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    Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) by Stafford, Eleanor J., Antar, Tarek, Vitale, Dan, Levine, Kristin, Pantazis, Caroline B., Wegel, Claire E., Nalls, Mike A., Blauwendraat, Cornelis, Morris, Huw R., Gatto, Emilia M., Khachatryan, Samson, Shepherd, Claire E., Koks, Sulev, Zimprich, Alexander, Awad, Paula Saffie, Tumas, Vitor, Camargos, Sarah, Fon, Edward A., Monchi, Oury, Fon, Ted, Galleguillos, Benjamin Pizarro, Miranda, Marcelo, Tang, Beisha, Luo, Wei, Arboleda, Gonzalo, Orozco, Jorge, Brice, Alexis, Westenberger, Ana, Klein, Christine, Vollstedt, Eva-Juliane, Trinh, Joanne, Junker, Johanna, Lohmann, Katja, Groppa, Sergiu, Gasser, Thomas, Fang, Zih-Hua, Akpalu, Albert, Hadjigorgiou, Georgios, Dagklis, Ioannis, Dadiotis, Efthymios, Chan, Germaine Hiu-Fai, Ip, Nancy, Cheung, Nelson Yuk-Fai, Zhou, Xiaopu, Kishore, Asha, Kukkle, Prashanth Lingappa, Salari, Mehri, Quattrone, Andrea, Schirinzi, Tommaso, Kaishibayeva, Gulnaz, Shambetova, Cholpon, Krüger, Rejko, Murad, Nor Azian Abdul, Lim, Shen-Yang, Martinez-Ramirez, Daniel, Sanyaolu, Arinola, Ojo, Oluwadamilola, Cornejo-Olivas, Mario, Rosales, Raymond, Iakovenko, Elena, Amod, Ferzana, Hoenicka, Janet, Beyer, Katrin, Lin, Chin-Hsien, Wu, Hsiu-Chuan, Wu, Yihru, Sassi, Samia Ben, Başak, A. Nazlı, Genc, Gencer, Noyce, Alastair, Schrag, Anette, Schapira, Anthony, Bale, Claire, Grosset, Donald, Hardy, John, Lewis, Patrick Alfryn, Kaiyrzhanov, Rauan, Weil, Rimona, Obese, Vida, Espay, Alberto, Sobering, Andrew K., Comart, Charisse, Wegel, Claire, Hernandez, Dena, Chen, Honglei, Williamson, Jared, Murphy, Kaileigh, Marek, Kenneth, Levine, Kristin S., Screven, Laurel, Ruffrage, Lauren, Shulman, Lisa, Kuhl, Maggie, Puckelwartz, Megan J., Louie, Naomi, Albin, Roger, Chowdhury, Sohini, Xie, Tao, Foroud, Tatiana, Sherer, Todd

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