Milovanovic Andona,...,Stankovic Iva D,Tamas Olivera S,Brankovic Marija,Marjanovic Ana,...,Brankovic Vesna,Novakovic Ivana V,Petrovic Igor N,Svetel Marina V,...,Kostic Vladimir S,Dragasevic-Miskovic Natasa T (2024) <i>ANO10</i>-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series, MOVEMENT DISORDERS, vol. 39, br. 5, str. 887-892 (Article) 

Djordjevic Stefan A,Milic-Rasic Vedrana M,Brankovic Vesna,Kosac Ana P,Dejanovic-Djordjevic Ivana,Bijelic Maja,Dimkic-Tomic Tijana J,Markovic-Denic Ljiljana N,Kovacevic Smiljka,Petrovic Hristina,Vitorovic S,Dobric Z,Zdravkovic Vera M (2022) Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3, ARCHIVES DE PEDIATRIE, vol. 29, br. 7, str. 480-483 (Article) 

Van de Vondel Liedewei,...,Brankovic Vesna,...,(broj koautora 38) (2022) De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia, MOVEMENT DISORDERS, vol. 37, br. 6, str. 1175-1186 (Article) 

Nuovo Sara,...,Brankovic Vesna,...,(broj koautora 35) (2022) Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study, JOURNAL OF MEDICAL GENETICS, vol. 59, br. 4, str. 399-409 (Article) 

Imbrici Paola,Conte Elena,Blunck Rikard,Stregapede Fabrizia,Liantonio Antonella,Tosi Michele,D'Adamo Maria Cristina,De Luca Annamaria,Brankovic Vesna,Zanni Ginevra (2021) A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, vol. 22, br. 18, str. - (Article) 

Nicita Francesco,...,Brankovic Vesna,...,(broj koautora 25) (2021) Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders, JOURNAL OF MEDICAL GENETICS, vol. 58, br. 7, str. 475-483 (Article) 

Djordjevic Stefan A,Milic-Rasic Vedrana M,Brankovic Vesna,Kosac Ana P,Dejanovic-Djordjevic Ivana,Markovic-Denic Ljiljana N,Djuricic Goran J,Milcanovic Natasa,Kovacevic Smiljka,Petrovic Hristina,Djukic Milan M,Zdravkovic Vera M (2021) Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3, NEUROMUSCULAR DISORDERS, vol. 31, br. 4, str. 291-299 (Article) 

Nuovo Sara,Brankovic Vesna,Caputi Caterina,Casella Antonella,Nigro Vincenzo,Leuzzi Vincenzo,Valente Enza Maria (2021) Novel unconventional variants expand the allelic spectrum of OPHN1 gene, AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol. 185, br. 5, str. 1575-1581 (Article) 

Djordjevic Stefan A,Milic-Rasic Vedrana M,Brankovic Vesna,Kosac Ana P,Vukomanovic Goran V,Topalovic Mirko,Marinkovic Dejan,Mladenovic Jelena M,Pavlovic Andrija S,Bijelic Maja,Djukic Milan M,Markovic-Denic Ljiljana N (2021) Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3, MUSCLE & NERVE, vol. 63, br. 1, str. 75-83 (Article) 

Balestrini Simona,...,Brankovic Vesna,...,Potic Ana D,...,(broj koautora 54) (2020) Cardiac phenotype in ATP1A3-related syndromes A multicenter cohort study, NEUROLOGY, vol. 95, br. 21, str. E2866-E2879 (Article) 

Bar Claire,...,Brankovic Vesna,...,(broj koautora 61) (2020) Developmental and epilepsy spectrum ofKCNB1encephalopathy with long-term outcome, EPILEPSIA, vol. 61, br. 11, str. 2461-2473 (Article) 

Dobricic Valerija S,Tomic Aleksandra D,Brankovic Vesna,Kresojevic Nikola D,Jankovic Milena Z,Westenberger Ana,Milic-Rasic Vedrana M,Klein Christine,Novakovic Ivana V,Svetel Marina V,Kostic Vladimir S (2017) GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia, PARKINSONISM & RELATED DISORDERS, vol. 45, br. , str. 81-84 (Article) 

Barresi S,Niceta M,Alfieri P,Brankovic Vesna,Piccini G,Bruselles A,Barone MR,Cusmai Raffaella,Tartaglia M,Bertini E,Zanni G (2017) Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia, CLINICAL GENETICS, vol. 91, br. 1, str. 86-91 (Article)