Author

S. McElroy

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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Bioengineering· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Organism:human· 2 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Approach:genetic perturbation / CRISPR· 1 Assay:organoid / primary culture· 1

Frequent Co-Authors

B. Xu· 2 shared C. Xu· 2 shared E. Azizi· 2 shared K. W. Leong· 2 shared R. Tomer· 2 shared S. Chauhan· 2 shared S. He· 2 shared Y.-H. Lao· 2 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersBioengineering

B. Xu

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Human vascular organoids with a mosaic AKT1 mutation recapitulate Proteus syndrome

S. He, Y. Zhu, S. Chauhan, D. N. Tavakol, J. H. Lee, R. B.-L. Berris, C. Xu, J. Lee, C. Lee, S. Cai, S. McElroy, G. Vunjak-Novakovic, R. Tomer, E. Azizi, B. Xu, , K. W. Leong

This paper creates a vascular organoid model with an AKT1 mutation to study Proteus syndrome and finds AKT inhibitors reverse vascular malformations.

bioRxiv · Jan 26, 2024 · PreprintBioengineering

Mapping morphological malformation to genetic dysfunction in blood vessel organoids with 22q11.2 Deletion Syndrome

S. He, C. Xu, Y.-H. Lao, S. Chauhan, Y. Xiao, M. J. Willner, Y. Jin, S. McElroy, S. Rao, J. Gogos, R. Tomer, E. Azizi, B. Xu, K. W. Leong

This study uses blood vessel organoids from 22q11.2 DS patients to link genetic dysfunction to vascular malformations through single-cell transcriptomics and imaging.

bioRxiv · Nov 17, 2021 · PreprintBioengineering