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Blauwendraat, Cornelis, Reed, Xylena, Kia, Demis A, Gan-Or, Ziv, Lesage, Suzanne, Pihistrom, Lasse, Guerreiro, Rita, Gibbs, J Raphael, Sabir, Marya, Ahmed, Sarah et al (show 19 more authors) , 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 and Cookson, Mark R (2018) Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease. JAMA NEUROLOGY, 75 (11). pp. 1416-1422.

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Grover, Sandeep, Kumar Sreelatha, Ashwin Ashok, Pihlstrom, Lasse, Domenighetti, Cloe, Schulte, Claudia, Sugier, Pierre-Emmanuel, Radivojkov-Blagojevic, Milena, Lichtner, Peter, Mohamed, Oceane, Portugal, Berta et al (show 73 more authors) , Landoulsi, Zied, May, Patrick, Bobbili, Dheeraj, Edsall, Connor, Bartusch, Felix, Hanussek, Maximilian, Krueger, Jens, Hernandez, Dena G, Blauwendraat, Cornelis, Mellick, George D, Zimprich, Alexander, Pirker, Walter, Tan, Manuela, Rogaeva, Ekaterina, Lang, Anthony, Koks, Sulev ORCID: 0000-0001-6087-6643, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean-Christophe, Chartier-Harlin, Marie-Christine, Mutez, Eugenie, Brockmann, Kathrin, Deutschlaender, Angela B, Hadjigeorgiou, Georges M, Dardiotis, Efthimos, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Straniero, Letizia, Zecchinelli, Anna, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Burbulla, Lena F, Matsuo, Hirotaka, Kawamura, Yusuke, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Pavelka, Lukas, van de Warrenburg, Bart PC, Bloem, Bastiaan R, Singleton, Andrew B, Aasly, Jan, Toft, Mathias, Guedes, Leonor Correia, Ferreira, Joaquim J, Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez-Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy L, Ran, Caroline, Belin, Andrea C, Puschmann, Andreas, Hellberg, Clara, Clarke, Carl E, Morrison, Karen E, Krainc, Dimitri, Farrer, Matt J, Kruger, Rejko, Elbaz, Alexis, Gasser, Thomas and Sharma, Manu (2022) Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Evidence From the COURAGE-PD Consortium. NEUROLOGY, 99 (7). E698-E710.

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Nalls, Mike A, Blauwendraat, Cornelis, Vallerga, Costanza L, Heilbron, Karl, Bandres-Ciga, Sara, Chang, Diana, Tan, Manuela, Kia, Demis A, Noyce, Alastair J, Xue, Angli et al (show 260 more authors) , Bras, Jose, Young, Emily, von Coelln, Rainer, Simón-Sánchez, Javier, Schulte, Claudia, Sharma, Manu, Krohn, Lynne, Pihlstrøm, Lasse, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Faghri, Faraz, Gibbs, J Raphael, Hernandez, Dena G, Scholz, Sonja W, Botia, Juan A, Martinez, Maria, Corvol, Jean-Christophe, Lesage, Suzanne, Jankovic, Joseph, Shulman, Lisa M, Sutherland, Margaret, Tienari, Pentti, Majamaa, Kari, Toft, Mathias, Andreassen, Ole A, Bangale, Tushar, Brice, Alexis, Yang, Jian, Gan-Or, Ziv, Gasser, Thomas, Heutink, Peter, Shulman, Joshua M, Wood, Nicholas W, Hinds, David A, Hardy, John A, Morris, Huw R, Gratten, Jacob, Visscher, Peter M, Graham, Robert R, Singleton, Andrew B, Adarmes-Gómez, Astrid D, Aguilar, Miquel, Aitkulova, Akbota, Akhmetzhanov, Vadim, Alcalay, Roy N, Alvarez, Ignacio, Alvarez, Victoria, Bandres-Ciga, Sara, Barrero, Francisco Javier, Bergareche Yarza, Jesús Alberto, Bernal-Bernal, Inmaculada, Billingsley, Kimberley, Blauwendraat, Cornelis, Blazquez, Marta, Bonilla-Toribio, Marta, Botía, Juan A, Boungiorno, María Teresa, Bras, Jose, Brice, Alexis, Brockmann, Kathrin, Bubb, Vivien ORCID: 0000-0003-2763-7004, Buiza-Rueda, Dolores, Cámara, Ana, Carrillo, Fátima, Carrión-Claro, Mario, Cerdan, Debora, Chelban, Viorica, Clarimón, Jordi, Clarke, Carl, Compta, Yaroslau, Cookson, Mark