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2. Genetska in farmakogenetska analiza izbranih genov pri bolnikih z astmo v SlovenijiMateja Žavbi, 2016, doctoral dissertation Keywords: astma, fenotip astme, rinitis, genetika, polimorfizem posameznega nukleotida, asociacijska raziskava, KOPB, kronična obstruktivna pljučna bolezen, ORMDL3, ORMDL - regulator biosinteze sfingolipidov 3, halotip, farmakogenetika, VEGFA, žilni endotelijski rastni dejavnik A, disertacije
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4. High burden of clonal mast cell disorders and hereditary α-tryptasemia in patients who need Hymenoptera venom immunotherapyPeter Korošec, Gunter J. Sturm, Jonathan J. Lyons, Tinkara Pirc Marolt, Manca Svetina, Mitja Košnik, Mihaela Zidarn, Mark Kačar, Nina Frelih, Nika Lalek, Ajda Demšar Luzar, Samo Zver, Matevž Škerget, Ewa Czarnobilska, Wojciech Dyga, Sanja Popović-Grle, Miroslav Samaržija, Lisa Arzt-Gradwohl, Urban Čerpes, Grzegorz Porebski, Branko Pevec, Eva Schadelbauer, Peter Kopač, Julij Šelb, Matija Rijavec, 2024, original scientific article Keywords: anaphylaxis, hereditary α-tryptasemia, hypersensitivity, immunotherapy, mast cell, mastocytosis, venom
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5. Gene expression levels of the prolyl hydroxylase domain proteins PHD1 and PHD2 but not PHD3 are decreased in primary tumours and correlate with poor prognosis of patients with surgically resected non-small-cell lung cancerAna Koren, Matija Rijavec, Tomaž Krumpestar, Izidor Kern, Aleksander Sadikov, Tanja Čufer, Peter Korošec, 2021, original scientific article Keywords: non-small-cell lung cancer, mRNA expression, prolyl hydroxylase domain proteins, carcinoma, prognosis
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6. Clonal mast cell disorders and hereditary α-tryptasemia as risk factors for anaphylaxisMark Kačar, Matija Rijavec, Julij Šelb, Peter Korošec, 2023, review article Keywords: anaphylaxis, venom, food, drugs, tryptase, mast cells, KIT p.D816V, hereditary α-tryptasemia, hypersensitivity, diagnosis, food hypersensitivity, drug hypersensitivity
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7. Integrative transcriptomic analysis in human and mouse model of anaphylaxis identifies gene signatures associated with cell movement, migration and neuroinflammatory signallingMatija Rijavec, Aleš Maver, Paul J. Turner, Keli Hočevar, Mitja Košnik, Amnah Yamani, Simon P. Hogan, Adnan Custovic, Borut Peterlin, Peter Korošec, 2022, original scientific article Keywords: transcriptome analysis, cell movement, migration, neuroinflammatory signaling, lipid activating nuclear receptors signaling, anaphylaxis, diagnosis, mast cells, basophils, neutrophils
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8. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiencyNina Rupar, Julij Šelb, Mitja Košnik, Mihaela Zidarn, Slađana Andrejević, Ljerka Čulav, Vesna Grivčeva-Panovska, Peter Korošec, Matija Rijavec, 2024, original scientific article Keywords: hereditary angioedema, C1 inhibitor deficiency, genetic modifiers, clinical phenotype, genotype-phenotype correlation, genetic variant, SERPING1, CC2D2B
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9. Fatal Hymenoptera venom–triggered anaphylaxis in patients with unrecognized clonal mast cell disorderMatija Rijavec, Jezerka Inkret, Urška Bidovec-Stojković, Tanja Carli, Nina Frelih, Andreja Kukec, Peter Korošec, Mitja Košnik, 2023, original scientific article Keywords: fatal anaphylaxis, Hymenoptera venom, mastocytosis, venom immunotherapy
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10. Evaluation of serum diamine oxidase as a diagnostic test for histamine intoleranceKristina Arih, Nina Đorđević, Mitja Košnik, Matija Rijavec, 2023, original scientific article Keywords: medicine, diamine oxidase, serum, diagnosis, histamine intolerance
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