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Jones, Lliwen, Baber, Wagaar, Wardle, Mark, Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909, Morris, Huw, Church, Alistair, Llewelyn, John and Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944 2019. A case of treatment resistance and complications in a patient with stiff person syndrome and cerebellar ataxia. Tremor and Other Hyperkinetic Movements 9 10.7916/tohm.v0.677
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Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Cross, William, Newsway, Victoria, Dillman, Allissa, Vandrovcova, Jana, Morris, Christopher M., Nalls, Michael A., Ferrucci, Luigi, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Cookson, Mark R., Singleton, Andrew B., de Silva, Rohan and Morris, Huw R. 2013. Variation in tau isoform expression in different brain regions and disease states. Neurobiology of Aging 34 (7) , 1922.e7-1922.e12. 10.1016/j.neurobiolaging.2013.01.017

Fawcett, Katherine, Mehrabian, Mohadeseh, Liu, Yo-Tsen, Hamed, Sherifa, Elahi, Elahe, Revesz, Tamas, Koutsis, Georgios, Herscheson, Joshua, Schottlaender, Lucia, Wardle, Mark, Morrison, Patrick J., Morris, Huw Rees, Giunti, Paola, Wood, Nicholas and Houlden, Henry 2013. The frequency of spinocerebellar ataxia type 23 in a UK population. Journal of Neurology 260 (3) , pp. 856-859. 10.1007/s00415-012-6721-1

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Sharma, Manu, Vedernikov, Alexey, Buchel, Finja, Sadd, Mohamad, Bras, Jose M., Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Morris, Huw Rees and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2013. A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Human Molecular Genetics 22 (5) , pp. 1039-1049. 10.1093/hmg/dds492

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Russo, Giancarlo, Vedernikov, Alexey, Sharma, Manu, Saad, Mohamad, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Bras, Jose M., Bettella, Francesco, Keller, Margaux F., Nicolaou, Nayia, Simón-Sánchez, Javier, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Peter, Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O’Donovan, Michael Conlon, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Morris, Huw and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2013. Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. JAMA Neurology 70 (10) , pp. 1268-1276. 10.1001/jamaneurol.2013.448

Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Smith, Daniel J., Kurian, Manju A., Wardle, Mark, Waite, Adrian James, Hedderly, Tammy, Lin, Jean-Pierre, Smith, Martin, Whone, Alan, Pall, Hardev, White, Cathy, Lux, Andrew, Jardine, Philip, Bajaj, Narinder, Lynch, Bryan, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Riordan, Sean, Samuel, Michael, Lynch, Timothy, King, Mary D., Chinnery, Patrick F., Warner, Thomas T., Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Morris, Huw Rees 2013. SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain 136 (1) , pp. 294-303. 10.1093/brain/aws308

Keller, Marguax F., Saad, Mohamad, Bras, Jose, Bettella, Francesco, Nicolaou, Nayia, Simon-Sanchez, Javier, Mittag, Florian, Buchel, Finja, Sharma, Manu, Gibbs, J. Raphael, Schulte, Claudia, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Durr, Alexandra, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kilarski, Laura, Guerreiro, Rita, Hernandez, Dena G., Brice, Alexis, Ylikotila, Pauli, Stefansson, Hreinn, Majamaa, Kari, Morris, Huw Rees, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Hardy, John, Martinez, Maria, Singleton, Andrew B. and Nalls, Michael A. 2012. Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Human Molecular Genetics 21 (22) , pp. 4996-5009. 10.1093/hmg/dds335

Kilarski, Laura, Pearson, Justin Peter, Newsway, Victoria Elizabeth, Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Knipe, M. Duleeka W., Misbahuddin, Anjum, Chinnery, Patrick F., Burn, David J., Clarke, Carl E., Marion, Marie-Helene, Lewthwaite, Alistair J., Nicholl, David J., Wood, Nicholas W., Morrison, Karen E., Williams-Gray, Caroline H., Evans, Jonathan R., Sawcer, Stephen J., Barker, Roger A., Wickremaratchi, Mirdhu M., Ben-Shlomo, Yoav, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Morris, Huw Rees 2012. Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1)andLRRK2in early-onset Parkinson's disease. Movement Disorders 27 (12) , pp. 1522-1529. 10.1002/mds.25132

