Author

M. Schnaubelt

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

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

A. H. Kim· 1 shared A. N. Reeb· 1 shared B. Friedrich· 1 shared C. C. Fronick· 1 shared C. Oh· 1 shared C. Zuo· 1 shared C.-K. Mo· 1 shared Ch· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperCancer Biology

A. H. Kim

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2 papers

Recent·Most cited

Spatial drivers and pre-cancer populations collaborate with the microenvironment in untreated and chemo-resistant pancreatic cancer

D. Cui Zhou, R. G. Jayasinghe, J. M. Herndon, E. Storrs, C.-K. Mo, Y. Wu, R. S. Fulton, M. A. Wyczalkowski, C. C. Fronick, L. A. Fulton, L. Thammavong, K. Sato, H. Zhu, H. Sun, L.-B. Wang, , Ch

This paper uses spatial single-cell omics to analyze PDAC tumors and microenvironment, identifying key populations and interactions that may inform treatment strategies.

bioRxiv · Jan 13, 2021Cancer Biology

Orthogonal proteomic platforms and their implications for the stable classification of high-grade serous ovarian cancer subtypes

S. N. Thomas, B. Friedrich, M. Schnaubelt, D. W. Chan, H. Zhang, R. Aebersold

This study compares two proteomic methods, 2DLC-MS/MS and SWATH-MS, showing they both identify differentially expressed proteins in HGSOC subtypes but differ in workflow complexity and proteome coverage.

bioRxiv · Oct 3, 2019Cancer Biology