Search Results - Perinan, Maria T
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Is SH3GL2 p.G276V the causal functional variant underlying Parkinson’s disease risk at this locus? by Lazaro-Figueroa, Alejandra, Hernandez-Medrano, Ana Jimena, Ramírez-Pineda, Diana Berenice, Navarro Cadavid, Andrés, Makarious, Mary, Foo, Jia Nee, Alvarado, Chelsea X., Bandres-Ciga, Sara, Periñan, Maria Teresa, Mohamed, Wael Mohamed Yousef
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Mendelian randomization and Parkinson’s disease by Sanyaolu, Arinola O, Mohamed, Wael Mohamed Yousef, Makarious, Mary B, August, Joanne L, Kekenadze, Mariam, Heilbron, Karl, Perinan, Maria T, Noyce, Alastair, Bandres-Ciga, Sara
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Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: a new generation of opportunities by Blauwendraat, Cornelis, Noyce, Alastair J., Mata, Ignacio F., Screven, Laurel A., Solle, J., Dumanis, Sonya B., Riley, Ekemini A., Perinan, Maria Teresa, Okubadejo, Njideka, Klein, Christine, Morris, Huw R., Singleton, Andrew B., Mohamed, Wael Mohamed Yousef
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Advancing Parkinson’s disease research in Africa: a strategic training framework of the global Parkinson’s genetics program by Step, Kathryn, Eltaraifee, Esraa, Elsayed, Inas, Rasaholiarison, Nomena, Okubadejo, Njideka Ulunma, Walker, Richard, Mohamed, Wael Mohamed Yousef, Rizig, Mie, Bandres-Ciga, Sara, Noyce, Alastair J., Dey, Sumit, Bardien, Soraya, Periñan, Maria Teresa
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