Browse by All Cardiff Authors

Tume, Claire E., Chick, Sophie L., Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Cameron, Darren and Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X 2024. Genetic implication of specific glutamatergic neurons of the prefrontal cortex in the pathophysiology of schizophrenia. Biological Psychiatry 4 (5) , 100345. 10.1016/j.bpsgos.2024.100345

Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Woolway, Grace, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Cardno, Alastair G., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael J. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2024. Genetic and phenotypic features of Schizophrenia in the UK Biobank. JAMA Psychiatry 81 , pp. 681-690. 10.1001/jamapsychiatry.2024.0200

Kappel, Djenifer, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Fenner, Eilidh, King, Adrian, Jansen, John, Helthius, Marinka, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590 2024. Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia. European Neuropsychopharmacology 80 , pp. 47-54. 10.1016/j.euroneuro.2023.12.007

Wellard, Natalie L., Clifton, Nicholas E. ORCID: https://orcid.org/0000-0003-2597-5253, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Thomas, Kerrie L. ORCID: https://orcid.org/0000-0003-3355-9583 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2024. The association of hippocampal long-term potentiation-induced gene expression with genetic risk for psychosis. International Journal of Molecular Sciences 25 (2) , 946. 10.3390/ijms25020946

Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Legge, Sophie, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2023. Genomic findings in schizophrenia and their implications. Molecular Psychiatry 28 , pp. 3638-3647. 10.1038/s41380-023-02293-8

Rammos, Alexandros, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Hubbard, Leon, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 2023. Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia. Molecular Psychiatry 28 , pp. 2081-2087. 10.1038/s41380-023-02013-2

Wadon, Megan, Fenner, Eilidh, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Bailey, Grace, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944 2022. Clinical and genotypic analysis in determining dystonia non-motor phenotypic heterogeneity: a UK Biobank study. Journal of Neurology 269 , pp. 6436-6451. 10.1007/s00415-022-11307-4

Clifton, Nicholas ORCID: https://orcid.org/0000-0003-2597-5253, Bosworth, Matthew ORCID: https://orcid.org/0000-0003-1391-7515, Haan, Niels, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Wilkinson, Lawrence ORCID: https://orcid.org/0000-0002-9337-6124, Isles, Anthony ORCID: https://orcid.org/0000-0002-7587-5712, Collins, Mark and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2022. Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function. Human Molecular Genetics 31 (18) , pp. 3095-3106. 10.1093/hmg/ddac105

Bracher-Smith, Matthew, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2022. Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK Biobank. Schizophrenia Research 246 , pp. 156-164. 10.1016/j.schres.2022.06.006

Creeth, Hugo D. J., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Legge, Sophie E., Dennison, Charlotte A. ORCID: https://orcid.org/0000-0002-7493-2041, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2022. Ultrarare coding variants and cognitive function in schizophrenia. JAMA Psychiatry 79 (10) , pp. 963-970. 10.1001/jamapsychiatry.2022.2289

McAllister, Branduff, Donaldson, Jasmine ORCID: https://orcid.org/0000-0001-6699-0674, Binda, Caroline, Powell, Sophie, Chughtai, Uroosa, Edwards, Gareth, Stone, Joseph, Lobanov, Sergey ORCID: https://orcid.org/0000-0002-3126-1903, Elliston, Linda, Schuhmacher, Laura, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Ciosi, Marc, Maxwell, Alastair, Chao, Michael, Eun Pyo, Hong, Lucente, Diane, Wheeler, Vanessa, Jong-Min, Lee, MacDonald, Marcy, Long, Jeffrey, Aylward, Elizabeth, Landwehrmeyer, G. Bernhard, Rosser, Anne ORCID: https://orcid.org/0000-0002-4716-4753, REGISTRY Investigators of the European Huntington’s disease netw, Paulsen, Jane, PREDICT-HD Investigators of the Huntington Study Group, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Gusella, James, Monckton, Darren, Allen, Nicholas, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 and Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 2022. Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset. Nature Neuroscience 25 , pp. 446-457. 10.1038/s41593-022-01033-5

Singh, Tarjinder, Schizophrenia Exome Meta-Analysis (SCHEMA) Consortium, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2022. Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 604 , pp. 509-516. 10.1038/s41586-022-04556-w

Sanders, Bret, D'Andrea, Daniel, Collins, Mark O., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Steward, Tom G. J., Zhu, Ying, Chapman, Gareth, Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Harwood, Adrian J. ORCID: https://orcid.org/0000-0003-3124-5169, Gray, William P. ORCID: https://orcid.org/0000-0001-7595-8887, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Errington, Adam C. ORCID: https://orcid.org/0000-0002-2171-389X, Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Whitcomb, Daniel J., Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452 and Shin, Eunju ORCID: https://orcid.org/0000-0002-8865-6834 2022. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature Communications 13 (1) , 27. 10.1038/s41467-021-27601-0