Wray, Selina, Self, Matthew, Lewis, Patrick A., Taanman, Jan-Willem, Ryan, Natalie S., Mahoney, Colin J., Liang, Yuying, Devine, Michael J., Sheerin, Una-Marie, Houlden, Henry, Morris, Huw Rees, Healy, Daniel, Marti-Masso, Jose-Felix, Preza, Elisavet, Barker, Suzanne, Sutherland, Margaret, Corriveau, Roderick A., D'Andrea, Michael, Schapira, Anthony H. V., Uitti, Ryan J., Guttman, Mark, Opala, Grzegorz, Jasinska-Myga, Barbara, Puschmann, Andreas, Nilsson, Christer, Espay, Alberto J., Slawek, Jaroslaw, Gutmann, Ludwig, Boeve, Bradley F., Boylan, Kevin, Stoessl, A. Jon, Ross, Owen A., Maragakis, Nicholas J., Van Gerpen, Jay, Gerstenhaber, Melissa, Gwinn, Katrina, Dawson, Ted M., Isacson, Ole, Marder, Karen S., Clark, Lorraine N., Przedborski, Serge E., Finkbeiner, Steven, Rothstein, Jeffrey D., Wszolek, Zbigniew K., Rossor, Martin N., Hardy, John, Kemp, Paul J. ORCID: https://orcid.org/0000-0003-2773-973X and Allen, Nicholas Denby ORCID: https://orcid.org/0000-0003-4009-186X 2012. Creation of an open-access, mutation-defined fibroblast resource for neurological disease research. PLoS ONE 7 (8) , e43099. 10.1371/journal.pone.0043099
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O'Dowd, Seán, Curtin, Denis, Waite, Adrian James, Roberts, Kinley, Pender, Niall, Reid, Valerie, O'Connell, Martin, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Morris, Huw Rees, Traynor, Bryan J. and Lynch, Timothy 2012. C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism. Movement Disorders 27 (8) , pp. 1072-1074. 10.1002/mds.25022

Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Waite, Adrian James, Kurian, Manju A., Wardle, Mark, Hedderly, Tammy, Lin, Jean-Pierre, Smith, Martin, Pall, Hardev, King, Mary D., Lynch, Timothy, White, Cathy, Chinnery, Patrick F., Warner, Thomas T., Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Morris, Huw Rees 2012. Myoclonus dystonia syndrome: SGCE mutations and psychiatric disease [Abstract]. Journal of Neurology 259 , S30-S30.

Simón-Sánchez, Javier, Kilarski, Laura, Nalls, Michael A., Martinez, Maria, Schulte, Claudia, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Gasser, Thomas, Hardy, John, Singleton, Andrew B., Wood, Nicholas W., Brice, Alexis, Heutink, Peter, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Morris, Huw Rees 2012. Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's Disease. PLoS ONE 7 (3) , e28787. 10.1371/journal.pone.0028787
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Mok, Kin, Traynor, Bryan J., Schymick, Jennifer, Tienari, Pentti J., Laaksovirta, Hannu, Peuralinna, Terhi, Myllykangas, Liisa, Chiò, Adriano, Shatunov, Aleksey, Boeve, Bradley F., Boxer, Adam L., DeJesus-Hernandez, Mariely, Mackenzie, Ian R., Waite, Adrian James, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Morris, Huw Rees, Simón-Sánchez, Javier, van Swieten, John C., Heutink, Peter, Restagno, Gabriella, Mora, Gabriele, Morrison, Karen E., Shaw, Pamela J., Rollinson, Pamela Sara, Al-Chalabi, Ammar, Rademakers, Rosa, Pickering-Brown, Stuart, Orrell, Richard W., Nalls, Michael A. and Hardy, John 2012. The chromosome 9 ALS and FTD locus is probably derived from a single founder. Neurobiology of Aging 33 (1) , 209.e3-209.e8. 10.1016/j.neurobiolaging.2011.08.005

