Author

Martina Markovska

ORCID 0009-0005-1246-7307Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aleksandra Stajkovska· 1 shared Goran KungulovskiiD· 1 shared Ivan KungulovskiiD· 1 shared Marija Janevska· 1 shared Rodney Alexander RosaliaiD· 1 shared Sanja Mehandziska· 1 shared Zan K. MitreviD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

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7 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Aleksandra Stajkovska

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintDec 3, 2019

Genetic aberrations in chromatin factors are pervasive, mutually exclusive, associated with a high mutational burden and improved response to checkpoint immunotherapy in cancer

Martina Markovska, Rodney Alexander Rosalia, Aleksandra Stajkovska…·Goran Kungulovski

The paper examines genetic aberrations in chromatin modifiers across cancer datasets, finding mutual exclusivity, higher prevalence in certain cancers, and links to mutational burden and immunotherapy response.

DOI 10.1101/861823

humanwhole-genome sequencing

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