Author

Zulema G. Romero

University of California, Los AngelesORCID 0000-0001-8305-8184Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Assay:CRISPR screen· 2 Organism:human· 2 Research Focus:variant calling· 2 Approach:deep learning· 1 Approach:experimental assay· 1

Frequent Co-Authors

Dario BoffelliiD· 2 shared David I. K. Martin· 2 shared Donald B. KohniD· 2 shared Mark C. WaltersiD· 2 shared Seok‐Jin HeoiD· 2 shared Stacia K. WymaniD· 2 shared Beatriz Campo-Fernández· 1 shared Fiona HennigiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Dario BoffelliORCID

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2 papers

Recent·Most cited

GenomicsGenesPeer-reviewedJun 24, 2026

Oligonucleotide synthesis errors are a source of untoward variation in HDR-mediated gene editing

Stacia K. Wyman, Zulema G. Romero, Seok‐Jin Heo…·Dario Boffelli

This study identifies synthesis errors in ssODNs used for HDR-mediated gene editing and shows they propagate into the genome, potentially causing disease alleles.

1 citation

humanCRISPR screen

𝕏 PostBluesky

GeneticsbioRxivPreprintJan 8, 2019

High-level correction of the sickle mutation amplified in vivo during erythroid differentiation

Wendy Magis, Mark A. DeWitt, Stacia K. Wyman…·David I. K. Martin

Cas9-mediated correction of the sickle mutation in human hematopoietic stem cells achieves curative levels of editing.

17 citations

humanCRISPR screen

𝕏 PostBluesky