V. Branković

500 total citations
9 papers, 79 citations indexed

About

V. Branković is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, V. Branković has authored 9 papers receiving a total of 79 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Genetics. Recurrent topics in V. Branković's work include Genetics and Neurodevelopmental Disorders (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA modifications and cancer (2 papers). V. Branković is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA modifications and cancer (2 papers). V. Branković collaborates with scholars based in Serbia, Italy and Czechia. V. Branković's co-authors include Ginevra Zanni, Marcello Niceta, Raffaella Cusmai, Sabina Barresi, Paolo Alfieri, Giorgia Piccini, Enrico Bertini, Alessandro Bruselles, Marco Tartaglia and Ljiljana Markovic‐Denic and has published in prestigious journals such as International Journal of Molecular Sciences, Movement Disorders and Muscle & Nerve.

In The Last Decade

V. Branković

8 papers receiving 79 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
V. Branković Serbia	5	50	26	26	14	14	9	79
Andrea Gangfuß Germany	6	51 1.0×	17 0.7×	14 0.5×	6 0.4×	14 1.0×	23	84
Abdulaziz Alsaman Saudi Arabia	7	93 1.9×	30 1.2×	14 0.5×	12 0.9×	9 0.6×	15	129
Ana Kosać Serbia	7	82 1.6×	53 2.0×	12 0.5×	31 2.2×	7 0.5×	15	120
Véronique Manel France	6	26 0.5×	10 0.4×	18 0.7×	14 1.0×	4 0.3×	7	54
F. Fortunato Italy	6	102 2.0×	13 0.5×	18 0.7×	12 0.9×	11 0.8×	12	122
Mai Thao Bui France	5	59 1.2×	16 0.6×	23 0.9×	10 0.7×	47 3.4×	10	108
Spencer Goodman United States	5	61 1.2×	6 0.2×	21 0.8×	5 0.4×	15 1.1×	7	105
Eugenia Borgione Italy	8	81 1.6×	13 0.5×	27 1.0×	5 0.4×	8 0.6×	19	125
S. Makri France	5	140 2.8×	12 0.5×	43 1.7×	9 0.6×	19 1.4×	8	156
Samineh Deheshi Canada	6	75 1.5×	10 0.4×	22 0.8×	5 0.4×	8 0.6×	15	140

Countries citing papers authored by V. Branković

Since Specialization

Citations

This map shows the geographic impact of V. Branković's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by V. Branković with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. Branković more than expected).

Fields of papers citing papers by V. Branković

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. Branković. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by V. Branković. The network helps show where V. Branković may publish in the future.

Co-authorship network of co-authors of V. Branković

This figure shows the co-authorship network connecting the top 25 collaborators of V. Branković. A scholar is included among the top collaborators of V. Branković based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with V. Branković. V. Branković is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

Westenberger, Ana, Iva Stanković, Björn‐Hergen Laabs, et al.. (2024). ANO10‐Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series. Movement Disorders. 39(5). 887–892.

Branković, V., et al.. (2022). Serum leptin levels in children and adolescents with spinal muscular atrophy types 2 and 3✰. Archives de Pédiatrie. 29(7). 480–483. 1 indexed citations

Imbrici, Paola, Elena Conte, Rikard Blunck, et al.. (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. 22(18). 9913–9913. 14 indexed citations

Branković, V., et al.. (2021). Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3. Neuromuscular Disorders. 31(4). 291–299. 15 indexed citations

Nuovo, Sara, et al.. (2021). Novel unconventional variants expand the allelic spectrum of OPHN1 gene. American Journal of Medical Genetics Part A. 185(5). 1575–1581. 1 indexed citations

Branković, V., et al.. (2020). Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3. Muscle & Nerve. 63(1). 75–83. 10 indexed citations

Kresojević, Nikola, Igor Petrović, Valerija Dobričić, et al.. (2018). Phenotype of PLP1‐related Disorder Caused by Novel Mutation: A Case Report. Movement Disorders Clinical Practice. 5(5). 548–550. 1 indexed citations

Dobričić, Valerija, Aleksandra Tomić, V. Branković, et al.. (2017). GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia. Parkinsonism & Related Disorders. 45. 81–84. 8 indexed citations

Barresi, Sabina, Marcello Niceta, Paolo Alfieri, et al.. (2016). Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia. Clinical Genetics. 91(1). 86–91. 29 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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