R, Corvol, Jean-Christophe, Craig, David W, Danjou, Fabrice, Diez-Fairen, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla-Sevilla, Francisco, Escott-Price, Valentina, Ezquerra, Mario, Faghri, Faraz, Feliz, Cici, Fernández, Manel, Fernández-Santiago, Rubén, Finkbeiner, Steven, Foltynie, Thomas, Gan-Or, Ziv, Garcia, Ciara, García-Ruiz, Pedro, Gasser, Thomas, Gibbs, J Raphael, Gomez Heredia, Maria Jose, Gómez-Garre, Pilar, González, Manuel Menéndez, Gonzalez-Aramburu, Isabel, Guelfi, Sebastian, Guerreiro, Rita, Hardy, John, Hassin-Baer, Sharon, Hernandez, Dena G, Heutink, Peter, Hoenicka, Janet, Holmans, Peter, Houlden, Henry, Infante, Jon, Iwaki, Hirotaka, Jesús, Silvia, Jimenez-Escrig, Adriano, Kaishybayeva, Gulnaz, Kaiyrzhanov, Rauan, Karimova, Altynay, Kia, Demis A, Kinghorn, Kerri J, Koks, Sulev ORCID: 0000-0001-6087-6643, Krohn, Lynne, Kulisevsky, Jaime, Labrador-Espinosa, Miguel A, Leonard, Hampton L, Lesage, Suzanne, Lewis, Patrick, Lopez-Sendon, Jose Luis, Lovering, Ruth, Lubbe, Steven, Lungu, Codrin, Macias, Daniel, Majamaa, Kari, Manzoni, Claudia, Marín, Juan, Marinus, Johan, Marti, Maria Jose, Martinez, Maria, Martínez Torres, Irene, Martínez-Castrillo, Juan Carlos, Mata, Marina, Mencacci, Niccolo E, Méndez-del-Barrio, Carlota, Middlehurst, Ben, Mínguez, Adolfo, Mir, Pablo, Mok, Kin Y, Morris, Huw R, Muñoz, Esteban, Nalls, Mike A, Narendra, Derek, Noyce, Alastair J, Ojo, Oluwadamilola O, Okubadejo, Njideka U, Pagola, Ana Gorostidi, Pastor, Pau, Perez Errazquin, Francisco, Periñán-Tocino, Teresa, Pihlstrom, Lasse, Plun-Favreau, Helene, Quinn, John ORCID: 0000-0003-3551-7803, R'Bibo, Lea, Reed, Xylena, Rezola, Elisabet Mondragon, Rizig, Mie, Rizzu, Patrizia, Robak, Laurie, Rodriguez, Antonio Sanchez, Rouleau, Guy A, Ruiz-Martínez, Javier, Ruz, Clara, Ryten, Mina, Sadykova, Dinara, Scholz, Sonja W, Schreglmann, Sebastian, Schulte, Claudia, Sharma, Manu, Shashkin, Chingiz, Shulman, Joshua M, Sierra, María, Siitonen, Ari, Simón-Sánchez, Javier, Singleton, Andrew B, Suarez-Sanmartin, Esther, Taba, Pille, Tabernero, Cesar, Tan, Manuela X, Tartari, Juan Pablo, Tejera-Parrado, Cristina, Toft, Mathias, Tolosa, Eduard, Trabzuni, Daniah, Valldeoriola, Francesc, van Hilten, Jacobus J, Van Keuren-Jensen, Kendall, Vargas-González, Laura, Vela, Lydia, Vives, Francisco, Williams, Nigel, Wood, Nicholas W, Zharkinbekova, Nazira, Zharmukhanov, Zharkyn, Zholdybayeva, Elena, Zimprich, Alexander, Ylikotila, Pauli, Shulman, Lisa M, von Coelln, Rainer, Reich, Stephen, Savitt, Joseph, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Elson, Sarah L, Fontanillas, Pierre, Furlotte, Nicholas A, Huber, Karen E, Hicks, Barry, Jewett, Ethan M, Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K, McCreight, Jennifer C, McIntyre, Matthew H, McManus, Kimberly F, Mountain, Joanna L, Noblin, Elizabeth S, Northover, Carrie AM, Pitts, Steven J, Poznik, G David, Sathirapongsasuti, J Fah, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce, Vacic, Vladimir, Wang, Xin, Wilson, Catherine H, Anderson, Tim, Bentley, Steven, Dalrymple-Alford, John, Fowdar, Javed, Gratten, Jacob, Halliday, Glenda, Henders, Anjali K, Hickie, Ian, Kassam, Irfahan, Kennedy, Martin, Kwok, John, Lewis, Simon, Mellick, George, Montgomery, Grant, Pearson, John, Pitcher, Toni, Sidorenko, Julia, Silburn, Peter A, Vallerga, Costanza L, Visscher, Peter M, Wallace, Leanne, Wray, Naomi R, Xue, Angli, Yang, Jian and Zhang, Futao (2019) Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 18 (12). pp. 1091-1102.

