S. Todorović

917 total citations
27 papers, 458 citations indexed

About

S. Todorović is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, S. Todorović has authored 27 papers receiving a total of 458 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 8 papers in Neurology. Recurrent topics in S. Todorović's work include Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (7 papers) and Muscle Physiology and Disorders (6 papers). S. Todorović is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (7 papers) and Muscle Physiology and Disorders (6 papers). S. Todorović collaborates with scholars based in Serbia, United States and United Kingdom. S. Todorović's co-authors include Edward Perez‐Reyes, Michael T. Nelson, Stanka Romac, Hanns Lochmüller, Slobodan Apostolski, Vesna Jevtovic‐Todorovic, C. F. Zorumski, Steven Mennerick, Jelena Mladenović and Tatjana Pekmezović and has published in prestigious journals such as The Journal of Cell Biology, Neurology and Annals of the New York Academy of Sciences.

In The Last Decade

S. Todorović

22 papers receiving 445 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Todorović Serbia	14	314	201	85	79	60	27	458
Mikko Kärppä Finland	14	651 2.1×	133 0.7×	75 0.9×	92 1.2×	70 1.2×	38	951
Verena Theis Germany	12	227 0.7×	90 0.4×	57 0.7×	59 0.7×	27 0.5×	19	372
Zivotije Radisavljevic United States	9	228 0.7×	183 0.9×	39 0.5×	41 0.5×	85 1.4×	13	577
Tohru Ibi Japan	12	363 1.2×	215 1.1×	34 0.4×	104 1.3×	56 0.9×	33	554
Katherine A. Dick United States	5	479 1.5×	463 2.3×	63 0.7×	158 2.0×	80 1.3×	5	606
M.L. Mostacciuolo Italy	12	289 0.9×	113 0.6×	119 1.4×	45 0.6×	31 0.5×	18	466
Valentina Pegoraro Italy	14	399 1.3×	91 0.5×	86 1.0×	164 2.1×	103 1.7×	25	626
Marie‐Christine Arné‐Bes France	9	164 0.5×	229 1.1×	103 1.2×	85 1.1×	14 0.2×	16	527
Zhen Zhi Tang United States	9	498 1.6×	217 1.1×	207 2.4×	34 0.4×	33 0.6×	12	546
Jian‐Guo Qi China	12	182 0.6×	155 0.8×	30 0.4×	39 0.5×	82 1.4×	27	552

Countries citing papers authored by S. Todorović

Since Specialization

Citations

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

Fields of papers citing papers by S. Todorović

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Todorović

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Todorović, S.. (2019). Troyer Syndrome. Definitions. 50(5). 482–8.

Oury, Julien, Yun Liu, Ana Töpf, et al.. (2019). MACF1 links Rapsyn to microtubule- and actin-binding proteins to maintain neuromuscular synapses. The Journal of Cell Biology. 218(5). 1686–1705. 38 indexed citations

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

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

Mladenović, Jelena, Stanka Romac, S. Todorović, et al.. (2011). Epidemiology of Charcot-Marie-Tooth Disease in the Population of Belgrade, Serbia. Neuroepidemiology. 36(3). 177–182. 16 indexed citations

Todorović, Nataša, Sofija Forkapić, I. Bikit, et al.. (2010). Monitoring for exposures to TENORM sources in Vojvodina region. Radiation Protection Dosimetry. 144(1-4). 655–658. 13 indexed citations

Todorović, S., et al.. (2009). Eosinophilic myositis as presenting symptom in γ-sarcoglycanopathy. Neuromuscular Disorders. 19(2). 167–171. 18 indexed citations

Prelević, Gordana M., et al.. (2009). Prolactin Secretion in Myotonic Dystrophy. Experimental and Clinical Endocrinology & Diabetes. 96(6). 247–252.

Mladenović, Jelena, et al.. (2006). Survival and mortality of myotonic dystrophy type 1 (Steinert's disease) in the population of Belgrade. European Journal of Neurology. 13(5). 451–454. 24 indexed citations

10.

Mladenović, Jelena, Tatjana Pekmezović, S. Todorović, et al.. (2006). Epidemiology of myotonic dystrophy type 1 (Steinert disease) in Belgrade (Serbia). Clinical Neurology and Neurosurgery. 108(8). 757–760. 14 indexed citations

11.

Nelson, Michael T., S. Todorović, & Edward Perez‐Reyes. (2006). The Role of T-Type Calcium Channels in Epilepsy and Pain. Current Pharmaceutical Design. 12(18). 2189–2197. 92 indexed citations

12.

Müller, Juliane S., Sabine Krause, S. Todorović, et al.. (2006). Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations. Neurology. 67(7). 1159–1164. 26 indexed citations

13.

Savić‐Pavićević, Dušanka, et al.. (2006). CLINICAL CASE REPORT ATYPICAL MYOPATHY IN A YOUNG GIRL WITH 91 CTG REPEATS IN DM1 LOCUS AND A POSITIVE DM1 FAMILY HISTORY. International Journal of Neuroscience. 116(12). 1509–1518. 4 indexed citations

14.

Krndija, Denis, Jelena Mladenović, Vidosava Rakočević-Stojanović, et al.. (2005). Haplotype analysis of the DM1 locus in the Serbian population. Acta Neurologica Scandinavica. 111(4). 274–277. 5 indexed citations

15.

Novaković, Ivana, et al.. (2005). Proximal Dystrophin Gene Deletions and Protein Alterations in Becker Muscular Dystrophy. Annals of the New York Academy of Sciences. 1048(1). 406–410. 13 indexed citations

16.

Jović, N., et al.. (2004). The Recurrence Risk of Ischemic Stroke in Childhood. Medical Principles and Practice. 13(3). 153–158. 13 indexed citations

17.

Savić‐Pavićević, Dušanka, Ivan Topisirović, Tamara Major, et al.. (2001). Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?. Psychiatric Genetics. 11(4). 201–205. 4 indexed citations

18.

Todorović, S., et al.. (1996). Association of Krabbe leukodystrophy and congenital fiber type disproportion. Pediatric Neurology. 15(1). 79–82. 6 indexed citations

19.

Todorović, S., et al.. (1993). Association of progressive myoclonic epilepsy and spinal muscular atrophy. Pediatric Neurology. 9(2). 147–150. 7 indexed citations

20.

Todorović, S. & Snežana Đorđević. (1986). [Late neurologic consequence of triorthocresyl phosphate (TOCP)].. PubMed. 43(2). 124–7. 1 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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