Author

A. H. Jonsson

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· 6 Cell Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 7 Research Focus:cell type annotation· 6 Research Focus:differential expression· 4 Approach:statistical model· 4 Approach:experimental assay· 3 Assay:scRNA-seq· 3 Assay:bulk RNA-seq· 2 Research Focus:cell-cell communication· 2

Frequent Co-Authors

D. A. Rao· 6 shared M. B. Brenner· 5 shared S. Raychaudhuri· 4 shared A. Nathan· 3 shared F. Zhang· 3 shared K. Wei· 3 shared L. T. Donlin· 3 shared G. F. M. Watts· 2 shared

Activity by Year

2018-2023 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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6 shared papersImmunology

D. A. Rao

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Author profile →

7 papers

Recent·Most cited

Adipocytes regulate fibroblast function, and their loss contributes to fibroblast dysfunction in inflammatory diseases

H. Faust, T.-Y. Cheng, I. Korsunsky, G. F. M. Watts, S. T. Gal-Oz, W. Trim, K. Kongthong, A. H. Jonsson, D. P. Simmons, F. Zhang, R. Padera, S. Chubinskaya, Accelerating Medicines Partnership Program, K. Wei, S. Raychaudhuri, , M. B. Brenner

The paper shows adipocytes regulate fibroblast function through cortisol signaling, and their loss leads to fibroblast dysfunction in inflammatory diseases.

bioRxiv · May 16, 2023Cell Biology

The Chromatin Landscape of Pathogenic Transcriptional Cell States in Rheumatoid Arthritis

K. Weinand, S. Sakaue, A. Nathan, A. H. Jonsson, F. Zhang, G. F. M. Watts, Z. Zhu, Accelerating Medicines Partnership Program: RA and SLE Network, D. A. Rao, J. H. Anolik, M. B. Brenner, L. T. Donlin, K. Wei, S. Raychaudhuri

The paper identifies chromatin classes in RA synovial tissue and links them to transcriptional cell states and genetic variants.

bioRxiv · Apr 7, 2023 · PreprintImmunology

Clonal associations of lymphocyte subsets and functional states revealed by single cell antigen receptor profiling of T and B cells in rheumatoid arthritis synovium

G. S. Dunlap, A. Wagner, N. Meednu, F. Zhang, A. H. Jonsson, K. Wei, S. Sakaue, A. Nathan, Accelerating Medicines Partnership Program: Rheumatoid Arthritis and Systemic Lupus Erythematosus (A, V. P. Bykerk, L. T. Donlin, S. M. Goodman, G. S. Firestein, D. L. Boyle, V. M. Holers, , J. Anolik

This study uses single-cell antigen receptor profiling to identify clonal relationships and functional states of T and B cells in RA synovium.

bioRxiv · Mar 18, 2023 · PreprintImmunology

Aging and interferon gamma response drive the phenotype of neutrophils in the inflamed joint

R. Grieshaber-Bouyer, T. Exner, N. S. Hackert, F. A. Radtke, S. A. Jelinsky, O. Halyabar, A. Wactor, E. Karimizadeh, J. Schettini, A. H. Jonsson, D. A. Rao, L. A. Henderson, C. Mueller-Tidow, H.-M. Lorenz, G. Wabnitz, , P. A. Nigrovic

This study identifies transcriptional and phenotypic changes in synovial fluid neutrophils from arthritis patients, highlighting IFNγ response and aging as key drivers.

bioRxiv · Nov 16, 2021 · PreprintImmunology

Clonally expanded CD38hi cytotoxic CD8 T cells define the T cell infiltrate in checkpoint inhibitor-associated arthritis

R. Wang, A. Singaraju, K. E. Marks, L. Shakib, G. S. Dunlap, A. Cunningham-Bussel, L. Chen, A. Tirpack, M. R. Fein, D. J. Todd, L. MacFarlane, S. M. Goodman, E. F. DiCarlo, E. M. Massarotti, J. A. Sparks, , D. A. Rao

This study identifies a distinct CD38hi cytotoxic CD8 T cell subset in ICI-induced arthritis, showing clonal expansion and IFN-driven activation.

bioRxiv · Oct 19, 2021 · PreprintImmunology

Repertoire analyses reveal TCR sequence features that influence T cell fate

K. A. Lagattuta, J. B. Kang, A. Nathan, K. E. Pauken, A. H. Jonsson, D. A. Rao, K. Ishigaki, S. Raychaudhuri

The paper identifies TCR sequence features that influence T cell fate by analyzing TCR sequences from human cells and developing a scoring system for regulatory potential.

bioRxiv · Jun 23, 2021Immunology

The immune cell landscape in kidneys of lupus nephritis patients

A. Arazi, D. A. Rao, C. C. Berthier, A. Davidson, Y. Liu, P. J. Hoover, A. Chicoine, T. M. Eisenhaure, A. H. Jonsson, S. Li, D. J. Lieb, E. P. Browne, A. Noma, D. Sutherby, S. Steelman, , B. Diamond

This study uses single-cell RNA-seq to analyze immune cell subsets in lupus nephritis kidneys, identifying pro-inflammatory and resolving responses and potential therapeutic targets.

bioRxiv · Jul 7, 2018Immunology