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Creeth, Hugo, Hwo, Hai-Gwo, Chen, Wei J., Tsuang, Ming, Glatt, Stephen J., Rey, Romain, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2021. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations. Nature Communications 12 , 5353. 10.1038/s41467-021-25532-4

Legge, Sophie, Cardno, Alastair, Allardyce, Judith ORCID: https://orcid.org/0000-0003-4094-552X, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Hubbard, Leon, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Associations between schizophrenia polygenic liability, symptom dimensions, and cognitive ability in schizophrenia. JAMA Psychiatry 78 (10) , pp. 1143-1151. 10.1001/jamapsychiatry.2021.1961

Clifton, Nicholas E. ORCID: https://orcid.org/0000-0003-2597-5253, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Pardinas, Antonio. F. ORCID: https://orcid.org/0000-0001-6845-7590, Harwood, Janet, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O’Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452 2021. Genetic association of FMRP targets with psychiatric disorders. Molecular Psychiatry 26 , pp. 2977-2990. 10.1038/s41380-020-00912-2

Hubbard, Leon, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Morris, Derek W., Lynham, Amy J. ORCID: https://orcid.org/0000-0002-3189-6888, Richards, Alex L., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Legge, Sophie E., Harold, Denise, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Donohoe, Gary, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452 and Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 90 (1) , pp. 28-34. 10.1016/j.biopsych.2020.11.025

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2021. Copy number variation and neuropsychiatric illness. Current Opinion in Genetics and Development 68 , pp. 57-63. 10.1016/j.gde.2021.02.014

Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Legge, Sophie E., Bracher-Smith, Matthew, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Murphy, Kevin ORCID: https://orcid.org/0000-0002-6516-313X 2021. 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 218 (2) , pp. 104-111. 10.1192/bjp.2020.139

Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, John, Ann, Lee, Sze Chim, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Del Pozo Banos, Marcos, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O’Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lloyd, Keith, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Legge, Sophie E. and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2020. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: a data linkage study. BJPsych Open 6 (6) , e139. 10.1192/bjo.2020.42

Legge, Sophie, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Hopkins, Lucinda, Bates, Lesley, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2020. Clinical indicators of treatment-resistant psychosis. British Journal of Psychiatry 216 (5) , pp. 259-266. 10.1192/bjp.2019.120

Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Hosking, Grace, Wadon, Megan, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2020. A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder. Translational Psychiatry 10 , 135. 10.1038/s41398-020-0821-y

Warland, Anthony, Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891 2020. Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank. Molecular Psychiatry 25 (4) , pp. 854-862. 10.1038/s41380-019-0355-y

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. Translating insights from neuropsychiatric genetics and genomics for precision psychiatry. Genome Medicine 12 (1) , 43. 10.1186/s13073-020-00734-5

Szatkiewicz, Jin P., Fromer, Menachem, Nonneman, Randal J., Ancalade, NaEshia, Johnson, Jessica S., Stahl, Eli A., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Bergen, Sarah, Hultman, Christina, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Sklar, Pamela, Sullivan, Patrick F., Purcell, Shaun M., Crowley, James J. and Ruderfer, Douglas M. 2020. Characterization of single gene copy number variants in schizophrenia. Biological Psychiatry 87 (8) , pp. 736-744. 10.1016/j.biopsych.2019.09.023

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, GROUP Investigators, Han, Jun, Morgan, Joanne, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Golimbat, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Nature Neuroscience 23 (2) , pp. 179-184. 10.1038/s41593-019-0565-2

Hall, Lynsey S, Medway, Christopher W ORCID: https://orcid.org/0000-0002-1764-0587, Pain, Oliver, Pardinas, Antonio F ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott G ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Bray, Nicholas J ORCID: https://orcid.org/0000-0002-4357-574X, Holmans, Peter A ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T R ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2020. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia. Human Molecular Genetics 29 (1) , pp. 159-167. 10.1093/hmg/ddz253

Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Bracher-Smith, Matthew, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Davis, Katrina A., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2019. Association of genetic liability to psychotic experiences with neuropsychotic disorders and traits. JAMA Psychiatry 76 (12) , pp. 1256-1265. 10.1001/jamapsychiatry.2019.2508

Chapman, Ria M, Tinsley, Caroline L, Hill, Matthew J ORCID: https://orcid.org/0000-0001-6776-8709, Forrest, Marc P, Tansey, Katherine E, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Doyle, A. Michelle, Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731 2019. Convergent evidence that ZNF804A is a regulator of pre-messenger RNA processing and gene expression. Schizophrenia Bulletin 45 (6) , pp. 1267-1278. 10.1093/schbul/sby183

Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Bracher-Smith, Matthew, Fitzpatrick, Harry, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2019. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank. British Journal of Psychiatry 214 (05) , pp. 297-304. 10.1192/bjp.2018.301

