The Progressive Supranuclear Palsy Clinical Deficits Scale von Piot, Ines, Schweyer, Kerstin, Respondek, Gesine, Stamelou, Maria, Sckopke, Philipp, Schenk, Thomas, Goetz, Christopher G., Stebbins, Glenn T., Höglinger, Günter U., Gasser, Thomas, Hermann, Andreas, Höglinger, Günter, Höllerhage, Matthias, Kimmich, Okka, Klockgether, Thomas, Levin, Johannes, Machetanz, Gerrit, Osterrath, Antje, Palleis, Carla, Prudlo, Johannes, Spottke, Annika, Berg, Daniela, Bürk, Katrin, Claßen, Joseph, Eggers, Carsten, Greuel, Andrea, Grimm, Max‐Joseph, Hermann, Lennard, Iankova, Vassilena, Jahn, Klaus, Jost, Wolfgang, Klietz, Martin, Kühn, Andrea, Marxreiter, Franz, Paschen, Steffen, Poetter‐Nerger, Monika, Preisl, Marie‐Therese, Prilop, Lisa, Tönges, Lars, Trenkwalder, Claudia, Warnecke, Tobias, Wegner, Florian, Winkler, Jürgen, Antonini, Angelo, P, Kailash P., L, Adam L., Colosimo, Carlo, Compta, Yaroslau, Corvol, Jean‐Christophe, I, Lawrence I., Höglinger, Günter U., E, Anthony E., Litvan, Irene, R, Huw R., Nilsson, Christer, Pantelyat, Alexander, Respondek, Gesine, Stamelou, Maria

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Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria von Höglinger, Günter U., Respondek, Gesine, Stamelou, Maria, Kurz, Carolin, Josephs, Keith A., Lang, Anthony E., Mollenhauer, Brit, Müller, Ulrich, Nilsson, Christer, Whitwell, Jennifer L., Arzberger, Thomas, Englund, Elisabet, Gelpi, Ellen, Giese, Armin, Irwin, David J., Meissner, Wassilios G., Pantelyat, Alexander, Rajput, Alex, Swieten, John C., Troakes, Claire, Antonini, Angelo, Bhatia, Kailash P., Bordelon, Yvette, Compta, Yaroslau, Corvol, Jean‐Christophe, Colosimo, Carlo, Dickson, Dennis W., Dodel, Richard, Ferguson, Leslie, Grossman, Murray, Kassubek, Jan, Krismer, Florian, Levin, Johannes, Lorenzl, Stefan, Morris, Huw R., Nestor, Peter, Oertel, Wolfgang H., Poewe, Werner, Rabinovici, Gil, Rowe, James B., Schellenberg, Gerard D., Seppi, Klaus, Eimeren, Thilo, Wenning, Gregor K., Boxer, Adam L., Golbe, Lawrence I., Litvan, Irene, Boxer, Adam L., Rajput, Alex, Pantelyat, Alexander, Antonini, Angelo, Lang, Anthony E., Giese, Armin, Mollenhauer, Brit, Colosimo, Carlo, Kurz, Caroline, Nilsson, Christer, Troakes, Claire, Irwin, David J., Dickson, Dennis W., Gelpi, Ellen, Krismer, Florian, Schellenberg, Gerard D., Respondek, Gesine, Rabinovici, Gil, Wenning, Gregor K., Höglinger, Günter U., Morris, Huw R., Litvan, Irene, Rowe, James B., Kassubek, Jan, Corvol, Jean‐Christophe, Whitwell, Jennifer L., Levin, Johannes, van Swieten, John, Bhatia, Kailash P., Josephs, Keith A., Seppi, Klaus, Golbe, Lawrence I., Stamelou, Maria, Grossman, Murray, Nestor, Peter, Dodel, Richard, Lorenzl, Stefan, van Eimeren, Thilo, Arzberger, Thomas, Müller, Ulrich, Meissner, Wassilios G., Poewe, Werner, Oertel, Wolfgang H., Compta, Yaroslau, Bordelon, Yvette

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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease von Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B

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Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease von Robak, Laurie A, Jansen, Iris E, van Rooij, Jeroen, Uitterlinden, André G, Kraaij, Robert, Jankovic, Joseph, Heutink, Peter, Shulman, Joshua M

