Sanja Mehandziska

University Clinic of Traumatology — Austria

Biochemistry, Genetics and Molecular Biology · Life Sciences

5h-index116citations16works0.32yr avg
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Research Topics

Cancer Genomics and Diagnostics(6), COVID-19 Clinical Research Studies(3), Bacterial Genetics and Biotechnology(3), SARS-CoV-2 and COVID-19 Research(2), Cancer Immunotherapy and Biomarkers(2)

Publications16 total

Tumors with mutations in chromatin regulators are associated with higher mutational burden and improved response to checkpoint immunotherapy
Clinical Epigenetics·2025Open Access
Tumors with mutations in chromatin regulators are associated with higher mutational burden and improved response to checkpoint immunotherapy
2025Open Access
Development of a molecular assay for multiomic detection of cfDNA signals in blood samples from skin cancer patients
EJC Skin Cancer·2025Open Access
Tumors with mutations in chromatin regulators are associated with higher mutational burden and improved response to checkpoint immunotherapy
2024· 1 citedOpen Access
Case Report: Omicron BA.2 Subvariant of SARS-CoV-2 Outcompetes BA.1 in Two Co-infection Cases
Frontiers in Genetics·2022· 8 citedOpen Access
Composition of Transcription Machinery and Its Crosstalk with Nucleoid-Associated Proteins and Global Transcription Factors
Biomolecules·2021· 13 citedOpen Access
Early Initiation of Extracorporeal Blood Purification Using the AN69ST (oXiris®) Hemofilter as a Treatment Modality for COVID-19 Patients: a Single-Centre Case Series
Brazilian Journal of Cardiovascular Surgery·2020· 18 citedOpen Access
Early initiation of Extracorporeal Blood Purification using the AN69ST (oXiris®) hemofilter as a treatment modality for COVID - 19 patients: a single-centre case series
Research Square (Research Square)·2020· 3 citedOpen Access
Workflow for the Implementation of Precision Genomics in Healthcare
Frontiers in Genetics·2020· 5 citedOpen Access
Genetic aberrations in chromatin factors are pervasive, mutually exclusive, associated with a high mutational burden and improved response to checkpoint immunotherapy in cancer
Research Square (Research Square)·2020Open Access
Genetic aberrations in chromatin factors are pervasive, mutually exclusive, associated with a high mutational burden and improved response to checkpoint immunotherapy in cancer
2019Open Access
A Pediatric Case of Glioblastoma Multiforme Associated With a Novel Germline p.His112CysfsTer9 Mutation in the MLH1 Gene Accompanied by a p.Arg283Cys Mutation in the TP53 Gene: A Case Report
Frontiers in Genetics·2019· 5 citedOpen Access
P961CYP2C19-dependent clopidogrel resistance is a possible cause for coronary stent and peripheral bypass occlusion
European Heart Journal·2018· 1 citedOpen Access
Trio Clinical Exome Sequencing in a Patient With Multicentric Carpotarsal Osteolysis Syndrome: First Case Report in the Balkans
Frontiers in Genetics·2018· 21 citedOpen Access
Isolation and Analysis of RNA Polymerase Supramolecular Complex with Associated Proteins
Methods in molecular biology·2017· 3 cited
Structural Coupling between RNA Polymerase Composition and DNA Supercoiling in Coordinating Transcription: a Global Role for the Omega Subunit?
mBio·2011· 38 citedOpen Access

Frequent Co-authors

Goran Kungulovski(11), Ivan Kungulovski(8), Aleksandra Stajkovska(7), Rodney Alexander Rosalia(7), Zan Mitrev(6), Zan Mitrev(5), Marija Gjorgjievska(5), Margarita Stavrevska(4), Marija Janevska(4), Georgi Muskhelishvili(3), Kristina Jakovleva(3), Martina Markovska(3), Djansel Bukovec(3), Milan Risteski(3), Andrew Travers(2), Patrick Sobetzko(2), Petar Ugurov(2), Dijana Popevski(2), Tanja Gramosli(2), Dragica Vuckova(2)