Jovan Pešović

542 total citations
32 papers, 391 citations indexed

About

Jovan Pešović is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Jovan Pešović has authored 32 papers receiving a total of 391 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Cellular and Molecular Neuroscience, 21 papers in Neurology and 17 papers in Molecular Biology. Recurrent topics in Jovan Pešović's work include Genetic Neurodegenerative Diseases (23 papers), Parkinson's Disease Mechanisms and Treatments (17 papers) and Mitochondrial Function and Pathology (7 papers). Jovan Pešović is often cited by papers focused on Genetic Neurodegenerative Diseases (23 papers), Parkinson's Disease Mechanisms and Treatments (17 papers) and Mitochondrial Function and Pathology (7 papers). Jovan Pešović collaborates with scholars based in Serbia, Italy and Bosnia and Herzegovina. Jovan Pešović's co-authors include Dušanka Savić‐Pavićević, Stojan Perić, Vidosava Rakočević-Stojanović, Goran Brajušković, Vidosava Rakočević Stojanović, Dragana Lavrnić, G. Meola, Ivana Basta, Vera Ilic and Ana Kosać and has published in prestigious journals such as Nature Communications, International Journal of Molecular Sciences and Journal of the Neurological Sciences.

In The Last Decade

Jovan Pešović

29 papers receiving 384 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jovan Pešović Serbia 13 278 275 182 36 21 32 391
Elisabetta Bucci Italy 12 174 0.6× 271 1.0× 229 1.3× 14 0.4× 7 0.3× 23 404
Simone van de Loo Germany 7 126 0.5× 209 0.8× 272 1.5× 10 0.3× 29 1.4× 8 441
Teresa Tempkin United States 5 140 0.5× 179 0.7× 110 0.6× 44 1.2× 16 0.8× 6 268
C. Marchini Italy 9 135 0.5× 165 0.6× 228 1.3× 55 1.5× 11 0.5× 28 456
Phillip A. Starr United States 7 181 0.7× 226 0.8× 202 1.1× 22 0.6× 13 0.6× 10 444
Namiko Nishida Japan 12 86 0.3× 78 0.3× 188 1.0× 41 1.1× 40 1.9× 38 465
Barbara Merico Italy 5 272 1.0× 87 0.3× 31 0.2× 72 2.0× 14 0.7× 6 339
J. F. Aita United States 8 151 0.5× 168 0.6× 157 0.9× 9 0.3× 22 1.0× 19 378
David Pellerin Canada 13 219 0.8× 150 0.5× 55 0.3× 10 0.3× 9 0.4× 37 344
Elisabeth Dirren Switzerland 10 112 0.4× 102 0.4× 90 0.5× 58 1.6× 7 0.3× 16 312

Countries citing papers authored by Jovan Pešović

Since Specialization
Citations

This map shows the geographic impact of Jovan Pešović'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 Jovan Pešović with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jovan Pešović more than expected).

Fields of papers citing papers by Jovan Pešović

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jovan Pešović. 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 Jovan Pešović. The network helps show where Jovan Pešović may publish in the future.