Charlesworth, Gavin, Gandhi, Sonia, Bras, Jose M., Barker, Roger A., Burn, David J., Chinnery, Patrick F., Gentleman, Stephen M., Guerreiro, Rita, Hardy, John, Holton, Janice L., Lees, Andrew, Morrison, Karen, Sheerin, Una-Marie, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Morris, Huw Rees, Revesz, Tamas and Wood, Nicholas W. 2012. Tau acts as an independent genetic risk factor in pathologically proven PD. Neurobiology of Aging 33 (4) , 838.e7-838.e11. 10.1016/j.neurobiolaging.2011.11.001

Morris, Huw Rees, Waite, Adrian James, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Neal, James William and Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731 2012. Recent advances in the genetics of the ALS-FTLD complex. Current Neurology and Neuroscience Reports 12 (3) , pp. 243-250. 10.1007/s11910-012-0268-5

Renton, Alan E., Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Waite, Adrian James, Simón-Sánchez, Javier, Rollinson, Sara, Gibbs, J. Raphael, Schymick, Jennifer C., Laaksovirta, Hannu, van Swieten, John C., Myllykangas, Liisa, Kalimo, Hannu, Paetau, Anders, Abramzon, Yevgeniya, Remes, Anne M., Kaganovich, Alice, Scholz, Sonja W., Duckworth, Jamie, Ding, Jinhui, Harmer, Daniel W., Hernandez, Dena G., Johnson, Janel O., Mok, Kin, Ryten, Mina, Trabzuni, Danyah, Guerreiro, Rita J., Orrell, Richard W., Neal, James William, Murray, Alexandra, Pearson, Justin Peter, Jansen, Iris E., Sondervan, David, Seelaar, Harro, Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Young, Kate, Halliwell, Nicola, Callister, Janis Bennion, Toulson, Greg, Richardson, Anna, Gerhard, Alex, Snowden, Julie, Mann, David, Neary, David, Nalls, Michael A., Peuralinna, Terhi, Jansson, Lilja, Isoviita, Veli-Matti, Kaivorinne, Anna-Lotta, Hölttä-Vuori, Maarit, Ikonen, Elina, Sulkava, Raimo, Benatar, Michael, Wuu, Joanne, Chiò, Adriano, Restagno, Gabriella, Borghero, Giuseppe, Sabatelli, Mario, Heckerman, David, Rogaeva, Ekaterina, Zinman, Lorne, Rothstein, Jeffrey D., Sendtner, Michael, Drepper, Carsten, Eichler, Evan E., Alkan, Can, Abdullaev, Ziedulla, Pack, Svetlana D., Dutra, Amalia, Pak, Evgenia, Hardy, John, Singleton, Andrew, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Heutink, Peter, Pickering-Brown, Stuart, Morris, Huw Rees, Tienari, Pentti J. and Traynor, Bryan J. 2011. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72 (2) , pp. 257-268. 10.1016/j.neuron.2011.09.010

Pearson, Justin P., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Waite, Adrian James, Stott, Jennifer, Newsway, Victoria, Murray, Alexandra, Hernandez, Dena, Guerreiro, Rita, Singleton, Andrew B., Neal, James William and Morris, Huw Rees 2011. Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p. Journal of Neurology 258 (4) , pp. 647-655. 10.1007/s00415-010-5815-x

Wickremaratchi, Mirdhu M., Knipe, Megan Duleeka W., Sastry, B. S. Dwarakanath, Morgan, Elizabeth, Jones, Anne Maria, Salmon, Rachel, Weiser, Richard, Moran, Maralyn, Davies, Debbie, Ebenezer, Louise, Raha, Sandip, Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909, Butler, Christopher Collett ORCID: https://orcid.org/0000-0002-0102-3453, Ben-Shlomo, Yoav and Morris, Huw Rees 2011. The motor phenotype of Parkinson's disease in relation to age at onset. Movement Disorders 26 (3) , pp. 457-463. 10.1002/mds.23469

