Author

Meriam A. Waqas

University of British ColumbiaORCID 0000-0001-7617-4179Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Anna F. LeeiD· 1 shared Anna LehmaniD· 1 shared Anthony Philip CooperiD· 1 shared Areesha SalmaniD· 1 shared Ashish SharmaiD· 1 shared Audi SetiadiiD· 1 shared Bhavi P. ModiiD· 1 shared Christina MichalskiiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anna F. LeeORCID

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1 paper

Recent·Most cited

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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