No Evidence for Association with Parkinson Disease for 13 Single-Nucleotide Polymorphisms Identified by Whole-Genome Association Screening

di Goris, A., Williams-Gray, C. H., Foltynie, T., Compston, D. A. S., Barker, R. A., Sawcer, S. J.
Pubblicazione 2006

Putative cortical dopamine levels affect cortical recruitment during planning()

di Fallon, S.J., Hampshire, A., Williams-Gray, C.H., Barker, R.A., Owen, A.M.
Pubblicazione 2013

Abnormalities of age-related T cell senescence in Parkinson’s disease

di Williams-Gray, C. H., Wijeyekoon, R. S., Scott, K. M., Hayat, S., Barker, R. A., Jones, J. L.
Pubblicato in J Neuroinflammation (2018)

The val(158)met COMT polymorphism's effect on atrophy in healthy aging and Parkinson's disease

di Rowe, J.B., Hughes, L., Williams-Gray, C.H., Bishop, S., Fallon, S., Barker, R.A., Owen, A.M.
Pubblicazione 2010

Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson's disease cohort

di Williams‐Gray, C H, Goris, A, Foltynie, T, Brown, J, Maranian, M, Walton, A, Compston, D A S, Sawcer, S J, Barker, R A
Pubblicazione 2006

Parkinson's disease and dopaminergic therapy—differential effects on movement, reward and cognition

di Rowe, J. B., Hughes, L., Ghosh, B. C. P., Eckstein, D., Williams-Gray, C. H., Fallon, S., Barker, R. A., Owen, A. M.
Pubblicazione 2008

Saccadic latency distributions in Parkinson's disease and the effects of l-dopa

di Michell, A. W., Xu, Z., Fritz, D., Lewis, S. J. G., Foltynie, T., Williams-Gray, C. H., Robbins, T. W., Carpenter, R. H. S., Barker, R. A.
Pubblicazione 2006

Progression of Neuropsychiatric Symptoms over Time in an Incident Parkinson’s Disease Cohort (ICICLE-PD)

di Dlay, J. K., Duncan, G. W., Khoo, T. K., Williams-Gray, C. H., Breen, D. P., Barker, R. A., Burn, D. J., Lawson, R. A., Yarnall, A. J.
Pubblicato in Brain Sci (2020)

Early constipation predicts faster dementia onset in Parkinson’s disease

di Camacho, M., Macleod, A. D., Maple-Grødem, J., Evans, J. R., Breen, D. P., Cummins, G., Wijeyekoon, R. S., Greenland, J. C., Alves, G., Tysnes, O. B., Lawson, R. A., Barker, R. A., Williams-Gray, C. H.
Pubblicato in NPJ Parkinsons Dis (2021)

Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

di Liu, Ganqiang, Boot, Brendon, Locascio, Joseph J., Jansen, Iris E., Winder‐Rhodes, Sophie, Eberly, Shirley, Elbaz, Alexis, Brice, Alexis, Ravina, Bernard, van Hilten, Jacobus J., Cormier‐Dequaire, Florence, Corvol, Jean‐Christophe, Barker, Roger A., Heutink, Peter, Marinus, Johan, Williams‐Gray, Caroline H., Scherzer, Clemens R., Scherzer, C., Hyman, B.T., Ivinson, A.J., Trisini‐Lipsanopoulos, A., Franco, D., Burke, K., Sudarsky, L.R., Hayes, M.T., Umeh, C.C., Growdon, J.H., Schwarzschild, M.A., Hung, A.Y., Flaherty, A.W., Wills, A.‐M., Mejia, N.I., Gomperts, S.N., Khurana, V., Selkoe, D.J., Yi, T., Page, K., Liao, Z., Barker, R., Foltynie, T., Williams‐Gray, C.H., Mason, S., Winder‐Rhodes, S., Barker, R., Williams‐Gray, C.H., Breen, D., Cummins, G., Evans, J., Winder‐Rhodes, S., Corvol, J.‐C., Brice, A., Elbaz, A., Mallet, A., Vidailhet, M., Bonnet, A.‐M., Bonnet, C., Grabli, D., Hartmann, A., Klebe, S., Lacomblez, L., Mangone, G., Bourdain, F., Brandel, J.‐P., Derkinderen, P., Durif, F., Mesnage, V., Pico, F., Rascol, O., Forlani, S., Lesage, S., Tahiri, K., van Hilten, J.J., Marinus, J., Liao, Z., Page, K., Franco, D., Duong, K., Yi, T., Trisini‐Lipsanopoulos, A., Dong, X., Sudarsky, L.R., Hutten, S.J., Amr, S.S., Shoulson, I., Tanner, C.M., Lang, A.E., Nalls, M.A.
Pubblicato in Ann Neurol (2016)