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Ana Marjanović

Observed names: A. Marjanovic, Ana Marjanovic
ORCID: 0000-0002-0182-7822
Observed ORCID: 0000-0002-0182-7822
OpenAlex ID: A5083356308
Five-year study of quality of life in myotonic dystrophy
2015 · S. Peric, M. Vujnic, et al. · Acta Neurologica Scandinavica · 30
Neuropathic pain in patients with Charcot-Marie-Tooth type 1A
2019 · Bogdan Bjelica, Stojan Peric, et al. · Neurological Sciences · 26
Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited
2015 · Valerija Dobričić, Nikola Kresojević, et al. · Parkinsonism & Related Disorders · 25
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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Prospective measurement of quality of life in myotonic dystrophy type 1
2017 · S. Peric, C. Heatwole, et al. · Acta Neurologica Scandinavica · 23
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Myotonic Dystrophy Type 2 – Data from the Serbian Registry
2018 · Ivo Bozovic, Stojan Peric, et al. · Journal of Neuromuscular Diseases · 16
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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HPCA‐related dystonia: Too rare to be found?
2016 · Valerija Dobričić, Nikola Kresojević, et al. · Movement Disorders · 11
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
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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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
Contribution to the knowledge on the distribution of freshwater sponges – the Danube and Sava rivers case study
2017 · Stefan Andjus, Nadja Nikolic, et al. · Journal of Limnology · 4
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GLUT1 deficiency syndrome: A case report with a novel SLC2A1 mutation
2017 · Nikola Ivancevic, Natasa Cerovac, et al. · Vojnosanitetski pregled · 4
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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C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia
2023 · Ana Marjanovic, Aleksa Palibrk, et al. · Genetika · 2
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Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism
2021 · Milica Pešić, Nataša Dragašević Mišković, et al. · Neurological Research · 2
Yield of the PMP22 deletion analysis in patients with compression neuropathies
2020 · Vukan Ivanovic, Marija Brankovic, et al. · Journal of Neurology · 2
First record of freshwater sponge Trochospongilla horrida Weltner, 1893 in Serbia – A morphological and genetic study
2019 · Stefan Andjus, Nadja Nikolic, et al. · Limnologica · 2
Works count: 44
Citation count: 250
H-index: 9
I10-index: 9
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