Author

Raúl E. Cachau

Frederick National Laboratory for Cancer ResearchORCID 0000-0001-9260-2102Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Cell Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:experimental assay· 2 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Approach:genetic perturbation / CRISPR· 1 Assay:protein structure· 1 Assay:proteomics· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Alison A. McBrideiD· 1 shared Alix WarburtoniD· 1 shared Ashley N. Della FeraiD· 1 shared Cheryl Ann WinkleriD· 1 shared Daeui ParkiD· 1 shared Do Hyeon ChaiD· 1 shared Heon Yung GeeiD· 1 shared Jiyao WangiD· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperCell Biology

Alison A. McBrideORCID

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3 papers

Recent·Most cited

Cell BiologyJournal of Biological ChemistryPeer-reviewedOct 13, 2025

Sp100A isoform promotes HIRA histone chaperone localization to PML nuclear bodies

Ashley N. Della Fera, Warda Arman, Maceo E. Powers…·Alison A. McBride

The paper shows Sp100A promotes HIRA localization to PML-NBs in keratinocytes, with the SUMO interacting motif being critical for this function.

2 citations

humanproteomics

BioinformaticsbioRxivPreprintJul 1, 2020

Using iCn3D and the World Wide Web for structure-based collaborative research: Analyzing molecular interactions at the root of COVID-19

Philippe Youkharibache, Raúl E. Cachau, Tom Madej, Jiyao Wang

The paper introduces iCn3D, a web-based tool for collaborative structural analysis of molecular interactions related to COVID-19, enabling efficient sharing and visualization of 3D data and sequence annotations.

2 citations

humanprotein structure

GeneticsbioRxivPreprintNov 8, 2018

Genetic predisposition to hypouricemia on whole-exome sequencing analysis and its utilities in primary screening purposes

Do Hyeon Cha, Heon Yung Gee, Raúl E. Cachau…·Sung Kweon Cho

This paper uses whole-exome sequencing to identify genetic markers for hypouricemia and shows that screening two SNPs can detect 87.7% of cases.

3 citations

humanwhole-exome sequencing