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Number of items: 14.

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. 2020. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 10.1016/j.biopsych.2020.11.025
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Tan, Manuela M.X., Lawton, Michael A., Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Pollard, Miriam I., Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams-Gray, Caroline H., Hardy, John, Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M., Ben-Shlomo, Yoav, Hu, Michele T.M., Grosset, Donald G., Shoai, Maryam and Morris, Huw R. 2020. Genome-wide association studies of cognitive and motor progression in Parkinson's disease. Movement Disorders 10.1002/mds.28342

Williams, Nigel M., Hubbard, Leon, Sandor, Cynthia, Webber, Caleb, Hendry, Hannah, Lawton, Michael, Carroll, Camille, Chaudhuri, K. Ray, Morris, Huw, Hu, Michele T., Grosset, Donald G., Kobylecki, Christopher and Silverdale, Monty 2020. Genome‐wide association study of pain in Parkinson's disease implicates TRPM8 as a risk factor. Movement Disorders 35 (4) , pp. 705-707. 10.1002/mds.28001

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

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) , -. 10.1001/jamanetworkopen.2019.6118

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

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

Pardinas, Antonio F., Holmans, Peter, Pocklington, Andrew J., 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, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda, Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nichols G., McIntosh, Andrew M., Plomin, Robert P., Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Eeben A., Als, Thomas P., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bocker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Giørtz Pedersenu, Marianne, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Søholm Hansen, Christine, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Consortium, GERAD, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J, O'Donovan, Michael C., Walters, James T. R. and Williams, Julie 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

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

Martin, Joanna, Tilling, Kate, Hubbard, Leon, Stergiakouli, Evie, Thapar, Anita, Davey Smith, George, O'Donovan, Michael C. 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

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

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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