The CamPaIGN study of Parkinson's disease: 10-year outlook in an incident population-based cohort von Williams-Gray, Caroline H, Mason, Sarah L, Evans, Jonathan R, Foltynie, Thomas, Brayne, Carol, Robbins, Trevor W, Barker, Roger A

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The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort von Williams-Gray, Caroline H., Evans, Jonathan R., Goris, An, Foltynie, Thomas, Ban, Maria, Robbins, Trevor W., Brayne, Carol, Kolachana, Bhaskar S., Weinberger, Daniel R., Sawcer, Stephen J., Barker, Roger A.

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Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort von WINDER-RHODES, Sophie E, EVANS, Jonathan R, BAN, Maria, MASON, Sarah L, WILLIAMS-GRAY, Caroline H, FOLTYNIE, Tom, DURAN, Raquel, MENCACCI, Niccolo E, SAWCER, Stephen J, BARKER, Roger A

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Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease von Hudson, Gavin, Nalls, Mike, Evans, Jonathan R, Breen, David P, Winder-Rhodes, Sophie, Morrison, Karen E, Morris, Huw R, Williams-Gray, Caroline H, Barker, Roger A, Singleton, Andrew B, Hardy, John, Wood, Nicholas E, Burn, David J, Chinnery, Patrick F

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Determinants of delayed diagnosis in Parkinson’s disease von Breen, David P., Evans, Jonathan R., Farrell, Krista, Brayne, Carol, Barker, Roger A.

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Neurotrophic factors as a therapeutic target for Parkinson's disease von Evans, Jonathan R, Barker, Roger A

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Addenbrooke's Cognitive Examination-Revised for mild cognitive impairment in Parkinson's disease von McColgan, Peter, Evans, Jonathan R., Breen, David P., Mason, Sarah L., Barker, Roger A., Williams-Gray, Caroline H.

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Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome von Winder-Rhodes, Sophie E., Garcia-Reitböck, Pablo, Ban, Maria, Evans, Jonathan R., Jacques, Thomas S., Kemppinen, Anu, Foltynie, Thomas, Williams-Gray, Caroline H., Chinnery, Patrick F., Hudson, Gavin, Burn, David J., Allcock, Liesl M., Sawcer, Stephen J., Barker, Roger A., Spillantini, Maria Grazia

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Serum immune markers and disease progression in an incident Parkinson's disease cohort (ICICLE-PD) von Williams-Gray, Caroline H., Wijeyekoon, Ruwani, Yarnall, Alison J., Lawson, Rachael A., Breen, David P., Evans, Jonathan R., Cummins, Gemma A., Duncan, Gordon W., Khoo, Tien K., Burn, David J., Barker, Roger A.

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Characterizing mild cognitive impairment in incident Parkinson disease: The ICICLE-PD Study von Yarnall, Alison J, Breen, David P, Duncan, Gordon W, Khoo, Tien K, Coleman, Shirley Y, Firbank, Michael J, Nombela, Cristina, Winder-Rhodes, Sophie, Evans, Jonathan R, Rowe, James B, Mollenhauer, Brit, Kruse, Niels, Hudson, Gavin, Chinnery, Patrick F, O’Brien, John T, Robbins, Trevor W, Wesnes, Keith, Brooks, David J, Barker, Roger A, Burn, David J

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Peripheral innate immune and bacterial signals relate to clinical heterogeneity in Parkinson’s disease von Wijeyekoon, Ruwani S., Kronenberg-Versteeg, Deborah, Scott, Kirsten M., Hayat, Shaista, Kuan, Wei-Li, Evans, Jonathan R., Breen, David P., Cummins, Gemma, Jones, Joanne L., Clatworthy, Menna R., Floto, R. Andres, Barker, Roger A., Williams-Gray, Caroline H.

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The natural history of treated Parkinson's disease in an incident, community based cohort von Evans, Jonathan R, Mason, Sarah L, Williams-Gray, Caroline H, Foltynie, Thomas, Brayne, Carol, Robbins, Trevor W, Barker, Roger A

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Systematic Review and UK-Based Study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease von Kilarski, Laura L., Pearson, Justin P., Newsway, Victoria, Majounie, Elisa, 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 M., Morris, Huw R.

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Development and external validation of a prognostic model in newly diagnosed Parkinson disease von Velseboer, Daan C, de Bie, Rob M.A, Wieske, Luuk, Evans, Jonathan R, Mason, Sarah L, Foltynie, Thomas, Schmand, Ben, de Haan, Rob J, Post, Bart, Barker, Roger A, Williams-Gray, Caroline H

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Validation of a 5‐Year Prognostic Model for Parkinson's Disease von Ribeiro, Joana, Camacho, Marta, Scott, Kirsten M., Greenland, Julia C., Evans, Jonathan R., Breen, David P., Wijeyekoon, Ruwani S., Barker, Roger A., Williams‐Gray, Caroline H.

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Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts von Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Kim, Jonggeol J., Liu, Ganqiang, Maple‐Grødem, Jodi, Corvol, Jean‐Christophe, Pihlstrøm, Lasse, Nimwegen, Marlies, Hutten, Samantha J., Nguyen, Khanh‐Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Gibbs, J. Raphael, Chitrala, Kumaraswamy Naidu, Day‐Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole‐Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Andreassen, Ole, Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams‐Gray, Caroline H., Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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Differences in the Presentation and Progression of Parkinson's Disease by Sex von Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Makarious, Mary B., Kim, Jonggeol J., Liu, Ganqiang, Maple‐Grødem, Jodi, Corvol, Jean‐Christophe, Pihlstrøm, Lasse, Nimwegen, Marlies, Smolensky, Luba, Amondikar, Ninad, Hutten, Samantha J., Frasier, Mark, Nguyen, Khanh‐Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Gibbs, Raphael J., Day‐Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole‐Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Andreassen, Ole A., Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams‐Gray, Caroline H., Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy von Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.

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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies von Nalls, Michael A, Plagnol, Vincent, Hernandez, Dena G, Sharma, Manu, Sheerin, Una-Marie, Saad, Mohamad, Simón-Sánchez, J, Schulte, Claudia, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Stefánsson, Kári, Martinez, Maria, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B, Wood, Nicholas W

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Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts von Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L, Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J, Nguyen, Khanh-Dung H, Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M, Wijeyekoon, Ruwani, Van Deerlin, Vivianna M, Hernandez, Dena G, Day-Williams, Aaron G, Brice, Alexis, Alves, Guido, Noyce, Alastair J, Tysnes, Ole-Bjørn, Evans, Jonathan R, Breen, David P, Estrada, Karol, Wegel, Claire E, Danjou, Fabrice, Simon, David K, Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R, Weintraub, Daniel, Barker, Roger A, Williams-Gray, Caroline H, van de Warrenburg, Bart P, Van Hilten, Jacobus J, Scherzer, Clemens R, Singleton, Andrew B, Nalls, Mike A

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