Kirov, George

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

Mullins, N., Kang, J., Campos, A. I., Coleman, J. R. I., Edwards, A. C., Galfalvy, H., Levey, D. F., Lori, A., Shabalin, A., Starnawska, A., et al. (2022) · Biological Psychiatry

Suicide and Self-Harm StudiesGenetic Associations and Epidemiology

Cited by 238

Neurexin 1 (NRXN1) Deletions in Schizophrenia

Kirov, G., Rujescu, D., Ingason, A., Collier, D. A., O'Donovan, M. C., & Owen, M. J. (2009) · Schizophrenia Bulletin

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 235

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

Kendall, K. M., Rees, E., Escott-Price, V., Einon, M., Thomas, R., Hewitt, J., O’Donovan, M. C., Owen, M. J., Walters, J. T. R., & Kirov, G. (2017) · Biological Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 226

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

Abraham, R., Moskvina, V., Sims, R., Hollingworth, P., Morgan, A., Georgieva, L., Dowzell, K., Cichon, S., Hillmer, A. M., O'Donovan, M. C., et al. (2008) · BMC Medical Genomics

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 195

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

Pocklington, A. J., Rees, E., Walters, J. T. R., Han, J., Kavanagh, D. H., Chambert, K. D., Holmans, P., Moran, J. L., McCarroll, S. A., Kirov, G., et al. (2015) · Neuron

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 193

Evidence that duplications of 22q11.2 protect against schizophrenia

Wellcome Trust Case Control Consortium, Rees, E., Kirov, G., Sanders, A., Walters, J. T. R., Chambert, K. D., Shi, J., Szatkiewicz, J., O'Dushlaine, C., Richards, A. L., et al. (2014) · Molecular Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 183

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

Crawford, K., Bracher-Smith, M., Owen, D., Kendall, K. M., Rees, E., Pardiñas, A. F., Einon, M., Escott-Price, V., Walters, J. T. R., O’Donovan, M. C., et al. (2019) · Journal of Medical Genetics

Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Cited by 175

Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia

Rees, E., Kendall, K., Pardiñas, A. F., Legge, S. E., Pocklington, A., Escott-Price, V., MacCabe, J. H., Collier, D. A., Holmans, P., O’Donovan, M. C., et al. (2016) · JAMA Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 162

CNVs in neuropsychiatric disorders

Kirov, G. (2015) · Human Molecular Genetics

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 159

Association of Rare Copy Number Variants With Risk of Depression

Kendall, K. M., Rees, E., Bracher-Smith, M., Legge, S., Riglin, L., Zammit, S., O’Donovan, M. C., Owen, M. J., Jones, I., Kirov, G., et al. (2019) · JAMA Psychiatry

Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Cited by 144

Common alleles contribute to schizophrenia in CNV carriers

Tansey, K. E., Rees, E., Linden, D. E., Ripke, S., Chambert, K. D., Moran, J. L., McCarroll, S. A., Holmans, P., Kirov, G., Walters, J., et al. (2016) · Molecular Psychiatry

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 132

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

GROUP Investigators, Rees, E., Han, J., Morgan, J., Carrera, N., Escott-Price, V., Pocklington, A. J., Duffield, M., Hall, L. S., Legge, S. E., et al. (2020) · Nature Neuroscience

Schizophrenia research and treatmentGenetic Associations and Epidemiology

Cited by 129

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

Richards, A. L., Jones, L., Moskvina, V, Kirov, G., Gejman, P. V., Levinson, D. F., Sanders, A. R., Molecular Genetics of Schizophrenia Collaboration (MGS), International Schizophrenia Consortium (ISC), Purcell, S., et al. (2012) · Molecular Psychiatry

Genetic Associations and EpidemiologySchizophrenia research and treatment

Cited by 123

SGCE mutations cause psychiatric disorders: clinical and genetic characterization

Peall, K. J., Smith, D. J., Kurian, M. A., Wardle, M., Waite, A. J., Hedderly, T., Lin, J.-P., Smith, M., Whone, A., Pall, H., et al. (2013) · Brain

Deep Brain Stimulation and Movement DisordersGenetic Neurodegenerative Diseases

Cited by 116

Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness

Ingason, A., Kirov, G., Giegling, I., Hansen, T., Isles, A. R., Jakobsen, K. D., Kristinsson, K. T., le Roux, L., Gustafsson, O., Craddock, N., et al. (2011) · American Journal of Psychiatry

Genomic variations and chromosomal abnormalitiesGenetic Syndromes and Imprinting

Cited by 114

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

Kirov, G., Ebmeier, K. P., Scott, A. I. F., Atkins, M., Khalid, N., Carrick, L., Stanfield, A., O'Carroll, R. E., Husain, M. M., & Lisanby, S. H. (2008) · British Journal of Psychiatry

Electroconvulsive Therapy StudiesTranscranial Magnetic Stimulation Studies

Cited by 108

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

Rees, E., Moskvina, V., Owen, M. J., O'Donovan, M. C., & Kirov, G. (2011) · Biological Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 94

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

Kirov, G., Tredget, J., John, R., Owen, M. J., & Lazarus, J. H. (2005) · Journal of Affective Disorders

Bipolar Disorder and TreatmentThyroid Disorders and Treatments

Cited by 90

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

Carroll, L. S., Woolf, R., Ibrahim, Y., Williams, H. J., Dwyer, S., Walters, J., Kirov, G., O’Donovan, M. C., & Owen, M. J. (2016) · Psychiatric Genetics

Schizophrenia research and treatmentIon channel regulation and function

Cited by 54

The role of copy number variation in schizophrenia

Kirov, G. (2010) · Expert Review of Neurotherapeutics

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 52

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

Morris, D. W., Pearson, R. D., Cormican, P., Kenny, E. M., O'Dushlaine, C. T., Perreault, L.-P. L., Giannoulatou, E., Tropea, D., Maher, B. S., Wormley, B., et al. (2014) · Human Molecular Genetics

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 42

Genetic Differences between Five European Populations

Moskvina, V., Smith, M., Ivanov, D., Blackwood, D., StClair, D., Hultman, C., Toncheva, D., Gill, M., Corvin, A., O’Dushlaine, C., et al. (2010) · Human Heredity

Forensic and Genetic ResearchGenetic Associations and Epidemiology

Cited by 38

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

Ruderfer, D. M., Kirov, G., Chambert, K., Moran, J. L., Owen, M. J., O'Donovan, M. C., Sklar, P., & Purcell, S. M. (2011) · Molecular Psychiatry

Genetic Associations and EpidemiologySchizophrenia research and treatment

Cited by 28