Co-authorship network of co-authors of Jovan Pešović

This figure shows the co-authorship network connecting the top 25 collaborators of Jovan Pešović. A scholar is included among the top collaborators of Jovan Pešović 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 Jovan Pešović. Jovan Pešović is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sekulić, Aleksandar, et al.. (2025). Screening for Pompe disease in Serbian patients with limb-girdle muscle weakness. Clinical Neurology and Neurosurgery. 254. 108950–108950.
2.
Pešović, Jovan, Dušanka Savić‐Pavićević, Stojan Perić, et al.. (2025). Evaluation of Sleep-Disordered Breathing and Respiratory Dysfunction in Children with Myotonic Dystrophy Type 1—A Retrospective Cross-Sectional Study. Biomedicines. 13(4). 966–966.
3.
Martínez‐Piñeiro, Alicia, Jovan Pešović, Estefanía Cerro-Herreros, et al.. (2024). Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity. iScience. 27(6). 109930–109930. 4 indexed citations
4.
Meola, G., et al.. (2024). Main features and disease outcome of congenital myotonic dystrophy - experience from a single tertiary center. Neuromuscular Disorders. 40. 16–23. 3 indexed citations
5.
Perić, Stojan, Jovan Pešović, Dragana Lavrnić, et al.. (2024). Association between Cytotoxic T-Lymphocyte-Associated Antigen 4 (CTLA-4) Locus and Early-Onset Anti-acetylcholine Receptor-Positive Myasthenia Gravis in Serbian Patients. Molecular Neurobiology. 61(11). 9539–9547. 1 indexed citations
6.
Kosać, Ana, Stojan Perić, Jovan Pešović, et al.. (2024). Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma as a Nusinersen treatment response marker in childhood-onset SMA individuals from Serbia. Frontiers in Neurology. 15. 1394001–1394001. 6 indexed citations
7.
Kabić, Jovana, Gianuário Fortunato, Ivone Vaz‐Moreira, et al.. (2023). Dissemination of Metallo-β-Lactamase-Producing Pseudomonas aeruginosa in Serbian Hospital Settings: Expansion of ST235 and ST654 Clones. International Journal of Molecular Sciences. 24(2). 1519–1519. 15 indexed citations
8.
Perić, Stojan, et al.. (2022). Cognitive assessment in patients with myotonic dystrophy type 2. Neuromuscular Disorders. 32(9). 743–748. 4 indexed citations
9.
Perić, Stojan, Jovan Pešović, Ivo Božović, et al.. (2022). Clinical score for early diagnosis of myotonic dystrophy type 2. Neurological Sciences. 44(3). 1059–1067. 1 indexed citations
10.
Perić, Stojan, et al.. (2022). Autoimmune Diseases in Patients With Myotonic Dystrophy Type 2. Frontiers in Neurology. 13. 932883–932883. 1 indexed citations
11.
Perić, Stojan, Jovan Pešović, Dušanka Savić‐Pavićević, Vidosava Rakočević Stojanović, & G. Meola. (2021). Molecular and Clinical Implications of Variant Repeats in Myotonic Dystrophy Type 1. International Journal of Molecular Sciences. 23(1). 354–354. 18 indexed citations
12.
Perić, Stojan, Ivo Božović, Jovan Pešović, et al.. (2019). Body composition analysis in patients with myotonic dystrophy types 1 and 2. Neurological Sciences. 40(5). 1035–1040. 12 indexed citations
13.
Pešović, Jovan, et al.. (2018). Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic Cells. Frontiers in Genetics. 9. 601–601. 35 indexed citations
14.
Pešović, Jovan, et al.. (2017). Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions. Neurogenetics. 18(4). 207–218. 27 indexed citations
15.
Perić, Stojan, Ružica Maksimović, Bogdan Bjelica, et al.. (2017). Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies. Journal of Neurology. 264(9). 1899–1908. 21 indexed citations
16.
Stojanović, Vidosava Rakočević, Stojan Perić, Jovan Pešović, et al.. (2016). Quality of life in patients with myotonic dystrophy type 2. Journal of the Neurological Sciences. 365. 158–161. 26 indexed citations
17.
Perić, Stojan, Vidosava Rakočević Stojanović, Vera Ilic, et al.. (2016). Clusters of cognitive impairment among different phenotypes of myotonic dystrophy type 1 and type 2. Neurological Sciences. 38(3). 415–423. 39 indexed citations
18.
Kosać, Ana, Vladimir Jovanović, Jovan Pešović, et al.. (2015). Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients. Journal of Human Genetics. 60(11). 723–728. 16 indexed citations
19.
Vojinović, Dina, Jovan Pešović, Vesna Lukić, et al.. (2014). Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location. Balkan Journal of Medical Genetics. 17(2). 25–35. 32 indexed citations
20.
Perić, Stojan, Elka Stefanova, Dušanka Savić‐Pavićević, et al.. (2014). Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2. Journal of Neurology. 262(1). 142–148. 33 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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