Researchers
Janković, Milena
Results 1-20 of 106
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 | Congenital clubfoot: Etiopathogenetic mechanisms and treatment challenges | Milanović, Filip; Dučić, Siniša ; Janković, Milena ; Nikolić, Dejan | Article | 52M52 |
| 2025 | The prevalence of spinal muscular atrophy carriers in pregnant women in Serbia | Mandic, Ratka; Jankovic, Milena | Conference Paper | Mp. category will be shown later |
| 2025 | Whole-exome sequencing in pediatric patients with glomerulonephritis | Perić, Marina; Branković, Marija ; Stajić, Nataša; Putnik, Jovana; Paripović, Aleksandra; Janković, Milena ; Nikolić, Dejan ; Milanović, Filip; Novaković, Ivana ; Vukomanović, Vladislav | Article | 22M22 |
| 2025 | Genetic Susceptibility to Glomerulonephritis in Children: Analysis of Structural Kidney Genes and Immune System Genes | Perić, Marina; Aničin, Aleksandra ; Branković, Marija ; Stajić, Nataša; Putnik, Jovana; Paripović, Aleksandra; Janković, Milena ; Božović, Ivo ; Perović, Vladimir S. ; Novaković, Ivana ;
Vukomanović, Vladislav A.
; Milošević, Emina ; | Article | 21M21 |
| 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 | 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 |
| 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 | Clinical Characteristics and Whole Exome Sequencing Analysis in Serbian Cases of Clubfoot Deformity—Single Center Study | Milanović, Filip; Dučić, Siniša ; Janković, Milena ; Sinđić-Antunović, Sanja ; Dubljanin-Raspopović, Emilija ; Aleksić, Milica; Đuričić, Goran; Nikolić, Dejan | Article | 21M21 |
| 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 | First Experience with the Implementation of Pharmacogenetics (TPMT, DPYD, and UGT1A1) | Mandic, Ratka; Jankovic, Milena Z ; Obradovic, Svetlana; Sakic, Mirjana | 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 |
| 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 | A Review of Current Perspectives on Motoric Insufficiency Rehabilitation following Pediatric Stroke | Čolović, Hristina ; Zlatanović, Dragan ; Živković, Vesna ; Janković, Milena ; Radosavljević, Nataša ; Dučić, Siniša ; Dučić, Jovan; Stojković, Jasna; Jovanović, Kristina; Nikolić, Dejan | Article | 21M21 |