Researchers
Marjanović, Ana
Results 1-20 of 101
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Hidden diagnoses among patients with double seronegative myasthenia gravis | Ivanović, Vukan  ; Perić, Stojan Z.  ; Briggs, Caitlin; Marjanović, Ana ; Pešović, Jovan ; Basta, Ivana ; Jansson, Johan; Randhawa, Simrat; Rajić, Sonja ; Gokhale, Sankalp | Article | 22M22 |
| 2026 | Disease burden in Serbian patients with facioscapulohumeral muscular dystrophy | Ralic, Branislav; Albano, Noemi; Viric, Vanja; Nuredini, Andi; Arsic-Azanjac, Ana; Rajic, Sonja; Marjanovic, Ana ; Tupler, Rossella; Heatwole, Chad; Peric, Stojan | Article | 22M22 |
| 2025 | Chorea in Hereditary Leukodystrophies - Overview of Two Cases | Milovanović, Andona ; Ječmenica-Lukić, Milica ; Mazalica, Nina; Radišić, Vanja ; Đorđević-Milošević, Maja ; Marjanović, Ana ; Branković, Marija ; Marković, Vladana ; Kresojević, Nikola ; Kostić, Vladimir ;
Dragašević-Mišković, Nataša T.
; | Article | 22M22 |
| 2025 | Secondary findings in 443 exome sequencing data | Branković, Marija ; Han, Heonjong; Janković, Milena ; Marjanović, Ana ; Andrejić, Nikola; Gunjić, Ilija ; Virić, Vanja ; Palibrk, Aleksa; Lee, Hane; Perić, Stojan | Article | 23M23 |
| 2025 | Hereditary neuropathies in Serbian population | Vukojević, Milica ; Marjanović, Ana ; Ivanović, Vukan ; Janković, Milena ; Kačar, Aleksandra ; Basta, Ivana ; Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2025 | The role of genetic factors in the occurrence of levodopa-induced motor complications in Parkinson's disease | Radojević, Branislava ; Milovanović, Andona ; Petrović, Igor N. ; Svetel, Marina V. ; Marjanović, Ana ; Jančić, Ivan ; Stanisavljevic, Dejana M ; Milićević, Ognjen S. ; Savić, Miroslav ; Kostić, Vladimir S. ;
Dragašević-Mišković, Nataša T.
; | Article | 22M22 |
| 2025 | The pleiotropy of C9orf72 repeat expansions in neurodegenerative diseases | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2025 | APOE, APP, and PSEN1 mutation screening in Alzheimer’s disease: a 15-year experience in Serbia | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2025 | Clinical exome sequencing identifies pathogenic SQSTM1 variant in a patient with chorea and gaze palsy | Stojadinović, Lenka ; Petrović, Igor ; Dragašević-Mišković, Nataša ; Jovanović, Emilija; Marković, Vladana ; Janković, Milena ; Novaković, Ivana ; Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2025 | Frequency of TREM2 and APOE rare variants in patients with Alzheimer’s disease in Serbia | Stojadinović, Lenka ; Marjanović, Ana ; Branković, Marija ; Mandić, Gorana ; Stojković, Tanja ; Jovanović, Emilija; Novaković, Ivana ; Stefanova, Elka ; Janković, Milena | Conference Paper | Mp. category will be shown later |
| 2025 | Genetic and Clinical Insights into ALS/FTD: Profiling a Rare Cohort to Explore Spectrum Heterogeneity | Marjanović, Ana ; Stefanova, Elka ; Virić, Vanja ; Palibrk, Aleksa; Mandić-Stojmenović, Gorana ; Stojković, Tanja ; Stojadinović, Lenka ; Basta, Ivana ; Novaković, Ivana ; Stević, Zorica ;
Janković, Milena
; | Article | 21M21 |
| 2025 | APOE, ATXN1 and ATXN2 genetic analysis in ALS/FTD patients | Marjanović, Ana ; Virić, Vanja ; Mandić, Gorana ; Stojković, Tanja ; Perić, Stojan ; Basta, Ivana ; Janković, Milena ; Stojadinović, Lenka ; Jovanović, Emilija; Branković, Marija ;
Novaković, Ivana
; Stević, Zorica ; Stefanova, Elka ; | Conference Paper | Mp. category will be shown later |
| 2025 | C9orf72–Associated ALS/FTD: From Genetic Diagnosis to Therapeutic Opportunities and Challenges | Marjanović, Ana ; Stojadinović, Lenka ; Janković, Milena | Book parts | Mp. category will be shown later |
| 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 | Disease burden in Serbian patients with facioscapulohumeral muscular dystrophy | Ralić, Branislav; Albano, N.; Virić, Vanja ; Nuredini, A.; Azanjac, Ana ; Rajić, Sonja ; Marjanović, Ana ; Tupler, R.; Heatwole, C.; Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2024 | Secondary findings in 443 whole exome sequencing data | Branković, Marija ; Janković, Milena ; Marjanovic, Ana ; Andrejić, Nikola; Gunjić, Nikola ; Virić, Vanja ; Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 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 | 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 | APOE genotype, ATXN1 and ATXN2 repeats size in C9orf72 expansion carriers | Marjanović, Ana ; Mandić-Stojmenović, Gorana ; Virić, Vanja ; Branković, Marija ; Janković, Milena ; Stojković, Tanja ; Novaković, Ivana ; Stević, Zorica ; Stefanova, Elka | Conference Paper | Mp. category will be shown later |
| 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 |