Researchers
Novaković, Ivana
Results 41-60 of 392
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2024 | A Machine Learning Approach to Gene Expression in Hypertrophic Cardiomyopathy | Pavić, Jelena   ; Živanović, Marko ; Tanasković, Irena ; Pavić, Ognjen ; Stanković, Vesna ; Virijević, Katarina ; Mladenović, Tamara ; Košarić, Jelena ; Milićević, Bogdan ; Qamar, Safi Ur Rehman ;
Velicki, Lazar
; Novaković, Ivana ; Preveden, Andrej ; Popović, Dejana ; Tesić, Milorad ; Seman, Stefan; Filipović, Nenad ; | Article | 21aM21a |
| 2024 | Sleep problems in female carriers of premutation in the FMR1 gene | Pešić, Milica ; Stevanović, Milena; Andrejić, Nikola; Pešović, Jovan ; Ćirković, Sanja; Dimitrijević, Sanja S.; Baščarević, Danijela; Dragašević-Mišković, Nataša ; Novaković, Ivana V. ; Protić, Dragana | Conference Paper | Mp. category will be shown later |
| 2024 | Wilson’s disease | Svetel, Marina ; Kresojević, Nikola ; Tomić, Aleksandra ; Ječmenica-Lukić, Milica ; Marković, Vladana ; Stanković, Iva ; Petrović, Igor ; Pekmezović, Tatjana ; Novaković, Ivana ; Božić, Marija ;
Svetel, Marko
; Vitković, Jelena; Dragašević, Nataša ; | Article | 23M23 |
| 2024 | C9orf72 genetic screening in patients with ALS/FTD phenotype from Serbia | Marjanović, Ana ; Mandić-Stojmenović, Gorana ; Milićević, Ognjen ; Stojković, Tanja ; Virić, Vanja ; Janković, Milena ; Branković, Marija ; Palibrk, Aleksa ; Ivanović, Vukan ; Dobričić, Valerija ;
Perić, Stojan
; Novaković, Ivana ; Stević, Zorica ; Stefanova, Elka ; | Conference Paper | Mp. category will be shown later |
| 2024 | Rare and Uncommon Gene Variants Associated with Familial Multiple Sclerosis: A Case-Control Study | Jovanović, Aleksa ; Turk, Aleksander; Novaković, Ivana V. ; Mesaroš, Šarlota T. ; Veselinović, Nikola ; Tamaš, Olivera S.; Marić, Gorica ; Andabaka, Marko M. ; Momčilović, Nikola; Pekmezović, Tatjana D. ;
Peterlin, Borut; Drulović, Jelena S.
; | Conference Paper | Mp. category will be shown later |
| 2024 | Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control study | Jovanović, Aleksa Lj. ; Pekmezović, Tatjana D. ; Mesaroš, Šarlota T. ; Novaković, Ivana V. ; Peterlin, Borut; Veselinović, Nikola D. ; Tamaš, Olivera S.; Ivanović, Jovana B. ; Marić, Gorica D. ; Andabaka, Marko M. ;
Momčilović, Nikola; Drulović, Jelena S.
; | Article | 21M21 |
| 2024 | Physical activity and mental health of medical students | Stratakis, Konstantinos; Terzić-Šupić, Zorica ; Todorović, Jovana ; Nešić, Dejan ; Novaković, Ivana | Article | 23M23 |
| 2023 | International Genetic Testing and Counseling Practices for Parkinson's Disease | Saunders-Pullman, Rachel; ...; Novaković, Ivana V. ; ...; (broj koautora 29) | Article | 21a+M21a+ |
| 2023 | CYP2C9 screening: important step in siponimod treatment of secondary progressive multiple sclerosis | Janković, Milena ; Branković, Marija ; Marjanović, Ana ; Drulović, Jelena ; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2023 | Genetic Testing in Parkinson's Disease | Pal, Gian; ...; Novakovicć, Ivana V. ; ...; (broj koautora 27) | Article | 21a+M21a+ |
| 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 | C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia | Marjanović, Ana ; Palibrk, Aleksa; Dobričić, Valerija ; Milićević, Ognjen ; Branković, Marija ; Virić, Vanja ; Drinić, Aleksandra; Mandić-Stojmenović, Gorana ; Janković, Milena ; Basta, Ivana ;
Perić, Stojan
; Novaković, Ivana ; Stefanova, Elka ; Stević, Zorica ; | Article | 22M22 |
| 2023 | LGALS3 RS4644 gene polymorphism is associated with obesity related metabolic traits in Serbian adolescent population | Damnjanović, Tatjana ; Vidović, Vanja; Vidović, Stojko; Salihović, Ajla; Maksimović, Nela ; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 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 | 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 | 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 variants in established epilepsy genes in focal epilepsy | Kovačević, Maša ; Milićević, Ognjen ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Sokić, Dragoslav ; Ristić, Aleksandar ; Shamsani, Jannah; Vojvodić, Nikola | Article | 22M22 |
| 2023 | C9ORF72 intermediate repats in neurodegenerative disorders from Serbia | Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Perić, Stojan ; Dragašević-Mišković, Nataša ; Mandić, Gorana ; Ječmenica-Lukić, Milica ; Stanković, Iva ; Stefanova, Elka ; Stević, Zorica ;
Novaković, Ivana
; Svetel, Marina ; Kostić, Vladimir ; | 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 | EPR-210 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 |