Author

Terri G. Thompson

University of California, IrvineORCID 0000-0002-5970-6601Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 2 Research Focus:differential expression· 2 Organism:human· 2 Assay:proteomics· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Organism:Drosophila· 1 Approach:experimental assay· 1

Frequent Co-Authors

Aaron P. Frank· 1 shared Alex Lenail· 1 shared Alyssa N. CoyneiD· 1 shared Andrea D. MatlockiD· 1 shared Andrew Tai-Ann ChengiD· 1 shared Artur ShvetcoviD· 1 shared Berhan Mandefro· 1 shared Brandon Shelley· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperNeuroscience

Aaron P. Frank

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2 papers

Recent·Most cited

APOE ε4 defines a systemic immune endophenotype independent of clinical trajectory in amyotrophic lateral sclerosis

Artur Shvetcov, Shannon Thomson, Sterling Kwan, Terri G. Thompson, Jeffery D. Rothstein, Caitlin A. Finney

This study identifies an APOE ε4-associated systemic immune proteomic signature in ALS that predicts disease progression independently of clinical features.

bioRxiv · Feb 4, 2026 · PreprintNeuroscience

An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients

Loren Ornelas, Emilda Gomez, Lindsay Panther, Aaron P. Frank, Susan Lei, Berhan Mandefro, Maria G. Bañuelos, Brandon Shelley, Julia Kaye, Leandro de Araújo Lima, Stacia K. Wyman, Ryan G. Lim, Jie Wu, Jennifer T. Stocksdale, Malcolm Casale, , Leslie Michels Thompson

The paper performs an integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients to identify dysregulated pathways and validate them in vivo and in postmortem data.

bioRxiv · Nov 1, 2020 · PreprintNeuroscience