Morris, Huw Rees, Pearson, Justin P., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Wickremaratchi, Mirdhu, International Parkinson's Disease Genomics Consortium (IPDGC) and Wellcome Trust Case Control Consortium (WTCCC) 2011. A two-stage meta-analysis identifies several new loci for Parkinson's Disease. PLoS Genetics 7 (6) , e1002142. 10.1371/journal.pgen.1002142
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Knipe, Megan Duleeka W., Wickremaratchi, Mirdhu M., Wyatt-Haines, Emma, Morris, Huw Rees and Ben-Shlomo, Yoav 2011. Quality of life in young- compared with late-onset Parkinson's disease. Movement Disorders 26 (11) , pp. 2011-2018. 10.1002/mds.23763

Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Waite, Adrian James, Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Morris, Huw Rees 2011. Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review. Movement Disorders 26 (10) , pp. 1939-1942. 10.1002/mds.23791

Höglinger, Günter U., Melhem, Nadine M., Dickson, Dennis W., Sleiman, Patrick M. A., Wang, Li-San, Klei, Lambertus, Rademakers, Rosa, de Silva, Rohan, Litvan, Irene, Riley, David E., van Swieten, John C., Heutink, Peter, Wszolek, Zbigniew K., Uitti, Ryan J., Vandrovcova, Jana, Hurtig, Howard I., Gross, Rachel G., Maetzler, Walter, Goldwurm, Stefano, Tolosa, Eduardo, Borroni, Barbara, Pastor, Pau, Albin, Roger L., Alonso, Elena, Antonini, Angelo, Apfelbacher, Manuela, Arnold, Steven E., Avila, Jesus, Beach, Thomas G., Beecher, Sherry, Berg, Daniela, Bird, Thomas D., Bogdanovic, Nenad, Boon, Agnita J. W., Bordelon, Yvette, Brice, Alexis, Budka, Herbert, Canesi, Margherita, Chiu, Wang Zheng, Cilia, Roberto, Colosimo, Carlo, De Deyn, Peter P., de Yebenes, Justo García, Kaat, Laura Donker, Duara, Ranjan, Durr, Alexandra, Engelborghs, Sebastiaan, Fabbrini, Giovanni, Finch, NiCole A., Flook, Robyn, Frosch, Matthew P., Gaig, Carles, Galasko, Douglas R., Gasser, Thomas, Gearing, Marla, Geller, Evan T., Ghetti, Bernardino, Graff-Radford, Neill R., Grossman, Murray, Hall, Deborah A., Hazrati, Lili-Naz, Höllerhage, Matthias, Jankovic, Joseph, Juncos, Jorge L., Karydas, Anna, Kretzschmar, Hans A., Leber, Isabelle, Lee, Virginia M., Lieberman, Andrew P., Lyons, Kelly E., Mariani, Claudio, Masliah, Eliezer, Massey, Luke A., McLean, Catriona A., Meucci, Nicoletta, Miller, Bruce L., Mollenhauer, Brit, Möller, Jens C., Morris, Huw Rees, Morris, Chris, O'Sullivan, Sean S., Oertel, Wolfgang H., Ottaviani, Donatella, Padovani, Alessandro, Pahwa, Rajesh, Pezzoli, Gianni, Pickering-Brown, Stuart, Poewe, Werner, Rabano, Alberto, Rajput, Alex, Reich, Stephen G., Respondek, Gesine, Roeber, Sigrun, Rohrer, Jonathan D., Ross, Owen A., Rossor, Martin N., Sacilotto, Giorgio, Seeley, William W., Seppi, Klaus, Silveira-Moriyama, Laura, Spina, Salvatore, Srulijes, Karin, St. George-Hyslop, Peter, Stamelou, Maria, Standaert, David G., Tesei, Silvana, Tourtellotte, Wallace W., Trenkwalder, Claudia, Troakes, Claire, Trojanowski, John Q., Troncoso, Juan C., Van Deerlin, Vivianna M., Vonsattel, Jean Paul G., Wenning, Gregor K., White, Charles L., Winter, Pia, Zarow, Chris, Zecchinelli, Anna L., Cantwell, Laura B., Han, Mi Ryung, Dillman, Allissa, van der Brug, Marcel P., Gibbs, J Raphael, Cookson, Mark R., Hernandez, Dena G., Singleton, Andrew B., Farrer, Matthew J., Yu, Chang-En, Golbe, Lawrence I., Revesz, Tamas, Hardy, John, Lees, Andrew J., Devlin, Bernie, Hakonarson, Hakon, Müller, Ulrich and Schellenberg, Gerard D. 2011. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy [Letter]. Nature Genetics 43 (7) , pp. 699-705. 10.1038/ng.859

