Psychiatry.

Erratum: Arc expression identifies the lateral amygdala fear memory trace

G. Kirov, K. Tansey, S. Mccarroll, 2015, Molecular Psychiatry.

Automated genotyping of single-nucleotide polymorphisms by extension of fluorescently labelled primers: analysis of individual and pooled DNA samples

G. Kirov, M. Owen, N. Williams, 2000 .

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

G. Kirov, M. Gill, N. Craddock, 2005, Molecular Psychiatry.

Plasma magnesium levels in a population of psychiatric patients: correlations with symptoms.

G. Kirov, R. Ramsey, N. J. Birch, 1994, Neuropsychobiology.

Genetic association study of psychotic experiences in UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, bioRxiv.

Prevalence of delusional misidentification syndromes.

G. Kirov, S. Lewis, P. Jones, 1994, Psychopathology.

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

D. Geschwind, J. Suvisaari, E. Bramon, 2017, Nature Genetics.

The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay

G. Kirov, M. Owen, M. O’Donovan, 2014, Biological Psychiatry.

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

S. Gabriel, M. Daly, D. Collier, 2008, Nature Genetics.

The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls.

Melissa J. Green, Janice M. Fullerton, Robert C. Thompson, 2019, Biological psychiatry.

Bmc Medical Genomics a Genome-wide Association Study for Late-onset Alzheimer's Disease Using Dna Pooling

S. Cichon, G. Kirov, M. Owen, 2008 .

Schizophrenia genetic variants are not associated with intelligence

P. Donnelly, P. Visscher, H. Stefánsson, 2013, Psychological Medicine.

1 Sex-biased reduction in reproductive success drives selective constraint on 2 human genes

M. Hurles, G. Kirov, K. Samocha, 2020 .

Clinical indicators of treatment-resistant psychosis

G. Kirov, M. Owen, M. O’Donovan, 2019, The British Journal of Psychiatry.

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

G. Kirov, M. Owen, P. Holmans, 2016, BMC Medical Genetics.

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2018, Journal of Medical Genetics.

Frontiers in TMS technology development: Controllable pulse shape TMS (cTMS) and magnetic seizure therapy (MST) at 100 Hz

Klaus P. Ebmeier, G. Kirov, M. Husain, 2007 .

Transcranial magnetic stimulation for patients with depression.

G. Kirov, E. Dunn, J. Tredget, 2005, Nursing standard (Royal College of Nursing (Great Britain) : 1987).

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

M C O'Donovan, P M Visscher, P. Visscher, 2011, Molecular Psychiatry.

De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes

Tomas W. Fitzgerald, G. Kirov, Tesca Fitzgerald, 2019, European Journal of Human Genetics.

A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

S. Cichon, G. Kirov, M. Owen, 2008, BMC Medical Genomics.

Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank

G. Kirov, M. Owen, M. O’Donovan, 2019, Molecular Psychiatry.

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

G. Kirov, M. Owen, M. O’Donovan, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

M91 POLYGENIC RISK FOR SCHIZOPHRENIA AND SEASON OF BIRTH WITHIN THE UK BIOBANK COHORT

G. Kirov, M. Owen, M. O’Donovan, 2018, European Neuropsychopharmacology.