The International Parkinson Disease Genomics Consortium Africa von Rizig, Mie, Okubadejo, Njideka, Salama, Mohamed, Thomas, Omotola, Akpalu, Albert, Gouider, Riadh

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Leucine rich repeat kinase 2 (LRRK2) GLY2019SER mutation is absent in a second cohort of Nigerian Africans with Parkinson disease von Okubadejo, Njideka U, Rizig, Mie, Ojo, Oluwadamilola O, Jonvik, Hallgeir, Oshinaike, Olajumoke, Brown, Emmeline, Houlden, Henry

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Prevalence of Fabry Disease among Patients with Parkinson’s Disease von Lackova, Alexandra, Beetz, Christian, Oppermann, Sebastian, Bauer, Peter, Pavelekova, Petra, Lorincova, Tatiana, Ostrozovicova, Miriam, Kulcsarova, Kristina, Cobejova, Jana, Cobej, Martin, Levicka, Petra, Liesenerova, Simona, Sendekova, Daniela, Sukovska, Viktoria, Gdovinova, Zuzana, Han, Vladimir, Rizig, Mie, Houlden, Henry, Skorvanek, Matej

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Comparing fluid biomarkers of Alzheimer's disease between African American or Black African and white groups: A systematic review and meta-analysis von Chaudhry, Aiysha, Rizig, Mie

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Metabolomic profiling reveals altered phenylalanine metabolism in Parkinson's disease in an Egyptian cohort von Shebl, Nourhan, El-Jaafary, Shaimaa, Saeed, Ayman A, Elkafrawy, Passent, El-Sayed, Amr, Shamma, Samir, Elnemr, Rasha, Mekky, Jaidaa, Mohamed, Lobna A, Kittaneh, Omar, El-Fawal, Hassan, Rizig, Mie, Salama, Mohamed

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A gene expression and systems pathway analysis of the effects of clozapine compared to haloperidol in the mouse brain implicates susceptibility genes for schizophrenia von Rizig, Mie A, McQuillin, Andrew, Ng, Aylwin, Robinson, Michelle, Harrison, Andrew, Zvelebil, Marketa, Hunt, Steve P, Gurling, Hugh M

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Parkinson’s Disease in Central Asian and Transcaucasian Countries: A Review of Epidemiology, Genetics, Clinical Characteristics, and Access to Care von Ganieva, Manizha, Rasulova, Khurshidakhon, Houlden, Henry, Khaibullin, Talgat, Karimova, Altynay, Kaishibayeva, Gulnaz, Shashkin, Chingiz, Zharkinbekova, Nazira, Aitkulova, Akbota, Rizig, Mie, Kaiyrzhanov, Rauan, Sadykova, Dinara

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The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson’s disease von William, Martina B., Hamed, Sharifa, Shalash, Ali, Khedr, Eman M., Yousef, Mohamed H., El-Jaafary, Shaimaa, Fawi, Gharib, Helmy, Asmaa, Hamid, Eman, Essam, Mohamed, Lee, Hamin, Jama, Alina, Koraym, Mohamed, Mahmoud, Doaa M., Elfarrash, Sara, Elsaid, Yasmin, Gabr, Asmaa S., Shebl, Nourhan, Abdelwahhab, Nesreen, Belal, Tamer M., Elsayed, Nehal A. B., El-Gamal, Mohamed, Elgamal, Shimaa, Ragab, Salma, Mekky, Jaidaa, Aly, Lobna, Nabhan, Samir, Ragab, Gaafar, Hussein, Mohamed A., Hegazy, Mohamed Tharwat, Houlden, Henry, Salama, Mohamed, Rizig, Mie

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LRRK2 Mutations and Asian Disease-Associated Variants in the First Parkinson’s Disease Cohort from Kazakhstan von Kaishibayeva, Gulnaz, Khaibullin, Talgat, Karimova, Altynay, Bralov, Askhat, Kissamedenov, Nurlan, Seidinova, Zhanar, Taskinbayeva, Anjela, Muratbaikyzy, Aliya, Houlden, Henry, Akhmetzhanov, Vadim, Jarmukhanov, Zharkyn, Zholdybayeva, Elena, Rizig, Mie, Zharkinbekova, Nazira, Shashkin, Chingiz, Aitkulova, Akbota, Kaiyrzhanov, Rauan, Akshulakov, Serik

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A health literacy campaign for Parkinson's disease in Africa: a novel campaign to break down language barriers von Rizig, Mie, Thomas, Omotola

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Novel fluid biomarkers to differentiate frontotemporal dementia and dementia with Lewy bodies from Alzheimer's disease: A systematic review von Chaudhry, Aiysha, Houlden, Henry, Rizig, Mie

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Ethnicity as a predictor of nonmotor symptoms impact on quality of life in patients with Parkinson's disease: A systematic review von Aldeen, Huda, Houlden, Henry, Rizig, Mie

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Therapeutic Challenges of Huntington’s Disease in Guinea: Study of HD Confirmed Cases in a Country with Limited Resources (P2-11.013) von Othon, GUELNGAR Carlos, Muthinja, Mendi Julianne, Rizig, Mie, Cisse, Abass Fode, cisse, Amara

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Feeding dystonia, chorea, psychosis, and self-mutilation in an African patient with neuroacanthocytosis syndrome von Fall, Maouly, Seck, Moussa, Diop, Alassane Mamadou, Kahwagi, Jamil, Yimta, Grace Tsemo, Guéye, Allé, Cruz, Pedro Rodriguez, Rizig, Mie

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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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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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Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G-protein signaling 4 protein (RGS... von Rizig, Mie A., McQuillin, Andrew, Puri, Vinay, Choudhury, Khalid, Datta, Susmita, Thirumalai, Srinivasa, Lawrence, Jacob, Quested, Digby, Pimm, Jonathan, Bass, Nicholas, Lamb, Graham, Moorey, Helen, Badacsonyi, Allison, Kelly, Katie, Morgan, Jenny, Punukollu, Bhaskar, Kandasami, Gomathinayagam, Curtis, David, Gurling, Hugh

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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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Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders von Mencacci, Niccolo E., Reynolds, Regina, Ruiz, Sonia Garcia, Vandrovcova, Jana, Forabosco, Paola, Sanchez-Ferrer, Alvaro, Volpato, Viola, Weale, Michael E., Bhatia, Kailash P., Webber, Caleb, Hardy, John, Botia, Juan A., Ryten, Mina

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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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