Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome von Jabbari, Edwin, Holland, Negin, Chelban, Viorica, Jones, P. Simon, Lamb, Ruth, Rawlinson, Charlotte, Guo, Tong, Costantini, Alyssa A, Tan, Manuela M. X, Heslegrave, Amanda J, Roncaroli, Federico, Klein, Johannes C, Ansorge, Olaf, Allinson, Kieren S. J, Jaunmuktane, Zane, Holton, Janice L, Revesz, Tamas, Warner, Thomas T, Lees, Andrew J, Zetterberg, Henrik, Russell, Lucy L, Bocchetta, Martina, Rohrer, Jonathan D, Williams, Nigel M, Grosset, Donald G, Burn, David J, Pavese, Nicola, Gerhard, Alexander, Kobylecki, Christopher, Leigh, P. Nigel, Church, Alistair, Hu, Michele T. M, Woodside, John, Houlden, Henry, Rowe, James B, Morris, Huw R

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Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease von Tan, Manuela M.X., Lawton, Michael A., Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Pollard, Miriam I., Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams‐Gray, Caroline H., Hardy, John, Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M., Ben‐Shlomo, Yoav, Hu, Michele T.M., Grosset, Donald G., Shoai, Maryam, Morris, Huw R.

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Lysosomal Polygenic Burden Drives Cognitive Decline in Parkinson's Disease with Low Alzheimer Risk von Tunold, Jon‐Anders, Tan, Manuela M.X., Toft, Mathias, Ross, Owen, Berg, Wilma D.J., Pihlstrøm, Lasse

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Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease von Tunold, Jon-Anders, Tan, Manuela M X, Koga, Shunsuke, Geut, Hanneke, Rozemuller, Annemieke J M, Valentino, Rebecca, Sekiya, Hiroaki, Martin, Nicholas B, Heckman, Michael G, Bras, Jose, Guerreiro, Rita, Dickson, Dennis W, Toft, Mathias, van de Berg, Wilma D J, Ross, Owen A, Pihlstrøm, Lasse

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Sequence of clinical and neurodegeneration events in Parkinson's disease progression von Oxtoby, Neil P., Leyland, Louise-Ann, Aksman, Leon M., Thomas, George E. C., Bunting, Emma L., Wijeratne, Peter A., Young, Alexandra L., Zarkali, Angelika, Tan, Manuela M. X., Bremner, Fion D., Keane, Pearse A., Morris, Huw R., Schrag, Anette E., Alexander, Daniel C., Weil, Rimona S.

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Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study von Tan, Manuela M X, Malek, Naveed, Lawton, Michael A, Hubbard, Leon, Pittman, Alan M, Joseph, Theresita, Hehir, Jason, Swallow, Diane M A, Grosset, Katherine A, Marrinan, Sarah L, Bajaj, Nin, Barker, Roger A, Burn, David J, Bresner, Catherine, Foltynie, Thomas, Hardy, John, Wood, Nicholas, Ben-Shlomo, Yoav, Grosset, Donald G, Williams, Nigel M, Morris, Huw R

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Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia von Real, Raquel, Martinez-Carrasco, Alejandro, Reynolds, Regina H, Lawton, Michael A, Tan, Manuela M X, Shoai, Maryam, Corvol, Jean-Christophe, Ryten, Mina, Bresner, Catherine, Hubbard, Leon, Brice, Alexis, Lesage, Suzanne, Faouzi, Johann, Elbaz, Alexis, Artaud, Fanny, Williams, Nigel, Hu, Michele T M, Ben-Shlomo, Yoav, Grosset, Donald G, Hardy, John, Morris, Huw R

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The genetic and clinico‐pathological profile of early‐onset progressive supranuclear palsy von Jabbari, Edwin, Woodside, John, Tan, Manuela M.X., Pavese, Nicola, Bandmann, Oliver, Ghosh, Boyd C.P., Massey, Luke A., Capps, Erica, Warner, Tom T., Lees, Andrew J., Revesz, Tamas, Holton, Janice L., Williams, Nigel M., Grosset, Donald G., Morris, Huw R.

