Author

E. J. Rushing

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

Biology Disciplines

Click to filter author papers

Cancer Biology· 3

Signature Assays, Organisms & Methods

Click to filter · or open tag

Assay:bulk RNA-seq· 3 Organism:human· 2 Approach:statistical model· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:development & morphogenesis· 1

Frequent Co-Authors

A. Burger· 1 shared A. Ferguson· 1 shared A. Fleischmann· 1 shared A. Garofoli· 1 shared A. Rodriguez· 1 shared A. van Drogen· 1 shared B. Augustynek· 1 shared B. Snijder· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperCancer Biology

A. Burger

Author profile →

3 papers

Recent·Most cited

Targeting tumour-intrinsic neural vulnerabilities of glioblastoma

S. Lee, T. Weiss, M. Buehler, J. Mena, Z. Lottenbach, R. Wegmann, M. Sun, M. Bihl, B. Augustynek, S. Baumann, S. Goetze, A. van Drogen, P. Pedrioli, D. Kirschenbaum, F. Vasella, , B. Snijder

This study identifies neural vulnerabilities in glioblastoma by analyzing patient samples and model systems, revealing drug targets and pathways that can be exploited for treatment.

bioRxiv · Oct 7, 2022 · PreprintCancer Biology

The Genomic Landscape of Prostate Cancer Brain Metastases

A. Rodriguez, J. Gallon, D. Akhoundova, S. Maletti, A. Ferguson, J. Cyrta, U. Amstutz, A. Garofoli, V. Paradiso, S. Tomlins, E. Hewer, V. Genitsch, A. Fleischmann, E. J. Rushing, R. Grobholz, , M. A. Rubin

This study identifies genomic alterations in prostate cancer brain metastases, highlighting mutations in NF1 and RICTOR and DNA homologous repair defects as potential drivers.

bioRxiv · May 12, 2020 · PreprintCancer Biology

Active Receptor Tyrosine Kinases, but not Brachyury, are sufficient to trigger chordoma in zebrafish

G. D'Agati, E. M. Cabello, K. Frontzek, E. J. Rushing, R. Klemm, M. Robinson, R. M. White, C. Mosimann, A. Burger

This study identifies that RTKs EGFR and KDR/VEGFR2, not Brachyury, can induce chordoma in zebrafish by disrupting notochord differentiation through RTK/Ras signaling.

bioRxiv · Nov 29, 2018Cancer Biology