Author

Brice Calco

National Institutes of Health

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

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Neuroscience· 1

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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 Benjamin M. GreenbergiD· 1 shared Bianca Palicha· 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

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1 shared paperNeuroscience

Avindra NathORCID

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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