| Phenotype of non-c. 907_909delGAG mutations in TOR1A: DYT1 dystonia revisited V Dobričić, N Kresojević, M Žarković, A Tomić, A Marjanović, ... Parkinsonism & related disorders 21 (10), 1256-1259, 2015 | 29 | 2015 |
| Five‐year study of quality of life in myotonic dystrophy S Peric, M Vujnic, V Dobricic, A Marjanovic, I Basta, I Novakovic, ... Acta Neurologica Scandinavica 134 (5), 346-351, 2016 | 27 | 2016 |
| Prospective measurement of quality of life in myotonic dystrophy type 1 S Peric, C Heatwole, E Durovic, A Kacar, A Nikolic, I Basta, A Marjanovic, ... Acta Neurologica Scandinavica 136 (6), 694-697, 2017 | 21 | 2017 |
| Neuropathic pain in patients with Charcot-Marie-Tooth type 1A B Bjelica, S Peric, I Basta, I Bozovic, A Kacar, A Marjanovic, V Ivanovic, ... Neurological Sciences 41, 625-630, 2020 | 19 | 2020 |
| Myotonic Dystrophy Type 2–Data from the Serbian Registry I Bozovica, S Perica, J Pesovicb, B Bjelicaa, M Brkusaninb, I Bastaa, ... Methods 14, 15, 2018 | 19 | 2018 |
| Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia S PERIC, J STEVANOVIC, K JOHNSON, ANA KOSAC, M PERIC, ... Acta Myologica 38 (3), 163, 2019 | 13 | 2019 |
| HPCA‐related dystonia: Too rare to be found? V Dobričić, N Kresojević, A Marjanović, A Tomić, M Svetel, I Novaković, ... Movement Disorders 31 (7), 1071-1071, 2016 | 13 | 2016 |
| Clinical and Genetic Analysis of Psychosis in Parkinson’s Disease B Radojević, NT Dragašević-Mišković, A Marjanović, M Branković, ... Journal of Parkinson's Disease 11 (4), 1973-1980, 2021 | 12 | 2021 |
| Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy PGA Dawod, J Jancic, A Marjanovic, M Brankovic, M Jankovic, ... Genes 11 (9), 1037, 2020 | 7 | 2020 |
| Contribution to the knowledge on the distribution of freshwater sponges–the Danube and Sava rivers case study S Anđus, N Nikolić, V Dobričić, A Marjanović, Z Gačić, G Branković, ... Journal of Limnology 77 (2), 199-208, 2018 | 5 | 2018 |
| Reply to:" Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism" N Kresojević, V Marković, V Dobričić, I Stanković, T Stojković, A Tomić, ... Movement disorders: official journal of the Movement Disorder Society 38 (4 …, 2023 | 3 | 2023 |
| Yield of the PMP22 deletion analysis in patients with compression neuropathies V Ivanovic, M Brankovic, B Bjelica, A Kacar, R Tubic, M Jankovic, ... Journal of Neurology 267, 3617-3623, 2020 | 3 | 2020 |
| First record of freshwater sponge Trochospongilla horrida Weltner, 1893 in Serbia–A morphological and genetic study S Andjus, N Nikolic, A Marjanovic, M Brankovic, V Lazovic, B Tubić, ... Limnologica 76, 48-51, 2019 | 3 | 2019 |
| Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience N Kresojević, V Dobričić, MJ Lukić, A Tomić, I Petrović, N Dragašević, ... Journal of neurology, 1-8, 2022 | 2 | 2022 |
| Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review PGA Dawod, J Jancic, A Marjanovic, M Brankovic, M Jankovic, ... Diagnostics 11 (11), 1969, 2021 | 2 | 2021 |
| Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit A Miletic, JR Stojanovic, V Parezanovic, S Rsovac, D Drakulic, ... European Journal of Pediatrics 180 (10), 3219-3227, 2021 | 2 | 2021 |
| HTERT promoter methylation and single nucleotide polymorphism (-245 T> C) affect renal cell carcinoma behavior in Serbian population J Trifunovic, G Basta Jovanovic, N Nikolic, J Carkic, A Marjanovic, ... Journal of BUON 22, 270-277, 2018 | 2 | 2018 |
| The importance of direct genetic testing for determining female carriers of the mutation in dystrophinopathies J Maksić, N Maksimović, L Rasulić, O Milankov, A Marjanović, ... Vojnosanitetski pregled 80 (3), 201-207, 2023 | 1* | 2023 |
| The correlation between genetic factors and freezing of gait in patients with Parkinson's disease B Radojević, NT Dragašević-Mišković, A Marjanović, M Branković, ... Parkinsonism & Related Disorders 98, 7-12, 2022 | 1 | 2022 |
| Clinical exome sequencing in Serbian patients with movement disorders: Single centre experience M Branković, N Dragašević, V Dobričić, A Maver, G Bergant, I Petrović, ... Genetika 54 (1), 395-409, 2022 | 1 | 2022 |
