| 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 | 56 | 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 | 42 | 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 | 27 | 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 | 27 | 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 | 26 | 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 | 24 | 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 | 23 | 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 | 17 | 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 | 16 | 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 | 14 | 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 | 14 | 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 | 14 | 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 | 13 | 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 | 13 | 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 | 13 | 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 | 12 | 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 | 11 | 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 | 10 | 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 | 10 | 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 | 9 | 2015 |
MIGUEL INCA-MARTINEZResearcher, Cleveland ClinicVerified email at CCF.ORG
