Craddock, Nick
Cardiff University
57 papers on CoChatORCID 0000-0003-2171-0610
Most cited papers
- Verified
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
eQTLGen, Wray, N. R., 23andMe, the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E. M., Abdellaoui, A., Adams, M. J., et al. (2018) · Nature Genetics
Genetic Associations and EpidemiologyTreatment of Major Depression
Cited by 3,005
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Analysis of shared heritability in common disorders of the brain
The Brainstorm Consortium, Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., Duncan, L., Escott-Price, V., Falcone, G. J., Gormley, P., et al. (2018) · Science
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 1,924
- Verified
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Multicenter Genetic Studies of Schizophrenia Consortium, Ripke, S., Psychosis Endophenotypes International Consortium, Wellcome Trust Case Control Consortium 2, O'Dushlaine, C., Chambert, K., Moran, J. L., Kähler, A. K., Akterin, S., Bergen, S. E., et al. (2013) · Nature Genetics
Schizophrenia research and treatmentGenetic Associations and Epidemiology
Cited by 1,496
- Verified
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Psychiatric GWAS Consortium Bipolar Disorder Working Group, Sklar, P., Ripke, S., Scott, L. J., Andreassen, O. A., Cichon, S., Craddock, N., Edenberg, H. J., Nurnberger, J. I., Rietschel, M., et al. (2011) · Nature Genetics
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 1,344
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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Vilhjálmsson, B. J., Yang, J., Finucane, H. K., Gusev, A., Lindström, S., Ripke, S., Genovese, G., Loh, P.-R., Bhatia, G., Do, R., et al. (2015) · The American Journal of Human Genetics
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 1,303
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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
Wellcome Trust Case Control Consortium, Ferreira, M. A. R., O'Donovan, M. C., Meng, Y. A., Jones, I. R., Ruderfer, D. M., Jones, L., Fan, J., Kirov, G., Perlis, R. H., et al. (2008) · Nature Genetics
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 1,237
- Verified
A mega-analysis of genome-wide association studies for major depressive disorder
Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Ripke, S., Wray, N. R., Lewis, C. M., Hamilton, S. P., Weissman, M. M., Breen, G., Byrne, E. M., Blackwood, D. H. R., Boomsma, D. I., et al. (2013) · Molecular Psychiatry
Genetic Associations and EpidemiologyBipolar Disorder and Treatment
Cited by 1,120
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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Marshall, C. R., Howrigan, D. P., Merico, D., Thiruvahindrapuram, B., Wu, W., Greer, D. S., Antaki, D., Shetty, A., Holmans, P. A., Pinto, D., et al. (2017) · Nature Genetics
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 1,058
- Verified
The UK10K project identifies rare variants in health and disease
The UK10K Consortium, Writing group, Walter, K., Min, J. L., Huang, J., Crooks, L., Memari, Y., McCarthy, S., Perry, J. R. B., Xu, C., et al. (2015) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 1,040
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Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease
Sakuntabhai, A., Ruiz-Perez, V., Carter, S., Jacobsen, N., Burge, S., Monk, S., Smith, M., Munro, C. S., O'Donovan, M., Craddock, N., et al. (1999) · Nature Genetics
Genetic and rare skin diseases.Skin and Cellular Biology Research
Cited by 740
- Verified
Microduplications of 16p11.2 are associated with schizophrenia
Wellcome Trust Case Control Consortium, McCarthy, S. E., Makarov, V., Kirov, G., Addington, A. M., McClellan, J., Yoon, S., Perkins, D. O., Dickel, D. E., Kusenda, M., et al. (2009) · Nature Genetics
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 711
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The Kraepelinian dichotomy – going, going … but still not gone
Craddock, N., & Owen, M. J. (2010) · British Journal of Psychiatry
Schizophrenia research and treatmentMental Health and Psychiatry
Cited by 587
