Author

Ty Schroeder

University of Minnesota

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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Immunology· 2 Bioinformatics· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 4 Organism:human· 4 Approach:statistical model· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:metabolomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

Christopher M. BastingiD· 3 shared Erik Swanson· 3 shared Garritt Wieking· 3 shared Jodi L. Anderson· 3 shared Kevin Escandón-VargasiD· 3 shared Melanie L. GrahamiD· 3 shared Nichole R. KlattiD· 3 shared Timothy W. SchackeriD· 3 shared

Activity by Year

2026-2026 · peak 4/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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Curved chords = mutual co-authorship

3 shared papersBioinformatics

Christopher M. BastingORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Anorectal care products cause variable inflammation and adverse barrier effects in a mucosal epithelial model

Erik Swanson, Christopher M Basting, Ty Schroeder, Greg Lam, Evan Goldstein, Nichole R. Klatt

This study evaluates the effects of anorectal care products on mucosal epithelial models, finding that hyperosmolar and surfactant-containing products cause inflammation and barrier disruption, while isotonic formulations are less harmful.

bioRxiv · Nov 3, 2026 · PreprintImmunology

Spatial Transcriptomics Reveals Compartment-Specific Immune Activation Signatures in Ileal and Lymph Node Tissue in Treated HIV Infection

Maura Barrett, Jodi L. Anderson, Kevin Escandón-Vargas, Garritt Wieking, Ty Schroeder, Erik Swanson, Melanie L. Graham, Michael Gale, Timothy W. Schacker, Nichole R. Klatt, Christopher M. Basting

This study uses spatial transcriptomics to identify compartment-specific immune activation signatures in ileal and lymph node tissues of HIV-treated patients, revealing tissue-specific transcriptional differences linked to immune activation and microbial translocation.

bioRxiv · Sep 1, 2026 · PreprintBioinformatics

Plasma metabolomics reveals lipid-predominant metabolic disruptions in virologically suppressed people with HIV

Christopher M. Basting, Candace Guerrero, Kevin Escandón-Vargas, Jodi L. Anderson, Garritt Wieking, Erik Swanson, Ty Schroeder, Charlotte R. Hemmila, Ross T. Cromarty, Fernanda Torres-Ruiz, Maribel Soto-Nava, Lady Ruiz-Carbajal, Karla Krystel Ordaz-Candelario, Olivia Briceño, Nicholas Funderburg, , Nichole R. Klatt

The paper uses metabolomics to show that HIV-treated individuals have metabolic disruptions, including lipid changes and inflammation markers, despite viral suppression.

bioRxiv · Aug 20, 2026 · PreprintMicrobiology

Multi-omics links microbial dysbiosis, systemic inflammation and metabolomic disruptions to SNAE risk in treated HIV

Christopher M. Basting, Jodi L. Anderson, Kevin Escandón-Vargas, Garritt Wieking, Candace Guerrero, Jarrett Reichel, Ross T. Cromarty, Erik Swanson, Ty Schroeder, Elaina Creagan, Maura Barrett, Fernanda Torres-Ruiz, Maribel Soto-Nava, Lady Ruiz-Carbajal, Karla Krystel Ordaz-Candelario, , Nichole R. Klatt

This study links microbial dysbiosis, systemic inflammation, and metabolomic disruptions to SNAE risk in treated HIV patients through multi-omic analysis.

JCI Insight · Jul 21, 2026Peer-reviewedImmunology