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GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians

by Crea, Peter Wild, Noyce, Alastair J., Kauffman, Marcelo, Tavadyan, Zaruhi, Hunter, Julie, Rentería, Miguel E., Koks, Sulev, Rieder, Carlos, Awad, Paula Saffie, Fon, Ted, Olguin, Patricio, Chan, Piu, Luo, Wei, Arboleda, Gonzalo, Hernandez, Alvaro, Salama, Mohamed, Westenberger, Ana, Illarionova, Anastasia, Hopfner, Franziska, Madoev, Harutyun, Junker, Johanna, Fang, Zih‐Hua, Xiromerisiou, Georgia, Dagklis, Ioannis, Stefanis, Leonidas, Medina, Alex, Divya, KP, Rajan, Roopa, Borgohain, Rupam, Salari, Mehri, Quattrone, Andrea, Hattori, Nobutaka, Shiraishi, Tomotaka, Krüger, Rejko, Ahmad‐Annuar, Azlina, Norlinah, Mohamed Ibrahim, Azmin, Shahrul, Lim, Shen‐Yang, Ojha, Rajeev, Okubadejo, Njideka, Cornejo‐Olivas, Mario, Rosales, Raymond, Iakovenko, Elena, Bardien, Soraya, Jeon, Beomseok, Cubo, Esther, Beyer, Katrin, Zweier, Christiane, Tinkhauser, Gerd, Lin, Chin‐Hsien, Amouri, Rim, Başak, A. Nazlı, Genc, Gencer, Çakmak, Özgür Öztop, Ertan, Sibel, Grosset, Donald, Morris, Huw R, Williams, Nigel, Lewis, Patrick Alfryn, Weil, Rimona, Stott, Simon, Jasaityte, Simona, Obese, Vida, Espay, Alberto, O'Grady, Alyssa, Fiske, Brian, Jonas, Cabell, Cruchaga, Carlos, Pantazis, Caroline B., Blauwendraat, Cornelis, Vitale, Dan, Mata, Ignacio F., Sarmiento, Ignacio Juan Keller, Kim, Jonggeol Jeff, Jankovic, Joseph, Murphy, Kaileigh, Kieburtz, Karl, Andersh, Kate, Markopoulou, Katerina, Levine, Kristin S., Ibanez, Laura, Marsili, Luca, Makarious, Mary B, Nalls, Mike A., Mencacci, Niccolò Emanuele, Albin, Roger, Chowdhury, Sohini, Foroud, Tatiana, Njideka, Okubadejo, Sani, Abubakar, Uchechi, Agulanna, Rufus, Akinyemi, Abiodun, Bello, Daniel, Ezuduemoih, Evewero, Ikwenu, Morenikeji, Komolafe, Paul, Nwani, Franscisca, Nwaokorie, Godwin, Osaigbovo, Simon, Ozomma
Published in Movement disorders (01.04.2024)

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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
Published in NPJ Parkinson's Disease (12.09.2023)

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Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

by Ellis, Melina, Illarionova, Anastasia, Tan, Ai-Huey, Roopnarain, Karisha, Valente, Enza Maria, Blauwendraat, Cornelis, Gatto, Emilia M., Khachatryan, Samson, Shepherd, Claire E., Tumas, Vitor, Fon, Edward A., Monchi, Oury, Galleguillos, Benjamin Pizarro, Miranda, Marcelo, Bustamante, Maria Leonor, Chana, Pedro, Tang, Beisha, Shang, Huifang, Orozco, Jorge, Kamel, Walaa A., Brice, Alexis, Corvol, Jean-Christophe, Mollenhauer, Brit, Klein, Christine, Höglinger, Günter, Trinh, Joanne, Sharma, Manu, Fang, Zih-Hua, Xiromerisiou, Georgia, Stefanis, Leonidas, Chan, Germaine Hiu-Fai, Kishore, Asha, KP, Divya, Pal, Pramod, Rajan, Roopa, Borgohain, Rupam, Salari, Mehri, Quattrone, Andrea, Funayama, Manabu, Karimova, Altynay, Kaishibayeva, Gulnaz, Shambetova, Cholpon, Krüger, Rejko, Ahmad-Annuar, Azlina, Norlinah, Mohamed Ibrahim, Azmin, Shahrul, Mohamed, Wael, Martinez-Ramirez, Daniel, Anderson, Tim J., Sanyaolu, Arinola, Okubadejo, Njideka, Cornejo-Olivas, Mario, Rosales, Raymond, Iakovenko, Elena, Umair, Muhammad, Tan, Eng-King, Amod, Ferzana, Bardien, Soraya, Jeon, Beomseok, Cubo, Esther, Hoenicka, Janet, El-Sadig, Sarah, Zweier, Christiane, Paul, Krack, Lin, Chin-Hsien, Amouri, Rim, Çakmak, Özgür Öztop, Noyce, Alastair, Schapira, Anthony, Carroll, Camille, Stafford, Eleanor J., Houlden, Henry, Hardy, John, Williams, Nigel, Kaiyrzhanov, Rauan, Love, Seth, Stott, Simon, Jasaitye, Simona, Obese, Vida, Espay, Alberto, O’Grady, Alyssa, Sobering, Andrew K., Hall, Deborah, Hernandez, Dena, Shiamim, Ejaz, Serrano, Geidy E., Chen, Honglei, Shulman, Joshua, Marek, Kenneth, Levine, Kristin S., Ruffrage, Lauren, Nalls, Mike A., Mencacci, Niccolò Emanuele, Albin, Roger, Bandres-Ciga, Sara, Chowdhury, Sohini, Xie, Tao, Foroud, Tatiana, Sherer, Todd, Song, Yeajin
Published in NPJ Parkinson's Disease (13.09.2023)

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