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Marija Branković

Observed names: Branković, Marija, Marija Branakovic, Marija Brankovic
ORCID: 0000-0001-5208-147X
Observed ORCID: 0000-0001-5208-147X
OpenAlex ID: A5071834258
Neuropathic pain in patients with Charcot-Marie-Tooth type 1A
2019 · Bogdan Bjelica, Stojan Peric, et al. · Neurological Sciences · 26
A multicenter study of genetic testing for Parkinson’s disease in the clinical setting
2022 · Anja Kovanda, Valentino Rački, et al. · npj Parkinson s Disease · 24
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RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia
2024 · Andona Milovanović, Nataša Dragaševic‐Mišković, et al. · Movement Disorders Clinical Practice · 23
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Body composition analysis in patients with myotonic dystrophy types 1 and 2
2019 · Stojan Peric, Ivo Bozovic, et al. · Neurological Sciences · 18
Myotonic Dystrophy Type 2 – Data from the Serbian Registry
2018 · Ivo Bozovic, Stojan Peric, et al. · Journal of Neuromuscular Diseases · 16
Physical and Mental Aspects of Quality of Life in Patients With Charcot-Marie-Tooth Disease Type 1A
2022 · Vukan Ivanovic, Bogdan Bjelica, et al. · Frontiers in Neurology · 14
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Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia
2019 · Stojan Peric, Jelena Stevanovic, et al. · PubMed Central · 11
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Clinical and Genetic Analysis of Psychosis in Parkinson’s Disease
2021 · Branislava Radojević, Nataša T. Dragašević-Mišković, et al. · Journal of Parkinson s Disease · 10
Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center
2024 · Elka Stefanova, Ana Marjanović, et al. · Neurogenetics · 9
ANO10 ‐Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series
2024 · Andona Milovanović, Ana Westenberger, et al. · Movement Disorders · 9
Novel GATOR1 variants in focal epilepsy
2023 · Maša Kovačević, Milena Janković, et al. · Epilepsy & Behavior · 9
Quality of life in hereditary neuropathy with liability to pressure palsies is as impaired as in Charcot–Marie–Tooth disease type 1A
2020 · Bogdan Bjelica, Stojan Peric, et al. · Acta Neurologica Belgica · 9
Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy
2020 · Phepy G. A. Dawod, Jasna Jancic, et al. · Genes · 8
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Novel variants in established epilepsy genes in focal epilepsy
2023 · Maša Kovačević, Ognjen Milićević, et al. · Seizure · 5
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Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism”
2023 · Nikola Kresojević, Vladana Marković, et al. · Movement Disorders · 5
Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit
2021 · Aleksandra Miletic, Jelena Ruml Stojanovic, et al. · European Journal of Pediatrics · 5
Secondary findings in 443 exome sequencing data
2024 · Marija Branković, Heonjong Han, et al. · Annals of Human Genetics · 4
Whole exome sequencing in Serbian patients with hereditary spastic paraplegia
2024 · Marija Brankovic, Vukan Ivanovic, et al. · Neurogenetics · 4
The correlation between genetic factors and freezing of gait in patients with Parkinson's disease
2022 · Branislava Radojević, Nataša T. Dragašević-Mišković, et al. · Parkinsonism & Related Disorders · 4
Employment status of patients with Charcot-Marie-Tooth type 1A
2021 · Bogdan Bjelica, Marija Brankovic, et al. · Acta Neurologica Belgica · 4
GLUT1 deficiency syndrome: A case report with a novel SLC2A1 mutation
2017 · Nikola Ivancevic, Natasa Cerovac, et al. · Vojnosanitetski pregled · 4
Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson’s Disease
2026 · Gaber Bergant, Vesna M. van Midden, et al. · Genes · 3
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FIC Domain Protein Adenylyltransferase (FICD) ‐Related Complex Hereditary Spastic Paraplegia with Diabetes Mellitus
2025 · Adriana P. Rebelo, Adel Alawwadh, et al. · Movement Disorders Clinical Practice · 3
Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience
2022 · Nikola Kresojević, Valerija Dobričić, et al. · Journal of Neurology · 3
Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review
2021 · Phepy G. A. Dawod, Jasna Jancic, et al. · Diagnostics · 3
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Works count: 44
Citation count: 244
H-index: 9
I10-index: 8
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