Author

Emilia Mabel Gatto

Hospital Ramos MejíaORCID 0000-0002-1346-5443Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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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:benchmarking· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Marcelo Andrés KauffmaniD· 5 shared Vítor TumasiD· 5 shared Alexander A. ZimprichiD· 4 shared Andrew SingletoniD· 4 shared Artur Francisco Schumacher SchuhiD· 4 shared Carlos Roberto de Mello RiederiD· 4 shared Claire E. ShepherdiD· 4 shared Edward A. FoniD· 4 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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5 shared papersGenetic & Genomic Medicine

Marcelo Andrés KauffmanORCID

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5 papers

Recent·Most cited

Genomic Landscape of Early-Onset and Familial Latin American Parkinson's Patients

Emily Waldo, Henry Mauricio Chaparro-Solano, Mariam Isayan, Thiago Peixoto Leal, Felipe Duarte-Zambrano, Miguel Inca‐Martinez, Janvi Ramchandra, Maria Paz, Mary B. Makarious, Carlos F. Hernández, Emilia Mabel Gatto, Natalia Gonzalez Rojas, Martin Cesarini, Bruno Lopes Santos‐Lobato, Grace Helena Letro, , 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.

medRxiv · Sep 22, 2026 · PreprintGenetic & Genomic Medicine

TMEM175, SCARB2 and CTSB associations with Parkinson's disease risk across populations.

Wenhua Sun, Claudia Schulte, Thomas Gasser, Manuela M. X. Tan, the Global Parkinson’s Genetic Program (GP2), Lasse Pihlstrøm, Pedro Chaná, Yeajin Song, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Andrew Singleton, Mike A. Nalls, Hampton L. Leonard, Mie Rizig, Hirotaka Iwaki, , Rejko Krüger

This study identifies genetic associations between lysosomal genes and Parkinson's disease risk across diverse populations using GWAS and whole genome sequencing data.

npj Parkinson s Disease · Dec 2, 2025Peer-reviewedGenetic & Genomic Medicine

Insights into Ancestral Diversity in Parkinsons Disease Risk: A Comparative Assessment of Polygenic Risk Scores

Paula Saffie Awad, Spencer M. Grant, Mary B. Makarious, Inas Elsayed, Arinola O. Sanyaolu, Peter Wild Crea, Artur Francisco Schumacher Schuh, Kristin S. Levine, Dan Vitale, Mathew J. Koretsky, Jeffrey Kim, Thiago Peixoto Leal, María Teresa Periñán, Sumit Dey, Alastair John Noyce, , Edward A. Fon

This study compares polygenic risk scores for Parkinson's disease across seven ancestries, finding varying predictive accuracy and highlighting the need for ancestry-specific models.

npj Parkinson s Disease · Jul 3, 2025Peer-reviewedGenetic & Genomic Medicine

Multi-ancestry genome-wide meta-analysis in Parkinson's disease

Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, Stella W. Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Paul Cannon, Daniella Coker, Gabriel Cuéllar-Partida, , Piu Chan

This paper conducts a multi-ancestry genome-wide meta-analysis of Parkinson's disease, identifying 78 independent loci and 23 genes associated with PD risk.

Nature Genetics · Dec 28, 2023Peer-reviewedGenetic & Genomic Medicine

Global Parkinson's Genetics Program (GP2) Complex Network Protocol: Defining the causes of sporadic Parkinson's disease

Clodagh Towns, Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar, Alejandro Martínez-Carrasco, Mary B. Makarious, Bradford H. Casey, Dan Vitale, Kristin S. Levine, Hampton L. Leonard, Caroline B. Pantazis, Laurel A. Screven, Dena G. Hernandez, , Andrea Quattrone

The paper outlines the protocol for integrating genetic and clinical data from a global cohort of over 150,000 participants to study the genetic causes of sporadic Parkinson's disease.

npj Parkinson s Disease · Sep 12, 2023Peer-reviewedGenetic & Genomic Medicine