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1. Shared genetic risk factors between cancer and cardiovascular diseases Aleksander Turk, Tanja Kunej, 2022, izvirni znanstveni članek Ključne besede: cancer, cardiovascular disease, risk factor, chemotherapy, comorbidity, genetic variant, interaction
network, cardio-oncology |
2. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency Nina Rupar, Julij Šelb, Mitja Košnik, Mihaela Zidarn, Slađana Andrejević, Ljerka Čulav, Vesna Grivčeva-Panovska, Peter Korošec, Matija Rijavec, 2024, izvirni znanstveni članek Ključne besede: hereditary angioedema, C1 inhibitor deficiency, genetic modifiers, clinical phenotype, genotype-phenotype correlation, genetic variant, SERPING1, CC2D2B |