NeuroBooster Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations von Bandres‐Ciga, Sara, Faghri, Faraz, Majounie, Elisa, Koretsky, Mathew J., Kim, Jeffrey, Levine, Kristin S., Leonard, Hampton, Makarious, Mary B., Iwaki, Hirotaka, Crea, Peter Wild, Hernandez, Dena G., Arepalli, Sampath, Billingsley, Kimberley, Lohmann, Katja, Klein, Christine, Lubbe, Steven J., Jabbari, Edwin, Saffie‐Awad, Paula, Narendra, Derek, Reyes‐Palomares, Armando, Quinn, John P., Schulte, Claudia, Morris, Huw R., Traynor, Bryan J., Scholz, Sonja W., Houlden, Henry, Hardy, John, Dumanis, Sonya, Riley, Ekemini, Blauwendraat, Cornelis, Singleton, Andrew, Nalls, Mike, Jeff, Janina, Vitale, Dan

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RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses von Gustavsson, Emil K, Follett, Jordan, Trinh, Joanne, Barodia, Sandeep K, Real, Raquel, Liu, Zhiyong, Grant-Peters, Melissa, Fox, Jesse D, Appel-Cresswell, Silke, Stoessl, A Jon, Rajput, Alex, Rajput, Ali H, Auer, Roland, Tilney, Russel, Sturm, Marc, Haack, Tobias B, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Vilariño-Güell, Carles, Ryten, Mina, Goldberg, Matthew S, West, Andrew B, Hu, Michele T, Morris, Huw R, Sharma, Manu, Gan-Or, Ziv, Samanci, Bedia, Lis, Pawel, Periñan, Maria Teresa, Amouri, Rim, Ben Sassi, Samia, Hentati, Faycel, Tonelli, Francesca, Alessi, Dario R, Farrer, Matthew J

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The Black and African American Connections to Parkinson's Disease (BLAAC PD) study protocol von Chahine, Lana M, Louie, Naomi, Solle, J, Akçimen, Fulya, Ameri, Andrew, Augenbraun, Samantha, Avripas, Sabrina, Breaux, Sarah, Causey, Christopher, Chandra, Shivika, Dean, Marissa, Disbrow, Elizabeth A, Fanty, Lauren, Fernandez, Jessica, Foster, Erin R, Furr Stimming, Erin, Hall, Deborah, Hinson, Vanessa, Johnson-Turbes, Ashani, Jonas, Cabell, Kilbane, Camilla, Norris, Scott A, Nguyen, Bao-Tran, Padmanaban, Mahesh, Paquette, Kimberly, Parry, Carly, Pessoa Rocha, Natalia, Rawls, Ashley, Shamim, Ejaz A, Shulman, Lisa M, Sipma, Rebeka, Staisch, Julia, Traurig, Rami, von Coelln, Rainer, Wild Crea, Peter, Xie, Tao, Fang, Zih-Hua, O'Grady, Alyssa, Kopil, Catherine M, McGuire Kuhl, Maggie, Singleton, Andrew, Blauwendraat, Cornelis, Bandres-Ciga, Sara

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Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus? von Lázaro‐Figueroa, Alejandra, Hernández‐Medrano, Ana Jimena, Ramírez‐Pineda, Diana Berenice, Navarro Cadavid, Andrés, Makarious, Mary, Foo, Jia Nee, Alvarado, Chelsea X., Bandres‐Ciga, Sara, Periñan, Maria Teresa

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Global Perspectives on Returning Genetic Research Results in Parkinson Disease von Tan, Ai Huey, Saffie-Awad, Paula, Schumacher Schuh, Artur F, Lim, Shen-Yang, Madoev, Harutyun, Ahmad-Annuar, Azlina, Solle, J, Wegel, Claire E, Doquenia, Maria Leila, Dey, Sumit, Perinan, Maria Teresa, Makarious, Mary B, Fiske, Brian, Morris, Huw R, Noyce, Alastair J, Alcalay, Roy N, Kumar, Kishore Raj, Klein, Christine

