Author

A. M. Robinson

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 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Research Focus:development & morphogenesis· 2 Assay:scRNA-seq· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

A. G. Shuparski· 2 shared B. W. Higgins· 2 shared K. B. Miller· 2 shared L. J. McHeyzer-Williams· 2 shared M. G. McHeyzer-Williams· 2 shared C. Buenaventura· 1 shared C. K. Thompson· 1 shared H. Bailey· 1 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

9 top collaborators · 16 mutual co-author links

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2 shared papersImmunology

A. G. Shuparski

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Lead (Pb) impairs thyroid hormone mediated changes in brain development and body length in Xenopus laevis tadpoles

L. I. Dahora, A. M. Robinson, C. Buenaventura, H. Bailey, C. K. Thompson

bioRxiv · Sep 27, 2022 · PreprintPharmacology & Toxicology

Evolution of antigen-specific follicular helper T cell transcriptional programs across effector function and through to memory

A. M. Robinson, B. W. Higgins, A. G. Shuparski, K. B. Miller, L. J. McHeyzer-Williams, M. G. McHeyzer-Williams

This study identifies antigen-specific transcriptional programs in follicular helper T cells across effector function and memory development, revealing distinct inflammatory and anti-inflammatory modules.

bioRxiv · Sep 17, 2021 · PreprintImmunology

Programming isotype specific plasma cell differentiation

B. W. Higgins, A. G. Shuparski, K. B. Miller, A. M. Robinson, L. J. McHeyzer-Williams, M. G. McHeyzer-Williams

This study identifies isotype-specific molecular programs in murine plasma cells, revealing distinct pathways for IgM, IgG1, IgG2a/b, and IgA that govern antigen clearance and immune protection.

bioRxiv · Aug 31, 2021 · PreprintImmunology