Author
Cleveland ClinicORCID 0000-0003-3770-0476Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
6 papers
Recent·Most cited
Emily Waldo, Henry Mauricio Chaparro-Solano, Mariam Isayan…·Ignacio Fernandez Mata
The paper screens variants in PD-related genes in Latin American EOPD and familial PD patients, identifying pathogenic variants and contributing to the genetic characterization of these conditions in the region.
Paula Saffie Awad, Peter Wild Crea, Spencer M. Grant…·Pedro Chaná‐Cuevas
The paper characterizes the genetic landscape of Parkinson's disease in a Chilean cohort, identifying common pathogenic variants in LRRK2 and GBA1.
Thiago Peixoto Leal, Jennifer N. French, Mateus Henrique Gouveia…·Ignacio Fernandez Mata
The paper conducts an X-chromosome association study in Latin American cohorts, identifying new loci linked to Parkinson Disease and replicating previous findings.
Douglas P. Loesch, Andréa R. V. R. Horimoto, Elif Irem Sarihan…·Timothy D. O’Connor
The paper constructs and validates a polygenic risk score for Parkinson's disease in a Latino cohort, finding ancestry-related biases and haplotype associations at the SNCA locus.
Douglas P. Loesch, Andréa R. V. R. Horimoto, Karl Heilbron…·Ignacio Fernandez Mata
This study conducts the first GWAS of Parkinson's disease in Latinos, identifies SNCA as significant, and finds genetic overlap with Europeans.
Elif Irem Sarihan, Eduardo Pérez‐Palma, Lisa‐Marie Niestroj…·Ignacio Fernandez Mata
The paper analyzes copy number variants in Latin American Parkinson's disease patients and finds enrichment of variants overlapping known Parkinson's genes, particularly PARK2, associated with early-onset disease.