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Domenighetti, Cloe, Douillard, Venceslas, Sugier, Pierre-Emmanuel, Sreelatha, Ashwin Ashok Kumar, Schulte, Claudia, Grover, Sandeep, May, Patrick, Bobbili, Dheeraj R, Radivojkov-Blagojevic, Milena, Lichtner, Peter et al (show 70 more authors) , Singleton, Andrew B, Hernandez, Dena G, Edsall, Connor, Gourraud, Pierre-Antoine, Mellick, George D, Zimprich, Alexander, Pirker, Walter, Rogaeva, Ekaterina, Lang, Anthony E, Koks, Sulev ORCID: 0000-0001-6087-6643, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean-Christophe, Chartier-Harlin, Marie-Christine, Mutez, Eugenie, Brockmann, Kathrin, Deutschlander, Angela B, Hadjigeorgiou, Georges M, Dardiotis, Efthimos, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Duga, Stefano, Straniero, Letizia, Zecchinelli, Anna, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Matsuo, Hirotaka, Nakayama, Akiyoshi, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Kolber, Pierre, van de Warrenburg, Bart PC, Bloem, Bastiaan R, Aasly, Jan, Toft, Mathias, Pihlstrom, Lasse, Correia Guedes, Leonor, Ferreira, Joaquim J, Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez-Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy L, Ran, Caroline, Belin, Andrea C, Puschmann, Andreas, Ygland Rodstrom, Emil, Clarke, Carl E, Morrison, Karen E, Tan, Manuela, KraincMD, Dimitri, Burbulla, Lena F, Farrer, Matt J, Kruger, Rejko, Gasser, Thomas, Sharma, Manu, Vince, Nicolas and Elbaz, Alexis (2022) The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited. MOVEMENT DISORDERS, 37 (9). pp. 1929-1937.

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Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Iwaki, Hirotaka ORCID: 0000-0002-8982-7885, Makarious, Mary B, Bandres-Ciga, Sara, Leonard, Hampton L, Grenn, Francis P, Lake, Julie ORCID: 0000-0002-3441-2455, Krohn, Lynne ORCID: 0000-0001-6554-1666, Tan, Manuela, Kim, Jonggeol J et al (show 28 more authors) , Gibbs, Jesse R, Hernandez, Dena G, Ruskey, Jennifer A, Pihlstrøm, Lasse ORCID: 0000-0002-7635-8645, Toft, Mathias ORCID: 0000-0002-6723-6865, van Hilten, Jacobus J, Marinus, Johan, Schulte, Claudia, Brockmann, Kathrin ORCID: 0000-0002-7515-8596, Sharma, Manu ORCID: 0000-0002-1260-5416, Siitonen, Ari, Majamaa, Kari, Eerola-Rautio, Johanna, Tienari, Pentti J, Grosset, Donald G, Lesage, Suzanne, Corvol, Jean-Christophe, Brice, Alexis, Wood, Nick, Hardy, John, Gan-Or, Ziv ORCID: 0000-0003-0332-234X, Heutink, Peter, Gasser, Thomas, Morris, Huw R, Noyce, Alastair J ORCID: 0000-0003-3027-5497, Nalls, Mike A, Singleton, Andrew B and International Parkinson's Disease Genomics Consortium (IPDGC), (2021) Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease. Annals of neurology, 90 (1). pp. 35-42.

