T. Stojkovic

1.0k total citations
25 papers, 428 citations indexed

About

T. Stojkovic is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, T. Stojkovic has authored 25 papers receiving a total of 428 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 8 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in T. Stojkovic's work include Myasthenia Gravis and Thymoma (6 papers), Cardiomyopathy and Myosin Studies (6 papers) and Muscle Physiology and Disorders (5 papers). T. Stojkovic is often cited by papers focused on Myasthenia Gravis and Thymoma (6 papers), Cardiomyopathy and Myosin Studies (6 papers) and Muscle Physiology and Disorders (5 papers). T. Stojkovic collaborates with scholars based in France, Japan and Switzerland. T. Stojkovic's co-authors include Didier Leys, Didier Chavot, Thierry Moulin, A. Destée, J. de Sèze, P. Vermersch, D. Ferriby, Pierre‐Yves Hatron, B. Wallaert and É. Hachulla and has published in prestigious journals such as Neurology, Journal of Neuropathology & Experimental Neurology and Journal of Neurology.

In The Last Decade

T. Stojkovic

20 papers receiving 412 citations

Peers

T. Stojkovic

NEURO

PRM

PHYSI

CCM

Marcus Vinícius Pinto United States

M Zavanone Italy

Philippe Petiot France

Judith A. Fryer Australia

Ryoji Nishi Japan

Judith M.A. Verhagen Netherlands

Susanne Gaertner Germany

Chuanqiang Pu China

Jun Morioka Japan

C Vital France

Marcus Vinícius Pinto United States

T. Stojkovic

127 ×0.6

NEURO

140 ×1.0

48 ×0.3

PRM

58 ×0.6

PHYSI

19 ×0.3

CCM

Citations per year, relative to T. Stojkovic T. Stojkovic (= 1×) peers Marcus Vinícius Pinto

Countries citing papers authored by T. Stojkovic

Since Specialization

Citations

This map shows the geographic impact of T. Stojkovic'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 T. Stojkovic with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Stojkovic more than expected).

Fields of papers citing papers by T. Stojkovic

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Stojkovic

This figure shows the co-authorship network connecting the top 25 collaborators of T. Stojkovic. A scholar is included among the top collaborators of T. Stojkovic 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 T. Stojkovic. T. Stojkovic 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

Stojkovic, T., et al.. (2024). 234P Congenital myasthenic syndromes in adults: clinical features, diagnosis and long-term prognosis. Neuromuscular Disorders. 43. 104441.617–104441.617. 1 indexed citations

Voermans, Nicol C., Jean‐Yves Hogrel, Marc Jeanpierre, et al.. (2019). Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations. Journal of Neurology. 266(12). 2987–2996.

Jacobs, Marni, M. James, Anna Mayhew, et al.. (2019). P.183Functional progression in dysferlinopathy: results of a 3-year natural history study. Neuromuscular Disorders. 29. S102–S102.

Carvalho, Alzira Alves de Siqueira, Guy Brochier, Konstantinos Papadopoulos, et al.. (2018). Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French Cohort. Genetic Testing and Molecular Biomarkers. 22(6). 374–383. 16 indexed citations

Wahbi, Karim, Raphaël Porcher, T. Stojkovic, et al.. (2017). Venous thromboembolism in adult patients with inherited myopathies: a high-risk in myotonic dystrophy. Neuromuscular Disorders. 27. S179–S179. 1 indexed citations

Devic, Perrine, P. Petiot, Thomas Simonet, et al.. (2013). Antibodies to clustered acetylcholine receptor: expanding the phenotype. European Journal of Neurology. 21(1). 130–134. 47 indexed citations

Jacquin, Agnès, Olivier Rouaud, P Soichot, et al.. (2013). Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family. Case Reports in Neurology. 5(3). 187–194. 13 indexed citations

Outteryck, Olivier, J. de Sèze, T. Stojkovic, et al.. (2012). Methionine Synthase Deficiency (cblG): A Rare Cause of Adult Onset Leukoencephalopathy with Reversible Neurological Deficit (P01.124). Neurology. 78(Meeting Abstracts 1). P01.124–P01.124.

Wargon, I., Pascale Richard, Thierry Küntzer, et al.. (2011). P5.17 Congenital Myasthenic Syndromes with COLQ mutations: Long term follow-up. Neuromuscular Disorders. 21(9-10). 728–729. 1 indexed citations

10.

Stojkovic, T. & Anthony Béhin. (2010). Myasthénies oculaires : diagnostic et traitement. Revue Neurologique. 166(12). 987–997. 5 indexed citations

11.

Toussaint, Anne, Marie Maurer, Belinda S. Cowling, et al.. (2010). P1.35 Amphiphysin 2 (BIN1) and triad defects in several forms of centronuclear myopathies. Neuromuscular Disorders. 20(9-10). 611–611. 2 indexed citations

12.

Béhin, Anthony, T. Stojkovic, Kristl G. Claeys, et al.. (2008). Desminopathies : What can we learn from a long term follow-up?. Neuromuscular Disorders. 18. 765.

13.

Wahbi, Karim, Christophe Meune, T. Stojkovic, et al.. (2008). Cardiac assessment of limb–girdle muscular dystrophy 2I patients: An echography, Holter ECG and magnetic resonance imaging study. Neuromuscular Disorders. 18(8). 650–655. 45 indexed citations

14.

Sèze, J. de, T. Stojkovic, S. Delalande, et al.. (2006). Myasthénie auto-immune et grossesse : évolution clinique, accouchement et post-partum. Revue Neurologique. 162(3). 330–338. 15 indexed citations

15.

Stojkovic, T.. (2005). Les neuropathies périphériques : orientations et moyens diagnostiques. La Revue de Médecine Interne. 27(4). 302–312. 8 indexed citations

16.

Zéphir, Hélène, J. de Sèze, D. Ferriby, T. Stojkovic, & P. Vermersch. (2002). [Epstein-Barr meningoencephaloradiculitis in a immunocompetent woman].. PubMed. 158(8-9). 830–2. 3 indexed citations

17.

Sèze, J. de, T. Stojkovic, Christine Delmaire, et al.. (2002). [Candida albicans meningoencephalomyeloradiculitis].. PubMed. 158(4). 473–6. 1 indexed citations

18.

Ferriby, D., J. de Sèze, T. Stojkovic, et al.. (2001). Long-term follow-up of neurosarcoidosis. Neurology. 57(5). 927–929. 83 indexed citations

19.

Quilliet, Xavier, Odile Chevallier-Lagente, Éric Eveno, et al.. (1996). Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene. Mutation Research/DNA Repair. 364(3). 161–169. 29 indexed citations

20.

Leys, Didier, et al.. (1995). Follow-Up of Patients with History of Cervical Artery Dissection. Cerebrovascular Diseases. 5(1). 43–49. 116 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.

Explore authors with similar magnitude of impact