Search Results - Mohamed Nor, Lisa

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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 by 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

    Published in Lancet neurology
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    Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) by Richer, Madeleine, Antar, Tarek, Makarious, Mary B, Levine, Kristin, Leonard, Hampton, Hernandez, Dena G, Blauwendraat, Cornelis, Singleton, Andrew B, Tan, Manuela, Iwaki, Hirotaka, Morris, Huw R, Shepherd, Claire E, Hunter, Julie, Kumar, Kishore, Ellis, Melina, Rentería, Miguel E, Schumacher-Schuh, Artur F, Rieder, Carlos, Camargos, Sarah, Fon, Edward A, Chana, Pedro, Guo, Jifeng, Luo, Wei, Orozco, Jorge, del Rio, Marlene Jimenez, Hernandez, Alvaro, Kamel, Walaa A, Brice, Alexis, Corvol, Jean-Christophe, Mollenhauer, Brit, Klein, Christine, Hopfner, Franziska, Madoev, Harutyun, Trinh, Joanne, Groppa, Sergiu, Gasser, Thomas, Hadjigorgiou, Georgios, Stamelou, Maria, Dadiotis, Efthymios, Medina, Alex, Ip, Nancy, Cheung, Nelson Yuk-Fai, Kp, Divya, Pal, Pramod, Kukkle, Prashanth Lingappa, Quattrone, Andrea, Avenali, Micol, Kaishibayeva, Gulnaz, Tay, Yi Wen, Ojha, Rajeev, Anderson, Tim J, Pitcher, Toni L, Sanyaolu, Arinola, Pihlstrøm, Lasse, Doquenia, Maria Leila, Rosales, Raymond, Vinuela, Angel, Iakovenko, Elena, Mubarak, Bashayer Al, Bardien, Soraya, Kim, Yun Joong, Periñan, Maria Teresa, Pastor, Pau, Wu, Hsiu-Chuan, Wu, Ruey-Meei, Wu, Yihru, Başak, A. Nazlı, Schrag, Anette, Bale, Claire, Hardy, John, Mok, Kin Ying, Wood, Nicholas, Williams, Nigel, Okunoye, Olaitan, Weil, Rimona, Jasaitye, Simona, O’Grady, Alyssa, Sobering, Andrew K, Jonas, Cabell, Comart, Charisse, Wegel, Claire, Hall, Deborah, Hernandez, Dena, Shulman, Joshua, Solle, Justin C, Nuytemans, Karen, Chahine, Lana M, Screven, Laurel, Marsili, Luca, Kuhl, Maggie, Dean, Marissa, Mencacci, Niccolò Emanuele, Albin, Roger, Alcalay, Roy, Lubbe, Steven, Foroud, Tatiana, Sherer, Todd, Song, Yeajin, Nguyen, Duan, Nguyen, Toan

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