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Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale von Junker, Johanna, Lange, Lara M., Vollstedt, Eva‐Juliane, Roopnarain, Karisha, Doquenia, Maria Leila M., Annuar, Azlina Ahmad, Avenali, Micol, Bardien, Soraya, Bahr, Natascha, Ellis, Melina, Galandra, Caterina, Gasser, Thomas, Heutink, Peter, Illarionova, Anastasia, Kanana, Yuliia, Keller Sarmiento, Ignacio J., Kumar, Kishore R., Lim, Shen‐Yang, Madoev, Harutyun, Mata, Ignacio F., Mencacci, Niccolò E., Nalls, Mike A., Padmanabhan, Shalini, Shambetova, Cholpon, Solle, J. C., Tan, Ai‐Huey, Trinh, Joanne, Valente, Enza Maria, Singleton, Andrew, Blauwendraat, Cornelis, Lohmann, Katja, Fang, Zih‐Hua, Klein, Christine, Junker, Johanna, Lange, Lara M., Vollstedt, Eva‐Juliane, Roopnarain, Karisha, Doquenia, Maria Leila M., Annuar, Azlina Ahmad, Avenali, Micol, Bardien, Soraya, Bahr, Natascha, Ellis, Melina, Galandra, Caterina, Gasser, Thomas, Heutink, Peter, Illarionova, Anastasia, Kanana, Yuliia, Keller, Ignacio J., Kumar, Kishore R., Lim, Shen‐Yang, Madoev, Harutyun, Mata, Ignacio F., Mencacci, Niccolò E., Nalls's, Mike A., Padmanabhan, Shalini, Shambetova, Cholpon, Solle, J., Tan, Ai‐Huey, Trinh, Joanne, Valente, Enza Maria, Singleton, Andrew, Blauwendraat, Cornelis, Lohmann, Katja, Fang, Zih‐Hua, Klein, Christine

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Author Correction: The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data von Leonard, Hampton L., Murtadha, Ruqaya, Martinez-Carrasco, Alejandro, Jama, Alina, Müller-Nedebock, Amica Corda, Gil-Martinez, Ana-Luisa, Illarionova, Anastasia, Moore, Anni, Bustos, Bernabe I., Jadhav, Bharati, Huxford, Brook, Storm, Catherine, Towns, Clodagh, Vitale, Dan, Chetty, Devina, Yu, Eric, Grenn, Francis P., Salazar, Gabriela, Rateau, Geoffrey, Iwaki, Hirotaka, Elsayed, Inas, Foote, Isabelle Francesca, Jansen van Rensburg, Zuné, Kim, Jonggeol Jeff, Yuan, Jie, Lake, Julie, Brolin, Kajsa, Senkevich, Konstantin, Wu, Lesley, Tan, Manuela M. X., Periñán, María Teresa, Makarious, Mary B., Ta, Michael, Pillay, Nikita Simone, Betancor, Oswaldo Lorenzo, Reyes-Pérez, Paula R., Alvarez Jerez, Pilar, Saini, Prabhjyot, al-Ouran, Rami, Sivakumar, Ramiya, Real, Raquel, Reynolds, Regina H., Hu, Ruifneg, Abrahams, Shameemah, Rao, Shilpa C., Antar, Tarek, Leal, Thiago Peixoto, Iankova, Vassilena, Scotton, William J., Song, Yeajin, Singleton, Andrew, Nalls, Mike A., Dey, Sumit, Bandres-Ciga, Sara, Blauwendraat, Cornelis, Noyce, Alastair J.

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African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1 von Álvarez Jerez, Pilar, Wild Crea, Peter, Ramos, Daniel M., Gustavsson, Emil K., Radefeldt, Mandy, Damianov, Andrey, Makarious, Mary B., Ojo, Oluwadamilola O., Billingsley, Kimberley J., Malik, Laksh, Daida, Kensuke, Bromberek, Sarah, Hu, Fangle, Schneider, Zachary, Surapaneni, Aditya L., Stadler, Julia, Rizig, Mie, Morris, Huw R., Pantazis, Caroline B., Leonard, Hampton L., Screven, Laurel, Qi, Yue A., Nalls, Mike A., Bandres-Ciga, Sara, Hardy, John, Houlden, Henry, Eng, Celeste, Burchard, Esteban González, Kachuri, Linda, Lin, Chia-Ho, Black, Douglas L., Singleton, Andrew B., Fischer, Steffen, Bauer, Peter, Reed, Xylena, Ryten, Mina, Beetz, Christian, Ward, Michael, Okubadejo, Njideka U., Blauwendraat, Cornelis

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The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson’s disease data von Leonard, Hampton L., Murtadha, Ruqaya, Martinez-Carrasco, Alejandro, Jama, Alina, Müller-Nedebock, Amica Corda, Gil-Martinez, Ana-Luisa, Illarionova, Anastasia, Moore, Anni, Bustos, Bernabe I., Jadhav, Bharati, Huxford, Brook, Storm, Catherine, Towns, Clodagh, Vitale, Dan, Chetty, Devina, Yu, Eric, Grenn, Francis P., Salazar, Gabriela, Rateau, Geoffrey, Iwaki, Hirotaka, Elsayed, Inas, Foote, Isabelle Francesca, Jansen van Rensburg, Zuné, Kim, Jonggeol Jeff, Yuan, Jie, Lake, Julie, Brolin, Kajsa, Senkevich, Konstantin, Wu, Lesley, Tan, Manuela M. X., Periñán, María Teresa, Makarious, Mary B., Ta, Michael, Pillay, Nikita Simone, Betancor, Oswaldo Lorenzo, Reyes-Pérez, Paula R., Alvarez Jerez, Pilar, Saini, Prabhjyot, al-Ouran, Rami, Sivakumar, Ramiya, Real, Raquel, Reynolds, Regina H., Hu, Ruifneg, Abrahams, Shameemah, Rao, Shilpa C., Antar, Tarek, Leal, Thiago Peixoto, Iankova, Vassilena, Scotton, William J., Song, Yeajin, Singleton, Andrew, Nalls, Mike A., Dey, Sumit, Bandres-Ciga, Sara, Blauwendraat, Cornelis, Noyce, Alastair J.

