Author

Bilal K. AlWattar

Boston Children's HospitalORCID 0009-0007-8942-983XUnclaimed 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:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Alexandra K. BlomfieldiD· 1 shared Anne B. FultoniD· 1 shared Jasmine LiniD· 1 shared Jing CheniD· 1 shared Kiran BoraiD· 1 shared Pankaj B. AgrawaliD· 1 shared Qifei LiiD· 1 shared Shiyu LuoiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetics

Alexandra K. BlomfieldORCID

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintOct 18, 2023

Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion

Shiyu Luo, Bilal K. AlWattar, Qifei Li…·Pankaj B. Agrawal

This study investigates the effects of HBS1L deficiency on retinal dystrophy, showing proteomic changes and photoreceptor cell loss in both human and mouse models.

1 citation

mousehuman

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