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Browsing by Author "Zabetian, Cyrus P."

Browsing by Author "Zabetian, Cyrus P."

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  • Loesch, Douglas P.; Horimoto, Andrea R. V. R.; Heilbron, Karl; Sarihan, Elif I.; Inca-Martinez, Miguel; Mason, Emily; Cornejo-Olivas, Mario; Torres, Luis; Mazzetti, Pilar; Cosentino, Carlos; Sarapura-Castro, Elison; Rivera-Valdivia, Andrea; Medina, Angel C.; Dieguez, Elena; Raggio, Victor; Lescano, Andres; Tumas, Vitor; Borges, Vanderci; Ferraz, Henrique B.; Rieder, Carlos R.; Schumacher-Schuh, Artur; Santos-Lobato, Bruno L.; Velez-Pardo, Carlos; Jimenez-Del-Rio, Marlene; Lopera, Francisco; Moreno, Sonia; Chana-Cuevas, Pedro; Fernandez, William; Arboleda, Gonzalo; Arboleda, Humberto; Arboleda-Bustos, Carlos E.; Yearout, Dora; Zabetian, Cyrus P.; Cannon, Paul; Thornton, Timothy A.; O'Connor, Timothy D.; Mata, Ignacio F.; Latin Amer Res Consortium Genetics (Wiley, 2021)
    Objective This work was undertaken in order to identify Parkinson's disease (PD) risk variants in a Latino cohort, to describe the overlap in the genetic architecture of PD in Latinos compared to European-ancestry subjects, ...
  • Velez-Pardo, Carlos; Lorenzo-Betancor, Oswaldo; Jimenez-Del-Rio, Marlene; Moreno, Sonia; Lopera, Francisco; Cornejo-Olivas, Mario; Torres, Luis; Inca-Martinez, Miguel; Mazzetti, Pilar; Cosentino, Carlos; Yearout, Dora; Waldherr, Sarah M.; Zabetian, Cyrus P.; Mata, Ignacio F. (Elsevier, 2019)
    Background: Mutations in the glucocerebrosidase (GBA) gene are an important risk factor for Parkinson's disease (PD). However, most GBA genetic studies in PD have been performed in patients of European origin and very few ...
  • Cornejo-Olivas, Mario; Torres, Luis; Velit-Salazar, Mario R.; Inca-Martinez, Miguel; Mazzetti, Pilar; Cosentino, Carlos; Micheli, Federico; Perandones, Claudia; Dieguez, Elena; Raggio, Victor; Tumas, Vitor; Borges, Vanderci; Ferraz, Henrique B.; Rieder, Carlos R. M.; Shumacher-Schuh, Artur; Velez-Pardo, Carlos; Jimenez-Del-Rio, Marlene; Lopera, Francisco; Chang-Castello, Jorge; Andreé-Munoz, Brennie; Waldherr, Sarah; Yearout, Dora; Zabetian, Cyrus P.; Mata, Ignacio F. (Springer, 2017)
    Mutations in Leucine-Rich Repeat Kinase 2 (LRRK2), primarily located in codons G2019 and R1441, represent the most common genetic cause of Parkinson's disease in European-derived populations. However, little is known about ...

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