Author

Benjamin M. Greenberg

The University of Texas Southwestern Medical CenterORCID 0000-0002-2091-8201Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1

Frequent Co-Authors

Avindra NathiD· 1 shared Bianca Palicha· 1 shared Brice Calco· 1 shared Christa S. ZerbeiD· 1 shared Colin L. SweeneyiD· 1 shared Farinaz SafaviiD· 1 shared Joseph P. SteineriD· 1 shared Kelsey Yoo· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 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

1 shared paperNeuroscience

Avindra NathORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

A novel frameshift mutation in Phosphoinositide 3-kinase regulatory subunit 1 (PIK3R1) causes immunodeficiency and Amyotrophic Lateral Sclerosis (ALS)

Brice Calco, Colin L. Sweeney, Joseph P. Steiner, Tongguang Wang, Tovah E. Markowitz, Subrata Paul, Bianca Palicha, Sara Dinges, Kelsey Yoo, Lisa J. Henderson, Valerie McDonald, Suk See De Ravin, Benjamin M. Greenberg, Christa S. Zerbe, Luigi Daniele Notarangelo, , Farinaz Safavi

The paper identifies a novel PIK3R1 frameshift mutation linked to immunodeficiency and ALS, showing haploinsufficiency causes neuronal dysfunction and apoptosis.

bioRxiv · May 23, 2025 · PreprintNeuroscience