Mapping the Diverse and Inclusive Future of Parkinson’s Disease Genetics and Its Widespread Impact

por Elsayed, Inas, Martinez-Carrasco, Alejandro, Cornejo-Olivas, Mario, Bandres-Ciga, Sara
Publicado 2021

Editorial: Monogenic vs. Oligogenic Reclassification

por Messaoud, Olfa, Dutta, Atanu Kumar, Cornejo-Olivas, Mario Reynaldo, Bhuiyan, Zahurul A.
Publicado 2021

Economic burden of Huntington’s disease in Peru

por Silva-Paredes, Gustavo, Urbanos-Garrido, Rosa M., Inca-Martinez, Miguel, Rabinowitz, Danielle, Cornejo-Olivas, Mario R.
Publicado 2019

The first report of CADASIL in Peru: Olfactory dysfunction on initial presentation

por Vishnevetsky, Anastasia, Inca-Martinez, Miguel, Milla-Neyra, Karina, Barrientos-Iman, Danny Moises, Cornejo-Herrera, Ivan, Cosentino, Carlos, Cornejo-Olivas, Mario
Publicado 2016

Knowledge and Attitudes for the Management of Behavioral Variant of Frontotemporal Dementia

por Castro-Suarez, Sheila, Guevara-Silva, Erik, Caparó-Zamalloa, César, Osorio-Marcatinco, Victor, Meza-Vega, Maria, Miller, Bruce, Cornejo-Olivas, Mario
Publicado 2022

Guillain–Barre syndrome outbreak in Peru: Association with polymorphisms in IL‐17, ICAM1, and CD1

por Jaramillo‐Valverde, Luis, Levano, Kelly S., Villanueva, Isolina, Hidalgo, Meylin, Cornejo, Marco, Mazzetti, Pilar, Cornejo‐Olivas, Mario, Sanchez, Cesar, Poterico, Julio A., Valdivia‐Silva, Julio, Guio, Heinner
Publicado 2019

Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population

por Figueroa-Ildefonso, Erick, Bademci, Guney, Rajabli, Farid, Cornejo-Olivas, Mario, Chacón Villanueva, Ruy Diego, Badillo-Carrillo, Rodolfo, Inca-Martinez, Miguel, Milla Neyra, Karina, Sineni, Claire, Tekin, Mustafa
Publicado 2019

C9orf72 Hexanucleotide Repeat in Huntington-Like Patients: Systematic Review and Meta-Analysis

por Alva-Diaz, Carlos, Alarcon-Ruiz, Christoper A., Pacheco-Barrios, Kevin, Mori, Nicanor, Pacheco-Mendoza, Josmel, Traynor, Bryan J., Rivera-Valdivia, Andrea, Lertwilaiwittaya, Pongtawat, Bird, Thomas D., Cornejo-Olivas, Mario
Publicado 2020

MLPA followed by target‐NGS to detect mutations in the dystrophin gene of Peruvian patients suspected of DMD/DMB

por Guevara‐Fujita, María Luisa, Huaman‐Dianderas, Francia, Obispo, Daisy, Sánchez, Rodrigo, Barrenechea, Victor, Rojas‐Málaga, Diana, Estrada‐Cuzcano, Alejandro, Trubnykova, Milana, Cornejo‐Olivas, Mario, Marca, Victoria, Gallardo, Bertha, Dueñas‐Roque, Milagros, Protzel, Ana, Castañeda, Carlos, Abarca, Hugo, Celis, Luis, La Serna‐Infantes, Jorge, Fujita, Ricardo
Publicado 2021

Genetics and genomics in Peru: Clinical and research perspective

por Guio, Heinner, Poterico, Julio A., Levano, Kelly S., Cornejo‐Olivas, Mario, Mazzetti, Pilar, Manassero‐Morales, Gioconda, Ugarte‐Gil, Manuel F., Acevedo‐Vásquez, Eduardo, Dueñas‐Roque, Milagros, Piscoya, Alejandro, Fujita, Ricardo, Sanchez, Cesar, Casavilca‐Zambrano, Sandro, Jaramillo‐Valverde, Luis, Sullcahuaman‐Allende, Yasser, Iglesias‐Pedraz, Juan M., Abarca‐Barriga, Hugo
Publicado 2018

