GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10‐Year Population‐Based Study by Szwedo, Aleksandra A., Dalen, Ingvild, Pedersen, Kenn Freddy, Camacho, Marta, Bäckström, David, Forsgren, Lars, Tzoulis, Charalampos, Winder‐Rhodes, Sophie, Hudson, Gavin, Liu, Ganqiang, Scherzer, Clemens R., Lawson, Rachael A., Yarnall, Alison J., Williams‐Gray, Caroline H., Macleod, Angus D., Counsell, Carl E., Tysnes, Ole‐Bjørn, Alves, Guido, Maple‐Grødem, Jodi

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

Motor complications in Parkinson's disease: 13‐year follow‐up of the CamPaIGN cohort by Kim, Han‐Joon, Mason, Sarah, Foltynie, Thomas, Winder‐Rhodes, Sophie, Barker, Roger A., Williams‐Gray, Caroline H.

Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohort by 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.

Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome by 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

Genetic impact on cognition and brain function in newly diagnosed Parkinson’s disease: ICICLE-PD study by Nombela, Cristina, Rowe, James B., Winder-Rhodes, Sophie E., Hampshire, Adam, Owen, Adrian M., Breen, David P., Duncan, Gordon W., Khoo, Tien K., Yarnall, Alison J., Firbank, Michael J., Chinnery, Patrick F., Robbins, Trevor W., O’Brien, John T., Brooks, David J., Burn, David J., Barker, Roger A.

Translational Approaches to Frontostriatal Dysfunction in Attention-Deficit/Hyperactivity Disorder Using a Computerized Neuropsychological Battery by Chamberlain, Samuel R., Robbins, Trevor W., Winder-Rhodes, Sophie, Müller, Ulrich, Sahakian, Barbara J., Blackwell, Andrew D., Barnett, Jennifer H.

Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease by 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.

Association between MAPT haplotype and memory function in patients with Parkinson's disease and healthy aging individuals by Winder-Rhodes, Sophie E., Hampshire, Adam, Rowe, James B., Peelle, Jonathan E., Robbins, Trevor W., Owen, Adrian M., Barker, Roger A.

The role of tau in the pathological process and clinical expression of Huntington’s disease by Vuono, Romina, Winder-Rhodes, Sophie, de Silva, Rohan, Cisbani, Giulia, Drouin-Ouellet, Janelle, Spillantini, Maria G., Cicchetti, Francesca, Barker, Roger A.

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy by 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.

Characterizing mild cognitive impairment in incident Parkinson disease: The ICICLE-PD Study by 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.

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease by Beilina, Alexandria, Rudenko, Iakov N., Kaganovich, Alice, Civiero, Laura, Chau, Hien, Kalia, Suneil K., Kalia, Lorraine V., Lobbestael, Evy, Chia, Ruth, Ndukwe, Kelechi, Ding, Jinhui, Nalls, Mike A., Olszewski, Maciej, Hauser, David N., Kumaran, Ravindran, Lozano, Andres M., Baekelandt, Veerle, Greene, Lois E., Taymans, Jean-Marc, Greggio, Elisa, Cookson, Mark R.

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease by van Rooij, Jeroen, Uitterlinden, André G, Kraaij, Robert, Heutink, Peter, Nalls, Mike A, Plagnol, Vincent, Sharma, Manu, Saad, Mohamad, Simón-Sánchez, Javier, Schulte, Claudia, Lesage, Suzanne, Arepalli, Sampath, Barker, Roger, Ben, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Majounie, Elisa, Charlesworth, Gavin, Lungu, Codrin, Chen, Honglei, Chong, Sean, Clarke, Carl E, Mark Cooper, J, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Dexter, David T, van Dijk, Karin D, Durif, Frank, Dürr, Alexandra, Evans, Jonathan R, Foltynie, Thomas, Gardner, Michelle, Raphael Gibbs, J, Gray, Emma, Guerreiro, Rita, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Wurster, Isabel, Hudson, Gavin, Hunt, Sarah E, Lees, Andrew, Lichtner, Peter, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Riess, Olaf, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Shulman, Joshua, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Bettella, Francesco, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Trabzuni, Daniah, Uitterlinden, André G, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Martinez, Maria, Wood, Nicholas W, Brice, Alexis, Gasser, Thomas

Association between intravascular thermoregulation devices and the development of venous thrombo-embolic phenomenon by Winder-Rhodes, Sophie, Lotay, Rosamund, Doyle, James

Neuropathic Gaucher’s Mutations: Shifting Parkinson’s Into High Gear (S1.002) by Liu, Ganqiang, Boot, Brendon, Locascio, Joseph J., Liao, Zhixiang, Franco, Daly, Duong, Karen, Page, Kara, Jansen, Iris, Yi, Tom, Trisini-Lipsanopoulos, Ana, Dong, Xianjun, Hutten, Samantha J., Winder-Rhodes, Sophie, Amr, Sami, Tanner, Caroline, Lang, Anthony, Nalls, Mike, Eberly, Shirley, Sudarsky, Lewis, Elbaz, Alexis, Brice, Alexis, Ravina, Bernard, Shoulson, Ira, van Hilten, Jacobus, Cormier-Dequaire, Florence, Corvol, Jean-Christophe, Barker, Roger, Heutink, Peter, Marinus, Johan, Williams-Gray, Caroline, Scherzer, Clemens R.

Translational Approaches to Frontostriatal Dysfunction in Attention-Deficit/Hyperactivity Disorder Using a Computerized Neuropsychological Battery: Prefrontal Cortical Circuits Reg... by CHAMBERLAIN, Samuel R, ROBBINS, Trevor W, WINDER-RHODES, Sophie, MÜLLER, Ulrich, SAHAKIAN, Barbara J, BLACKWELL, Andrew D, BARNETT, Jennifer H