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Autori: Brankovic Marija

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Naslov Multi-Strain Probiotic Intervention Modestly Modulates Microbial Composition and Inflammatory Profile in Individuals with Long COVID (Article)
Autori Bacic Ana  Gmizic Tijana  Brankovic Marija  Rajilic-Stojanovic Mirjana D 
Info MICROORGANISMS, (2026), vol. 14 br. 4, str. -
Projekat AbelaPharm Probiotic Excellence Center; Ministry of Education, Science and Technological Development of the Republic of Serbia [451-03-34/2026-03/200135]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease (Article)
Autori Bergant Gaber  ...  Brankovic Marija  Jankovic Milena Z  Svetel Marina V  ...  Dragasevic-Miskovic Natasa T  Petrovic Igor N  ...  Novakovic Ivana V  ...  (broj koautora 19) 
Info GENES, (2026), vol. 17 br. 4, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Digital Transformation in Pharmaceutical and Medical Device Regulation: Building Resilience During the COVID-19 Crisis in Serbia (Proceedings Paper)
Autori Stojadinovic Tatjana  Antovic Ilija  Brankovic Marija 
Info BUILDING RESILIENCE IN A DYNAMIC CRITICAL INFRASTRUCTURE LANDSCAPE, (2026), vol. br. , str. 155-171
Ispravka ISI/Web of Science   Članak  
Naslov A Novel 4.2 kb deletion of the 3′UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3′UTR (Article)
Autori Mijovic Marija  Cuturilo Goran  Ruml-Stojanovic Jelena  Brankovic Marija  Miletic A  Bosankic Brankica  Dedovic Maja  Perovic D  Maksimovic N  Damnjanovic Tatjana M 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2025), vol. 28 br. 2, str. 107-112
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Diagnostic challenges in skeletal dysplasia: a clinical overview based on a 10-year retrospective study of single genetic department (Meeting Abstract)
Autori Mijovic Marija  Cuturilo Goran  Ruml-Stojanovic Jelena  Miletic Aleksandra  Bosankic Brankica  Dedovic Maja  Brankovic Marija 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 668-668
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov The coexistence of APC and FH germline variants: a case report of cooccurrence of two hereditary cancer predisposition syndromes in a single patient (Meeting Abstract)
Autori Bosankic Brankica  Cuturilo Goran  Mijovic Marija  Ruml-Stojanovic Jelena  Miletic Aleksandra  Dedovic Maja  Brankovic Marija 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 563-563
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Chorea in Hereditary Leukodystrophies - Overview of Two Cases (Article)
Autori Milovanovic Andona  Jecmenica-Lukic Milica V  Mazalica Nina  Radisic Vanja  Djordjevic-Milosevic Maja  Marjanovic Ana  Brankovic Marija  Markovic Vladana V  Kresojevic Nikola D  Kostic Vladimir K  Dragasevic-Miskovic Natasa T 
Info TREMOR AND OTHER HYPERKINETIC MOVEMENTS, (2025), vol. 15 br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Utilizing Fuzzy Logic for Enhanced Characterization of Ovarian Tumors (Proceedings Paper)
Autori Brankovic Marija  Miric Ana N  Geroski Tijana  Zivanovic Marko N  Filipovic Nenad D 
Info APPLIED ARTIFICIAL INTELLIGENCE 4: MEDICINE, BIOLOGY, CHEMISTRY, FINANCIAL, GAMES, ENGINEERING, SICAAI, (2025), vol. 1446 br. , str. 192-202
Projekat Ministry of Science, Technological Development and Innovation of the Republic of Serbia [451-03-66/2024-03/200378, 451-03-65/2024-03/200107]
Ispravka ISI/Web of Science   Članak  
Naslov Whole-exome sequencing in pediatric patients with glomerulonephritis (Article)
Autori Peric Marina  Brankovic Marija  Stajic Natasa  Putnik Jovana  Paripovic Aleksandra  Jankovic Milena Z  Nikolic Dejan  Milanovic Filip  Novakovic Ivana  Vukomanovic Vladislav A 
Info FRONTIERS IN GENETICS, (2025), vol. 16 br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov FIC Domain Protein Adenylyltransferase (FICD)-Related Complex Hereditary Spastic Paraplegia with Diabetes Mellitus (Letter)
Autori Rebelo Adriana P  Alawwadh Adel  Hakami Ali  Viric Vanja  Alshahrani Saeed  Brankovic Marija  Stevic Zorica D  Zuchner Stephan  Al-Shehri Abdulaziz  Peric Stojan Z 
Info MOVEMENT DISORDERS CLINICAL PRACTICE, (2025), vol. 12 br. 8, str. 1193-1195
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