Researchers
Novaković, Ivana
Issue Date | Title | Author(s) | Type | М-cat. |
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2023 | The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti (✓) | Minić, Snežana B. ; Cerovac, Nataša M. ; Novaković, Ivana V. ; Gazikalović, Slobodan; Popadić, Svetlana P. ; Trpinac, Dušan P. | Article | 21M21 |
2023 | miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome (✓) | Janković, Milena ; Nikolić, Dejan ; Novaković, Ivana ; Petrović, Bojana ; Lacković, Milan ; Šantrić-Milićević, Milena | Article | 21M21 |
2022 | Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia (✓) | Perić, Stojan ; Marković, Vladana ; Candayan, Ayse; De Vriendt, Els; Momčilović, Nikola; Savić, Andrija; Dragašević-Mišković, Nataša ; Svetel, Marina ; Stević, Zorica ; Božović, Ivo ; | Article | 21M21 |
2022 | The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options (✓) | Janković, Milena ; Petrović, Bojana ; Novaković, Ivana ; Branković, Slavko ; Radosavljević, Nataša ; Nikolić, Dejan | Article | 21M21 |
2022 | Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation (✓) | Minić, Snežana B. ; Trpinac, Dušan P. ; Novaković, Ivana V. ; Cerovac, Nataša M. ; Dobrosavljević-Vukojević, Danijela ; Rosain, Jeremie | Article | 21M21 |
2022 | Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages (✓) | Pereza, Nina; Terzic, Rifet; Plaseska-Karanfilska, Dijana; Miljanovic, Olivera; Novaković, Ivana V. ; Poslon, Zeljka; Ostojic, Sasa; Peterlin, Borut | Article | 21M21 |
2022 | Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience (✓) | Kresojević, Nikola ; Dobričić, Valerija ; Ječmenica-Lukić, Milica ; Tomić, Aleksandra ; Petrović, Igor ; Dragašević, Nataša ; Perović, Ivana; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; | Article | 21M21 |
2021 | Genetic and epigenomic modifiers of diabetic neuropathy (✓) | Janković, Milena ; Novaković, Ivana ; Nikolić, Dejan ; Mitrović-Maksić, Jasmina ; Branković, Slavko ; Petronić, Ivana ; Ćirović, Dragana ; Dučić, Siniša ; Grajić, Mirko ; Bogićević, Dragana | Article | 21M21 |
2021 | The FKBP5 genotype and childhood trauma effects on FKBP5 DNA methylation in patients with psychosis, their unaffected siblings, and healthy controls (✓) | Mihaljević, Marina ; Franić, Dušanka ; Soldatović, Ivan ; Lukić, Iva ; Andrić-Petrović, Sanja ; Mirjanić, Tijana; Stanković, Biljana ; Žukić, Branka ; Zeljić, Katarina ; Gašić, Vladimir ; | Article | 21M21 |
2021 | Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA (✓) | Đurić, Olivera ; Anđelković, Marina ; Vreća, Miša ; Skakić, Anita ; Pavlović, Sonja ; Novaković, Ivana ; Jovanović, Bojan ; Škodrić-Trifunović, Vesna ; Marković-Denić, Ljiljana | Article | 21M21 |
2021 | Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis (✓) | Janković, Milena ; Novaković, Ivana ; Gamil Anwar Dawod, Phepy; Gamil Anwar Dawod, Ayman; Drinić, Aleksandra; Abdel Motaleb, Fayda I.; Dučić, Sinisa ; Nikolić, Dejan | Article | 21M21 |
2021 | Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents (✓) | Maksimović, Nela ; Vidović, Vanja; Damnjanović, Tatjana ; Jekić, Biljana ; Majkić-Singh, Nada ; Simeunović, Slavko ; Savić-Božović, Dara; Vidović, Stojko; Novaković, Ivana | Article | 21M21 |
2021 | Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review (✓) | Dawod, Phepy; Jančić, Jasna ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Samardžić, Janko ; Dawod, Ayman Gamil Anwar; Novaković, Ivana ; Abdel Motaleb, Fayda I.; Radlović, Vladimir; | Article | 21M21 |
2020 | Yield of the PMP22 deletion analysis in patients with compression neuropathies (✓) | Ivanović, Vukan ; Branković. Marija ; Bjelica, Bogdan ; Kačar, Aleksandra ; Tubić, Radoje ; Janković, Milena ; Marjanović, Ana ; Novaković, Ivana ; Rakočević-Stojanović, Vidosava ; Perić, Stojan | Article | 21M21 |
2020 | Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentation (✓) | Jančić, Jasna B. ; Rovčanin, Branislav R.; Đurić, Vesna; Pepić, Ana; Samardžić, Janko S. ; Nikolić, Blažo ; Novaković, Ivana V. ; Kostić, Vladimir S. | Article | 21M21 |
2020 | In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber's hereditary optic neuropathy (✓) | Rovčanin, Branislav R.; Jančić, Jasna B. ; Samardžić, Janko M. ; Rovčanin, Marija G. ; Nikolić, Blažo ; Ivančević, Nikola ; Novaković, Ivana V. ; Kostić, Vladimir K. | Article | 21M21 |
2020 | Analysis of association of ADORA2A and ADORA3 polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis (✓) | Grk, Milka ; Milic, Vera ; Dolzan, Vita; Maksimović, Nela ; Damnjanović, Tatjana ; Dušanović-Pjević, Marija ; Pešić, Milica ; Novaković, Ivana ; Jekić, Biljana | Article | 21M21 |
2020 | Genetic Aspects of Inflammation and Immune Response in Stroke (✓) | Nikolić, Dejan ; Janković, Milena ; Petrović, Bojana ; Novaković, Ivana | Article | 21M21 |