Listar por autor "Inca-Martinez, Miguel"

Ordenar por:Orden:Resultados:

  • ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population 
    Veliz-Otani, Diego; Inca-Martinez, Miguel; Bampi, Giovana B.; Ortega, Olimpio; Jardim, Laura B.; Saraiva-Pereira, Maria Luiza; Mazzetti, Pilar; Cornejo-Olivas, Mario (Springer, 2019)
    Spinocerebellar ataxia type 10 (SCA10) is a repeat expansion disease occurring mostly in Latin America, suggesting that the mutation spread with the peopling of the Americas, or that Amerindian populations, have a higher ...
  • Characterizing the Genetic Architecture of Parkinson's Disease in Latinos 
    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, Andrés; 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, ...
  • The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru 
    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 ...
  • Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population 
    Figueroa Ildefonso, Erick Gianpierre; Bademci, Guney; Rajabli, Farid; Cornejo-Olivas, Mario; Villanueva, Ruy Diego Chacon; Badillo-Carrillo, Rodolfo; Inca-Martinez, Miguel; Neyra, Karina Milla; Sineni, Claire; Tekin, Mustafa (MDPI, 2019)
    Hearing loss (HL) is a common sensory disorder affecting over 5% of the global population. The etiology underlying HL includes congenital and acquired causes; genetic factors are the main cause in over 50% of congenital ...
  • Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort 
    Loesch, Douglas P.; Horimoto, Andrea R. V. R.; Sarihan, Elif Irem; 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, Andrés; 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; Thornton, Timothy A.; Mata, Ignacio F.; O'Connor, Timothy D.; International Parkinson Disease Genomics Consortium (IPDGC); Latin American Research Consortium on the Genetics of Parkinson's Disease (LARGE-PD) (Elsevier, 2022)
    Background: Large-scale Parkinson's disease (PD) genome-wide association studies (GWAS) have, until recently, only been conducted on subjects with European-ancestry. Consequently, polygenic risk scores (PRS) constructed ...
  • Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry 
    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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