Mario Cornejo-Olivas,MD
Mario Cornejo-Olivas,MD
Neurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas
Verified email at - Homepage
Cited by
Cited by
Age-and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease
X Hou, FC Fiesel, D Truban, M Castanedes Casey, W Lin, AI Soto, P Tacik, ...
Autophagy 14 (8), 1404-1418, 2018
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population
C Kay, JA Collins, GEB Wright, F Baine, Z Miedzybrodzka, F Aminkeng, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018
A Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristics
MR Cornejo-Olivas, L Torres, IF Mata, P Mazzetti, D Rivas, C Cosentino, ...
Parkinsonism & related disorders 21 (5), 444-448, 2015
Clinical and molecular features of late onset Huntington disease in a Peruvian cohort
MR Cornejo-Olivas, MA Inca-Martinez, K Espinoza-Huertas, D Veliz-Otani, ...
Journal of Huntington's disease 4 (1), 99-105, 2015
The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru
C Velez-Pardo, O Lorenzo-Betancor, M Jimenez-Del-Rio, S Moreno, ...
Parkinsonism & related disorders 63, 204-208, 2019
Genetics and genomics in Peru: Clinical and research perspective
H Guio, JA Poterico, KS Levano, M Cornejo‐Olivas, P Mazzetti, ...
Molecular genetics & genomic medicine 6 (6), 873-886, 2018
Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry
M Cornejo-Olivas, L Torres, MR Velit-Salazar, M Inca-Martinez, P Mazzetti, ...
NPJ Parkinson's disease 3 (1), 1-6, 2017
Using global team science to identify genetic Parkinson’s disease worldwide
EJ Vollstedt, M Kasten, C Klein
Annals of neurology 86 (2), 153, 2019
Huntington's disease-like disorders in Latin America and the Caribbean
RH Walker, EM Gatto, ML Bustamante, O Bernal-Pacheco, F Cardoso, ...
Parkinsonism & related disorders 53, 10-20, 2018
A comprehensive haplotype-targeting strategy for allele-specific HTT suppression in Huntington disease
C Kay, JA Collins, NS Caron, L de Andrade Agostinho, H Findlay-Black, ...
The American Journal of Human Genetics 105 (6), 1112-1125, 2019
Haplotype study in SCA10 families provides further evidence for a common ancestral origin of the mutation
GB Bampi, R Bisso-Machado, T Hünemeier, TC Gheno, GV Furtado, ...
Neuromolecular Medicine 19 (4), 501-509, 2017
The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America
C Kay, I Tirado-Hurtado, M Cornejo-Olivas, JA Collins, G Wright, ...
European Journal of Human Genetics 25 (3), 332-340, 2017
Characterizing the genetic architecture of Parkinson's disease in Latinos
DP Loesch, ARVR Horimoto, K Heilbron, EI Sarihan, M Inca‐Martinez, ...
Annals of Neurology 90 (3), 353-365, 2021
Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil
TC Gheno, GV Furtado, JAM Saute, KC Donis, AMV Fontanari, VE Emmel, ...
European Journal of Neurology 24 (7), 892-e36, 2017
Lrrk2 p. Q1111H substitution and Parkinson’s disease in Latin America
IF Mata, GJ Wilhoite, D Yearout, JA Bacon, M Cornejo-Olivas, P Mazzetti, ...
Parkinsonism & related disorders 17 (8), 629-631, 2011
Genetic polymorphism of apolipoprotein E in a Peruvian population
V Marca, O Acosta, M Cornejo-Olivas, O Ortega, D Huerta, P Mazzetti
Revista Peruana de Medicina Experimental y Salud Publica 28 (4), 589-594, 2011
Clinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimer's disease
MR Cornejo-Olivas, CE Yu, P Mazzetti, IF Mata, M Meza, ...
Neuroscience letters 563, 140-143, 2014
ATXN3, ATXN7, CACNA1A, and RAI1 genes and mitochondrial polymorphism A10398G did not modify age at onset in Spinocerebellar Ataxia Type 2 patients from South America
FS Pereira, TL Monte, LD Locks-Coelho, ASP Silva, O Barsottini, ...
The Cerebellum 14 (6), 728-730, 2015
Polimorfismo genético de la apolipoproteína E en una población peruana
V Marca, O Acosta, M Cornejo-Olivas, O Ortega, D Huerta, P Mazzetti
Revista Peruana de Medicina Experimental y Salud Pública 28, 589-594, 2011
Neurogenetics in Peru: clinical, scientific and ethical perspectives
M Cornejo-Olivas, K Espinoza-Huertas, MR Velit-Salazar, D Veliz-Otani, ...
Journal of community genetics 6 (3), 251-257, 2015
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