Истраживачи
Novaković, Ivana
Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
---|---|---|---|---|
2022 | Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience (✓) | Kresojević, Nikola ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2022 | Clinical exome sequencing in Serbian patients with movement disorders – Single centre experience (✓) | Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2022 | Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia (✓) | Perić, Stojan ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2022 | The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options (✓) | Janković, Milena ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2022 | C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population (✓) | Marjanović, Ana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2022 | Impact of the Fetuin Gene Polymorphisms in Coronary Artery Calcification and Mortality of Patients with Chronic Kidney Disease and Renal Transplant (✓) | Jovičić-Pavlović, Svetlana; Simić-Ogrizović, Sanja P. ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2022 | Analysis of “clinical exome” panel in Serbian patients with cognitive disorders (✓) | Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2022 | Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients (✓) | Perović, Dijana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
2022 | Correlation between leukocyte-platelet aggregates and thrombosis in myeloproliferative neoplasms (✓) | Šefer, Dijana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
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. ![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2022 | Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation (✓) | Minić, Snežana B. ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21M21 - Рад у врхунском међ. часопису |
2022 | PPARGC1A gene polymorphism and its association with obesity-related metabolic traits in Serbian adolescent population (✓) | Vidović, Vanja; Maksimović, Nela S. ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 23M23 - Рад у међ. часопису |
2022 | KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizure (✓) | Dimitrijević, Sanja; Jekić, Biljana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 22M22 - Рад у истакнутом међ. часопису |
2022 | A multicenter study of genetic testing for Parkinson’s disease in the clinical setting (✓) | Kovanda, Anja; Rački, Valentino; Bergant, Gaber; Georgiev, Dejan; Flisar, Dušan; Papić, Eliša; Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() | Научни чланак | 21aM21a - Рад у међ. часопису изузетних вредности |