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Sugier, Pierre-Emmanuel, Lucotte, Elise H, Domenighetti, Cloe M, Law, Matthew, Iles, Mark, Brown, Kevin D, Amos, Christopher J, McKay, James, Hung, Rayjean, Karimi, Mojgan et al (show 84 more authors) , Bacq-Daian, Delphine, Boland-Auge, Anne, Olaso, Robert, Deleuze, Jean-francois, Lesueur, Fabienne, Ostroumova, Evgenia, Kesminiene, Ausrele, de Vathaire, Florent, Guenel, Pascal, Sreelatha, Ashwin Ashok Kumar, Schulte, Claudia, Grover, Sandeep R, May, Patrick, Bobbili, Dheeraj, Radivojkov-Blagojevic, Milena B, Lichtner, Peter G, Singleton, Andrew, Hernandez, Dena D, Edsall, Connor, Mellick, George, Zimprich, Alexander, Pirker, Walter E, Rogaeva, Ekaterina, Lang, Anthony, Koks, Sulev ORCID: 0000-0001-6087-6643, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean-Christophe, Chartier-Harlin, Marie-Christine, Mutez, Eugenie B, Brockmann, Kathrin M, Deutschlaender, Angela, Hadjigeorgiou, Georges, Dardiotis, Efthimios, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Straniero, Letizia, Zecchinelli, Anna, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Matsuo, Hirotaka, Nakayama, Akiyoshi, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Kolber, Pierre R, van de Warrenburg, Bart PC, Bloem, Bastiaan, Aasly, Jan, Toft, Mathias, Pihlstrom, Lasse J, Guedes, Leonor Correia, Ferreira, Joaquim, Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez-Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy C, Ran, Caroline, Belin, Andrea, Puschmann, Andreas E, Roedstroem, Emil Ygland E, Clarke, Carl, Morrison, Karen, Tan, Manuela F, Krainc, Dimitri J, Burbulla, Lena, Farrer, Matt, Kruger, Rejko, Gasser, Thomas, Sharma, Manu, Truong, Therese and Elbaz, Alexis (2023) Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. MOVEMENT DISORDERS, 38 (4). pp. 604-615.

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Liu, Hui ORCID: 0000-0001-5308-0874, Dehestani, Mohammad, Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Makarious, Mary B, Leonard, Hampton, Kim, Jonggeol J, Schulte, Claudia, Noyce, Alastair ORCID: 0000-0003-3027-5497, Jacobs, Benjamin M, Foote, Isabelle ORCID: 0000-0002-0253-4116 et al (show 6 more authors) , Sharma, Manu ORCID: 0000-0002-1260-5416, International Parkinson's Disease Genomics Consortium; Comprehen, , Nalls, Mike, Singleton, Andrew, Gasser, Thomas and Bandres-Ciga, Sara ORCID: 0000-0003-0056-1361 (2022) Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors. Annals of neurology, 92 (2). pp. 270-278.

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Fernandez-Santiago, Ruben, Martin-Flores, Nuria, Antonelli, Francesca, Cerquera, Catalina, Moreno, Veronica, Bandres-Ciga, Sara, Manduchi, Elisabetta, Tolosa, Eduard, Singleton, Andrew B, Moore, Jason H et al (show 152 more authors) , Noyce, Alastair J, Kaiyrzhanov, Rauan, Middlehurst, Ben, Kia, Demis A, Tan, Manuela, Houlden, Henry, Morris, Huw R, Plun-Favreau, Helene, Holmans, Peter, Hardy, John, Trabzuni, Daniah, Bras, Jose, Quinn, John ORCID: 0000-0003-3551-7803, Mok, Kin Y, Kinghorn, Kerri J, Billingsley, Kimberley, Wood, Nicholas W, Lewis, Patrick, Schreglmann, Sebastian, Guerreiro, Rita, Lovering, Ruth, R'Bibo, Lea, Manzoni, Claudia, 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, Corvol, Jean-Christophe, Martinez, Maria, Schulte, Claudia, Brockmann, Kathrin, Simon-Sanchez, Javier, Heutink, Peter, Rizzu, Patrizia, Sharma, Manu, Gasser, Thomas, Nicolas, Aude, Cookson, Mark