Author

Neal S. Young

National Institutes of HealthORCID 0009-0007-0999-2519Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Zhijie WuiD· 2 shared Aaron B. Schultz· 1 shared Alejandro V. VillarinoiD· 1 shared Alyssa C. IndartiD· 1 shared Amy E. KeatingiD· 1 shared Benjamin TerrieriD· 1 shared Carolyne CroizieriD· 1 shared Catherine J. PotenskiiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetics

Zhijie WuORCID

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2 papers

Recent·Most cited

GeneticsLife Science AlliancePeer-reviewedApr 14, 2025

STAT5B leukemic mutations, altering SH2 tyrosine 665, have opposing impacts on immune gene programs

Hye‐Kyung Lee, Jichun Chen, Rachael Laura Philips…·Lothar G. Hennighausen

The paper investigates two STAT5B mutations in T cell leukemias, showing one causes gain-of-function and the other loss-of-function, with distinct impacts on immune cell populations and transcriptional activity.

8 citations

humanmouse

𝕏 PostBluesky

GenomicsbioRxivPreprintMay 19, 2024

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

Saravanan Ganesan, Rebecca M. Murray, Jesús Alfonso López Sotélo…·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.

16 citations

humanscRNA-seq

𝕏 PostBluesky