Search Results - Singleton, Andrew B.

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) by Towns, Clodagh, Richer, Madeleine, Jasaityte, Simona, Mohamed, Wael Mohamed Yousef, 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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The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population by Lange, Lara M., Levine, Kristin, Fox, Susan H., Marras, Connie, Ahmed, Nazish, Kuznetsov, Nicole, Vitale, Dan, Iwaki, Hirotaka, Lohmann, Katja, Marsili, Luca, Espay, Alberto J., Bauer, Peter, Beetz, Christian, Martin, Jessica, Factor, Stewart A., Higginbotham, Lenora A., Chen, Honglei, Leonard, Hampton, Nalls, Mike A., Mencacci, Niccolo E., Morris, Huw R., Singleton, Andrew B., Klein, Christine, Blauwendraat, Cornelis, Fang, Zih-Hua, Mohamed, Wael Mohamed Yousef

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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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GBA1 rs3115534 is associated with REM sleep behavior disorder in Parkinson’s disease in Nigerians by 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, Mohamed, Wael Mohamed Yousef

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