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Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype von Jabbari, Edwin, Woodside, John, Tan, Manuela M. X., Shoai, Maryam, Pittman, Alan, Ferrari, Raffaele, Mok, Kin Y., Zhang, David, Reynolds, Regina H., de Silva, Rohan, Grimm, Max‐Joseph, Respondek, Gesine, Müller, Ulrich, Al‐Sarraj, Safa, Gentleman, Stephen M., Lees, Andrew J., Warner, Thomas T., Hardy, John, Revesz, Tamas, Höglinger, Günter U., Holton, Janice L., Ryten, Mina, Morris, Huw R.

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Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease von Brown, Emmeline E., Blauwendraat, Cornelis, Trinh, Joanne, Rizig, Mie, Nalls, Mike A., Leveille, Etienne, Ruskey, Jennifer A., Jonvik, Hallgeir, Tan, Manuela M.X., Bandres-Ciga, Sara, Hassin-Baer, Sharon, Brockmann, Kathrin, Infante, Jon, Tolosa, Eduardo, Ezquerra, Mario, Ben Romdhan, Sawssan, Benmahdjoub, Mustapha, Arezki, Mohamed, Mhiri, Chokri, Hardy, John, Singleton, Andrew B., Alcalay, Roy N., Gasser, Thomas, Grosset, Donald G., Williams, Nigel M., Pittman, Alan, Gan-Or, Ziv, Fernandez-Santiago, Ruben, Brice, Alexis, Lesage, Suzanne, Farrer, Matthew, Wood, Nicholas, Morris, Huw R.

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Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk von Lubbe, Steven J, Bustos, Bernabe I, Hu, Jing, Krainc, Dimitri, Joseph, Theresita, Hehir, Jason, Tan, Manuela, Zhang, Weijia, Escott-Price, Valentina, Williams, Nigel M, Blauwendraat, Cornelis, Singleton, Andrew B, Morris, Huw R

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Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease von Martinez-Carrasco, Alejandro, Real, Raquel, Lawton, Michael, Iwaki, Hirotaka, Tan, Manuela M. X., Wu, Lesley, Williams, Nigel M., Carroll, Camille, Hu, Michele T. M., Grosset, Donald G., Hardy, John, Ryten, Mina, Foltynie, Tom, Ben-Shlomo, Yoav, Shoai, Maryam, Morris, Huw R.

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Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study von Jabbari, Edwin, Koga, Shunsuke, Valentino, Rebecca R, Reynolds, Regina H, Ferrari, Raffaele, Tan, Manuela M X, Rowe, James B, Dalgard, Clifton L, Scholz, Sonja W, Dickson, Dennis W, Warner, Thomas T, Revesz, Tamas, Höglinger, Günter U, Ross, Owen A, Ryten, Mina, Hardy, John, Shoai, Maryam, Morris, Huw R, Mok, Kin Y., Murphy, David P., Al-Sarraj, Safa, Troakes, Claire, Gentleman, Steve M., Allinson, Kieren S.J., Jaunmuktane, Zane, Holton, Janice L., Lees, Andrew J., Morris, Christopher M., Compta, Yaroslau, Gelpi, Ellen, van Swieten, John C., Rajput, Alex, Ferguson, Leslie, Cookson, Mark R., Gibbs, J. Raphael, Blauwendraat, Cornelis, Ding, Jinhui, Chia, Ruth, Traynor, Bryan J., Pantelyat, Alexander, Viollet, Coralie, Pletnikova, Olga, Troncoso, Juan C., Rosenthal, Liana S., Boxer, Adam L., Respondek, Gesine, Arzberger, Thomas, Roeber, Sigrun, Giese, Armin, Burn, David J., Pavese, Nicola, Gerhard, Alexander, Kobylecki, Christopher, Leigh, P. Nigel, Church, Alistair, T.M. Hu, Michele

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RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts von Brolin, Kajsa, Bandres-Ciga, Sara, Leonard, Hampton, Makarious, Mary B., Blauwendraat, Cornelis, Mata, Ignacio F, Foo, Jia Nee, Pihlstrøm, Lasse, Swanberg, Maria, Gan-Or, Ziv, Tan, Manuela MX

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Parkinson’s families project: a UK-wide study of early onset and familial Parkinson’s disease von Towns, Clodagh, Fang, Zih-Hua, Tan, Manuela M. X., Jasaityte, Simona, Schmaderer, Theresa M., Stafford, Eleanor J., Pollard, Miriam, Tilney, Russel, Hodgson, Megan, Wu, Lesley, Labrum, Robyn, Hehir, Jason, Polke, James, Lange, Lara M., Schapira, Anthony H. V., Bhatia, Kailash P., Singleton, Andrew B., Blauwendraat, Cornelis, Klein, Christine, Houlden, Henry, Wood, Nicholas W., Jarman, Paul R., Morris, Huw R., Real, Raquel

