Author

Martin Cesarini

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· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Jorge OrozcoiD· 2 shared Mary B. MakariousiD· 2 shared Natalia Gonzalez Rojas· 2 shared Thiago Peixoto LealiD· 2 shared Alan Osvaldo Espinal MartineziD· 1 shared Alex MedinaiD· 1 shared Alicia ColomboiD· 1 shared Álvaro Hernandez-Guillen· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Jorge OrozcoORCID

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2 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

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