Author

Lauren Rose Wilkes

New York University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Aravinda ChakravartiiD· 2 shared Gabriel GrulloniD· 2 shared Sumantra ChatterjeeiD· 2 shared Aamir R. ZuberiiD· 1 shared Hanna Berk-RauchiD· 1 shared Jarod A. RollinsiD· 1 shared Lauren E. FriesiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

7 top collaborators · 17 mutual co-author links

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2 shared papersGenomics

Aravinda ChakravartiORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintJan 28, 2026

Sod1 trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal Ret suppression and glial remodeling

Gabriel Grullon, Jarod A. Rollins, Lauren Rose Wilkes…·Sumantra Chatterjee

This study shows that SOD1 trisomy disrupts ENS development and increases HSCR risk by reducing RET expression and altering glial states.

DOI 10.64898/2026.01.26.701837

𝕏 PostBluesky

GeneticsbioRxivPreprintJan 23, 2025

Combined effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system

Lauren E. Fries, Gabriel Grullon, Lauren Rose Wilkes…·Sumantra Chatterjee

The paper investigates how a non-coding variant in a RET enhancer and a coding null allele together cause loss of inhibitory motor neurons in the enteric nervous system, leading to Hirschsprung disease.

3 citations

mousebulk RNA-seq

𝕏 PostBluesky