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    Genome sequence analyses identify novel risk loci for multiple system atrophy von Ray, Anindita, Shah, Zalak, Ruffo, Paola, Fujita, Masashi, Menon, Vilas, Saez-Atienzar, Sara, Reho, Paolo, Kaivola, Karri, Walton, Ronald L, Reynolds, Regina H, Karra, Ramita, Sait, Shaimaa, Akcimen, Fulya, Diez-Fairen, Monica, Alvarez, Ignacio, Fanciulli, Alessandra, Stefanova, Nadia, Seppi, Klaus, Duerr, Susanne, Leys, Fabian, Krismer, Florian, Sidoroff, Victoria, Zimprich, Alexander, Pirker, Walter, Rascol, Olivier, Foubert-Samier, Alexandra, Meissner, Wassilios G, Tison, François, Pavy-Le Traon, Anne, Pellecchia, Maria Teresa, Barone, Paolo, Russillo, Maria Claudia, Marín-Lahoz, Juan, Torres, Soraya, Mir, Pablo, Periñán, Maria Teresa, Proukakis, Christos, Chelban, Viorica, Wu, Lesley, Goh, Yee Y, Parkkinen, Laura, Hu, Michele T, Kobylecki, Christopher, Saxon, Jennifer A, Rollinson, Sara, Garland, Emily, Biaggioni, Italo, Litvan, Irene, Rubio, Ileana, Alcalay, Roy N, Kwei, Kimberly T, Lubbe, Steven J, Mao, Qinwen, Flanagan, Margaret E, Castellani, Rudolph J, Khurana, Vikram, Ndayisaba, Alain, Calvo, Andrea, Mora, Gabriele, Floris, Gianluca, Bohannan, Ryan C, Moore, Anni, Norcliffe-Kaufmann, Lucy, Palma, Jose-Alberto, Kaufmann, Horacio, Kim, Changyoun, Iba, Michiyo, Dawson, Ted M, Rosenthal, Liana S, Pantelyat, Alexander, Albert, Marilyn S, Pletnikova, Olga, Troncoso, Juan C, Infante, Jon, Lage, Carmen, Sánchez-Juan, Pascual, Serrano, Geidy E, Beach, Thomas G, Pastor, Pau, Morris, Huw R, Albani, Diego, Clarimon, Jordi, Wenning, Gregor K, Hardy, John A, Ryten, Mina, Topol, Eric, Torkamani, Ali, Chiò, Adriano, Bennett, David A, De Jager, Philip L, Singer, Wolfgang, Cheshire, William P, Wszolek, Zbigniew K, Dickson, Dennis W, Traynor, Bryan J, Gibbs, J Raphael, Dalgard, Clifton L, Ross, Owen A, Houlden, Henry, Scholz, Sonja W

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