Author

Hara Levy

National Jewish HealthORCID 0000-0002-3784-0711Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Justin E. Ideozu· 2 shared Aparna VasanthakumariD· 1 shared Ashvani K. SinghiD· 1 shared Bridget M. Riley-GillisiD· 1 shared Camille M. MooreiD· 1 shared Erwin W. GelfandiD· 1 shared Fedik RahimoviD· 1 shared Jeffrey F. WaringiD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Justin E. Ideozu

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences

Justin E. Ideozu, Mengzhen Liu, Bridget M. Riley-Gillis, Sri R. Paladugu, Fedik Rahimov, Preethi Krishnan, Rakesh L. Tripathi, Patrick K. Dorr, Hara Levy, Ashvani K. Singh, Jeffrey F. Waring, Aparna Vasanthakumar

The paper characterizes CFTR variant diversity across six ancestries using UK Biobank whole exome sequences, identifying ancestry-specific variants and associations with CF-related phenotypes.

medRxiv · Mar 10, 2023 · PreprintGenetic & Genomic Medicine

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