Researchers
Novaković, Ivana
| Issue Date | Title | Author(s) | Type | М-cat. |
|---|---|---|---|---|
| 2023 | The importance of direct genetic testing to determine female carriers in dystrophinopathies (✓) | Maksić, Jasmina   ; Maksimović, Nela ; Rasulić, Lukas ; Milankov, Olgica; Marjanović, Ana ; Cvetković, Dragana ; Rakočević-Stojanović, Vidosava ; Novaković, Ivana | Article | 23M23 |
| 2023 | Novel GATOR1 variants in focal epilepsy (✓) | Kovačević, Maša ; Janković, Milena ; Branković, Marija ; Milićević, Ognjen ; Novaković, Ivana ; Sokić, Dragoslav ; Ristić, Aleksandar ; Shamsani, Jannah; Vojvodić, Nikola | Article | 22M22 |
| 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 |
| 2023 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia (✓) | Ivanović, Vukan ; Branković, Marija ; Božović, Ivo ; Stević, Zorica ; Basta, Ivana ; Marković, Vladana ; Svetel, Marina ; Tubić, Radoje ; Marjanović, Ana ; Veselinović, Nikola ;
Mesaroš, Šarlota
; Janković, Milena ; Rakočević-Stojanović, Vidosava ; Savić-Pavićević, Dušanka ; Novaković, Ivana ; Perić, Stojan ; | Conference Paper | Mp. category will be shown later |
| 2023 | Analysis of clinical exome panel in rare neurodegenerative disorders in Serbian population (✓) | Branković, Marija ; Dragašević, Nataša ; Svetel, Marina ; Milovanović, Andona ; Marković, Vladana ; Janković, Milena ; Marjanović, Ana ; Dobričić, Valerija ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2023 | Genetic Testing in Parkinson's Disease (✓) | Pal, Gian; ...; Novakovicć, Ivana V. ; ...; (broj koautora 27) | Article | 21aM21a |
| 2023 | Yield of GATOR1 gene sequencing in a Serbian focal epilepsy cohort (✓) | Kovačević, Maša ; Janković, Milena ; Branković, Marija ; Milićević, Ognjen S. ; Novaković, Ivana V. ; Sokić, Dragoslav V. ; Ristić, Aleksandar J. ; Berisavac, Ivana I. ; Vojvodić, Nikola M. | Conference Paper | Mp. category will be shown later |
| 2023 | Motor neuron involvement in facial muscles as characteristic of ANO10 mutation (✓) | Dragašević-Mišović, Nataša ; Milovanović, Andona ; Stanković, Iva ; Marjanović, Ana ; Branković, Marija ; Dobričić, Valerija S. ; Petrović, Igor N. ; Svetel, Marina V. ; Novaković, Ivana ; Kostić, Vladimir | Conference Paper | Mp. category will be shown later |
| 2023 | Clinical and genetic features of Huntington’s disease patients from Serbia: A single-center experience (✓) | Kresojević, Nikola ; Perović, Ivana; Stanković, Iva ; Tomić, Aleksandra ; Ječmenica-Lukić, Milica ; Marković, Vladana ; Stojković, Tanja ; Mandić, Gorana ; Janković, Milena ; Marjanović, Ana ;
Branković, Marija
; Novaković, Ivana ; Petrović, Igor ; Dragašević, Nataša ; Stefanova, Elka ; Svetel, Marina ; Kostić, Vladimir ; | Article | 22M22 |
| 2023 | TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients (✓) | Pešić, Milica ; Andrejić, Nikola; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka | Conference Paper | Mp. category will be shown later |
| 2023 | Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism” (✓) | Kresojević, Nikola ; Marković, Vladana ; Dobričić, Valerija ; Stanković, Iva ; Stojković, Tanja; Tomić, Aleksandra ; Ječmenica-Lukić, MIlica ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ;
Novaković, Ivana
; Petrović, Igor ; Dragašević, Nataša ; Svetel, Marina ; Kostić, Vladimir ; | Article | 21aM21a |
| 2023 | The association of R47H variant in the TREM2 gene and genetic susceptibility to Alzheimer's disease in Serbian population (✓) | Andrejić, Nikola; Pešić, Milica ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka | Article | 53M53 |
| 2022 | Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients (✓) | Perović, Dijana ; Damnjanović, Tatjana M. ; Jekić, Biljana B. ; Dušanović-Pjević, Marija G. ; Grk, Milka B. ; Đuranovic, Ana S. ; Rašić, Milica ; Novaković, Ivana V. ; Maksimović, Nela S. | Article | 22M22 |
| 2022 | Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans (✓) | Maver, Aleš; Kovanda, Anja; Bergant, Gaber; Teran, Nataša; Vrečar, Irena; Branković, Marija ; Janković, Milena Z. ; Svetel, Marina V. ; Kostić, Vladimir S. ; Novaković, Ivana V. ;
Rački, Valentino; Vuletić, Vladimira; Peterlin, Borut;
| Conference Paper | Mp. category will be shown later |
| 2022 | Correlation between leukocyte-platelet aggregates and thrombosis in myeloproliferative neoplasms (✓) | Šefer, Dijana ; Miljić, Predrag ; Kraguljac-Kurtović, Nada ; Bižić-Radulović, Sandra; Bogdanović, Andrija ; Knežević, Vesna; Marković, Dragana ; Beleslin-Čokić, Bojana ; Novaković, Ivana ; Marinković, Jelena ;
Leković, Danijela
; Gotić, Mirjana ; Čokić, Vladan ; | Article | 22M22 |
| 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 ;
Novaković, Ivana
; Svetel, Marina ; Kostić, Vladimir S. ; | Article | 21M21 |
| 2022 | Clinical exome sequencing in Serbian patients with movement disorders – Single centre experience (✓) | Branković, Marija ; Dragašević, Nataša ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Petrović, Igor ; Perić, Stojan ; Marjanović, Ana ; Janković, Milena ; Jančić, Jasna ;
Novaković, Ivana
; Peterlin, Borut; Svetel, Marina ; Kostić, Vladimir ; | Article | 23M23 |
| 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 | PPARGC1A gene polymorphism and its association with obesity-related metabolic traits in Serbian adolescent population (✓) | Vidović, Vanja; Maksimović, Nela S. ; Vidović, Stojko; Damnjanović, Tatjana M. ; Milovac, Irina; Novaković, Ivana V. | Article | 23M23 |