GP2: The Global Parkinson's Genetics Program von Tan, Ai Huey, Noyce, Alastair, Carrasco, Alejandro Martinez, Brice, Alexis, Reimer, Alyssa, Illarionova, Anastasia, Singleton, Andrew, Schumacher-Schuh, Artur, Stecher, Benjamin, Siddiqi, Bernadette, Casey, Bradford, Fiske, Brian, Pantazis, Caroline, Klein, Christine, Bale, Claire, Wegel, Claire, Blauwendraat, Cornelis, Vitale, Dan, Hernandez, Dena, Riley, Ekemini, Fisher, Emily, Valente, Enza Maria, Vollstedt, Eva Juliane, Faghri, Faraz, Leonard, Hampton, Iwaki, Hirotaka, Morris, Huw, Sarmiento, Ignacio Juan Keller, Mata, Ignacio, Kim, Jeff, Hardy, John, Murphy, Kaileigh, Lohmann, Katja, Marek, Ken, Mok, Kin, Kumar, Kishore, Lange, Lara, Kuhl, Maggie, Sharma, Manu, Tan, Manuela, Makarious, Mary, Durborow, Michelle, Avenali, Micol, Rizig, Mie, Nalls, Mike, Mencacci, Niccolo, Wood, Nicholas, Williams, Nigel, Okubadejo, Njideka, Okunoye, Olaitan, Lewis, Patrick, Heutink, Peter, Prashanth, L. K., Kruger, Rejko, Rajan, Roopa, Murtadha, Ruqaya, Adams, Sabina, Bandres-Ciga, Sara, Fox, Schuyler, Lim, Shen-Yang, Stott, Simon, Bardien, Soraya, Foroud, Tatiana, Gasser, Thomas, Sherer, Todd, Song, Yeajin, Fang, Zih-Hua

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

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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) von Towns, Clodagh, Richer, Madeleine, Jasaityte, Simona, Stafford, Eleanor J., Joubert, Julie, Antar, Tarek, Martinez-Carrasco, Alejandro, Makarious, Mary B., Casey, Bradford, Vitale, Dan, Levine, Kristin, Leonard, Hampton, Pantazis, Caroline B., Screven, Laurel A., Hernandez, Dena G., Wegel, Claire E., Solle, Justin, Nalls, Mike A., Blauwendraat, Cornelis, Singleton, Andrew B., Tan, Manuela M. X., Iwaki, Hirotaka, Morris, Huw R.

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Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) von Lange, Lara M., Avenali, Micol, Ellis, Melina, Illarionova, Anastasia, Keller Sarmiento, Ignacio J., Tan, Ai-Huey, Madoev, Harutyun, Galandra, Caterina, Junker, Johanna, Roopnarain, Karisha, Solle, Justin, Wegel, Claire, Fang, Zih-Hua, Heutink, Peter, Kumar, Kishore R., Lim, Shen-Yang, Valente, Enza Maria, Nalls, Mike, Blauwendraat, Cornelis, Singleton, Andrew, Mencacci, Niccolo, Lohmann, Katja, Klein, Christine

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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) von 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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