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Mario Cornejo-Olivas

Explore the profile of Mario Cornejo-Olivas including associated specialties, affiliations and a list of published articles. Areas
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Articles 59
Citations 369
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Recent Articles
1.
Cruz-Criollo L, Davila-Salazar W, Sarapura-Castro E, Rivera-Valdivia A, Bazalar-Montoya J, Bluske K, et al.
Clin Neurol Neurosurg . 2025 Mar; 251:108823. PMID: 40068357
Introduction: Ataxia with oculomotor apraxia type 2 (AOA2) is a rare autosomal recessive cerebellar ataxia characterized by progressive cerebellar ataxia, sensorimotor peripheral neuropathy, and occasional oculomotor apraxia. Case Report: A...
2.
Ramchandra J, Inca-Martinez M, Leal T, Chaparro-Solano H, Salim A, Gatto E, et al.
Parkinsonism Relat Disord . 2025 Mar; 134:107344. PMID: 40058072
Background: Age and sex are known risk factors for Parkinson's Disease (PD), but it remains controversial if there are sex differences in the diagnosis latency. The objective of this study...
3.
Milla-Neyra K, Araujo-Aliaga I, Manrique-Enciso C, Sarapura-Castro E, Illanes-Manrique M, Veliz-Otani D, et al.
Cerebellum . 2025 Feb; 24(2):44. PMID: 39918768
Spinocerebellar ataxia type 10 (SCA10) is a neurodegenerative disease predominant in Latin American individuals with Indigenous American ancestry. SCA10 is caused by an expansion of ATTCT repeat within the ATXN10...
4.
Anis S, Chaparro-Solano H, Leal T, Sperling S, Sonneborn C, Callegari Piccinin C, et al.
Clin Neuropsychol . 2025 Jan; 1-21. PMID: 39825715
Despite significant progress in understanding the factors influencing cognitive function in Parkinson's disease (PD), there is a notable gap in data representation for the Latinx population. This study aims to...
5.
Ramirez A, Bertholim-Nasciben L, Moura S, Coombs L, Rajabli F, DeRosa B, et al.
Res Sq . 2024 Dec; PMID: 39678342
Background: This study aims to elucidate ancestry-specific changes to the genomic regulatory architecture in induced pluripotent stem cell (iPSC)-derived oligodendroglia, focusing on their implications for Alzheimer's disease (AD). This work...
6.
Bazalar-Montoya J, Cornejo-Olivas M, Duenas-Roque M, Purizaca-Rosillo N, Rodriguez R, Milla-Neyra K, et al.
NPJ Genom Med . 2024 Oct; 9(1):51. PMID: 39468051
There is limited access to molecular genetic testing in most low- and middle-income countries. The iHope program provides clinical genome sequencing (cGS) to underserved individuals with signs or symptoms of...
7.
Lorenzo-Betancor O, Mehta S, Ramchandra J, Mumuney S, Schumacher-Schuh A, Cornejo-Olivas M, et al.
Mov Disord . 2024 Jul; 39(10):1843-1855. PMID: 39051491
Background: Parkinson's disease (PD) is the second most common neurodegenerative disease following Alzheimer's disease. Nearly 30 causative genes have been identified for PD and related disorders. However, most of these...
8.
Medina Escobar A, Pringsheim T, Gautreau S, Rivera-Duarte J, Amorelli G, Cornejo-Olivas M, et al.
Mov Disord . 2024 Jul; 39(11):1907-1921. PMID: 39044616
Background: Latin America has played a crucial role in advancing our understanding of Huntington's disease (HD). However, previous global reviews include limited data from Latin America. It is possible that...
9.
Thorpe E, Williams T, Shaw C, Chekalin E, Ortega J, Robinson K, et al.
Am J Hum Genet . 2024 Jun; 111(7):1271-1281. PMID: 38843839
There is mounting evidence of the value of clinical genome sequencing (cGS) in individuals with suspected rare genetic disease (RGD), but cGS performance and impact on clinical care in a...
10.
Sosa A, Brucki S, Crivelli L, Lopera F, Acosta D, Acosta-Uribe J, et al.
Alzheimers Dement . 2024 May; 20(7):5009-5026. PMID: 38801124
Introduction: While Latin America (LatAm) is facing an increasing burden of dementia due to the rapid aging of the population, it remains underrepresented in dementia research, diagnostics, and care. Methods:...