Genetic Dystonias: Update on Classification and New Genetic Discoveries von Keller Sarmiento, Ignacio Juan, Mencacci, Niccolò Emanuele

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YY1‐Related Dystonia: Clinical Aspects and Long‐Term Response to Deep Brain Stimulation von Zorzi, Giovanna, Keller Sarmiento, Ignacio Juan, Danti, Federica Rachele, Bustos, Bernabe I., Invernizzi, Federica, Panteghini, Celeste, Reale, Chiara, Garavaglia, Barbara, Chiapparini, Luisa, Lubbe, Steven J., Nardocci, Nardo, Mencacci, Niccolò E.

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Childhood‐Onset Chorea Caused by a Recurrent De Novo DRD2 Variant von Mencacci, Niccolò E., Steel, Dora, Magrinelli, Francesca, Hsu, Jerry, Keller Sarmiento, Ignacio Juan, Troncoso Schifferli, Mónica, Muñoz, Daniela, Stefanis, Leonidas, Lubbe, Steven J., Wood, Nicholas W., Kurian, Manju A., Stamelou, Maria

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Childhood‐Onset Lower Limb Focal Dystonia Due to a NAA15 Variant: A Case Report von Danti, Federica Rachele, Sarmiento, Ignacio Juan Keller, Moloney, Patrick B., Colangelo, Isabel, Graziola, Federica, Garavaglia, Barbara, Zorzi, Giovanna, Mencacci, Niccolò E., Lubbe, Steven J.

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Rising evidence for neurological involvement in COVID-19 pandemic von Calcagno, Narghes, Colombo, Eleonora, Maranzano, Alessio, Pasquini, Jacopo, Keller Sarmiento, Ignacio Juan, Trogu, Francesca, Silani, Vincenzo

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Efficacy and safety of nabiximols (Sativex®) on multiple sclerosis spasticity in a real-life Italian monocentric study von Ferrè, Laura, Nuara, Arturo, Pavan, Giulia, Radaelli, Marta, Moiola, Lucia, Rodegher, Mariaemma, Colombo, Bruno, Keller Sarmiento, Ignacio Juan, Martinelli, Vittorio, Leocani, Letizia, Martinelli Boneschi, Filippo, Comi, Giancarlo, Esposito, Federica

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GP2: The Global Parkinson's Genetics Program

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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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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 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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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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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease von Vitale, Dan, Otani, Diego Véliz, Aslibekyan, Stella, Babalola, Elizabeth, Bell, Robert K, Bryc, Katarzyna, Dhamija, Devika, Elson, Sarah L, Eriksson, Nicholas, Fontanillas, Pierre, Freyman, Will, Granka, Julie M, Hicks, Barry, Hinds, David A, Llamas, Bianca A, Nandakumar, Priyanka, Nguyen, Dominique T, Poznik, G. David, Shastri, Anjali J, Shringarpure, Suyash, Tung, Joyce Y, Wang, Wei, Weldon, Catherine H, Wilton, Peter, Makarious, Mary B, Gatto, Emilia M, Shepherd, Claire E, Hunter, Julie, Koks, Sulev, Fon, Ted, Galleguillos, Benjamin Pizarro, Bustamante, Maria Leonor, Chana, Pedro, Chan, Piu, Luo, Wei, del Rio, Marlene Jimenez, Hernandez, Alvaro, Corvol, Jean-Christophe, Illarionova, Anastasia, Mollenhauer, Brit, Lohmann, Katja, Fang, Zih-Hua, Hadjigorgiou, Georgios, Dagklis, Ioannis, Dadiotis, Efthymios, Cheung, Nelson Yuk-Fai, Zhou, Xiaopu, Salari, Mehri, Valente, Enza Maria, Parnetti, Lucilla, Schirinzi, Tommaso, Hattori, Nobutaka, Tan, Ai Huey, Murad, Nor Azian Abdul, Azmin, Shahrul, Lim, Shen-Yang, Martinez-Ramirez, Daniel, Rodriguez-Violante, Mayela, Reyes-Pérez, Paula, Tserensodnom, Bayasgalan, Ojha, Rajeev, Pitcher, Toni L, Sanyaolu, Arinola, Ur-Rehman, Shoaib, Cornejo-Olivas, Mario, Doquenia, Maria Leila, Vinuela, Angel, Iakovenko, Elena, Jeon, Beomseok, Cubo, Esther, Beyer, Katrin, Tinkhauser, Gerd, Wu, Hsiu-Chuan, Wu, Yihru, Schrag, Anette, Schapira, Anthony, Bale, Claire, Morris, Huw R, Love, Seth, Jasaityte, Simona, O’Grady, Alyssa, Fiske, Brian, Cruchaga, Carlos, Faghri, Faraz, Serrano, Geidy E, Sarmiento, Ignacio Juan Keller, Williamson, Jared, Jankovic, Joseph, Nuytemans, Karen, Chahine, Lana M, Screven, Laurel, Ruffrage, Lauren, Dean, Marissa, Puckelwartz, Megan J, Louie, Naomi, Lubbe, Steven, Foroud, Tatiana, Nguyen, Toan, Blauwendraat, Cornelis, Nalls, Mike A

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YY1-Related Dystonia: Clinical Aspects and Long-Term Response to Deep Brain Stimulation von Zorzi, Giovanna, Keller Sarmiento, Ignacio Juan, Danti, Federica Rachele, Bustos, Bernabe I, Invernizzi, Federica, Panteghini, Celeste, Reale, Chiara, Garavaglia, Barbara, Chiapparini, Luisa, Lubbe, Steven J, Nardocci, Nardo, Mencacci, Niccolò E

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