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Articulatory Changes in Vowel Production following STN DBS and Levodopa Intake in Parkinson's Disease von Langlois, Mélanie, Prud’Homme, Michel, Cantin, Léo, Roy, Johanna-Pascale, Martel Sauvageau, Vincent, Macoir, Joël

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Postural and Balance Disorders in Patients with Parkinson's Disease: A Prospective Open-Label Feasibility Study with Two Months of Action Observation Treatment von Seripa, Davide, Panza, Francesco, Greco, Antonio, Fortunato, Francesca, De Sanctis, Jula Laura, Valeno, Giovanni, Stuppiello, Lucia Anna, Cinone, Nicoletta, Ranieri, Maurizio, Santamato, Andrea, Solfrizzi, Vincenzo

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Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets von Kia, Demis A, Zhang, David, Guelfi, Sebastian, Manzoni, Claudia, Hubbard, Leon, Reynolds, Regina H, Botía, Juan, Ryten, Mina, Ferrari, Raffaele, Lewis, Patrick A, Williams, Nigel, Trabzuni, Daniah, Hardy, John, Wood, Nicholas W

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Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome von Storm, Catherine S., Kia, Demis A., Almramhi, Mona M., Bandres-Ciga, Sara, Finan, Chris, Hingorani, Aroon D., Wood, Nicholas W.

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Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption von Cornelis, M C, Byrne, E M, Esko, T, Nalls, M A, Paynter, N, Monda, K L, Amin, N, Renstrom, F, Cavadino, A, Nolte, I M, Teumer, A, Yu, K, Manichaikul, A, Wojczynski, M K, Vink, J M, Zhao, J H, Burlutsky, G, Lahti, J, Lemaitre, R N, Eriksson, J, Musani, S K, Tanaka, T, Luan, J, Hui, J, Ho, W-K, Magnusson, P K E, Pedersen, N L, Couper, D, Oostra, B A, Tiemeier, H W, Uitterlinden, A G, Barroso, I, Xue, L, Kaakinen, M, Milani, L, Power, C, Baumeister, S E, Biffar, R, Kutalik, Z, Jacobs, D R, Lind, L, Jensen, M, Luben, R N, Wang, J J, Männistö, S, Lehtimäki, T, Viikari, J, Mozaffarian, D, Mukamal, K, Döring, A, Montgomery, G W, Dahmen, N, Tucker, K L, Ferrucci, L, Treur, J L, Mellström, D, Hottenga, J J, Tönjes, A, Deloukas, P, Kanoni, S, Lorentzon, M, Houston, D K, Liu, Y, Mason, M A, Zonderman, A B, Franke, L, Kristal, B S, Karjalainen, J, Reed, D R, Westra, H-J, Evans, M K, Dedoussis, G, Stumvoll, M, Bandinelli, S, Ordovas, J M, Chan, A T, Ohlsson, C, Gieger, C, Martin, N G, Siscovick, D S, Raitakari, O, Eriksson, J G, Mitchell, P, Hunter, D J, Rimm, E B, Borecki, I B, Vollenweider, P, Grabe, H J, Neuhouser, M L, Wolffenbuttel, B H R, Hyppönen, E, Cupples, L A, Franks, P W, van Duijn, C M, Heiss, G, Metspalu, A, North, K E, Ingelsson, E, Nettleton, J A, van Dam, R M

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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease von 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.

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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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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy von Müller, Ulrich, Schellenberg, Gerard D, 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, 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

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Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders von Mencacci, Niccolo E., Reynolds, Regina, Ruiz, Sonia Garcia, Vandrovcova, Jana, Forabosco, Paola, Sanchez-Ferrer, Alvaro, Volpato, Viola, Weale, Michael E., Bhatia, Kailash P., Webber, Caleb, Hardy, John, Botia, Juan A., Ryten, Mina