Silveira-Moriyama, Laura, Hughes, Graham, Church, Alistair, Ayling, Hilary, Williams, David R., Petrie, Aviva, Holton, Janice, Revesz, Tamas, Kingsbury, Ann, Morris, Huw Rees, Burn, David J. and Lees, Andrew J. 2010. Hyposmia in progressive supranuclear palsy. Movement Disorders 25 (5) , pp. 570-577. 10.1002/mds.22688

Newsway, Victoria Elizabeth, Fish, Mark, Rohrer, Jonathan D., Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Hack, Melissa Anne, Warren, Jason D. and Morris, Huw Rees 2010. Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure. Movement Disorders 25 (6) , pp. 767-770. 10.1002/mds.22950

Quinn, Lori ORCID: https://orcid.org/0000-0002-2982-923X, Busse, Monica, Khalil, Hanan, Richardson, Sue, Rosser, Anne Elizabeth ORCID: https://orcid.org/0000-0002-4716-4753 and Morris, Huw Rees 2010. Client and therapist views on exercise programmes for early-mid stage Parkinson's disease and Huntington's disease. Disability & Rehabilitation 32 (11) , pp. 917-928. 10.3109/09638280903362712

Momeni, Parastoo, Wickremaratchi, Mirdhu, Bell, Jason, Arnold, Richard, Beer, Roger, Hardy, John, Revesz, Tamas, Neal, James William and Morris, Huw Rees 2010. Familial early onset frontotemporal dementia caused by a novel S356T MAPT mutation, initially diagnosed as schizophrenia. Clinical Neurology and Neurosurgery 112 (10) , pp. 917-920. 10.1016/j.clineuro.2010.07.015

Spencer, C. C. A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., Barker, Roger, Bellenguez, C., Bhatia, K., Blackburn, H., Blackwell, J. M., Bramon, E., Brown, M. A, Brown, M. A., Burn, D., Casas, J.-P., Chinnery, P. F., Clarke, C. E., Corvin, A., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Deloukas, P., Edkins, S., Evans, J., Freeman, C., Gray, E., Hardy, J., Hudson, G., Hunt, S., Jankowski, J., Langford, C., Lees, A. J., Markus, H. S., Mathew, C. G., McCarthy, M. I., Morrison, K. E., Palmer, C. N. A., Pearson, J. P., Peltonen, L., Pirinen, M., Plomin, R., Potter, S., Rautanen, A., Sawcer, S. J., Su, Z., Trembath, R. C., Viswanathan, A. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Morris, Huw Rees, Donnelly, Peter and Wood, N. W. 2010. Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Human Molecular Genetics 20 (2) , pp. 345-353. 10.1093/hmg/ddq469

Graves, T. D., Rajakulendran, S., Zuberi, S. M., Morris, Huw Rees, Schorge, S., Hanna, M. G. and Kullmann, D. M. 2010. Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins. Neurology 75 (4) , pp. 367-372. 10.1212/WNL.0b013e3181ea9ee3

Hayesmoore, Jesse B. G., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Cross, William C., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Morris, Huw Rees 2009. The effect of age and the H1c MAPT haplotype on MAPT expression in human brain. Neurobiology of Aging 30 (10) , pp. 1652-1656. 10.1016/j.neurobiolaging.2007.12.017

Wardle, Mark, Morris, Huw Rees and Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 2009. Clinical and genetic characteristics of non-Asian dentatorubral-pallidoluysian atrophy: a systematic review. Movement Disorders 24 (11) , pp. 1636-1640. 10.1002/mds.22642

Wickremaratchi, Mirdhu M., Perera, Duleeka, O'Loghlen, Clare, Sastry, B. S. D., Morgan, E., Jones, A., Edwards, P., Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909, Butler, Christopher Collett ORCID: https://orcid.org/0000-0002-0102-3453, Morris, Huw Rees and Ben-Shlomo, Y. 2009. Prevalence and age of onset of Parkinson's disease in Cardiff: A community based cross sectional study and meta-analysis. Journal of Neurology, Neurosurgery & Psychiatry 80 (7) , pp. 805-807. 10.1136/jnnp.2008.162222

