Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Browse by Current Cardiff authors

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Number of items: 7.

Hong, Eun Pyo, Chao, Michael J., Massey, Thomas, McAllister, Branduff, Lobanov, Sergey, Jones, Lesley, Holmans, Peter, Kwak, Seung, Orth, Michael, Ciosi, Marc, Monckton, Darren G., Long, Jeffrey D., Lucente, Diane, Wheeler, Vanessa C., MacDonald, Marcy E., Gusella, James F. and Lee, Jong-Min 2021. Association analysis of chromosome X to identify genetic modifiers of Huntington's disease. Journal of Huntington's Disease 10.3233/JHD-210485
file

McAllister, Branduff, Gusella, James F., Landwehrmeyer, G. Bernhard, Lee, Jong-Min, MacDonald, Marcy E., Orth, Michael, Rosser, Anne E., Williams, Nigel M., Holmans, Peter, Jones, Lesley and Massey, Thomas H. 2021. Timing and impact of psychiatric, cognitive, and motor abnormalities in Huntington disease. Neurology 96 (19) , e2395-e2406. 10.1212/WNL.0000000000011893
file

Ellis, Natalie, Tee, Amelia, McAllister, Branduff, Massey, Thomas, McLauchlan, Duncan, Stone, Timothy, Correia, Kevin, Loupe, Jacob, Kim, Kyung-Hee, Barker, Douglas, Hong, Eun Pyo, Chao, Michael, Long, Jeffrey, Lucente, Diane, Vonsattel, Jean Paul, Pinto, Ricardo, Elneel, Kawther Abu, Ramos, Eliana Marisa, Mysore, Jayalakshmi Srinidhi, Gillis, Tammy, Wheeler, Vanessa, Medway, Christopher, Hall, Lynsey, Kwak, Seung, Sampaio, Cristina, Ciosi, Marc, Maxwell, Alastair, Chatzi, Afroditi, Monckton, Darren, Orth, Michael, Landwehrmeyer, G. Bernhard, Paulsen, Jane, Shoulson, Ira, Myers, Richard, van Duijn, Erik, Rickards, Hugh, MacDonald, Marcy, Lee, Jong-min, Gusella, James, Jones, Lesley and Holmans, Peter 2020. Genetic risk underlying psychiatric and cognitive symptoms in Huntington’s Disease. Biological Psychiatry 87 (9) , pp. 857-865. 10.1016/j.biopsych.2019.12.010
file

McAllister, Branduff, Gusella, James F., Landwehrmeyer, G. Bernhard, Lee, Jong-Min, MacDonald, Marcy E., Orth, Michael, Rosser, Anne E., Williams, Nigel M., Holmans, Peter, Jones, Lesley and Massey, Thomas H. 2020. The onset and prevalence of motor and psychiatric symptoms in Huntington’s disease. BioRxiv 10.1101/2020.05.26.116798
file

McAllister, William Branduff 2019. Identification and characterisation of genetic variation that modifies age at onset in Huntington’s disease. PhD Thesis, Cardiff University.
Item availability restricted.
filefile

Lee, Jong-Min, Correia, Kevin, Loupe, Jacob, Kim, Kyung, Barker, Douglas, Hong, Eun Pyo, Chao, Michael, Long, Jeffery, Lucente, Diane, Vonsattel, Jean, Pinto, Richardo, Ehiana, Ramos, Mysore, Jayalakshmi, Gillis, Tammy, Wheeler, Vanessa, MacDonald, Marcy, Gusella, James, McAllister, Branduff, Massey, Thomas, Medway, Christopher, Stone, Timothy, Hall, Lynsey, Jones, Lesley, Holmans, Peter, Kwark, Seung, Ehrhardt, Anka, Sampaio, Cristina, Ciosi, Marc, Maxwell, Alastair, Chatzi, Afroditi, Monckton, Darren, Orth, Michael, Landwehrmeyer, Bernhard and Paulsen, Jane 2019. CAG repeat not polyglutamine length determines timing of Huntington’s disease onset. Cell 178 (4) , 887-099.e14. 10.1016/j.cell.2019.06.036
file

Massey, Thomas, McAllister, Branduff and Jones, Lesley 2018. Methods for assessing DNA repair and repeat expansion in Huntington's Disease. In: Precious, Sophie V., Rosser, Anne E. and Dunnett, Stephen B. eds. Huntington’s Disease, Vol. 1780. Methods in Molecular Biology, Humana Press, pp. 483-495. (10.1007/978-1-4939-7825-0_22)
file

This list was generated on Sun Sep 19 04:38:54 2021 BST.