Violeta Mihaylova

1.5k total citations
22 papers, 424 citations indexed

About

Violeta Mihaylova is a scholar working on Molecular Biology, Neurology and Cell Biology. According to data from OpenAlex, Violeta Mihaylova has authored 22 papers receiving a total of 424 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Neurology and 5 papers in Cell Biology. Recurrent topics in Violeta Mihaylova's work include Muscle Physiology and Disorders (6 papers), Myasthenia Gravis and Thymoma (5 papers) and Mitochondrial Function and Pathology (5 papers). Violeta Mihaylova is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Myasthenia Gravis and Thymoma (5 papers) and Mitochondrial Function and Pathology (5 papers). Violeta Mihaylova collaborates with scholars based in Bulgaria, Germany and Switzerland. Violeta Mihaylova's co-authors include Hanns Lochmüller, Juliane S. Müller, Angela Abicht, Velina Guergueltcheva, Angela Huebner, Maja von der Hagen, Ulrike Schara, Amina Chaouch, Marina Dusl and Constanze Gallenmüller and has published in prestigious journals such as Brain, Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Violeta Mihaylova

19 papers receiving 419 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Violeta Mihaylova Bulgaria 12 210 172 122 76 37 22 424
Luca Chiveri Italy 9 199 0.9× 291 1.7× 41 0.3× 61 0.8× 68 1.8× 13 540
A. Al‐Memar United Kingdom 9 106 0.5× 138 0.8× 31 0.3× 125 1.6× 39 1.1× 13 336
Naoki Nakao Japan 9 154 0.7× 234 1.4× 39 0.3× 185 2.4× 37 1.0× 32 445
Milena Janković Serbia 12 152 0.7× 106 0.6× 29 0.2× 91 1.2× 79 2.1× 37 337
D. Schiffer Italy 12 129 0.6× 158 0.9× 69 0.6× 61 0.8× 70 1.9× 34 399
Michela Ripolone Italy 13 72 0.3× 349 2.0× 43 0.4× 121 1.6× 74 2.0× 40 526
Keiko Ishigaki Japan 13 68 0.3× 252 1.5× 45 0.4× 56 0.7× 110 3.0× 58 476
Ichiro Nozaki Japan 13 100 0.5× 350 2.0× 33 0.3× 32 0.4× 88 2.4× 33 510
Hannes Steinkellner Austria 11 83 0.4× 218 1.3× 43 0.4× 196 2.6× 78 2.1× 20 400
Christine Makowski Germany 10 95 0.5× 229 1.3× 21 0.2× 62 0.8× 51 1.4× 18 480

Countries citing papers authored by Violeta Mihaylova

Since Specialization
Citations

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

Fields of papers citing papers by Violeta Mihaylova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Violeta Mihaylova