Wickremaratchi, Mindhu M., Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Morris, Huw Rees, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Lewis, Helen, Gill, Steven S., Khan, Sadaquate, Heywood, Peter, Hardy, John, Wiles, Charles Mark, Singleton, Andrew B. and Quinn, Niall P. 2009. Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome [Letter]. Movement Disorders 24 (1) , pp. 138-140. 10.1002/mds.22181

Wardle, Mark, Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Muzaimi, Mustapha B., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Morris, Huw Rees and Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 2009. The genetic aetiology of late-onset chronic progressive cerebellar ataxia. Journal of Neurology 256 (3) , pp. 343-348. 10.1007/s00415-009-0015-2

Wickremaratchi, Mirdhu, Ben-Shlomo, Y. and Morris, Huw Rees 2009. The effect of onset age on the clinical features of Parkinson's disease. European Journal of Neurology 16 (4) , pp. 450-456. 10.1111/j.1468-1331.2008.02514.x

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Glaser, Beate, Morris, Huw Rees, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2008. Analysis of copy number variation using quantitative interspecies competitive PCR. Nucleic Acids Research 36 (17) , e112-e112. 10.1093/nar/gkn495

Wardle, M, Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Rosser, Anne Elizabeth ORCID: https://orcid.org/0000-0002-4716-4753, Morris, Huw Rees and Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 2008. Dentatorubral pallidoluysian atrophy in South Wales. Journal of Neurology, Neurosurgery and Psychiatry 79 (7) , pp. 804-807. 10.1136/jnnp.2007.128074

Singleton, A. and Morris, Huw Rees 2008. Association, expression, pathobiology: Is too much tau in PD a blueprint for genetic association? [Editorial]. Neurology 71 (1) , pp. 11-12. 10.1212/01.wnl.0000316388.84840.1f

Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Wardle, Mark, Muzaimi, M., Cross, W. C., Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Morris, Huw Rees 2007. Case control analysis of repeat expansion size in ataxia. Neuroscience Letters 429 (1) , pp. 28-32. 10.1016/j.neulet.2007.09.055

Morris, Huw Rees, Steele, John C., Crook, Richard, Wavrant-De Vrièze, Fabienne, Onstead-Cardinale, Luisa, Gwinn-Hardy, Katrina, Wood, Nick W., Farrer, Matthew, Lees, Andrew J., McGeer, P. L., Siddique, Teepu, Hardy, John and Perez-Tur, Jordi 2004. Genome-wide analysis of the parkinsonism-dementia complex of Guam. Archives of Neurology 61 (12) , pp. 1889-1897. 10.1001/archneur.61.12.1889

Morris, Huw Rees, Baker, M., Yasojima, K., Houlden, H., Khan, M. N., Wood, N. W., Hardy, J., Grossman, M., Trojanowski, J., Revesz, T., Bigio, E. H., Bergeron, C., Janssen, J. C., McGeer, P. L., Rossor, M. N., Lees, A. J., Lantos, P. L. and Hutton, M. 2002. Analysis of tau haplotypes in Pick's disease. Neurology 59 , pp. 443-445.

Morris, Huw Rees, Gibb, G., Katzenschlager, R., Wood, N. W., Hanger, D. P., Strand, C., Lashley, T., Daniel, S. E., Lees, A. J., Anderton, B. H. and Revesz, T. 2002. Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy. Brain 125 (5) , pp. 969-975. 10.1093/brain/awf109

Morris, Huw Rees, Al-Sarraj, S., Schwab, C., Gwinn-Hardy, Katrina, Perez-Tur, Jordi, Wood, Nick W., Hardy, John, Lees, Andrew J., McGeer, P. L., Daniel, S. E. and Steele, John C. 2001. A clinical and pathological study of motor neurone disease on Guam. Brain 124 (11) , pp. 2215-2222. 10.1093/brain/124.11.2215

This list was generated on Fri Apr 26 08:05:39 2024 BST.


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