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Validation of the movement disorder society criteria for the diagnosis of 4‐repeat tauopathies von Respondek, Gesine, Grimm, Max‐Joseph, Piot, Ines, Arzberger, Thomas, Compta, Yaroslau, Englund, Elisabet, Ferguson, Leslie W., Gelpi, Ellen, Roeber, Sigrun, Giese, Armin, Grossman, Murray, Irwin, David J., Meissner, Wassilios G., Nilsson, Christer, Pantelyat, Alexander, Rajput, Alex, Swieten, John C., Troakes, Claire, Höglinger, Günter U., Aiba, Ikuko, Antonini, Angelo, Arzberger, Thomas, Barone, Paolo, Bhatia, Kailash P., Boxer, Adam K., Colosimo, Carlo, Compta, Yaroslau, Corvol, Jean Christophe, Dickson, Dennis W., Gelpi, Ellen, Giese, Armin, Golbe, Lawrence I., Grossman, Murray, Höglinger, Günter U., Hopfner, Franziska, Irwin, David J., Josephs, Keith A., Kassubek, Jan, Kovacs, Gabor G., Lang, Anthony E., Levin, Johannes, Litvan, Irene, Höllerhage, Matthias, McFarland, Nikolaus, Meissner, Wassilios G., Morris, Huw R., Müller, Ulrich, Nilsson, Christer, Oertel, Wolfgang H., Pantelyat, Alexander, Rajput, Alex, Respondek, Gesine, Rowe, James B., Sakakibara, Ruji, Schellenberg, Gerard, Stamelou, Maria, Troakes, Claire, Eimeren, Thilo, Swieten, John C., Wenning, Gregor K., Whitwell, Jennifer L.

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Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing von Jansen, Iris E, Ye, Hui, Heetveld, Sasja, Lechler, Marie C, Michels, Helen, Seinstra, Renée I, Lubbe, Steven J, Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa, Gibbs, J Raphael, Nalls, Mike A, Ryten, Mina, Botia, Juan A, Vandrovcova, Jana, Simon-Sanchez, Javier, Castillo-Lizardo, Melissa, Rizzu, Patrizia, Blauwendraat, Cornelis, Chouhan, Amit K, Li, Yarong, Yogi, Puja, Amin, Najaf, van Duijn, Cornelia M, Morris, Huw R, Brice, Alexis, Singleton, Andrew B, David, Della C, Nollen, Ellen A, Jain, Shushant, Shulman, Joshua M, Heutink, Peter

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Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score von Iwaki, Hirotaka, Makarious, Mary B., Bandrés‐Ciga, Sara, Leonard, Hampton L., Gibbs, J. Raphael, Singleton, Andrew B., Middlehurst, Ben, Kia, Demis A, Houlden, Henry, Morris, Huw R, Plun‐Favreau, Helene, Quinn, John, Mok, Kin Y, Kinghorn, Kerri J., Wood, Nicholas W, Lewis, Patrick, Lovering, Ruth, Rizig, Mie, Ryten, Mina, Guelfi, Sebastian, Escott‐Price, Valentina, Chelban, Viorica, Foltynie, Thomas, Williams, Nigel, Morrison, Karen E., Clarke, Carl, Brice, Alexis, Danjou, Fabrice, Lesage, Suzanne, Martinez, Maria, Simón‐Sánchez, Javier, Heutink, Peter, Rizzu, Patrizia, Sharma, Manu, Gasser, Thomas, Bandres‐Ciga, Sara, Blauwendraat, Cornelis, Craig, David W., Billingsley, Kimberley, Narendra, Derek, Raphael Gibbs, J, Shulman, Joshua M., Iwaki, Hirotaka, Leonard, Hampton L., Nalls, Mike A., Finkbeiner, Steven, Lungu, Codrin, Singleton, Andrew B, Gan‐Or, Ziv, Rouleau, Guy A., Krohn, Lynne, Aguilar, Miquel, Alvarez, Ignacio, Alvarez, Victoria, Barrero, Francisco Javier, Yarza, Jesús Alberto Bergareche, Bonilla‐Toribio, Marta, Boungiorno, María Teresa, Buiza‐Rueda, Dolores, Cámara, Ana, Carrillo, Fátima, Carrión‐Claro, Mario, Cerdan, Debora, Diez‐Fairen, Monica, Dols‐Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla‐Sevilla, Francisco, Feliz, Cici, Fernández, Manel, Gonzalez‐Aramburu, Isabel, Pagola, Ana Gorostidi, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Jimenez‐Escrig, Adriano, Kulisevsky, Jaime, Labrador‐Espinosa, Miguel A., Lopez‐Sendon, Jose Luis, Torres, Irene Martínez, Mir, Pablo, Rezola, Elisabet Mondragon, Periñán‐Tocino, Teresa, Ruiz‐Martínez, Javier, Ruz, Clara, Rodriguez, Antonio Sanchez, Tabernero, Cesar, Tartari, Juan Pablo, Tolosa, Eduard, Valldeoriola, Francesc, Vela, Lydia, Vives, Francisco, Zimprich, Alexander, Koks, Sulev, Siitonen, Ari, Kaiyrzhanov, Coordinator ‐ Rauan, Zharkinbekova, Nazira, Aitkulova, Akbota, Kaishybayeva, Gulnaz, Karimova, Altynay

