Author

Julia M. Martínez Gómez

University of ZurichORCID 0000-0002-5684-3707Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:benchmarking· 2 Assay:bulk RNA-seq· 2 Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

Mitchell Paul LevesqueiD· 3 shared David J. AdamsiD· 2 shared Ingrid FerreiraiD· 2 shared Á.R. Rodríguez-Pérez· 1 shared Agshin Balayev· 1 shared Ala’a Al HroutiD· 1 shared Alejandro Jiménez-SáncheziD· 1 shared Alethia Álvarez‐CanoiD· 1 shared

Activity by Year

2020-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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3 shared papersCancer Biology

Mitchell Paul LevesqueORCID

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Author profile →

3 papers

Recent·Most cited

Melanoma Response to Immunotherapy is regulated by B Cell-Derived Extracellular Vesicles

Ala’a Al Hrout, Agshin Balayev, Karla Cervantes-Gracia, Konstantinos Gkelis, Stephan Benke-Bruderer, Julia M. Martínez Gómez, Karīna Siliņa, Mitchell Paul Levesque, Richard Chahwan

This study identifies B cell-derived extracellular vesicles and miR-99a-5p as key regulators of melanoma response to immunotherapy.

Science Advances · Oct 8, 2025Peer-reviewedCancer Biology

The microenvironment of ulcerated acral melanoma is characterised by an inflammatory milieu and an enhanced humoral immune response

Martha Estefania Vázquez‐Cruz, Patricia Basurto‐Lozada, Christian Molina‐Aguilar, Bram Van Haastrecht, Irving Simonin Wilmer, Sophia Orozco-Ruiz, Héctor Martínez‐Said, Alethia Álvarez‐Cano, Dorian Yarih García-Ortega, Ingrid Ferreira, Alfredo Hidalgo‐Miranda, Diego Hinojosa Ugarte, Luis Alberto Tavares-de-la-Paz, Jonadab E. Olguín, Isabella Salinas, , Carla Daniela Robles‐Espinoza

This study identifies immunological differences in ulcerated acral melanoma, showing increased humoral immunity and inflammation markers, and proposes potential therapeutic targets.

medRxiv · May 5, 2025 · PreprintGenetic & Genomic Medicine

Multi-site clonality analyses uncovers pervasive subclonal heterogeneity and branching evolution across melanoma metastases

Roy Rabbie, Naser Ansari‐Pour, Oliver M. Cast, Doreen Lau, Francis Scott, Sarah Joanne Welsh, Christine Parkinson, Leila Khoja, Luiza Moore, Mark Tullett, Kim Wong, Ingrid Ferreira, Julia M. Martínez Gómez, Mitchell Paul Levesque, Ferdia Aidan Gallagher, , David J. Adams

The paper analyzes whole-genome sequencing data from melanoma metastases to show that branched evolution is common and that subclonal heterogeneity is prevalent in metastatic melanoma.

Nature Communications · Aug 27, 2020Peer-reviewedGenomics