Author

Virginia Vega-Warner

University of MichiganORCID 0009-0007-6396-6717Unclaimed 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 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Assay:organoid / primary culture· 1 Approach:statistical model· 1

Frequent Co-Authors

Matthias KretzleriD· 2 shared Akihiro MinakawaiD· 1 shared Anja M. BillingiD· 1 shared Bradley GodfreyiD· 1 shared Brendan Crawford· 1 shared Catherine C Robertson· 1 shared Céline C. BerthieriD· 1 shared Chenchen HeiD· 1 shared

Activity by Year

2016-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersCell Biology

Matthias KretzlerORCID

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintJan 14, 2026

Dapagliflozin mitigates hypoxia-induced metabolic stress, kidney tubular cell death and fibrosis

Akihiro Minakawa, Jamal El Saghir, Céline C. Berthier…·Jennifer L. Harder

This study shows dapagliflozin reduces hypoxia-induced metabolic stress, cell death, and fibrosis in kidney organoids derived from human pluripotent stem cells.

1 citation

humanorganoid / primary culture

𝕏 PostBluesky

GeneticsPediatric NephrologyPeer-reviewedOct 20, 2016

Evaluating Mendelian nephrotic syndrome genes for evidence of risk alleles or oligogenicity that explain heritability

Brendan Crawford, Christopher E Gillies, Catherine C Robertson…·Matthew Sampson

This study evaluates whether risk alleles or oligogenicity in 21 Mendelian nephrotic syndrome genes explain NS heritability, but finds no significant burden or unique combinations in NS patients compared to a reference population.

DOI 10.1007/s00467-016-3513-3

humanwhole-exome sequencing

𝕏 PostBluesky