Author

María A. Gómez-Muñoz

NYU Langone HealthORCID 0000-0002-6478-8197Unclaimed 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· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Approach:statistical model· 2 Approach:biophysical modeling· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell-cell communication· 1 Approach:experimental assay· 1

Frequent Co-Authors

Eva HernandoiD· 2 shared Milad IbrahimiD· 2 shared Nicole M. EskowiD· 2 shared A. Paulina MedelliniD· 1 shared Adam Walker· 1 shared Aida Amador-ÁlvareziD· 1 shared Alcida KarziD· 1 shared Amanda Flores YankeiD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersCancer Biology

Eva HernandoORCID

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3 papers

Recent·Most cited

Cancer BiologybioRxivPreprintSep 19, 2026

Cross-species spatial profiling links progranulin to an immune suppressive niche in brain metastasis

Nicole M. Eskow, Kylie Prutisto-Chang, María A. Gómez-Muñoz…·Eva Hernando

The paper identifies progranulin as a mediator of immune suppressive niches in brain metastasis using cross-species spatial transcriptomics and functional analyses.

DOI 10.64898/2026.09.13.751277

mousehuman

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Cancer BiologyCell Communication and SignalingPeer-reviewedJan 10, 2026

Rho GTPases signaling mediates aggressiveness and differentiation in neuroblastoma tumors

María A. Gómez-Muñoz, Mónica Ojeda-Puertas, Luis Luna-Ramírez…·Francisco M. De La Vega

This study investigates Rho GTPase signaling in neuroblastoma, finding dysregulation associated with aggressiveness and identifying Cdc42 as a key regulator of differentiation and stemness.

1 citation

humanbulk RNA-seq

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Cancer BiologybioRxivPreprintMar 18, 2025

The carnosinase dipeptidase CNDP1 is a novel metabolic vulnerability in brain metastasis

María A. Gómez-Muñoz, Alcida Karz, Maya R. Navarro…·Eva Hernando

This study identifies CNDP1 as a metabolic vulnerability in brain metastasis, showing its inhibition suppresses metastasis and its expression confers metastatic potential.

1 citation

humanproteomics

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