Author

Carolyne Croizier

New York Genome CenterORCID 0000-0002-2932-2957Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:ATAC-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1

Frequent Co-Authors

Alyssa C. IndartiD· 1 shared Benjamin TerrieriD· 1 shared Catherine J. PotenskiiD· 1 shared Dan Avi LandauiD· 1 shared David B. BeckiD· 1 shared Eirini P. PapapetrouiD· 1 shared Elliot O. EtoniD· 1 shared Franco IzzoiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Alyssa C. IndartORCID

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1 paper

Recent·Most cited

Single-cell genotype-phenotype mapping identifies therapeutic vulnerabilities in VEXAS syndrome

Saravanan Ganesan, Rebecca M. Murray, Jesús Alfonso López Sotélo, Elliot O. Eton, Kouhei Takashima, Theo Botella, Kai Beattie, Alyssa C. Indart, Nada Chraiki, Carolyne Croizier, Franco Izzo, Catherine J. Potenski, Samuele G. Marro, Zhijie Wu, Shouguo Gao, , Dan Avi Landau

This study uses single-cell multi-omics to map genotype-to-phenotype relationships in VEXAS syndrome, identifying PERK pathway activation as a therapeutic target.

bioRxiv · May 19, 2024 · PreprintGenomics