This figure shows the co-authorship network connecting the top 25 collaborators of Violeta Mihaylova. A scholar is included among the top collaborators of Violeta Mihaylova 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 Violeta Mihaylova. Violeta Mihaylova 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.
Gresham, David, Velina Guergueltcheva, Teodora Chamova, et al.. (2024). Phenotypic Variability of LGMD 2C/R5 in a Genetically Homogenous Group of Bulgarian Muslim Roma. Genes. 15(9). 1144–1144.
2.
Chamova, Teodora, Violeta Mihaylova, Rachel Thompson, et al.. (2024). Characterization of Clinical Phenotypes in Congenital Myasthenic Syndrome Associated with the c.1327delG Frameshift Mutation in CHRNE Encoding the Acetylcholine Receptor Epsilon Subunit. Journal of Neuromuscular Diseases. 11(5). 1011–1020. 2 indexed citations
3.
Mihaylova, Violeta, Yvan Herenger, Tobias Bethge, & Stephan Bohlhalter. (2023). A Novel WARS2 Mutation in a Swiss Family With Predominant Generalized Dystonia Responsive to Trihexyphenidyl. Journal of Clinical Neurology. 19(4). 413–413. 1 indexed citations
4.
Mihaylova, Violeta, Juliane Bremer, Roman Guggenberger, et al.. (2021). Collagen VI-Related Myopathy Caused by Compound Heterozygous Mutations of COL6A3 in a Consanguineous Kurdish Family. Journal of Clinical Neuromuscular Disease. 22(3). 173–179. 3 indexed citations
5.
Mihaylova, Violeta, et al.. (2020). Novel truncating mutations of MYO18B causing congenital myopathy in a Swiss patient. Neurology Genetics. 6(4). e458–e458. 4 indexed citations
6.
Mihaylova, Violeta, et al.. (2018). Forced interventions against persons with mental disorders - medical-legal accents. Trakia Journal of Sciences. 16(Suppl.1). 110–116.
7.
Mueller, Sandro Manuel, Jens A. Petersen, Sebastian Frese, et al.. (2017). Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients. Orphanet Journal of Rare Diseases. 12(1). 184–184. 15 indexed citations
8.
Mihaylova, Violeta, Sebastian Frese, Sandro Manuel Mueller, et al.. (2016). Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy. Orphanet Journal of Rare Diseases. 11(1). 105–105. 14 indexed citations
9.
Frese, Sebastian, Jens A. Petersen, Sandro Manuel Mueller, et al.. (2016). Exercise effects in Huntington disease. Journal of Neurology. 264(1). 32–39. 33 indexed citations
10.
Chamova, Teodora, Velina Guergueltcheva, Мариана Господинова, et al.. (2015). GNE myopathy in Roma patients homozygous for the p.I618T founder mutation. Neuromuscular Disorders. 25(9). 713–718. 27 indexed citations
11.
Mihaylova, Violeta, et al.. (2013). Possible Toxicity of Tuberculostatic Agents in a Patient With a NovelTYMPMutation Leading to Mitochondrial Neurogastrointestinal Encephalomyopathy. Journal of Neurogenetics. 27(1-2). 19–22. 4 indexed citations
12.
13.
Abicht, Angela, Marina Dusl, Constanze Gallenmüller, et al.. (2012). Congenital myasthenic syndromes: Achievements and limitations of phenotype-guided gene-after-gene sequencing in diagnostic practice: A study of 680 patients. Human Mutation. 33(10). 1474–1484. 91 indexed citations
14.
Mihaylova, Violeta, et al.. (2012). Neurological Symptoms, Genotype-Phenotype Correlations and Ethnic-specific Differences in Bulgarian Patients With Wilson Disease. The Neurologist. 18(4). 184–189. 20 indexed citations
15.
Mihaylova, Violeta, Rosana Hermínia Scola, Paulo José Lorenzoni, et al.. (2010). Molecular characterisation of congenital myasthenic syndromes in Southern Brazil. Journal of Neurology Neurosurgery & Psychiatry. 81(9). 973–977. 44 indexed citations
16.
Angelicheva, Dora, Ivailo Tournev, Velina Guergueltcheva, et al.. (2009). Partial epilepsy syndrome in a Gypsy family linked to 5q31.3‐q32. Epilepsia. 50(7). 1679–1688. 15 indexed citations
17.
Guergueltcheva, Velina, Violeta Mihaylova, Т. Тодоров, et al.. (2009). Molecular Diagnostics of Duchenne/Becker Muscular Dystrophy Patients by Multiplex Ligation-Dependent Probe Amplification Analysis and Direct Sequencing. Balkan Journal of Medical Genetics. 12(2). 3–9. 1 indexed citations
18.
Sivadorai, Padma, Sylvia Cherninkova, Dora Angelicheva, et al.. (2008). Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies. Clinical Genetics. 74(1). 82–87. 15 indexed citations
19.
Müller, Juliane S., Violeta Mihaylova, Angela Abicht, & Hanns Lochmüller. (2007). Congenital myasthenic syndromes: spotlight on genetic defects of neuromuscular transmission. Expert Reviews in Molecular Medicine. 9(22). 1–20. 50 indexed citations
20.
Mihaylova, Violeta, Janina Hantke, Radka Tincheva, et al.. (2006). Highly variable neural involvement in sphingomyelinase-deficient Niemann-Pick disease caused by an ancestral Gypsy mutation. Brain. 130(4). 1050–1061. 31 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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