Researchers
Novaković, Ivana
Results 21-40 of 395
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | New evidence supporting female protective effect in patients with congenital anomalies and neurodevelopmental disorders | Maksimović, Nela   ; Damnjanović, Tatjana ; Jekić, Biljana ; Novaković, Ivana ; Đurić-Zdravković, Aleksandra ; Dušanović-Pjević, Marija ; Grk, Milka ; Pešić, Milica ; Đuranović-Uklein, Ana ; Rašić, Milica ;
Stojanovski, Nataša
; Perović, Dijana ; | Article | 21M21 |
| 2025 | A Specific Haplotype of the MMP2 Gene Promoter May Increase the Risk of Developing Cerebral Palsy | Đuranović-Uklein, Ana S. ; Cerovac, Nataša ; Perović, Dijana ; Maksimović, Nela S. ; Jekić, Biljana B. ; Grk, Milka B. ; Dušanović-Pjević, Marija G. ; Rašić, Milica ; Stojanovski, Nataša ; Pešić, Milica ;
Novaković, Ivana V.
; Damnjanović, Tatjana M. ; | Article | 21M21 |
| 2025 | Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease? | Kresojević, Nikola ; Marković, Vladana ; Geratović, Cveta; Ječmenica-Lukić, Milica ; Tomić, Aleksandra ; Dobričić, Valerija ; Stanković, Iva D. ; Stojkovic, Tanja ; Dragašević, Nataša ; Šarčević, Maksim;
Jankovic, Milena
; Marjanovic, Ana ; Novaković, Ivana ; Kostić, Vladimir ; Svetel, Marina ; Petrović, Igor ; | Article | 22M22 |
| 2025 | Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesis | Podgrajsek, Rebeka; Hodzic, Alenka; Maver, Aleš; Stimpfel, Martin; Andjelic, Aleksander; Miljanovic, Olivera; Ristanović, Momčilo ; Novaković, Ivana V. ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojic, Sasa; Buretic-Tomljanovic, Alena; Peterlin, Borut;
| Conference Paper | Mp. category will be shown later |
| 2025 | Chromosomal Microarray in Children Born Small for Gestational Age - Single Center Experience | Perović, Dijana ; Barzegar, P.; Damnjanović, Tatjana M. ; Jekić, Biljana B. ; Grk, Milka B. ; Dušanović-Pjević, Marija G. ; Cvetković, Dragana ; Đuranović-Uklein, Ana ; Stojanovski, Nataša ; Rašić, Milica ;
Novaković, Ivana V.
; Elhayani, B.; Maksimović, Nela S. ; | Article | 23M23 |
| 2024 | Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis | Grk, Milka ; Jekic, Biljana ; Dolzan, Vita; Maksimovic, Nela ; Damnjanovic, Tatjana ; Rasic, Milica ; Novakovic, Ivana ; Perovic, Dijana ; Carkic, Jelena ; Dusanovic Pjevic, Marija | Article | 23M23 |
| 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 | R47H TREM2 variant among Serbian Alzheimer's disease patients | Andrejić, Nikola ; Pešić, Milica ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka | Conference Paper | Mp. category will be shown later |
| 2024 | Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility | Podgrajšek, Rebeka; Hodžić, Alenka; Maver, Aleš; Štimpfel, Martin; Anđelić, Aleksander; Miljanović, Olivera; Ristanović, Momčilo ; Novaković, Ivana V. ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojić, Saša; Gršković, Antun; Buretić-Tomljanović, Alena; Peterlin, Borut;
| Conference Paper | Mp. category will be shown later |
| 2024 | Association of AQP-4 polymorphisms with the clinical and paraclinical characteristics of patients with NMOSD | Andabaka, Marko M. ; Novaković, Ivana V. ; Branković, Marija ; Mesaroš, Šarlota T. ; Veselinović, Nikola ; Tamaš, Olivera S.; Budimkić, Maja S. ; Martinović, Vanja ; Momčilović, Nikola; Marić, Gorica ;
Suknjaja, Vesna
; Sakalas, Lorand; Pekmezović, Tatjana D. ; Habek, Mario; Drulović, Jelena S. ; | Conference Paper | Mp. category will be shown later |
| 2024 | Continuous glucose monitoring in pregnancy | Novaković, Ivana ; Todorović, Jovana ; Dugalić, Stefan ; Macura, Maja; Milinčić, Miloš; Gojnić-Dugalić, Miroslava | Article | 23M23 |
| 2024 | NOTCH3 genetic analysis in patients with cerebral small vessel disease | Jovanović, Marija; Vojvodić, Ljubica; Marjanović, Ana ; Branković, Marija ; Cvetković, Dragana ; Novaković, Ivana ; Janković, Milena | Conference Paper | Mp. category will be shown later |
| 2024 | Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center | Stefanova, Elka D. ; Marjanović, Ana ; Dobričić, Valerija S. ; Mandić-Stojmenović, Gorana B. ; Stojković, Tanja ; Branković, Marija ; Šarčević, Maksim; Novaković, Ivana V. ; Kostić, Vladimir S. | Article | 22M22 |
| 2024 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia | Branković, Marija ; Ivanović, Vukan ; Basta, Ivana ; Khang, Rin; Lee, Eugene; Stević, Zorica ; Ralić, Branislav; Tubić, Radoje ; Seo, GoHun; Marković, Vladana ;
Božović, Ivo
; Svetel, Marina ; Marjanović, Ana ; Veselinović, Nikola; Mesaroš, Šarlota ; Janković, Milena ; Savić-Pavićević, Dušanka ; Jovin, Zita; Novaković, Ivana ; Lee, Hane; Perić, Stojan ; | Article | 22M22 |
| 2024 | Influence of polymorphisms in genes for interleukin-6 and interleukin-10 on dialysis patients survival | Jovičić-Pavlović, Svetlana M.; Simić-Ogrizović, Sanja P. ; Pavlović, Natalija; Bukumirić, Zoran M. ; Novaković, Ivana V. | Conference Paper | Mp. category will be shown later |
| 2024 | Analysis of clinical exome panel in rare movement and cognitive disorders | Branković, Marija ; Dragašević, Nataša ; Svetel, Marina ; Stefanova, Elka ; Mandić, Gorana ; Stojković, Tanja ; Milovanović, Andona ; Marković, Vladana ; Janković, Milena ; Marjanović, Ana ;
Dobričić, Valerija
; Novaković, Ivana ; Kostić, Vladimir ; | Conference Paper | Mp. category will be shown later |
| 2024 | Challenges in rare diseases: The example of mitochondrial diseases | Novaković, Ivana ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Svetel, Marina ; Jančić, Jasna | Conference Paper | Mp. category will be shown later |
| 2024 | Етички аспекти генетског тестирања | Новаковић, Ивана | Conference Paper | Mp. category will be shown later |
| 2024 | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series | Milovanović, Andona ; Westenberger, Ana; Stanković, Iva D. ; Tamaš, Olivera S.; Branković, Marija ; Marjanović, Ana ; ...; Branković, Vesna; Novaković, Ivana V. ; Petrović, Igor N. ;
Svetel, Marina V.
; Klein, Christine; Kostić, Vladimir S. ; Dragašević-Mišković, Nataša T. ; (broj koautora 18); | Article | 21a+M21a+ |
| 2024 | Earlier age of symptom onset in younger generation of familial cases of multiple sclerosis | 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 | 22M22 |