Ignacio Mata, PhD, is Assistant Professor at Cleveland Clinic Lerner College of Medicine. He hold a Bachelor of Science and PhD in Human/Medical Genetics from la Universidad de Oviedo in Asturias, Spain, and he received his PhD in Neurogenetics from Mayo Clinic. Dr. Mata's lab is working towards identifying and understanding the genes that play a role in those diseases that affect the brain (neurological disorders). These include the very well-known Parkinson’s disease (PD), but also other less common disorders such as a form of PD that presents with severe cognitive problems/dementia (PDD) and another type of dementia called Dementia with Lewy Bodies (DLB).
Recent Publications
- Barberena-Jonas, C, Flores-Ocampo, V, Ogonowski, NS, Piña-Escudero, SD, Mata, IF, Yokoyama, JS, García-García, L, Aguilar Salinas, CA, ENSANUT consortium, Tusié-Luna, MT et al.. Genetic analysis of APOE reveals distinct origins and distribution of ancestry-enrichment haplotypes in the Mexican Biobank. Genes Dis 2026; 13 (1): 101542. PubMed PMID:41049132 PubMed Central PMC12495275.
- Hernández, CF, Villaman, C, Tejos, C, Repetto, GM, Leu, C, Lal, D, Mata, IF, Klein, AD, Pérez-Palma, E. Polygenic scores contribution to Parkinson's disease comorbidities. Brain Commun 2025; 7 (5): fcaf325. PubMed PMID:40980402 PubMed Central PMC12448616.
- Sarapura-Castro, E, Milla-Neyra, K, Ríos-Pinto, J, Maguiña, JL, Rivera-Valdivia, A, Inca-Martinez, M, Illanes-Manrique, M, Galecio-Castillo, M, Montano, S, Mata, IF et al.. Prevalence of Parkinson's Disease in a Town of the Central Highlands of Peru: A Population-Based Study. Mov Disord Clin Pract 2025; : . PubMed PMID:40970415 .
- Chaparro-Solano, HM, Teixeira-Dos-Santos, D, Waldo, E, Leal, TP, Inca-Martinez, M, Alcauter, S, Medina-Rivera, A, Ruiz-Contreras, AE, Cornejo-Olivas, M, Mejia-Rojas, K et al.. EPIDEMIOLOGY OF LEVODOPA-INDUCED DYSKINESIA: PREVALENCE AND ASSOCIATED CLINICAL FACTORS IN LATIN AMERICA. medRxiv 2025; : . PubMed PMID:40909824 PubMed Central PMC12407593.
- Blauwendraat, C, Noyce, AJ, Mata, IF, Screven, LA, Solle, J, Dumanis, SB, Riley, EA, Periñan, MT, Okubadejo, N, Klein, C et al.. Tackling a disease on a global scale, the Global Parkinson's Genetics Program, GP2: A new generation of opportunities. Am J Hum Genet 2025; 112 (9): 1988-2000. PubMed PMID:40834859 PubMed Central PMC12461011.
- Step, K, Leal, TP, Kamel, WA, Waldo, E, Bardien, S, Mata, IF. X chromosome-wide association studies in neurological disorders: uncovering the hidden influence of the X chromosome. Front Genet 2025; 16 : 1650259. PubMed PMID:40809846 PubMed Central PMC12343220.
- Leal, TP, Waldo, E, Duarte-Zambrano, F, Inca-Martinez, M, Ramchandra, J, Chaparro-Solano, HM, Anello, AE, Borda, V, Gouveia, MH, Teixeira-Dos-Santos, D et al.. Genotype-phenotype association study conducted on LARGE-PD reveals novel loci associated with Parkinson's Disease. medRxiv 2025; : . PubMed PMID:40791673 PubMed Central PMC12338945.
- Step, K, Leal, TP, Waldo, E, Madula, L, Swart, Y, Hernández, CF, Kim, JJ, Bandres-Ciga, S, Global Parkinson’s Genetics Program (GP2), Mata, IF et al.. Genome-wide association analyses reveal susceptibility variants linked to Parkinson's disease in the South African population using inferred global and local ancestry. medRxiv 2025; : . PubMed PMID:40766124 PubMed Central PMC12324638.
- Saffie-Awad, P, Grant, SM, Makarious, MB, Elsayed, I, Sanyaolu, AO, Crea, PW, Schumacher Schuh, AF, Levine, KS, Vitale, D, Koretsky, MJ et al.. Insights into ancestral diversity in Parkinson's disease risk: a comparative assessment of polygenic risk scores. NPJ Parkinsons Dis 2025; 11 (1): 201. PubMed PMID:40610451 PubMed Central PMC12229533.
- Gouveia, MH, Meeks, KAC, Borda, V, Leal, TP, Kehdy, FSG, Mogire, R, Doumatey, AP, Tarazona-Santos, E, Kittles, RA, Mata, IF et al.. Subcontinental genetic variation in the All of Us Research Program: Implications for biomedical research. Am J Hum Genet 2025; 112 (6): 1286-1301. PubMed PMID:40480197 PubMed Central PMC12256905.
