Author

Tiger Zhou

Flinders UniversityORCID 0000-0001-6495-8865Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Alex William HewittiD· 3 shared David Anthony MackeyiD· 3 shared Jamie E. CraigiD· 3 shared Owen M. SiggsiD· 3 shared Anthony L. CookiD· 2 shared Connor J GreatbatchiD· 2 shared Guei‐Sheung LiuiD· 2 shared Helena Hai LiangiD· 2 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Alex William HewittORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

GeneticsOphthalmology SciencePeer-reviewedMar 5, 2024

Deep Learning-based Identification of Intraocular Pressure-Associated Genes Influencing Trabecular Meshwork Cell and Organelle Morphology

Connor J Greatbatch, Qinyi Lu, Sandy S. C. Hung…·Alex William Hewitt

The paper uses AI to identify genes associated with intraocular pressure by analyzing morphological changes in trabecular meshwork cells after gene knockouts.

9 citations

humanimaging

𝕏 PostBluesky

GeneticsHuman Molecular GeneticsPeer-reviewedJan 10, 2024

High throughput functional profiling of genes at intraocular pressure loci reveals distinct networks for glaucoma

Connor J Greatbatch, Qinyi Lu, Sandy S. C. Hung…·Alex William Hewitt

This study uses gene knockouts and single-cell RNA sequencing to identify genetic networks contributing to elevated intraocular pressure in glaucoma.

15 citationstop 3%

humanscRNA-seq

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GeneticsOphthalmologyPeer-reviewedJan 7, 2020

Congenital glaucoma with anterior segment dysgenesis in individuals with biallelic CPAMD8 variants

Owen M. Siggs, Emmanuelle Souzeau, Deepa Ajay Taranath…·Jamie E. Craig

The paper identifies biallelic CPAMD8 variants as a cause of congenital glaucoma with anterior segment dysgenesis in four individuals from three families.

72 citationstop 2%

humanwhole-exome sequencing

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