Author

L. O'Mahony

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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Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:proteomics· 2 Approach:statistical model· 2 Approach:experimental assay· 1

Frequent Co-Authors

B. Forde· 2 shared N. Lunjani· 2 shared A. Cerny· 1 shared A. Mortha· 1 shared A. U. Neumann· 1 shared C. A. Akdis· 1 shared C. Altunbulakli· 1 shared C. Garzoni· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

B. Forde

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Author profile →

3 papers

Recent·Most cited

A gut commensal protozoa remotely shapes a lung niche for asthma-promoting eosinophils.

K. Burrows, L. Ngai, P. Chiaranunt, E. Cao, C. Streutker, B. Forde, L. O'Mahony, A. Mortha

This study shows that the gut protozoa Tritrichomonas musculis exacerbates asthma by promoting lung eosinophilia through a tripartite immune network.

bioRxiv · Mar 25, 2022 · PreprintImmunology

Excessive inflammatory and metabolic responses to acute SARS-CoV-2 infection are associated with a distinct gut microbiota composition

W. C. Albrich, T. S. Ghosh, S. Ahearn-Ford, F. Mikaeloff, N. Lunjani, B. Forde, N. Suh, G.-R. Kleger, U. Pietsch, M. Frischknecht, C. Garzoni, R. Forlenza, M. Horgan, C. Sadlier, T. R. Negro, , L. O'Mahony

This study identifies distinct gut microbiota compositions and metabolic/cytokine profiles associated with severe outcomes in SARS-CoV-2 infection.

bioRxiv · Oct 26, 2021 · PreprintImmunology

Distribution of ACE2, CD147, cyclophilins, CD26 and other SARS-CoV-2 associated molecules in human tissues and immune cells in health and disease

U. Radzikowska, M. Ding, G. Tan, D. Zhakparov, Y. Peng, P. Wawrzyniak, M. Wang, S. Li, H. Morita, C. Altunbulakli, M. Reiger, A. U. Neumann, N. Lunjani, C. Traidl-Hoffmann, K. Nadeau, , M. Sokolowska

The paper examines the expression of SARS-CoV-2-related molecules in human tissues and immune cells across health and disease states, identifying age, comorbidities, and immune cell types associated with altered expression.

bioRxiv · May 14, 2020Immunology