Researchers
Janković, Milena
Results 1-20 of 107
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease | Bergant, Gaber; ...; Branković, Marija   ; Janković, Milena Z. ; Svetel, Marina ; ...; Dragašević-Mišković, Nataša ; Petrović, Igor ; ...; Novaković, Ivana ;
...; (broj koautora 19);
| Article | 22M22 |
| 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 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 | 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 | Congenital clubfoot: Etiopathogenetic mechanisms and treatment challenges | Milanović, Filip; Dučić, Siniša ; Janković, Milena ; Nikolić, Dejan | Article | 52M52 |
| 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 | 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 | 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 | The prevalence of spinal muscular atrophy carriers in pregnant women in Serbia | Mandic, Ratka; Jankovic, Milena | 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 | 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 |
| 2024 | Gestational Weight Gain, Pregnancy Related Complications and the Short-Term Risks for the Offspring | Lacković, Milan ; Janković, Milena ; Mihajlović, Slađana ; Milovanović, Zagorka; Rovčanin, Marija ; Mitić, Nikola; Nikolić, Dejan | Article | 21M21 |
| 2024 | Comparison of the ABC and ACMG systems for variant classification | Houge, Gunnar; Bratland, Eirik; Aukrust, Ingvild; Tveten, Kristian; Žukauskaitė, Gabrielė; Sansovic, Ivona; Brea-Fernández, Alejandro J; Mayer, Karin; Paakkola, Teija; McKenna, Caoimhe;
Wright, William; Keckarević-Marković, Milica
; Lildballe, Dorte L; Konecny, Michal; Smol, Thomas; Alhopuro, Pia; Gouttenoire, Estelle Arnaud; Obeid, Katharina; Todorova, Albena; Jankovic, Milena ; Lubieniecka, Joanna M; Stojiljkovic, Maja ; Buisine, Marie-Pierre; Haukanes, Bjørn Ivar; Lorans, Marie; Roomere, Hanno; Petit, François M; Haanpää, Maria K; Beneteau, Claire; Pérez, Belén; Plaseska-Karanfilska, Dijana; Rath, Matthias; Fuhrmann, Nico; Ferreira, Bibiana I; Stephanou, Coralea; Sjursen, Wenche; Maver, Aleš; Rouzier, Cécile; Chirita-Emandi, Adela; Gonçalves, João; Kuek, Wei Cheng David; Broly, Martin; Haer-Wigman, Lonneke; Thong, Meow-Keong; Tae, Sok-Kun; Hyblova, Michaela; den Dunnen, Johan T; Laner, Andreas; | Article | 21M21 |
| 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 | 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 | 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 | 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 |