Author

M. J. Willner

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Bioengineering· 1

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Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Organism:human· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1

Frequent Co-Authors

B. Xu· 1 shared C. Xu· 1 shared E. Azizi· 1 shared J. Gogos· 1 shared K. W. Leong· 1 shared R. Tomer· 1 shared S. Chauhan· 1 shared S. He· 1 shared

Activity by Year

2021-2021 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperBioengineering

B. Xu

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1 paper

Recent·Most cited

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