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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease von Kim, Jonggeol Jeffrey, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, Iwaki, Hirotaka, Lake, Julie, Solsberg, Caroline Warly, Leonard, Hampton, Makarious, Mary B., Tan, Eng-King, Singleton, Andrew B., Bandres-Ciga, Sara, Noyce, Alastair J., Blauwendraat, Cornelis, Nalls, Mike A., Foo, Jia Nee, Mata, Ignacio

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GBA 1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians von Ojo, Oluwadamilola Omolara, Bandres‐Ciga, Sara, Makarious, Mary B., Crea, Peter Wild, Hernandez, Dena G., Houlden, Henry, Rizig, Mie, Singleton, Andrew B., Noyce, Alastair J., Nalls, Mike A., Blauwendraat, Cornelis, Okubadejo, Njideka Ulunma

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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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Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions von Schumacher‐Schuh, Artur Francisco, Bieger, Andrei, Okunoye, Olaitan, Mok, Kin Ying, Lim, Shen‐Yang, Bardien, Soraya, Ahmad‐Annuar, Azlina, Santos‐Lobato, Bruno Lopes, Strelow, Matheus Zschornack, Salama, Mohamed, Rao, Shilpa C., Zewde, Yared Zenebe, Dindayal, Saiesha, Azar, Jihan, Prashanth, Lingappa Kukkle, Rajan, Roopa, Noyce, Alastair J., Okubadejo, Njideka, Rizig, Mie, Lesage, Suzanne, Mata, Ignacio Fernandez

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Advancing Parkinson's Disease Research in Africa: A Strategic Training Framework of the Global Parkinson's Genetics Program von Step, Kathryn, Eltaraifee, Esraa, Elsayed, Inas, Rasaholiarison, Nomena, Okubadejo, Njideka, Walker, Richard, Mohamed, Wael, Rizig, Mie, Bandres‐Ciga, Sara, Noyce, Alastair J., Dey, Sumit, Bardien, Soraya, Periñan, Maria Teresa

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Is SH3GL2 p. G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus? von Lázaro‐Figueroa, Alejandra, Hernández‐Medrano, Ana Jimena, Ramírez‐Pineda, Diana Berenice, Navarro Cadavid, Andrés, Makarious, Mary, Foo, Jia Nee, Alvarado, Chelsea X., Bandres‐Ciga, Sara, Periñan, Maria Teresa

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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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Parkinson’s families project: a UK-wide study of early onset and familial Parkinson’s disease von Towns, Clodagh, Fang, Zih-Hua, Tan, Manuela M. X., Jasaityte, Simona, Schmaderer, Theresa M., Stafford, Eleanor J., Pollard, Miriam, Tilney, Russel, Hodgson, Megan, Wu, Lesley, Labrum, Robyn, Hehir, Jason, Polke, James, Lange, Lara M., Schapira, Anthony H. V., Bhatia, Kailash P., Singleton, Andrew B., Blauwendraat, Cornelis, Klein, Christine, Houlden, Henry, Wood, Nicholas W., Jarman, Paul R., Morris, Huw R., Real, Raquel

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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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Lack of genetic evidence for NLRP3 inflammasome involvement in Parkinson’s disease pathogenesis von Senkevich, Konstantin, Liu, Lang, Alvarado, Chelsea X., Leonard, Hampton L., Nalls, Mike A., Gan-Or, Ziv

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3039 Monogenic Parkinson’s Disease Australia (MonoPDAus) initiative: study protocol von Yeow, Dennis, Rudaks, Laura I, García-Marín, Luis M, Flores-Ocampo, Victor, Morales-Briceño, Hugo, Yau, Wai Y, Kõks, Sulev, Mellick, George D, Fung, Victor SC, Tisch, Stephen, Wu, Kathy HC, Schofield, Deborah, Willis, Amanda M, Klein, Christine, Sue, Carolyn M, Davis, Ryan L, Young, Mary-Anne, Rentería, Miguel E, Kumar, Kishore R

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