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Genome-wide determinants of mortality and motor progression in Parkinson’s disease von Tan, Manuela M. X., Lawton, Michael A., Pollard, Miriam I., Brown, Emmeline, Real, Raquel, Carrasco, Alejandro Martinez, Bekadar, Samir, Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams-Gray, Caroline H., Andreassen, Ole A., Toft, Mathias, Elbaz, Alexis, Artaud, Fanny, Brice, Alexis, Corvol, Jean-Christophe, Aasly, Jan, Farrer, Matthew J., Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M., Ben-Shlomo, Yoav, Hardy, John, Hu, Michele T. M., Grosset, Donald G., Shoai, Maryam, Pihlstrøm, Lasse, Morris, Huw R.

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Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease von Stolp Andersen, Maren, Tan, Manuela, Holtman, Inge R., Hardy, John, Pihlstrøm, Lasse

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Proxy-analysis of the genetics of cognitive decline in Parkinson’s disease through polygenic scores von Faouzi, Johann, Tan, Manuela, Casse, Fanny, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Mangone, Graziella, Mariani, Louise-Laure, Iwaki, Hirotaka, Colliot, Olivier, Pihlstrøm, Lasse, Corvol, Jean-Christophe

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Early Onset Parkinson's Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report von Norman, Brendan P, Lubbe, Steven J, Tan, Manuela, Warren, Naomi, Morris, Huw R

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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies von Vallerga, Costanza L, Tan, Manuela, Kia, Demis A, Xue, Angli, Young, Emily, Sharma, Manu, Krohn, Lynne, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Botia, Juan A, Martinez, Maria, Jankovic, Joseph, Sutherland, Margaret, Majamaa, Kari, Andreassen, Ole A, Gan-Or, Ziv, Gasser, Thomas, Heutink, Peter, Gratten, Jacob, Alvarez, Ignacio, Alvarez, Victoria, Bandres-Ciga, Sara, Bergareche Yarza, Jesús Alberto, Billingsley, Kimberley, Bonilla-Toribio, Marta, Botía, Juan A, Boungiorno, María Teresa, Bras, Jose, Bubb, Vivien, Buiza-Rueda, Dolores, Cerdan, Debora, Chelban, Viorica, Corvol, Jean-Christophe, Craig, David W, Danjou, Fabrice, Diez-Fairen, Monica, Escott-Price, Valentina, Ezquerra, Mario, Fernández, Manel, Fernández-Santiago, Rubén, Gan-Or, Ziv, Garcia, Ciara, García-Ruiz, Pedro, Hernandez, Dena G, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Kaiyrzhanov, Rauan, Kia, Demis A, Leonard, Hampton L, Lewis, Patrick, Lopez-Sendon, Jose Luis, Lovering, Ruth, Lubbe, Steven, Majamaa, Kari, Manzoni, Claudia, Marti, Maria Jose, Méndez-del-Barrio, Carlota, Middlehurst, Ben, Mínguez, Adolfo, Muñoz, Esteban, Pagola, Ana Gorostidi, Pastor, Pau, Perez Errazquin, Francisco, Periñán-Tocino, Teresa, Reed, Xylena, Rezola, Elisabet Mondragon, Rodriguez, Antonio Sanchez, Ruiz-Martínez, Javier, Sadykova, Dinara, Shashkin, Chingiz, Sierra, María, Simón-Sánchez, Javier, Singleton, Andrew B, Suarez-Sanmartin, Esther, Tabernero, Cesar, Tolosa, Eduard, van Hilten, Jacobus J, Vargas-González, Laura, Wood, Nicholas W, Zimprich, Alexander, Reich, Stephen, Savitt, Joseph, Bryc, Katarzyna, Hicks, Barry, Jiang, Yunxuan, McCreight, Jennifer C., McIntyre, Matthew H., Noblin, Elizabeth S., Sathirapongsasuti, J. Fah, Tung, Joyce, Anderson, Tim, Bentley, Steven, Kennedy, Martin, Mellick, George, Sidorenko, Julia, Silburn, Peter A., Visscher, Peter M., Yang, Jian

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