Author

Rachel R. Brown

Stanford MedicineORCID 0000-0003-1364-9610Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:chromatin & epigenetic regulation· 1 Organism:human· 1 Assay:long-read sequencing· 1 Research Focus:protein structure prediction· 1 Assay:proteomics· 1 Organism:Xenopus· 1

Frequent Co-Authors

Aaron F. StraightiD· 2 shared Aaron StreetsiD· 1 shared Angela M. DetweileriD· 1 shared Annie MaslaniD· 1 shared Jacob Price SchwartziD· 1 shared Karen H. MigaiD· 1 shared Kousik SundararajaniD· 1 shared Lyin GhadriiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersCell Biology

Aaron F. StraightORCID

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintJul 15, 2025

Regulation of X. laevis M18BP1 centromeric localization and CENP-A assembly

Rachel R. Brown, Jacob Price Schwartz, Lyin Ghadri, Aaron F. Straight

This study identifies a cell cycle-dependent phosphorylation mechanism that regulates M18BP1 binding to CENP-A nucleosomes, controlling CENP-A assembly during interphase.

1 citation

Xenopusproteomics

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GenomicsNature MethodsPeer-reviewedApr 8, 2022

DiMeLo-seq: a long-read, single-molecule method for mappingprotein-DNA interactions genome-wide

Nicolas Altemose, Annie Maslan, Owen K. Smith…·Aaron Streets

DiMeLo-seq maps protein-DNA interactions genome-wide with single-molecule resolution by methylating DNA near binding sites and using long-read sequencing.

154 citationstop 1%

humanlong-read sequencing

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