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Number of items: 11.

Escott-Price, Valentina, Sims, Rebecca, Bannister, Christian, Harold, Denise, Vronskaya, Maria, Majounie, Elisa, Badarinarayan, Nandini, Morgan, Kevin, Passmore, Peter, Holmes, Clive, Powell, John, Brayne, Carol, Gill, Michael, Mead, Simon, Goate, Alison, Cruchaga, Carlos, Lambert, Jean-Charles, van Duijn, Cornelia, Maier, Wolfgang, Ramirez, Alfredo, Holmans, Peter Alan, Jones, Lesley, Hardy, John, Seshadri, Sudha, Schellenberg, Gerard D., Amouyel, Philippe and Williams, Julie 2015. Common polygenic variation enhances risk prediction for Alzheimer's disease. Brain 138 (12) , pp. 3673-3684. 10.1093/brain/awv268

Lee, J. M., Wheeler, V. C., Chao, M. J., Vonsattel, P., Pinto, R. M., Lucente, D., Abu-Elmeel, K., Ramos, E. M., Mysore, J. S., Gillis, T., MacDonald, M. E., Gusella, J. F., Harold, Denise, Stone, Timothy C., Escott-Price, Valentina, Han, Jun, Vedernikov, Alexey, Holmans, Peter Alan, Jones, Lesley, Kwak, S., Mahmoudi, M., Orth, M., Landwehmeyer, G. B., Paulsen, J. S., Dorsey, R., Shoulson, I. and Myers, R. H. 2015. Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease. Cell 162 (3) , pp. 516-26. 10.1016/j.cell.2015.07.003

Jones, Lesley, Lambert, J-C., Wang, L-S., Choi, S-H., Harold, Denise, Vedernikov, Alexey, Escott-Price, Valentina, Stone, Timothy C., Richards, Alexander, Bellenguez, C., Ibrahim-Verbaas, C. A., Naj, A. C., Sims, Rebecca, Gerrish, Amy, Jun, G., DeStefano, A. L., Bis, J. C., Beecham, G. W., Grenier-Boley, B., Russo, G., Thornton-Wells, T. A., Denning, Nicola, Smith, A. V., Chouraki, V., Thomas, Charlene, Ikram, M. A., Zelenika, D., Vardarajan, B. N., Kamatani, Y., Lin, C-F., Schmidt, H., Kunkle, B. W., Dunstan, Melanie, Ruiz, A., Bihoreau, M-T., Reitz, C., Pasquier, F., Hollingworth, P., Hanon, O., Fitzpatrick, A. L., Buxbaum, J. D., Campion, D., Crane, P. K., Becker, T., Gudnason, V., Cruchaga, C., Craig, D., Amin, N., Berr, C., Lopez, O. L., De Jager, P. L., Deramecourt, V., Johnston, J. A., Evans, D., Lovestone, S., Letteneur, L., Kornhuber, J., Tarraga, L., Rubinsztein, D. C., Eiriksdottir, G., Sleegers, K., Goate, A. M., Fievet, N., Heuntelman, M. J., Gill, M., Emilsson, V., Brown, K., Kamboh, M. I., Keller, L., Barberger-Gateau, P., McGuinness, B., Larson, E. B., Myers, A. J., Dufoil, C., Todd, S., Wallon, D., Love, S., Kehoe, P., Rogaeva, E., Gallacher, J., St George-Hyslop, P., Clarimon, J., Lleo, A., Bayer, Antony, Tsuang, D. W., Yu, L., Tsolaki, M., Bossu, P., Spalletta, G., Proitsi, P., Collinge, J., Sorbi, S., Sanchez Garcia, F., Fox, N., Hardy, J., Deniz Naranjo, M. C., Razquin, C., Bosco, P., Clarke, R., Brayne, C., Galimberti, D., Mancuso, M., Moebus, S., Mecocci, P., del Zompo, M., Maier, W., Hampel, H., Pilotto, A., Bullido, M., Panza, F., Caffarra, P., Nacmias, B., Gilbert, J. R., Mayhaus, M., Jessen, F., Dichgans, M., Lannfelt, L., Hakonarson, H., Pichier, S., Carrasquillo, M. M., Ingelsson, M., Beekly, D., Alavarez, V., Zou, F., Valadares, O., Younkin, S. G., Coto, E., Hamilton-Nelson, K. L., Mateo, I., Owen, Michael John, Faber, K. M., Jonsson, P. V., Combarros, O., O'Donovan, Michael Conlon, Cantwell, L. B., Soininen, H., Blacker, D., Mead, S., Mosley Jr., T. H., Bennett, D. A., Harris, T. B., Fratiglioni, L., Holmes, C., de Bruijn, R. F. A. G., Passmore, P., Montine, T. J., Bettens, K., Rotter, J. I., Brice, A., Morgan, K., Faroud, T. M., Kukull, W. A., Hannequin, D., Powell, J. F., Nalls, M. A., Ritchie, K., Lunetta, K. L., Kauwe, J. S. K., Boenwinkle, E., Riemenschneider, M., Boada, M., Hiltunen, M., Martin, E. R., Pastor, P., Schmidt, R., Rujescu, D., Dartigues, J-F., Mayeaux, R., Tzourio, C., Hofman, A., Nothen, M. M., Graff, C., Psaty, B. W., Haines, J. L., Lathrop, M., Pericak-Vance, M. A., Launer, L. J., Farren, L. A., van Duijn, C. M., Van Broeckhoven, C., Ramirez, A., Schellenberg, G. D., Seshadri, S., Amouye, P., Williams, Julie and Holmans, Peter Alan 2015. Convergent genetic and expression data implicate immunity in Alzheimer's disease. Alzheimer's and Dementia 11 (6) , pp. 658-671. 10.1016/j.jalz.2014.05.1757

