Author

Ashish Sharma

Emory UniversityORCID 0000-0001-9444-7046Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Ashish Sharma1 paper · University of Copenhagen

Biology Disciplines

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Genetic & Genomic Medicine· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Research Focus:cell-cell communication· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Henry Y. LuiD· 2 shared Joshua DalmanniD· 2 shared Kate L. Del BeliD· 2 shared Maggie P. FuiD· 2 shared Mehul SharmaiD· 2 shared Stuart E. TurveyiD· 2 shared Susan Xiaoqin LiniD· 2 shared Wyeth W. WassermaniD· 2 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Henry Y. LuORCID

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3 papers

Recent·Most cited

ImmunologyJournal of Clinical InvestigationPeer-reviewedJul 14, 2026

Neutralization activity in chronic HIV infection is characterized by a distinct programming of follicular helper CD4 T cells

Eirini Moysi, Ashish A. Sharma, Sijy J. O'Dell…·Constantinos Petrovas

The paper identifies distinct follicular helper CD4 T cell programming in HIV-positive individuals who produce broadly neutralizing antibodies, linking it to improved B cell follicle architecture and reduced suppressor cells.

1 citation

humanbulk RNA-seq

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Genetic & Genomic MedicineThe Journal of Experimental MedicinePeer-reviewedFeb 10, 2023

Human Germline Heterozygous Gain-of-Function STAT6 Variants Cause Severe Allergic Disease

Mehul Sharma, Daniel Leung, Mana Momenilandi…·Stuart E. Turvey

This study identifies heterozygous gain-of-function STAT6 variants in two patients with severe allergic disease and shows JAK inhibitors reduce the enhanced STAT6 responses.

125 citationstop 1%

humanstatistical model

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Genetic & Genomic MedicineBloodPeer-reviewedJul 5, 2022

Human germline biallelic complete NFAT1 deficiency causes the triad of progressive joint contractures, osteochondromas, and susceptibility to B cell malignancy

Mehul Sharma, Maggie P. Fu, Henry Y. Lu…·Stuart E. Turvey

The paper identifies a human with complete NFAT1 deficiency, revealing its role in joint contractures, osteochondromas, and B cell malignancy through single-cell omic analyses.

19 citations

humanbulk RNA-seq

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