George Kirov

发表

User Dependent Control of Dynamic Routing

D. Lakov, Margarita Raykova Saralieva, George Kirov, 2001 .

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.

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

Fikret Erdogan, Reinhard Ullmann, Wei Chen, 2007, 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.

Genetic Differences between Five European Populations

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

The role of copy number variation in schizophrenia

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

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.

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

Jakob Grove, Esben Agerbo, Robert Plomin, 2018, Nature 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.

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

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

Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

Naomi R. Wray, Robert Plomin, Stephan Ripke, 2016, bioRxiv.

Exome Aggregation Consortium

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

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.

De novo CNVs in bipolar affective disorder and schizophrenia

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

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.

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 .

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 identifies 30 Loci Associated with Bipolar Disorder

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

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 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.

Support for RGS4 as a susceptibility gene for schizophrenia

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

Genome-wide association study identifies five new schizophrenia loci

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

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.

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.

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

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

Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1)

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

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.

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

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

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

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