Prevalence of stroke survival in rural communities living in northern Peru

por Moyano, Luz M., Montano, Silvia M., Vilchez Barreto, Percy, Reto, Narcisa, Larrauri, Luis, Mori, Nicanor, Cornejo-Olivas, Mario, Guevara-Silva, Erik, Urizar, Fernando, Najar, Enrique, Gamboa, Ricardo, Azabache, Cintya, Herrer Ticse, Raquel, Bolivar-Herrada, Lucia, Doud, Alex, Martinez, Peggy, Miranda, J. Jaime, Zunt, Joseph R., García, Hector H.
Publicado 2021

Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry

por 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.
Publicado 2017

Erratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry

por 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.
Publicado 2018

Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease

por Hou, Xu, Fiesel, Fabienne C., Truban, Dominika, Castanedes Casey, Monica, Lin, Wen-lang, Soto, Alexandra I., Tacik, Pawel, Rousseau, Linda G., Diehl, Nancy N., Heckman, Michael G., Lorenzo-Betancor, Oswaldo, Ferrer, Isidre, Arbelo, José M., Steele, John C., Farrer, Matthew J., Cornejo-Olivas, Mario, Torres, Luis, Mata, Ignacio F., Graff-Radford, Neill R., Wszolek, Zbigniew K., Ross, Owen A., Murray, Melissa E., Dickson, Dennis W., Springer, Wolfdieter
Publicado 2018

Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson’s disease cohort

por 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, 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., Thornton, Timothy A., Mata, Ignacio F., O’Connor, Timothy D.
Publicado 2022

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Projec...

por Vollstedt, Eva-Juliane, Madoev, Harutyun, Aasly, Anna, Ahmad-Annuar, Azlina, Al-Mubarak, Bashayer, Alcalay, Roy N., Alvarez, Victoria, Amorin, Ignacio, Annesi, Grazia, Arkadir, David, Bardien, Soraya, Barker, Roger A., Barkhuizen, Melinda, Basak, A. Nazli, Bonifati, Vincenzo, Boon, Agnita, Brighina, Laura, Brockmann, Kathrin, Carmine Belin, Andrea, Carr, Jonathan, Clarimon, Jordi, Cornejo-Olivas, Mario, Correia Guedes, Leonor, Corvol, Jean-Christophe, Crosiers, David, Damásio, Joana, Das, Parimal, de Carvalho Aguiar, Patricia, De Rosa, Anna, Dorszewska, Jolanta, Ertan, Sibel, Ferese, Rosangela, Ferreira, Joaquim, Gatto, Emilia, Genç, Gençer, Giladi, Nir, Gómez-Garre, Pilar, Hanagasi, Hasmet, Hattori, Nobutaka, Hentati, Faycal, Hoffman-Zacharska, Dorota, Illarioshkin, Sergey N., Jankovic, Joseph, Jesús, Silvia, Kaasinen, Valtteri, Kievit, Anneke, Klivenyi, Peter, Kostic, Vladimir, Koziorowski, Dariusz, Kühn, Andrea A., Lang, Anthony E., Lim, Shen-Yang, Lin, Chin-Hsien, Lohmann, Katja, Markovic, Vladana, Martikainen, Mika Henrik, Mellick, George, Merello, Marcelo, Milanowski, Lukasz, Mir, Pablo, Öztop-Çakmak, Özgür, Pimentel, Márcia Mattos Gonçalves, Pulkes, Teeratorn, Puschmann, Andreas, Rogaeva, Ekaterina, Sammler, Esther M., Skaalum Petersen, Maria, Skorvanek, Matej, Spitz, Mariana, Suchowersky, Oksana, Tan, Ai Huey, Termsarasab, Pichet, Thaler, Avner, Tumas, Vitor, Valente, Enza Maria, van de Warrenburg, Bart, Williams-Gray, Caroline H., Wu, Ruey-Mei, Zhang, Baorong, Zimprich, Alexander, Solle, Justin, Padmanabhan, Shalini, Klein, Christine
Publicado 2023