Kendall, Kimberley M ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Bracher-Smith, Matthew, Legge, Sophie, Riglin, Lucy, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053 2019. Association of rare copy number variants with risk of depression. JAMA Psychiatry 76 (8) , pp. 818-825. 10.1001/jamapsychiatry.2019.0566

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Richards, Alexander, Leonenko, Ganna M ORCID: https://orcid.org/0000-0001-8025-661X, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Kavanagh, D, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Evans, Anna ORCID: https://orcid.org/0000-0002-2430-811X, Chambert, K. D., Moran, J. L., Goldstein, J., Neale, B. M., McCarroll, S. A., Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2016. Exome arrays capture polygenic rare variant contributions to schizophrenia. Human Molecular Genetics 25 (5) , pp. 1001-1007. 10.1093/hmg/ddv620

Tansey, Katherine E., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Linden, David Edmun Johannes ORCID: https://orcid.org/0000-0002-5638-9292, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2015. Common alleles contribute to schizophrenia in CNV carriers [Erratum]. Molecular Psychiatry 21 , 1153. 10.1038/mp.2015.170

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Isles, Anthony Roger ORCID: https://orcid.org/0000-0002-7587-5712, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2015. No evidence for enrichment in schizophrenia for common allelic associations at imprinted loci. PLoS ONE 10 (12) , -. 10.1371/journal.pone.0144172

Heyes, Samuel, Pratt, Wendy S., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Dahimene, Shehrazade, Ferron, Laurent, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Dolphin, Annette C. 2015. Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders. Progress in Neurobiology 134 , pp. 36-54. 10.1016/j.pneurobio.2015.09.002

Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Han, Jun, Kavanagh, David H., Chambert, Kimberly D., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Moran, Jennifer L., McCarroll, Steven A., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2015. Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia. Neuron 86 (5) , pp. 1203-1214. 10.1016/j.neuron.2015.04.022

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053 2015. What a psychiatrist needs to know about copy number variants. BJPscyh Advances 21 (3) , pp. 157-163. 10.1192/apt.bp.113.012039

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2015. Genetics of schizophrenia. Current Opinion in Behavioral Sciences 2 , pp. 8-14. 10.1016/j.cobeha.2014.07.001

Green, E. K., Rees, E. ORCID: https://orcid.org/0000-0002-6168-9222, Walters, J. T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Smith, K-G, Forty, L., Grozeva, D. ORCID: https://orcid.org/0000-0003-3239-8415, Moran, J. L., Sklar, P., Ripke, S., Chambert, K. D., Genovese, G., McCarroll, S. A., Jones, I. ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L. ORCID: https://orcid.org/0000-0001-5821-5889, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, N. ORCID: https://orcid.org/0000-0003-2171-0610 and Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950 2015. Copy number variation in bipolar disorder. Molecular Psychiatry 21 (1) , pp. 89-93. 10.1038/mp.2014.174

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Richards, Alexander, Howrigan, D., Kavanagh, D. H., Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Fromer, M., Ruderfer, D..M., Georgieva, Lyudmila, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Gormley, P., Palta, P., Williams, H., Dwyer, S., Johnson, J. S., Roussos, P., Barker, D. D., Banks, E., Milanova, V., Rose, S .A., Chambert, K., Mahajan, M, Scolnick, E. M., Moran, J. L., Tsuang, M. T., Glatt, S. J., Chen, W. J., Hwu, H.-G., Faraone, Stephen V., Roe, Cheri A., Chandler, Sharon D., Liu, Chih-Min, Liu, Chen-Chung, Yeh, Ling-Ling, Ouyang, Wen-Chen, Chan, Hung-Yu, Chen, Chun-Ying, Neale, B. M., Palotie, A., Sklar, P., Purcell, S. M., McCarroll, S .A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2015. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational Psychiatry 5 (7) , e607. 10.1038/tp.2015.99

Georgieva, Lyudmila, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Moran, Jennifer L., Chambert, Kimberly D., Milanova, Vihra, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Purcell, Shaun, Sklar, Pamela, McCarroll, Steven, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2014. De novo CNVs in bipolar affective disorder and schizophrenia. Human Molecular Genetics 23 (24) , pp. 6677-6683. 10.1093/hmg/ddu379

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Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Georgieva, Lyudmila, Isles, Anthony R. ORCID: https://orcid.org/0000-0002-7587-5712, Chambert, Kimberley D., Richards, Alexander L., Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Stephen A., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2014. Analysis of copy number variations at 15 schizophrenia-associated loci. British Journal of Psychiatry 204 (2) , pp. 108-114. 10.1192/bjp.bp.113.131052

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Chapman, J., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Harold, Denise, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Gerrish, Amy, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Hollingworth, P, Stretton, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2013. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics 22 (4) , pp. 816-824. 10.1093/hmg/dds476

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