Author
Ryan M. Boileau
Duke UniversityORCID 0000-0003-0670-3236Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
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2022-2026 · peak 2/yrCo-Author Collaboration Network
10 top collaborators · 15 mutual co-author links6 papers
Recent·Most cited
- BioengineeringbioRxivPreprint
An autonomous system for multi-objective continuous evolution at scale
Ryan M. Boileau, Stefan M. Golas, Qianni Ma…·Emma J. Chory
TurboPRANCE enables large-scale, multi-objective continuous evolution by integrating robotic systems with phage-assisted evolution, generating high-resolution evolutionary data across diverse selection regimes.
DOI 10.64898/2026.03.02.709196 - Developmental BiologyStem CellsPeer-reviewed
The miR-290 and miR-302 clusters are essential for reprogramming of fibroblasts to induced pluripotent stem cells
Julia Ye, Ryan M. Boileau, Ronald J. Parchem…·Robert H. Blelloch
This study shows that miR-290 and miR-302 clusters are essential for reprogramming fibroblasts to iPSCs, but individually are not required, while their combined loss blocks the process.
4 citations - Molecular BiologybioRxivPreprint
Synergy between cis-regulatory elements can render cohesin dispensable for distal enhancer function
Karissa L. Hansen, Annie S. Adachi, Luca Braccioli…·Elphège Pierre Nora
This study shows that cohesin is not always necessary for enhancer function, as some enhancers can act independently through synergy or insulators.
28 citations - GenomicsbioRxivPreprint
MLL3/MLL4 enzymatic activity shapes DNA replication timing
Deniz Gökbuget, Ryan M. Boileau, Kayla Lenshoek, Robert H. Blelloch
The paper identifies MLL3/MLL4 enzymatic activity as a regulator of DNA replication timing through H3K4me1 modification, showing its role in chromatin structure and replication dynamics during differentiation.
- GenomicsbioRxivPreprint
Loss of MLL3/4 decouples enhancer H3K4 monomethylation, H3K27 acetylation, and gene activation during ESC differentiation
Ryan M. Boileau, Kevin X. Chen, Robert H. Blelloch
This study shows that MLL3/4 are essential for dynamic enhancer histone modifications but not for stable ones, and their loss does not impair transcriptional activation of nearby genes.