Author

Robert J. Schneider

New York UniversityORCID 0000-0001-5807-5564Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Assay:bulk RNA-seq· 3 Approach:experimental assay· 3 Research Focus:cancer & tumor microenvironment· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

C. Theresa VincentiD· 2 shared A. Paulina MedelliniD· 1 shared Adam C. MariD· 1 shared Adam Walker· 1 shared Adler Guerrero· 1 shared Albert Jiang· 1 shared Alcida KarziD· 1 shared Alex Donovan· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersCancer Biology

C. Theresa VincentORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Cancer BiologybioRxivPreprintMay 15, 2026

Purinergic signaling promotes gliomagenesis through nuclear calcium transients

Shuai Wang, Jenna Richter, Claire Kim…·Dimitris G. Placantonakis

This study identifies purinergic signaling via P2RY1 receptors and nuclear calcium transients as a driver of glioblastoma tumorigenesis, with therapeutic potential through P2RY1 inhibition.

DOI 10.64898/2026.05.11.724407

humanbulk RNA-seq

𝕏 PostBluesky

Cancer BiologybioRxivPreprintMar 18, 2025

The carnosinase dipeptidase CNDP1 is a novel metabolic vulnerability in brain metastasis

María A. Gómez-Muñoz, Alcida Karz, Maya R. Navarro…·Eva Hernando

This study identifies CNDP1 as a metabolic vulnerability in brain metastasis, showing its inhibition suppresses metastasis and its expression confers metastatic potential.

1 citation

humanproteomics

𝕏 PostBluesky

Molecular BiologyCommunications BiologyPeer-reviewedMar 26, 2021

Inhibiting LXRα Phosphorylation in Hematopoietic Cells Reduces Inflammation and Attenuates Atherosclerosis and Obesity

Maud Voisin, Elina Shrestha, Claire Rollet…·Michael J. Garabedian

This study shows that inhibiting LXRα phosphorylation in hematopoietic cells reduces inflammation and improves atherosclerosis and obesity by altering macrophage and adipose tissue gene expression.

10 citations

mousebulk RNA-seq

𝕏 PostBluesky