Author

Sonia Moreno

Universidad de Antioquia

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 5

Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 5 Assay:GWAS summary statistics· 4 Research Focus:GWAS / association mapping· 3 Research Focus:polygenic risk· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andréa R. V. R. HorimotoiD· 4 shared Andrea Rivera‐ValdiviaiD· 4 shared Artur Francisco Schumacher SchuhiD· 4 shared Bruno Lopes Santos‐LobatoiD· 4 shared Carlos CosentinoiD· 4 shared Carlos Roberto de Mello RiederiD· 4 shared Carlos Velez‐PardoiD· 4 shared Cyrus P. ZabetianiD· 4 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Andréa R. V. R. HorimotoORCID

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5 papers

Recent·Most cited

Exploring MAPT-containing H1 and H2 haplotypes in Parkinson's disease across diverse populations

Paula Reyes‐Pérez, Jia Wei Hor, Tzi Shin Toh, Arinola O. Sanyaolu, Caroline B. Pantazis, Thiago Peixoto Leal, Sheila Yeboah, Sara Bandrés‐Ciga, Huw R. Morris, Mary B. Makarious, Konstantin A. Senkevich, Pedro Chana-Cuevas, Ximena Pizarro Correa, Angel Vinuela, Esther Colon, , Álvaro Hernandez-Guillen

The paper investigates the association of MAPT haplotypes H1 and H2 with Parkinson's disease risk across diverse populations using genetic data from multiple cohorts.

npj Parkinson s Disease · Jun 24, 2026Peer-reviewedGenetic & Genomic Medicine

X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson Disease

Thiago Peixoto Leal, Jennifer N. French, Mateus Henrique Gouveia, Víctor Borda, Miguel Inca‐Martinez, Emily A Mason, Andréa R. V. R. Horimoto, Douglas P. Loesch, Elif Irem Sarihan, Mario Cornejo‐Olivas, Luis Torres, Pilar Mazzetti, Carlos Cosentino, Elison H. Sarapura‐Castro, Andrea Rivera‐Valdivia, , 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.

medRxiv · Jan 31, 2023 · PreprintGenetic & Genomic Medicine

Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort

Douglas P. Loesch, Andréa R. V. R. Horimoto, Elif Irem Sarihan, Miguel Inca‐Martinez, Emily Mason, Mario Cornejo‐Olivas, Luis Torres, Pilar Mazzetti, Carlos Cosentino, Elison H. Sarapura‐Castro, Andrea Rivera‐Valdivia, Ángel C. Medina, Elena Diéguez, Víctor E. Raggio, Andres Lescano, , 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.

Parkinsonism & Related Disorders · Jun 18, 2022Peer-reviewedGenetic & Genomic Medicine

Characterizing the genetic architecture of Parkinson's disease in Latinos

Douglas P. Loesch, Andréa R. V. R. Horimoto, Karl Heilbron, Elif Irem Sarihan, Miguel Inca‐Martinez, Emily Mason, Mario Cornejo‐Olivas, Luis Torres, Pilar Mazzetti, Carlos Cosentino, Elison H. Sarapura‐Castro, Andrea Rivera‐Valdivia, Ángel C. Medina, Elena Diéguez, Víctor E. Raggio, , 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.

Annals of Neurology · Jul 6, 2021Peer-reviewedGenetic & Genomic Medicine

Genome-wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients

Elif Irem Sarihan, Eduardo Pérez‐Palma, Lisa‐Marie Niestroj, Douglas P. Loesch, Miguel Inca‐Martinez, Andréa R. V. R. Horimoto, Mario Cornejo‐Olivas, Luis Torres, Pilar Mazzetti, Carlos Cosentino, Elison H. Sarapura‐Castro, Andrea Rivera‐Valdivia, Elena Diéguez, Víctor E. Raggio, Andres Lescano, , 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.

Movement Disorders · Nov 5, 2020Peer-reviewedGenetic & Genomic Medicine