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    Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study von Rizig, Mie, Bandres-Ciga, Sara, Levine, Kristin S, Adeniji, Olaleye Akinmola, Agabi, Osigwe Paul, Arigbodi, Ohwotemu Michael, Erameh, Cyril Oshomah, Okunoye, Olaitan, Komolafe, Morenikeji Adeyoyin, Odeniyi, Olanike Adedoyin, Ojini, Francis Ibe, D'Souza, Andrea M, Osemwegie, Nosakhare, Leonard, Hampton L, Ozomma, Simon Izuchukwu, Zubair, Yusuf Agboola, Abiodun, Oladunni, Akinyemi, Rufus, Ali, Mohammed, Bello, Abiodun, Erameh, Cyril, Farombi, Temitope, Imarhiagbe, Frank, Iwuozo, Emmanuel, Nwazor, Ernest, Ojini, Francis, Onwuegbuzie, Gerald, Ozomma, Simon, Zubair, Yusuf, Gueumekane Bila lamou, Eric, Shalash, Ali, Khedr, Eman, El-Jaafary, Shaimaa, Hamed, Sharifa, Melka Oda, Dereje, Debebe Gelan, Yohanesse, Charway-Felli, Augustina, Stephen Sarfo, Fred, Koita, Abdou, Bell, Abiodun, Adebowale, Akintunde A., Akpekpe, John, Agu, Christian, Agabi Osigwe, Paul, Balarabe, Salisu, Williams, Uduak, Hilaire Dominique, Ewodo Touna, Mochan, Andre, Ben Djebara, Mouna, Kacem, Imen, Mkada, Imen, Atadzhanov, Masharip, Jama, Fatumah, Hall, Deborah A., Warren, Natalie, Chauppeta, Brian, Rawls, Ashley, O'Grady, Alyssa, Sherer, Todd, Blauwendraat, Cornelis, Brice, Alexis, Illarionova, Anastasia, Quattrone, Andrea, Kishore, Asha, Ahmad-Annuar, Azlina, Mollenhauer, Brit, Carroll, Camille, Rieder, Carlos, KP, Divya, Fon, Edward A., Gatto, Emilia M, Xiromerisiou, Georgia, Hiu-Fai Chan, Germaine, Kaishibayeva, Gulnaz, Leonard, Hampton, Iwaki, Hirotaka, Chen, Honglei, F. Mata, Ignacio, Aasly, Jan O., Kim, Jonggeol Jeff, Lohmann, Katja, Kumar, Kishore, Shulman, Lisa, Parnetti, Lucilla, Periñan Tocino, Maria Teresa, Ibrahim Norlinah, Mohamed, Williams, Nigel, Kaiyrzhanov, Rauan, Krüger, Rejko, Wu, Ruey-Meei, Bandres-Ciga, Sara, Wu, Serena, Lim, Shen-Yang, Ertan, Sibel, Foroud, Tatiana, Pitcher, Toni, Tumas, Vitor, Luo, Wei, Zhou, Xiaopu, Tavadyan, Zaruhi

    Veröffentlicht in Lancet neurology

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