Author

I. Damm

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· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell-cell communication· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

M. M. Sarwal· 3 shared P. Rashmi· 2 shared T. Sigdel· 2 shared A. A. da Silva· 1 shared A. A. Silva· 1 shared A. L. F. Gouvea· 1 shared A. L. Lourenco· 1 shared C. S. Craik· 1 shared

Activity by Year

2022-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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3 shared papersImmunology

M. M. Sarwal

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3 papers

Recent·Most cited

Perturbations in podocyte transcriptome and biological pathways induced by FSGS associated circulating factors.

P. Rashmi, T. K. Sigdel, D. Rychkov, I. Damm, A. A. da Silva, F. Vincenti, A. L. Lourenco, C. S. Craik, J. Reiser, M. M. Sarwal

This paper investigates how circulating factors like suPAR and CD40 autoantibodies induce podocyte injury in FSGS and identifies therapeutic targets for rFSGS.

Annals of Translational Medicine · Jun 1, 2023Peer-reviewedImmunology

Genetic deletion and pharmacologic inhibition of FcER1 reduces renal injury in mouse models of diabetic nephropathy.

P. Rashmi, A. A. Silva, T. Sigdel, I. Damm, A. L. F. Gouvea, S. Koliwad, V. Walavalkar, S. Hakroush, M. M. Sarwal

This study shows that reducing FcER1 signaling in mouse models of diabetic nephropathy decreases proteinuria and kidney damage.

bioRxiv · Sep 10, 2022 · PreprintImmunology

Perturbations of the T-cell immune repertoire in kidney transplant rejection

T. Sigdel, P. A. Fields, J. Liberto, I. Damm, M. Kerwin, J. Hood, P. Towfighi, M. Sirota, H. Robins, M. M. Sarwal

This study examines T-cell repertoire changes in kidney transplant recipients to understand rejection mechanisms, finding lower pre-transplant T-cell fractions and higher TCR turnover during acute rejection.

bioRxiv · Aug 24, 2022Immunology