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Di Florio, Arianna, Yang, Jessica M. K., Crawford, Karen, Bergink, Veerle, Leonenko, Ganna, Pardinas, Antonio, Escott-Price, Valentina, Gordon-Smith, Katherine, Owen, Michael J., Craddock, Nick, Jones, Lisa, O'Donovan, Michael and Jones, Ian 2021. Post-partum psychosis and its association with bipolar disorder in the UK: a case-control study using polygenic risk scores. The Lancet Psychiatry 8 (12) , pp. 1045-1052. 10.1016/S2215-0366(21)00253-4 |
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Alonso-Llamazares, Carmen, Blanco Márquez, Beatriz, Lopez, Belen and Pardinas, Antonio F. 2021. Assessing individual and population variability in degenerative joint disease prevalence using generalized linear mixed models. American Journal of Physical Anthropology 175 (3) , pp. 611-625. 10.1002/ajpa.24195 |
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Hubbard, Leon, Rees, Elliott, Morris, Derek W., Lynham, Amy J., Richards, Alex L., Pardinas, Antonio F., Legge, Sophie E., Harold, Denise, Zammit, Stanley, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Donohoe, Gary, Kirov, George, Pocklington, Andrew and Walters, James T.R. 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 |
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Hall, Lynsey S, Medway, Christopher W, Pain, Oliver, Pardinas, Antonio F, Rees, Elliott G, Escott-Price, Valentina, Pocklington, Andrew, Bray, Nicholas J, Holmans, Peter A, Walters, James T R, Owen, Michael and O'Donovan, Michael 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 |
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Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M., Pardinas, Antonio F., Menzies, Georgina, Bracher-Smith, Matthew, Escott-Price, Valentina, Rees, Elliott, Davis, Katrina A., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter, Kirov, George, Owen, Michael J., O'Donovan, Michael C., Zammit, Stanley and Walters, James T. R.
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Chapman, Ria M, Tinsley, Caroline L, Hill, Matthew J, Forrest, Marc P, Tansey, Katherine E, Pardinas, Antonio F., Rees, Elliott, Doyle, A. Michelle, Wilkinson, Lawrence S., Owen, Michael J., O'Donovan, Michael and Blake, Derek J.
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Convergent evidence that ZNF804A is a regulator of pre-messenger RNA processing and gene expression.
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D'Ambrosio, Enrico, Dahoun, Tarik, Pardinas, Antonio F., Veronese, Mattia, Bloomfield, Michael A.P., Jauhar, Sameer, Bonoldi, Ilaria, Rogdaki, Maria, Froudist-Walsh, Sean, Walters, James T. R. and Howes, Oliver D. 2019. The effect of a genetic variant at the schizophrenia associated AS3MT/BORCS7 locus on striatal dopamine function: A PET imaging study. Psychiatry Research: Neuroimaging 291 , pp. 34-41. 10.1016/j.pscychresns.2019.07.005 |
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Pain, Oliver, Pocklington, Andrew J., Holmans, Peter A., Bray, Nichloas J., O'Brian, Heath E., Hall, Lynsey S., Pardinas, Antonio F., O'Donovan, Michael C., Owen, Michael J. and Anney, Richard
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Novel insight into the etiology of autism spectrum disorder gained by integrating expression data with genome-wide association statistics.
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Escott-Price, Valentina, Pardinas, Antonio F., Santiago, Enrique, Walters, James, Kirov, George, Owen, Michael J. and O'Donovan, Michael C.
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The relationship between common variant schizophrenia liability and number of offspring in the UK Biobank.
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Pardinas, Antonio F., Nalmpanti, Mariana, Pocklington, Andrew J., Legge, Sophie E., Medway, Christopher, King, Adrian, Jansen, John, Helthuis, Marinka, Zammit, Stanley, MacCabe, James, Owen, Michael J., O'Donovan, Michael C. and Walters, James T. R
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Pharmacogenomic variants and drug interactions identified through the genetic analysis of clozapine metabolism.
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Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Agrawal, A., Børglum, A. D., Bulik, C. M., Daly, M. J., Davis, L. K., Demontis, D., Edenberg, H. J., Grove, J., Gelernter, J., Neale, B. M., Pardinas, A. F., Stahl, E., Walters, J. T. R., Walters, R., Sullivan, P. F., Posthuma, D. and Polderman, T. J. C.
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Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls.
