Author

Areesha Salman

University of British ColumbiaORCID 0000-0001-6362-2104Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Audi SetiadiiD· 2 shared Henry Y. LuiD· 2 shared Maggie P. FuiD· 2 shared Mehul SharmaiD· 2 shared Michael Steffen KoboriD· 2 shared Stuart E. TurveyiD· 2 shared Susan Xiaoqin LiniD· 2 shared Anna F. LeeiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Audi SetiadiORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of Clinical ImmunologyPeer-reviewedApr 28, 2025

A germline heterozygous dominant negative IKZF2 variant causing syndromic primary immune regulatory disorder and ICHAD

Henry Y. Lu, Maryam Vaseghi‐Shanjani, Avery J. Lam…·Stuart E. Turvey

The paper describes a germline variant in IKZF2 causing immune dysregulation, including AIHA and atopic dermatitis, and reports single-cell RNA sequencing findings on T cell dysfunction.

6 citations

humanbulk RNA-seq

𝕏 PostBluesky

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

𝕏 PostBluesky