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MD, School of Medicine, Aristotle University of Thessaloniki, Greece, 2012
M.Sc. in Research Methodology in Biomedicine, Biostatistics and Clinical Bioinformatics, University of Thessaly, 2016
M.Sc. in Clinical Applications of Molecular Medicine, School of Medicine, University of Thessaly, 2018
April 2018: Erasmus Research Scholarship, Division of Translational Medical Oncology, Deutsches Krebsforschungszentrum (DKFZ), Heidelberg, Germany. Supervisor: Prof. Dr. Stefan Fröhling
Ph.D. candidate in Medical Oncology, School of Medicine, University of Ioannina, Greece, 2019-
Title of PhD thesis: “Studying the role of cancer-related cell surface cluster of differentiation (CD) molecules on cancer cell growth: Role of canonical NF-κB signalling on CD regulation”, PhD in Medical Oncology, University of Ioannina
Kougioumtzi A.; Ntellas P, Papadopoulou E, Nasioulas G, Kampletsas E, Pentheroudakis G. (2019). Molecular findings reveal possible resistance mechanisms in a patient with ALK-rearranged lung cancer: A case report and literature review. ESMO Open 4, doi:10.1136/esmoopen-2019-000561.
Xiromerisiou G, Marogianni C, Dadouli K, et al. (2020). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy revisited: Genotype-phenotype correlations of all published cases. Neurol. Genet. 6(3):e434
Xiromerisiou G, Dadouli K, Marogianni C, Provatas A, Ntellas P, et al. (2020). A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published cases. J. Mol. Neurosci. 70(1):131-141.
Ntellas P, Mavroeidis L, Gkoura S, Gazouli I, Amylidou A-L, Papadaki A, Zarkavelis G, Mauri D, Karpathiou G, Kolettas E, Batistatou A and Pentheroudakis G. (2020). Old player-new tricks: Non angiogenic effects of the VEGF/VEGFR pathway in cancer. Cancers (Basel) 12(11):E3145
Marogianni C, Georgouli D, Dadouli K, Ntellas P, Rikos D, Hadjigeorgiou GM, Spanaki C, Xiromerisiou G. (2021). Identification of a novel de novo KMT2B variant in a Greek dystonia patient via exome sequencing genotype–phenotype correlations of all published cases. Mol. Biol. Rep. 8(1):371-79