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The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease von Saez‐Atienzar, Sara, Bonet‐Ponce, Luis, Vitale, Dan, Blauwendraat, Cornelis, Pihlstrøm, Lasse, Gan‐Or, Ziv, Noyce, Alastair J, Middlehurst, Ben, Kia, Demis A, Tan, Manuela, Houlden, Henry, Holmans, Peter, Hardy, John, Mok, Kin Y, Kinghorn, Kerri J., Wood, Nicholas W, Lovering, Ruth, RņBibo, Lea, Rizig, Mie, Ryten, Mina, Guelfi, Sebastian, Escott‐Price, Valentina, Chelban, Viorica, Foltynie, Thomas, Williams, Nigel, Morrison, Karen E., Brice, Alexis, Danjou, Fabrice, Corvol, Jean‐Christophe, Brockmann, Kathrin, Rizzu, Patrizia, Gasser, Thomas, Bandres‐Ciga, Sara, Blauwendraat, Cornelis, Craig, David W., Faghri, Faraz, Gibbs, J Raphael, Hernandez, Dena G., Shulman, Joshua M., Iwaki, Hirotaka, Robak, Laurie, Lubbe, Steven, Mencacci, Niccolo E., Lungu, Codrin, Scholz, Sonja W., Reed, Xylena, Alcalay, Roy N., Hilten, Jacobus J, Marinus, Johan, Aguilar, Miquel, Alvarez, Victoria, Barrero, Francisco Javier, Yarza, Jesɐs Alberto Bergareche, Bernal‐Bernal, Inmaculada, Blazquez, Marta, Bonilla‐Toribio, Marta, Buiza‐Rueda, Dolores, CarriɃn‐Claro, Mario, ClarimɃn, Jordi, Compta, Yaroslau, Casa, Beatrȷz, Dols‐Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Ezquerra, Mario, Feliz, Cici, Garcia, Ciara, Garcȷa‐Ruiz, Pedro, Heredia, Maria Jose Gomez, Gonzalez‐Aramburu, Isabel, Pagola, Ana Gorostidi, Infante, Jon, Jimenez‐Escrig, Adriano, Kulisevsky, Jaime, Munain Arregui, Adolfo LɃpez, Macias, Daniel, Torres, Irene Martȷnez, Marȷn, Juan, Marti, Maria Jose, Martȷnez‐Castrillo, Juan Carlos, Mȳndez‐del‐Barrio, Carlota, Mata, Marina, MuɁoz, Esteban, Pagonabarraga, Javier, Pascual‐Sedano, Berta, PeriɁȥn‐Tocino, Teresa, Ruiz‐Martȷnez, Javier, Rodriguez, Antonio Sanchez, Sierra, Marȷa, Tabernero, Cesar, Tartari, Juan Pablo, Tejera‐Parrado, Cristina, Valldeoriola, Francesc, Vargas‐Gonzȥlez, Laura, Vela, Lydia, Vives, Francisco, Zimprich, Alexander, Koks, Sulev, Hassin‐Baer, Sharon, Nalls, Mike A.

