Author

Carlos Frederico Martins Menck

Universidade de São PauloORCID 0000-0003-1941-0694Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:benchmarking· 1 Approach:biophysical modeling· 1 Research Focus:cell type annotation· 1 Assay:DNA methylation· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

Juliana Brandstetter VilariD· 2 shared Veridiana MunfordiD· 2 shared Alain R. SarasiniD· 1 shared Alexander A.L. JorgeiD· 1 shared Anthony Gabry da SilveiraiD· 1 shared Antonio Amorin· 1 shared Antônio Marcondes LerárioiD· 1 shared Ari WaismaniD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Juliana Brandstetter VilarORCID

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3 papers

Recent·Most cited

ImmunologyNature CommunicationsPeer-reviewedApr 1, 2026

Th17 cells require the DNA repair sensor XPC to control oxidative DNA damage

Jefferson Antônio Leite, Natalia Notarberardino Bos, Luísa Menezes-Silva…·Niels Olsen Saraiva Câmara

This study identifies XPC as essential for protecting Th17 cells from oxidative DNA damage, showing its role in DNA repair, differentiation, and function.

DOI 10.1038/s41467-026-69914-y

mouseDNA methylation

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Genetic & Genomic MedicineCarcinogenesisPeer-reviewedMay 17, 2023

Mutational signatures and increased retrotransposon insertions in Xeroderma Pigmentosum variant skin tumors

Camila Corradi, Juliana Brandstetter Vilar, Vanessa Candiotti Buzatto…·Carlos Frederico Martins Menck

The paper identifies mutational signatures and retrotransposon insertions in XP-V skin tumors, linking them to UV exposure and tobacco use, and suggests immunotherapy potential.

12 citations

humanwhole-exome sequencing

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Genetic & Genomic MedicinemedRxivPreprintOct 20, 2022

PCNA thermosensitivity underlies an Ataxia Telangiectasia-like disorder

Joe Magrino, Veridiana Munford, Davi Jardim Martins…·Brian A. Kelch

The paper identifies a second PCNA mutation, C148S, causing PARD, showing both variants have thermo-stability defects leading to reduced chromatin-bound PCNA and temperature-dependent phenotypes.

DOI 10.1101/2022.10.20.22281069

humanexperimental assay

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