Researchers
Komazec, Jovana
Results 1-20 of 50
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | Genomic profiling, implications for genotype-based treatment of 131 patients with phenylketonuria and characterization of novel p.Pro416Leu PAH variant | Klaassen, K | Article | 21M21 |
| 2025 | Role of Next-Generation Sequencing in Diagnosis of Familial Hypercholesterolemia in Serbia![]() | Lukac Singh, Sandra; Gašić, Vladimir | Article | 21M21 |
| 2025 | Advancing the IMGGE RD Biobank through BRIDGING-RD Project: Achieving full interoperability of genetic and phenotypic data to enhance participation in transnational research and innovation for human health | Komazec, Jovana | Conference Paper | Mp. category will be shown later |
| 2025 | ESTABLISHING IN VITRO MODELS FOR GLYCOGEN STORAGE DISEASE TYPE IB: A PLATFORM FOR THERAPEUTIC INVESTIGATIONS![]() | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2025 | ESTABLISHMENT OF AN IN VITRO INSULIN RESISTANCE MODEL IN HepG2 CELLS THROUGH GLUCOSE AND INSULIN COTREATMENT | Spasovski, Vesna | Conference Paper | Mp. category will be shown later |
| 2025 | BIOCHEMICAL CHARACTERISATION OF FAMILIAL HYPERCHOLESTEROLEMIA:ASSOCIATIONS BETWEEN GENETIC AND LIPID PROFILES![]() | Singh, Sandra; Gašić, Vladimir
Ilić, Katarina;
| Article | 23M23 |
| 2025 | MITOCHONDRIAL MYOPATHY CAUSED BY MT-ND5 VARIANT: INTEGRATING WES AND MITOCHONDRIAL DNA ANALYSIS | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2025 | PULMONARY IN VITRO MODEL SYSTEM ENABLES EXPLORATION OF INNOVATIVE TREATMENT STRATEGIES FOR RARE RESPIRATORY DISEASES | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2024 | WGS approach to identify potential genetic modifiers in Glycogen Storage Disease Ib![]() | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2024 | New TERT variant in a family with aplastic anemia![]() | Virijević, Marijana | Conference Paper | Mp. category will be shown later |
| 2024 | INVESTIGATING THE GENETIC COMPLEXITY OF NEUTROPENIA IN PEDIATRIC PATIENTS WITH GLYCOGEN STORAGE DISEASE IB: A MODIFIER GENE PERSPECTIVE | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2024 | GERMLINE VARIANTS IN CANCER PREDISPOSITION GENES IN PEDIATRIC PATIENTS WITH CENTRAL NERVOUS SYSTEM TUMORS | Marjanović, Irena | Conference Paper | Mp. category will be shown later |
| 2024 | Genetic landscape of phenylketonuria in Serbia![]() | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2023 | The role of MIR-34 family members on the mucociliary process in the cellular respiratory model system![]() | Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2023 | Molecular diagnosis of Fabry disease in patients with chronic renal failure of unknown etiology![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | Molecular basis of thalassemia syndromes in Serbia: an update![]() | Ugrin, Milena | Conference Paper | Mp. category will be shown later |
| 2023 | Improving the diagnostics of rare lung disorders using a uniquely designed pipeline for analysis of ngs data | Anđelković, Marina | Conference Paper | Mp. category will be shown later |
| 2023 | THE IMPACT OF NEXT-GENERATION SEQUENCING ON DIAGNOSIS AND TREATMENT OF RARE DISEASES | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2023 | Germline Variants in Cancer Predisposition Genes in Pediatric Patients with Central Nervous System Tumors![]() | Jovanović, Aleksa; Tošić, Nataša | Article | 21M21 |
| 2023 | High-risk population screening for fabry disease in patients with chronic renal failure of unknown etiology![]() | Parezanović, Marina | Conference Paper | Mp. category will be shown later |
