Author

F. Neri

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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Cell Biology· 3

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Assay:imaging· 1 Assay:proteomics· 1

Frequent Co-Authors

B. Schilling· 3 shared J. Campisi· 3 shared P.-Y. Desprez· 2 shared A. A. Gerencser· 1 shared A. Gerencser· 1 shared C. A. Lerner· 1 shared D. Wirtz· 1 shared J. Bons· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

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3 shared papersCell Biology

B. Schilling

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Senescent cell heterogeneity and responses to senolytic treatment are related to cell cycle status during cell growth arrest.

F. Neri, S. Zheng, M. Watson, P. Y. Desprez, A. Gerencser, J. Campisi, D. Wirtz, P.-H. Wu, B. Schilling

This study identifies functionally distinct senescent cell subpopulations based on cell cycle status, showing G2-arrested cells secrete more IL-6 and are more sensitive to senolytic treatment.

bioRxiv · Jun 22, 2024 · PreprintCell Biology

A Fully-Automated Senescence Test (FAST) for the high-throughput quantification of senescence-associated markers

F. Neri, S. N. Takajjart, C. A. Lerner, P.-Y. Desprez, B. Schilling, J. Campisi, A. A. Gerencser

The paper introduces FAST, an automated method for high-throughput senescence quantification using image-based markers, showing it accurately measures senescence burden across cell types and reduces false positives.

bioRxiv · Dec 22, 2023Cell Biology

Comprehensive Profiling of Plasma Exosomes Using Data Independent Acquisitions, New Tools for Aging Cohort Studies

S. K. Patel, R. Bruderer, N. Basisty, J. Bons, P.-Y. Desprez, F. Neri, L. Reiter, J. Campisi, B. Schilling

The paper develops a method to isolate and analyze plasma exosomes, identifying age-related protein and miRNA differences in an aging cohort.

bioRxiv · Feb 27, 2021 · PreprintCell Biology