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The genetics of schizophrenia and bipolar disorder: dissecting psychosis
Craddock, N., O’Donovan, M. C., & Owen, M. J. (2005) · Journal of Medical Genetics
Schizophrenia research and treatmentBipolar Disorder and Treatment
Cited by 574
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Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
Gusev, A., Lee, S. H., Trynka, G., Finucane, H., Vilhjálmsson, B. J., Xu, H., Zang, C., Ripke, S., Bulik-Sullivan, B., Stahl, E., et al. (2014) · The American Journal of Human Genetics
Genetic Associations and EpidemiologyGenomics and Chromatin Dynamics
Cited by 544
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The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia
Wellcome Trust Case Control Consortium, Green, E. K., Grozeva, D., Jones, I., Jones, L., Kirov, G., Caesar, S., Gordon-Smith, K., Fraser, C., Forty, L., et al. (2010) · Molecular Psychiatry
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 526
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Genes for Schizophrenia and Bipolar Disorder? Implications for Psychiatric Nosology
Craddock, N. (2005) · Schizophrenia Bulletin
Schizophrenia research and treatmentBipolar Disorder and Treatment
Cited by 496
- Verified
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Study, S. S., Singh, T., Study, I., Study, D., UK10 K Consortium, Kurki, M. I., Curtis, D., Purcell, S. M., Crooks, L., McRae, J., et al. (2016) · Nature Neuroscience
Schizophrenia research and treatmentGenomics and Rare Diseases
Cited by 452
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DSM-5 and RDoC: progress in psychiatry research?
Casey, B. J., Craddock, N., Cuthbert, B. N., Hyman, S. E., Lee, F. S., & Ressler, K. J. (2013) · Nature Reviews Neuroscience
Mental Health and PsychiatryMental Health Research Topics
Cited by 434
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Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
Kirov, G., Grozeva, D., Norton, N., Ivanov, D., Mantripragada, K. K., Holmans, P., International Schizophrenia Consortium, the Wellcome Trust Case Control Consortium, Craddock, N., Owen, M. J., et al. (2009) · Human Molecular Genetics
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 390
- Verified
Gene Ontology Analysis of GWA Study Data Sets Provides Insights into the Biology of Bipolar Disorder
Holmans, P., Green, E. K., Pahwa, J. S., Ferreira, M. A. R., Purcell, S. M., Sklar, P., Owen, M. J., O'Donovan, M. C., & Craddock, N. (2009) · The American Journal of Human Genetics
Bioinformatics and Genomic NetworksGenetic Associations and Epidemiology
Cited by 378
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Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151)
Davies, G., Marioni, R. E., Liewald, D. C., Hill, W. D., Hagenaars, S. P., Harris, S. E., Ritchie, S. J., Luciano, M., Fawns-Ritchie, C., Lyall, D., et al. (2016) · Molecular Psychiatry
Genetic Associations and EpidemiologyCognitive Abilities and Testing
Cited by 373
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Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia
Ruderfer, D. M., Fanous, A. H., Ripke, S., McQuillin, A., Amdur, R. L., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Cross-Disorder Working Group of the Psychiatric Genomics Consortium, Gejman, P. V., O'Donovan, M. C., et al. (2014) · Molecular Psychiatry
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 364
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Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk
Moskvina, V, Craddock, N., Holmans, P., Nikolov, I., Pahwa, J. S., Green, E., Wellcome Trust Case Control Consortium, Owen, M. J., & O'Donovan, M. C. (2009) · Molecular Psychiatry
Genetic Associations and EpidemiologySchizophrenia research and treatment
Cited by 363
- Verified
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
Cichon, S., Mühleisen, T. W., Degenhardt, F. A., Mattheisen, M., Miró, X., Strohmaier, J., Steffens, M., Meesters, C., Herms, S., Weingarten, M., et al. (2011) · The American Journal of Human Genetics
Bipolar Disorder and TreatmentGenetic Associations and Epidemiology
Cited by 286
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