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Number of items: 11.

Tan, Manuela M.X., Malek, Naveed, Lawton, Michael A., Hubbard, Leon, Pittman, Alan M., Joseph, Theresita, Hehir, Jason, Swallow, Diane M.A., Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Hardy, John, Wood, Nicholas, Ben-Shlomo, Yoav, Grosset, Donald G., Williams, Nigel M. and Morris, Huw R. 2019. Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study. Brain 142 (9) , pp. 2828-2844. 10.1093/brain/awz191
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Jones, Hannah J., Hubbard, Leon, Mitchell, Ruth E., Jones, Simon A., Williams, Nigel M., Zammit, Stanley and Hall, Jeremy 2019. Association of genetic risk for rheumatoid arthritis with cognitive and psychiatric phenotypes across childhood and adolescence. JAMA Network Open 2 (6) , e196118. 10.1001/jamanetworkopen.2019.6118
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Silverdale, Monty A., Kobylecki, Christopher, Kass-Iliyya, Lewis, Martinez-Martin, Pablo, Lawton, Michael, Cotterill, Sarah, Chaudhuri, K. Ray, Morris, Huw, Baig, Fahd, Williams, Nigel, Hubbard, Leon, Hu, Michele T. and Grosset, Donald G. 2018. A detailed clinical study of pain in 1957 participants with early/moderate Parkinson's disease. Parkinsonism & Related Disorders 56 , pp. 27-32. 10.1016/j.parkreldis.2018.06.001
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Lynham, Amy, Hubbard, Leon, Tansey, Katherine, Hamshere, Marian L., Legge, Sophie, Owen, Michael, Jones, Ian and Walters, James 2018. Examining cognition across the bipolar / schizophrenia diagnostic spectrum. Journal of Psychiatry and Neuroscience 43 (3) , 170076. 10.1503/jpn.170076
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Pardinas, Antonio, Holmans, Peter, Pocklington, Andrew, Escott-Price, Valentina, Ripke, S, Carrera, Noa, Legge, Sophie, Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, J, McCarroll, S, Baune, B, Breen, G, Byrne, E, Dannlowski, U, Eley, T, Hayward, C, Martin, N, McIntosh, M, Plomin, R, Porteous, D, Wray, N, Caballero, A, Geschwind, D, Huckins, L, Ruderfer, D, Santiago, E, Sklar, P, Stahl, E, Won, H, Agerbo, E, Als, T, Andreassen, O, Bækvad-Hansen, M, Mortensen, P, Pedersen, CB, Børglum, A, Bybjerg-Grauholm, J, Djurovic, S, Durmishi, N, Giørtz Pedersenu, M, Golimbet, V, Grove, J, Hougaard, M, Mattheisen, M, Molden, E, Mors, O, Nordentoft, M, Pejovic-Milovancevic, M, Sigurdsson, E, Silagadze, T, Søholm Hansen, C, Stefansson, K, Stefansson, H, Steinberg, S, Tosato, S, Werge, T, Consortium, GERAD, Collier, D, Rujescu, D, Kirov, George, Owen, Michael J and Walters, James 2018. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics 50 , pp. 381-389. 10.1038/s41588-018-0059-2
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Pardinas, Antonio, Holmans, Peter, Pocklington, Andrew, Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Stephen A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Consortium, , Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael, O'Donovan, Michael and Walters, James 2016. Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection. bioRxiv , -. 10.1101/068593
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Martin, Joanna, Tilling, Kate, Hubbard, Leon, Stergiakouli, Evie, Thapar, Anita, Davey Smith, George, O'Donovan, Michael Conlon and Zammit, Stanley 2016. Association of genetic risk for schizophrenia with nonparticipation over time in a population-based cohort study. American Journal of Epidemiology 183 (12) , pp. 1149-1158. 10.1093/aje/kww009
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Jones, Hannah J., Stergiakouli, Evie, Tansey, Katherine E., Hubbard, Leon, Heron, Jon, Cannon, Mary, Holmans, Peter Alan, Lewis, Glyn, Linden, David Edmund Johannes, Jones, Peter B., Davey Smith, George, O'Donovan, Michael Conlon, Owen, Michael John, Walters, James Tynan Rhys and Zammit, Stanley 2016. Phenotypic manifestation of genetic risk for schizophrenia during adolescence in the general population. JAMA Psychiatry 73 (3) , pp. 221-228. 10.1001/jamapsychiatry.2015.3058

Hubbard, Leon, Tansey, Katherine E., Rai, Dheeraj, Jones, Peter, Ripke, Stephan, Chambert, Kimberly D., Moran, Jennifer L., McCarroll, Steven A., Linden, David Edmund Johannes, Owen, Michael John, O'Donovan, Michael Conlon, Walters, James Tynan Rhys and Zammit, Stanley 2016. Evidence of common genetic overlap between schizophrenia and cognition. Schizophrenia Bulletin 42 (3) , pp. 832-842. 10.1093/schbul/sbv168
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Akpudo, Hilary, Aleksic, Branko, Alkelai, Anna, Burton, Christie, Carillo Roa, Tania, Chen, David T.W., Cheng, Min-Chih, Cocchi, Enrico, Davis, Lea K., Giori, Isabele G., Hubbard, Leon, Merikangas, Alison, Moily, Nagaraj S., Okewole, Adeniran, Olfson, Emily, Pappa, Irene, Reitt, Markus, Singh, Ajeet B., Steinberg, Julia, Strohmaier, Jana, Ting, Te-Tien, van Hulzen, Kimm J.E., O?Shea, Anne and DeLisi, Lynn E. 2014. Summaries of oral sessions at the XXI World Congress of Psychiatric Genetics, Boston, Massachusetts, 17-21 October 2013. Psychiatric Genetics 24 (4) , pp. 125-150. 10.1097/YPG.0000000000000043

Hubbard, Leon 2014. Common and rare genetic risk factors for schizophrenia and their associations with cognition. PhD Thesis, Cardiff University.
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This list was generated on Fri Dec 6 04:31:44 2019 GMT.