Author

Andrew E. Place

Boston Children's HospitalORCID 0000-0002-9604-4213Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Approach:experimental assay· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Marian H. HarrisiD· 2 shared Amy Guillaumet-AdkinsiD· 1 shared Annette S. KimiD· 1 shared Arnaldo ArbiniiD· 1 shared Barbara A. DegariD· 1 shared Birgit KnoecheliD· 1 shared Carlo BrugnaraiD· 1 shared Daniel R. BouéiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersCancer Biology

Marian H. HarrisORCID

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2 papers

Recent·Most cited

Altered immune and treatment response gene expression signatures among poverty-exposed children with B-ALL

Amy Guillaumet-Adkins, Noori Sotudeh, Sayalee V. Potdar, Tushara Vijaykumar, Monica S. Nair, Valeriya Dimitrova, Julia Frede, Yana Pikman, Marian H. Harris, Andrew E. Place, Lewis B. Silverman, Jens G. Lohr, Kira O'Neil Bona, Birgit Knoechel

This study identifies transcriptional signatures of steroid resistance and altered immune responses in poverty-exposed children with B-ALL using single-cell RNA sequencing.

bioRxiv · Jan 29, 2026 · PreprintCancer Biology

Acute promyelocytic leukemia with torque teno mini virus (TTMV)::RARA fusion: an approach to screening and diagnosis

Harrison Kwei Tsai, Mark F Sabbagh, Meagan Montesion, Erik Abraham Williams, Arnaldo Arbini, Daniel R. Boué, Emily M. Harris, Franziska Wachter, Leslie Grimmett, Andrew E. Place, Fabienne McClanahan Lucas, Valentina Nardi, Annette S. Kim, Carlo Brugnara, Barbara A. Degar, , Jacob R. Bledsoe

The paper describes a clinicopathologic approach and tools for diagnosing APL with TTMV::RARA fusion using NGS assays, identifying four cases with poor treatment outcomes.

medRxiv · Mar 29, 2024 · PreprintGenetic & Genomic Medicine