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Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease von Blauwendraat, Cornelis, Reed, Xylena, Kia, Demis A, Gan-Or, Ziv, Lesage, Suzanne, Pihlstrøm, Lasse, Guerreiro, Rita, Gibbs, J. Raphael, Sabir, Marya, Ahmed, Sarah, Ding, Jinhui, Alcalay, Roy N, Hassin-Baer, Sharon, Pittman, Alan M, Brooks, Janet, Edsall, Connor, Hernandez, Dena G, Chung, Sun Ju, Goldwurm, Stefano, Toft, Mathias, Schulte, Claudia, Bras, Jose, Wood, Nicholas W, Brice, Alexis, Morris, Huw R, Scholz, Sonja W, Nalls, Mike A, Singleton, Andrew B, Cookson, Mark R

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The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight von Ahmed, Sarah, Jesús, Silvia, Méndez‐del‐Barrio, Carlota, Vargas‐González, Laura, Tartari, Juan Pablo, Mondragon, Elisabet, Vinagre‐Aragon, Ana, Dols‐Icardo, Oriol, Pascual‐Sedano, Berta, Ezquerra, Mario, Cámara, Ana, Compta, Yaroslau, Fernández, Manel, Sierra, María, Menéndez‐González, Manuel, García‐Ruiz, Pedro, Vela‐Desojo, Lydia, Barrero, Francisco Javier, Mínguez‐Castellanos, Adolfo, Cerdan, Debora, Gomez Heredia, Maria Jose, Feliz, Cici, Lopez‐Sendon, Jose Luis, Martínez Torres, Irene, Kim, Jonggeol Jeffrey, Botia, Juan A., Morrison, Karen E., Morris, Huw, Edsall, Connor, Vives, Francisco, Duran, Raquel, Hoenicka, Janet, Alvarez, Victoria, Marti, Maria José, Singleton, Andrew, Noyce, Alastair J, Holmans, Peter, Trabzuni, Daniah, Bras, Jose, Wood, Nicholas W, Guerreiro, Rita, Guelfi, Sebastian, Chelban, Viorica, Foltynie, Thomas, Morrison, Karen E., Brockmann, Kathrin, Gasser, Thomas, Cookson, Mark R, Blauwendraat, Cornelis, Craig, David W., Faghri, Faraz, Gibbs, J Raphael, Shulman, Joshua M., Leonard, Hampton L., Nalls, Mike A., Robak, Laurie, Lubbe, Steven, Mencacci, Niccolo E., Alcalay, Roy N., Krohn, Lynne, Aguilar, Miquel, Alvarez, Ignacio, Yarza, Jesús Alberto Bergareche, Blazquez, Marta, Botía, Juan A., Boungiorno, María Teresa, Buiza-Rueda, Dolores, Clarimón, Jordi, Casa, Beatríz, Diez-Fairen, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Fernández, Manel, Heredia, Maria Jose Gomez, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Jimenez-Escrig, Adriano, Arregui, Adolfo López de Munain, Marín, Juan, Mata, Marina, Mínguez, Adolfo, Mir, Pablo, Pascual-Sedano, Berta, Pastor, Pau, Errazquin, Francisco Perez, Ruiz-Martínez, Javier, Rodriguez, Antonio Sanchez, Sierra, María, Suarez-Sanmartin, Esther, Tolosa, Eduard, Valldeoriola, Francesc, Vargas-González, Laura, Zimprich, Alexander, Taba, Pille, Dalgard, Clifton L., Adeleye, Adelani, Soltis, Anthony R., Bacikova, Dagmar, Wilkerson, Matthew D.

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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease von KELLER, Margaux F, SAAD, Mohamad, SCHULTE, Claudia, MOSKVINA, Valentina, DURR, Alexandra, HOLMANS, Peter, KILARSKI, Laura L, GUERREIRO, Rita, HERNANDEZ, Dena G, BRICE, Alexis, YLIKOTILA, Pauli, STEFANSSON, Hreinn, BRAS, Jose, MAJAMAA, Kari, MORRIS, Huw R, WILLIAMS, Nigel, GASSER, Thomas, HEUTINK, Peter, WOOD, Nicholas W, HARDY, John, MARTINEZ, Maria, SINGLETON, Andrew B, NALLS, Michael A, BETTELLA, Francesco, NICOLAOU, Nayia, SIMON-SANCHEZ, Javier, MITTAG, Florian, BÜCHEL, Finja, SHARMA, Manu, RAPHAEL GIBBS, J

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