R, Bandres-Ciga, Sara, Blauwendraat, Cornelis, Craig, David W, Faghri, Faraz, Gibbs, J Raphael, Hernandez, Dena G, Van Keuren-Jensen, Kendall, Shulman, Joshua M, Iwaki, Hirotaka, Leonard, Hampton L, Nalls, Mike A, Robak, Laurie, Lubbe, Steven, Finkbeiner, Steven, Mencacci, Niccolo E, Lungu, Codrin, Singleton, Andrew B, Scholz, Sonja W, Reed, Xylena, Alcalay, Roy N, Gan-Or, Ziv, Rouleau, Guy A, Krohn, Lynne, van Hilten, Jacobus J, Marinus, Johan, Adarmes-Gomez, Astrid D, Aguilar, Iquel, Alvarez, Ignacio, Alvarez, Victoria, Javier Barrero, Francisco, Bergareche Yarza, Jesus Alberto, Bernal-Bernal, Inmaculada, Blazquez, Marta, Bonilla-Toribio, Marta, Botia, Juan A, Teresa Boungiorno, Maria, Buiza-Rueda, Dolores, Camara, Ana, Carrillo, Fatima, Carrion-Claro, Mario, Cerdan, Debora, Clarimon, Jordi, Compta, Yaroslau, de la Casa, Beatriz, Diez-Fairen, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla-Sevilla, Francisco, Ezquerra, Mario, Feliz, Cici, Fernandez, Manel, Fernandez-Santiago, Ruben, Garcia, Ciara, Garcia-Ruiz, Pedro, Gomez-Garre, Pilar, Gomez Heredia, Maria Jose, Gonzalez-Aramburu, Isabel, Gorostidi Pagola, Ana, Hoenicka, Janet, Infante, Jon, Jesus, Silvia, Jimenez-Escrig, Adriano, Kulisevsky, Jaime, Labrador-Espinosa, Miguel A, Luis Lopez-Sendon, Jose, de Munain Arregui, Adolfo Lopez, Macias, Daniel, Martinez Torres, Irene, Marin, Juan, Jose Marti, Maria, Martinez-Castrillo, Carlos, Mendez-del-Barrio, Carlota, Menendez Gonzalez, Manuel, Mata, Marina, Minguez, Adolfo, Mir, Pablo, Mondragon Rezola, Elisabet, Munoz, Esteban, Pagonabarraga, Javier, Pascual-Sedano, Berta, Pastor, Pau, Perez Errazquin, Francisco, Perinan-Tocino, Teresa, Ruiz-Martinez, Javier, Ruz, Clara, Sanchez Rodriguez, Antonio, Sierra, Maria, Suarez-Sanmartin, Esther, Tabernero, Cesar, Pablo Tartari, Juan, Tejera-Parrado, Cristina, Tolosa, Eduard, Valldeoriola, Francesc, Vargas-Gonzalez, Laura, Vela, Lydia, Vives, Francisco, Zimprich, Alexander, Pihlstrom, Lasse, Toft, Mathias, Koks, Sulev ORCID: 0000-0001-6087-6643, Taba, Pille, Hassin-Baer, Sharon, Marti, Maria-Josep, Ezquerra, Mario and Malagelada, Cristina (2019) SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease. MOVEMENT DISORDERS, 34 (9). pp. 1333-1344.

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Sailer, Anna, Scholz, Sonja W, Nalls, Michael A, Schulte, Claudia, Federoff, Monica, Price, T Ryan, Lees, Andrew ORCID: 0000-0002-2476-4385, Ross, Owen A, Dickson, Dennis W, Mok, Kin et al (show 35 more authors) , Mencacci, Niccolo E, Schottlaender, Lucia, Chelban, Viorica, Ling, Helen, O'Sullivan, Sean S, Wood, Nicholas W, Traynor, Bryan J, Ferrucci, Luigi, Federoff, Howard J, Mhyre, Timothy R, Morris, Huw R, Deuschl, Gunther, Quinn, Niall, Widner, Hakan, Albanese, Alberto, Infante, Jon, Bhatia, Kailash P, Poewe, Werner, Oertel, Wolfgang, Hoglinger, Gunter U, Wullner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Ferreira, Joaquim, Tolosa, Eduardo, Bloem, Bastiaan R, Rascol, Olivier, Meissner, Wassilios G, Hardy, John A, Revesz, Tamas, Holton, Janice L, Gasser, Thomas, Wenning, Gregor K, Singleton, Andrew B and Houlden, Henry (2016) A genome-wide association study in multiple system atrophy. NEUROLOGY, 87 (15). pp. 1591-1598.