Author

Stephanie Jump

National Jewish Health

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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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Camille M. MooreiD· 1 shared Erwin W. GelfandiD· 1 shared Hara LevyiD· 1 shared Jennifer R. KnappiD· 1 shared Jeremy W. ProkopiD· 1 shared Joanne M. Domenico· 1 shared Justin E. Ideozu· 1 shared Kate A. Woods· 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

Camille M. MooreORCID

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Author profile →

1 paper

Recent·Most cited

CFTR-mediated monocyte-macrophage dysfunction revealed by cystic fibrosis proband-parent comparisons

Xi Zhang, Camille M. Moore, Laura D. Harmacek, Joanne M. Domenico, Vittobai Rashika Rangaraj, Justin E. Ideozu, Jennifer R. Knapp, Kate A. Woods, Stephanie Jump, Shuang Jia, Jeremy W. Prokop, Russell Paul Bowler, Martin J. Hessner, Erwin W. Gelfand, Hara Levy

The paper compares transcriptomic profiles of CF probands and their parents to healthy controls, revealing CFTR-related immune dysfunction in both homozygous and heterozygous carriers.

JCI Insight · Mar 21, 2022Peer-reviewedGenetic & Genomic Medicine