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Research outputs

Genetic Profiling and Performance Optimization in Elite Combat Sport Athletes: A Cross-Sectional Study Based on Total Genetic Score Analysis [2025]

Pagliaro, Andrea; Alioto, Anna; Boatta, Alessia; Messina, Giuseppe; Drid, Patrik ; Milazzo, Paolo; Cortis, Cristina; Fusco, Andrea; Vasto, Sonya; Proia, Patrizia;

Baldassano, Sara;

Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study [2024]

Ilić, Nikola; Krasić, Staša; Marić, Nina; Gašić, Vladimir V. ; Krstić, Jovana; Cvetković, Dimitrije; Miljković, Vesna; Zec, Boris; Maver, Ales; Vukomanović, Vladislav A. ;

Sarajlija, Adrijan ;

Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias [2017]

Hebert, Eva; ...; Kostic, Vladimir S; ...; (broj, koautora 24)

Nitric Oxide Synthase Dependency in Hydroxyurea Inhibition of Erythroid Progenitor Growth [2021]

Subotički, Tijana ; Mitrović-Ajtić, Olivera ; Đikić, Dragoslava ; Santibanez, Juan ; Tošić, Milica ; Čokić, Vladan

The Artificial Intelligence-Assisted Diagnosis of Skeletal Dysplasias in Pediatric Patients: A Comparative Benchmark Study of Large Language Models and a Clinical Expert Group [2025]

Ilić, Nikola A.; Marić, Nina; Cvetković, Dimitrije; Bogosavljević, Marko; Bukara-Radujković, Gordana; Krstić, Jovana; Paunović, Zoran; Begović, Ninoslav; Panić-Zarić, Sanja; Todorović, Slađana;

Mitrović, Katarina; Vlahović, Aleksandar ; Sarajlija, Adrijan ;

Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy [2020]

Dawod, Phepy G. A.; Jančić, Jasna ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Samardžić, Janko ; Potkonjak, Dario ; Đurić, Vesna; Mesaroš, Šarlota ; Novaković, Ivana ;

Abdel Motaleb, Fayda I.; Kostić, Vladimir S. ; Nikolić, Dejan ;

Origin and Genealogy of Rare mtDNA Haplotypes Detected in the Serbian Population [2025]

Davidović, Slobodan ; Aleksić, Jelena ; Tanasković, Marija ; Erić, Pavle ; Stevanović, Milena ; Kovačević-Grujičić, Nataša

Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease [2026]

Bergant, Gaber; ...; Branković, Marija ; Janković, Milena Z. ; Svetel, Marina ; ...; Dragašević-Mišković, Nataša ; Petrović, Igor ; ...; Novaković, Ivana ;

...; (broj koautora 19);

B Chromosomes in Populations of Mammals Revisited [2018]

Vujošević, Mladen ; Rajičić, Marija ; Blagojević, Jelena

LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients [2022]

Kosac, Ana ; Pešović, Jovan ; Radenković, Lana ; Brkušanin, Miloš ; Radovanović, Nemanja ; Đurišić, Marina; Radivojević, Danijela; Mladenović, Jelena; Ostojić, Slavica; Kovačević, Gordana;

Kravljanac, Ružica ; Savić-Pavićević, Dušanka ; Milić-Rašić, Vedrana ;