Author

E. H. Ahn

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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Cancer Biology· 2 Bioengineering· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:clustering· 2 Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1

Frequent Co-Authors

A. S. T. Smith· 1 shared B. Kohrn· 1 shared C. E. Murry· 1 shared C.-Y. Su· 1 shared D.-H. Kim· 1 shared E. C. Clark· 1 shared E. Choi· 1 shared J. C. Wu· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperBioengineering

A. S. T. Smith

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Changes of Mutations and Copy-number and Enhanced Cell Migration during Breast Tumorigenesis

S. H. T. Lee, J. Y. Kim, P. Kim, Z. Dong, C.-Y. Su, E. H. Ahn

This study identifies mutations and copy-number variations in breast tumorigenic cells and shows that ECM-mimetic platforms enhance their migration.

bioRxiv · Mar 27, 2022Cancer Biology

Unexpectedly High Subclonal Mutational Diversity in Human Colorectal Cancer and Its Significance

L. A. Loeb, B. Kohrn, K. J. Loubet-Senear, Y. J. Dunn, E. H. Ahn, J. N. O'Sullivan, J. J. Salk, M. P. Bronner, R. A. Beckman

This study quantifies subclonal mutations in colorectal cancer using Duplex Sequencing, revealing high mutation rates and confirming neutral evolution in tumors.

bioRxiv · Jun 21, 2019Cancer Biology

NanoMEA: a versatile platform for high-throughput analysis of structure-function relationships in human stem cell-derived excitable cells and tissues

A. S. T. Smith, E. Choi, K. Gray, J. Macadangdang, E. H. Ahn, E. C. Clark, P. Tyler, M. A. Laflamme, L. Tung, J. C. Wu, C. E. Murry, D.-H. Kim

This paper introduces nanoMEAs to enhance the structural and functional properties of hPSC-derived cardiomyocytes and neurons, improving their response to pharmacological agents.

bioRxiv · Oct 26, 2018 · PreprintBioengineering