Variants in ATP5F1B are associated with dominantly inherited dystonia by Nasca, Alessia, Mencacci, Niccolò E, Invernizzi, Federica, Zech, Michael, Keller Sarmiento, Ignacio J, Legati, Andrea, Frascarelli, Chiara, Bustos, Bernabe I, Romito, Luigi M, Krainc, Dimitri, Winkelmann, Juliane, Carecchio, Miryam, Nardocci, Nardo, Zorzi, Giovanna, Prokisch, Holger, Lubbe, Steven J, Garavaglia, Barbara, Ghezzi, Daniele

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De novo FRMD5 Missense Variants in Patients with Childhood‐Onset Ataxia, Prominent Nystagmus, and Seizures by Keller Sarmiento, Ignacio J., Bustos, Bernabe I., Blackburn, Joanna, Hac, Nicholas E.F., Ruzhnikov, Maura, Monroe, Matthea, Levy, Rebecca J., Kinsley, Lisa, Li, Megan, Silani, Vincenzo, Lubbe, Steven J., Krainc, Dimitri, Mencacci, Niccolò E.

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Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale by 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

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Novel THAP1 missense variant with incomplete penetrance in a case of generalized young onset dystonia showing good response to deep brain stimulation by Keller Sarmiento, Ignacio J., Fraint, Avram, Kinsley, Lisa, Akhtar, Rizwan S., Silani, Vincenzo, Lubbe, Steven J., Krainc, Dimitri, Mencacci, Niccolò E.

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Biallelic AOPEP Loss‐of‐Function Variants Cause Progressive Dystonia with Prominent Limb Involvement by Zech, Michael, Kumar, Kishore R., Reining, Sophie, Reunert, Janine, Tchan, Michel, Riley, Lisa G., Drew, Alexander P., Adam, Robert J., Berutti, Riccardo, Biskup, Saskia, Derive, Nicolas, Bakhtiari, Somayeh, Jin, Sheng Chih, Kruer, Michael C., Bardakjian, Tanya, Gonzalez‐Alegre, Pedro, Keller Sarmiento, Ignacio J., Mencacci, Niccolo E., Lubbe, Steven J., Kurian, Manju A., Clot, Fabienne, Méneret, Aurélie, Sainte Agathe, Jean‐Madeleine, Fung, Victor S.C., Vidailhet, Marie, Baumann, Matthias, Marquardt, Thorsten, Winkelmann, Juliane, Boesch, Sylvia

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Novel bi-allelic FBXO7 variants in a family with early-onset typical Parkinson's disease by Keller Sarmiento, Ignacio J., Afshari, Mitra, Kinsley, Lisa, Silani, Vincenzo, Akhtar, Rizwan S., Simuni, Tanya, Lubbe, Steven J., Krainc, Dimitri, Mencacci, Niccolò E.

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Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2) by 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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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

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Novel THAP1 missense variant with incomplete penetrance in a case of generalized young onset dystonia showing good response to deep brain stimulation by Keller Sarmiento, Ignacio J, Fraint, Avram, Kinsley, Lisa, Akhtar, Rizwan S, Silani, Vincenzo, Lubbe, Steven J, Krainc, Dimitri, Mencacci, Niccolò E

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YY1‐Related Dystonia: Clinical Aspects and Long‐Term Response to Deep Brain Stimulation by 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 by 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 by 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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Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions by 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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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

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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

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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease by 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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Childhood-Onset Lower Limb Focal Dystonia Due to a NAA15 Variant: A Case Report by 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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YY1-Related Dystonia: Clinical Aspects and Long-Term Response to Deep Brain Stimulation by 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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