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Huckins, Laura M., Dobbyn, Amanda, Ruderfer, Douglas M., Hoffman, Gabriel, Wang, Weiqing, Pardinas, Antonio F., Rajagopal, Veera M., Als, Thomas D., Tan Hoang, Hoang T., Girdhar, Kiran, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R., Purcell, Shaun, Demontis, Ditte, Borglum, Anders, Walters, James T. R., O'Donovan, Michael C., Sullivan, Patrick, Owen, Michael J., Devlin, Bernie, Sieberts, Solveig K., Cox, Nancy J., Kyung Im, Hae, Sklar, Pamela, Ayumi Stahl, Eli A., The Schizophrenia Working Group of the Psychiatric Genomics Cons and iPSYCH-GEMS Schizophrenia Working Group
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Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
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Targeted sequencing of 10,198 samples confirms abnormalities in neuronal activity and implicates voltage-gated sodium channels in schizophrenia pathogenesis.
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Legge, Sophie E., Pardinas, Antonio F., Helthuis, Marinka, Jansen, John A., Jollie, Karel, Knapper, Steven, MacCabe, James H., Rujescu, Dan, Collier, David A., O'Donovan, Michael C., Owen, Michael J. and Walters, James T. R.
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A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia.
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Li, Mingfeng, Santpere, Gabriel, Imamura Kawasawa, Yuka, Evgrafov, Oleg V., Gulden, Forrest O., Pochareddy, Sirisha, Sunkin, Susan M., Li, Zhen, Shin, Yurae, Zhu, Ying, Sousa, André M. M., Werling, Donna M., Kitchen, Robert R., Kang, Hyo Jung, Pletikos, Mihovil, Choi, Jinmyung, Muchnik, Sydney, Xu, Xuming, Wang, Daifeng, Lorente-Galdos, Belen, Liu, Shuang, Giusti-Rodríguez, Paola, Won, Hyejung, de Leeuw, Christiaan A., Pardinas, Antonio F., Hu, Ming, Jin, Fulai, Li, Yun, Owen, Michael J., O'Donovan, Michael C., Walters, James T. R., Posthuma, Danielle, Reimers, Mark A., Levitt, Pat, Weinberger, Daniel R., Hyde, Thomas M., Kleinman, Joel E., Geschwind, Daniel H., Hawrylycz, Michael J., State, Matthew W., Sanders, Stephan J., Sullivan, Patrick F., Gerstein, Mark B., Lein, Ed S., Knowles, James A. and Sestan, Nenad
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O'Brien, Heath E., Hannon, Eilis, Hill, Matthew J., Toste, Carolina C., Robertson, Matthew J., Morgan, Joanne E., McLaughlin, Gemma, Lewis, Cathryn M., Schalkwyk, Leonard C., Hall, Lynsey S., Pardinas, Antonio F., Owen, Michael J., O'Donovan, Michael C., Mill, Jonathan and Bray, Nicholas J.
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Dahoun, Tarik, Pardinas, Antonio F., Veronese, Mattia, Bloomfield, Michael A. P., Jauhar, Sameer, Bonoldi, Ilaria, Froudist-Walsh, Sean, Nosarti, Chiara, Korth, Carsten, Hennah, William, Walters, James, Prata, Diana and Howes, Oliver D.
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Alonso-Llamazares, Carmen, Gomez, Carlos, Garcia-Manrique, Pablo, Pardinas, Antonio F. and Lopez, Belen 2018. Medical diagnostic methods applied to a medieval female with vitamin D deficiency from the North of Spain. International Journal of Paleopathology 22 , pp. 109-120. 10.1016/j.ijpp.2018.07.007 |
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Skene, Nathan G., Bryois, Julien, Bakken, Trygve E., Breen, Gerome, Crowley, James J., Gaspar, Héléna A., Giusti-Rodriguez, Paola, Hodge, Rebecca D., Jeremy A., Miller, Muñoz-Manchado, Ana, O'Donovan, Michael C., Owen, Michael J., Pardinas, Antonio, Ryge, Jesper, Walters, James T. R., Linnarsson, Sten, Lein, Ed S., Sullivan, Patrick F. and Hjerling-Leffler, Jens
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Genetic identification of brain cell types underlying schizophrenia.
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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
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Gomes, Cláudia, Fondevila, Manuel, Palomo-Díez, Sara, Pardinas, Antonio, López-Matayoshi, César, Baeza-Richer, Carlos, López-Parra, Ana María, Lareu, María Victoria, López, Belén and Arroyo-Pardo, Eduardo 2017. Phenotyping the ancient world: the physical appearance and ancestry of very degraded samples from a chalcolithic human remains. Forensic Science International: Genetics Supplement Series 6 , e484-e486. 10.1016/j.fsigss.2017.09.188 |
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