Desikan, R S, Schork, A J, Wang, Y, Witoelar, A, Sharma, M, McEvoy, L K, Holland, D, Brewer, J B, Chen, C-H, Thompson, W K, Harold, Denise, Williams, Julie, Owen, Michael John, O'Donovan, Michael Conlon, Pericak-Vance, M A, Mayeux, R, Haines, J L, Farrer, L A, Schellenberg, G D, Heutink, P, Singleton, A B, Brice, A, Wood, N W, Hardy, J, Martinez, M, Choi, S H, DeStefano, A, Ikram, M A, Bis, J C, Smith, A, Fitzpatrick, A L, Launer, L, van Duijn, C, Seshadri, S, Ulstein, I D, Aarsland, D, Fladby, T, Djurovic, S, Hyman, B T, Snaedal, J, Stefansson, H, Stefansson, K, Gasser, T, Andreassen, O A and Dale, A M 2015. Genetic overlap between Alzheimer's Disease and Parkinson's Disease at the MAPT locus. Molecular Psychiatry 20 (12) , pp. 1588-1595. 10.1038/mp.2015.6

Correia, Kevin, Harold, Denise, Kim, Kyung-Hee, Holmans, Peter Alan, Jones, Lesley, Orth, Michael, Myers, Richard H., Kwak, Seung, Wheeler, Vanessa C., MacDonald, Marcy E., Gusella, James F. and Lee, Jong-Min 2015. The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease. Journal of Huntington's Disease 4 (3) , pp. 279-284. 10.3233/JHD-150169

Mok, Kin Y., Jones, Emma L., Hanney, Marisa, Harold, Denise, Sims, Rebecca, Williams, Julie, Ballard, Clive and Hardy, John 2014. Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome. Neurobiology of Aging 35 (6) , 1513.e1-5. 10.1016/j.neurobiolaging.2013.12.022

Chapman, J., Rees, Elliott, Harold, Denise, Ivanov, Dobril, Gerrish, Amy, Sims, Rebecca, Hollingworth, P, Stretton, A., Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon, Williams, Julie and Kirov, George 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

Harold, Denise, Jehu, Luke, Turic, Darko, Hollingworth, Paul, Moore, P., Summerhayes, P., Escott-Price, Valentina, Foy, C., Archer, N., Hamilton, B.A., Lovestone, S., Powell, J., Brayne, C., Rubinsztein, D.C., Jones, Lesley, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2007. Interaction between theADAM12 andSH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (4) , pp. 448-452. 10.1002/ajmg.b.30456

Harold, Denise, Macgregor, S., Patterson, C. E., Hollingworth, P., Moore, P., Owen, Michael John, Williams, Julie, O'Donovan, Michael Conlon, Passmore, P., McIlroy, S. and Jones, Lesley 2006. A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease. Pharmacogenetics and genomics 16 (2) , pp. 75-77.

Barratt, Bryan J., Payne, Felicity, Lowe, Chris E., Hermann, Robert, Healy, Barry C., Harold, Denise, Concannon, Patrick, Gharani, Neda, McCarthy, Mark I., Olavesen, Mark G., McCormack, Rose, Guja, Cristian, Ionescu-Tirgoviste, Constantin, Undlien, Dag E., Ronningen, Kjersti S., Gillespie, Kathleen M., Tuomilehto-Wolf, Eva, Tuomilehto, Jaakko, Bennett, Simon T., Clayton, David G., Cordell, Heather J. and Todd, John A. 2004. Remapping the insulin gene/IDDM2 locus in type 1 diabetes. Diabetes 53 (7) , pp. 1884-1889. 10.2337/diabetes.53.7.1884

Harold, Denise, Peirce, Timothy, Escott-Price, Valentina, Lovestone, Simon, Powell, John, Foy, Catherine, Archer, Nicola, Walter, Sarah, Edmonson, Amanda, McIlroy, Stephen, Craig, David, Passmore, Peter A., Goate, Alison, Hardy, John, O'Donovan, Michael Conlon, Williams, Julie, Liddell, Malcolm, Owen, Michael John, Jones, Lesley, Myers, Amanda, Jones, Susan, Hollingworth, Paul and Moore, Pamela 2003. Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. Human Genetics 113 (3) , pp. 258-267. 10.1007/s00439-003-0960-2

This list was generated on Wed Dec 11 09:18:21 2019 GMT.