Author

Madison M. Uyemura

Beth Israel Deaconess Medical Center

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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Cancer Biology· 1 Microbiology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Research Focus:cell signaling & trafficking· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1

Frequent Co-Authors

Frank John SlackiD· 3 shared João A. PauloiD· 2 shared Jonathan D. LeeiD· 2 shared Maria MavrikakiiD· 2 shared Ryan R. PoseyiD· 2 shared Amyah C. Harris· 1 shared Anupama RaiiD· 1 shared Arne M. MülleriD· 1 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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Curved chords = mutual co-authorship

3 shared papersCancer Biology

Frank John SlackORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Cancer BiologybioRxivPreprintSep 30, 2026

Tumor suppressor-like mutations mark a dosage-constrained dependency in leukemia

Jonathan D. Lee, Madison M. Uyemura, Francisca Lamini…·Frank John Slack

The paper shows that oncogene-imposed dosage constraints can lead to mutations resembling tumor suppressor loss, which are essential in APL.

DOI 10.64898/2026.09.29.755484

humanbulk RNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintMay 28, 2026

A microRNA atlas of the human prefrontal cortex across the adult lifespan

Irais E. Valenzuela-Arzeta, Pourya Naderi Yeganeh, Anupama Rai…·Maria Mavrikaki

The paper creates a miRNA atlas of the human prefrontal cortex across aging, identifying age-related miRNA changes and highlighting miR-34a-5p as a key upregulated miRNA in older individuals.

DOI 10.64898/2026.05.27.728239

humanbulk RNA-seq

𝕏 PostBluesky

MicrobiologyCell ReportsPeer-reviewedNov 21, 2023

Differences in syncytia formation by SARS-CoV-2 variants modify host chromatin accessibility and cellular senescence via TP53

Jonathan D. Lee, Bridget L. Menasché, Maria Mavrikaki…·Frank John Slack

This study shows that SARS-CoV-2 variants differ in syncytia formation, which affects host chromatin accessibility, cellular senescence, and inflammation via TP53.

17 citations

𝕏 PostBluesky