Author details

Full Name

George Kirov

Affiliation

ORCID

Career Start Year

1990

Papers

247

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36914811	Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia.		2023
36379544	Characterising heart rhythm abnormalities associated with Xp22.31 deletion.	Journal of Medical Genetics	2023
37881570	Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive Performance.		2023
36752340	DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts.		2023
35322230	Reduced reproductive success is associated with selective constraint on human genes.	Nature	2022
35396580	Mapping genomic loci implicates genes and synaptic biology in schizophrenia.	Nature	2022
35396579	Rare coding variants in ten genes confer substantial risk for schizophrenia.	Nature	2022
35779327	Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank.	Schizophrenia Research	2022
34099189	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	Biol Psychiatry	2022
35330591	Comorbid Medical Issues in X-Linked Ichthyosis.		2022
35220357	Electroconvulsive Therapy Reverses Cerebral Hypoperfusion in a Patient With Psychotic Depression and Catatonia.	Journal of ECT	2022
34504065	Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations.	Nat Commun	2021
33752146	Copy number variation and neuropsychiatric illness.	Current Opinion in Genetics and Development	2021
33678419	Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia.	Biological Psychiatry	2021
34002096	Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.	Nat Genet	2021
33931204	Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition.	Biol Psychiatry	2021
33077856	Genetic association of FMRP targets with psychiatric disorders.	Molecular Psychiatry	2021
32792019	Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank.	British Journal of Psychiatry	2021
35048876	Characterisation of age and polarity at onset in bipolar disorder.	Br J Psychiatry	2021
35048827	Electroconvulsive therapy for depression: 80 years of progress.	British Journal of Psychiatry	2021
31155017	Clinical indicators of treatment-resistant psychosis.	British Journal of Psychiatry	2020
31802253	International Consortium on the Genetics of Electroconvulsive Therapy and Severe Depressive Disorders (Gen-ECT-ic).	Eur Arch Psychiatry Clin Neurosci	2020
32139392	Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank.	Journal of Medical Genetics	2020
32398668	A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder.	Translational Psychiatry	2020
32051258	Contribution of de novo and inherited rare CNVs to very preterm birth.	Journal of Medical Genetics	2020
31767120	Characterization of Single Gene Copy Number Variants in Schizophrenia.	Biol Psychiatry	2020
32766777	Medical and neurobehavioural phenotypes in male and female carriers of Xp22.31 duplications in the UK Biobank.	Human Molecular Genetics	2020
33168126	Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study.	BJPsych Open	2020
30610204	Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank.	Molecular Psychiatry	2020
30679740	Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank.	Molecular Psychiatry	2020
30886340	De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes.	Eur J Hum Genet	2019
31553412	Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits.	JAMA Psychiatry	2019
30606050	The Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK Biobank.	American Journal of Psychiatry	2019
30343275	Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank.	Journal of Medical Genetics	2019
30420267	Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis.	Biological Psychiatry	2019
29501066	Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort.	Psychological Medicine	2019
30767844	Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.	British Journal of Psychiatry	2019
31160808	Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.	Nat Genet	2019
31256626	The Relationship Between Common Variant Schizophrenia Liability and Number of Offspring in the UK Biobank: Response to Lawn et al.	American Journal of Psychiatry	2019
30994872	Association of Rare Copy Number Variants With Risk of Depression.	JAMA Psychiatry	2019
29687944	Association of copy number variation across the genome with neuropsychiatric traits in the general population.	American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	2018
30509170	Effects of pathogenic CNVs on physical traits in participants of the UK Biobank.	BMC Genomics	2018
29897006	An InDel in Phospholipase-C-B-1 Is Linked with Euthyroid Multinodular Goiter.	Thyroid	2018
29483656	Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.	Nat Genet	2018
29296025	Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.	Mol Psychiatry	2018
27956746	Schizophrenia copy number variants and associative learning.	Molecular Psychiatry	2017
28632202	Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.	Transl Psychiatry	2017
28851079	Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type.	Am J Med Genet B Neuropsychiatr Genet	2017
28650482	The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.	Nat Genet	2017
27400856	Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.	Mol Psychiatry	2017