Boglárka Bánsági

898 total citations
16 papers, 515 citations indexed

About

Boglárka Bánsági is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Boglárka Bánsági has authored 16 papers receiving a total of 515 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 8 papers in Molecular Biology and 5 papers in Cell Biology. Recurrent topics in Boglárka Bánsági's work include Hereditary Neurological Disorders (8 papers), Mitochondrial Function and Pathology (5 papers) and Cellular transport and secretion (4 papers). Boglárka Bánsági is often cited by papers focused on Hereditary Neurological Disorders (8 papers), Mitochondrial Function and Pathology (5 papers) and Cellular transport and secretion (4 papers). Boglárka Bánsági collaborates with scholars based in United Kingdom, Germany and United States. Boglárka Bánsági's co-authors include Rita Horváth, Hanns Lochmüller, Veronika Boczonadi, Patrick F. Chinnery, Helen Griffin, Angela Pyle, Roger G. Whittaker, Léna Szabó, László Zubek and András Fogarasi and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Boglárka Bánsági

16 papers receiving 503 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Boglárka Bánsági United Kingdom	11	275	175	106	102	77	16	515
Inge A. Meijer Canada	14	369 1.3×	362 2.1×	138 1.3×	129 1.3×	79 1.0×	22	811
Stefania Bigoni Italy	14	190 0.7×	105 0.6×	53 0.5×	65 0.6×	82 1.1×	33	520
Dorota Hoffman‐Zacharska Poland	14	216 0.8×	169 1.0×	34 0.3×	186 1.8×	64 0.8×	53	541
Soraya Scuderi Italy	15	232 0.8×	217 1.2×	20 0.2×	45 0.4×	46 0.6×	21	508
Susanne Gydesen Denmark	8	289 1.1×	99 0.6×	158 1.5×	634 6.2×	102 1.3×	17	981
Pia Rossi Italy	10	216 0.8×	206 1.2×	79 0.7×	99 1.0×	110 1.4×	10	491
Gautam Wali Australia	12	119 0.4×	169 1.0×	50 0.5×	103 1.0×	28 0.4×	30	363
Daita Kaneda Japan	10	183 0.7×	79 0.5×	47 0.4×	110 1.1×	51 0.7×	39	402
Claude Mignard France	5	690 2.5×	688 3.9×	130 1.2×	238 2.3×	51 0.7×	7	865
Erin Feeney United States	6	129 0.5×	58 0.3×	76 0.7×	43 0.4×	80 1.0×	8	511

Countries citing papers authored by Boglárka Bánsági

Since Specialization

Citations

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

Fields of papers citing papers by Boglárka Bánsági

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Boglárka Bánsági

This figure shows the co-authorship network connecting the top 25 collaborators of Boglárka Bánsági. A scholar is included among the top collaborators of Boglárka Bánsági 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 Boglárka Bánsági. Boglárka Bánsági 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:

16 of 16 papers shown

1.

McMacken, Grace, Hanns Lochmüller, Boglárka Bánsági, et al.. (2020). Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion. Journal of Neurology. 267(12). 3643–3649. 5 indexed citations

2.

Bánsági, Boglárka, Mark R. Baker, Julia O’Sullivan, et al.. (2018). Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo PTEN mutation. Neurology. 90(21). e1842–e1848. 5 indexed citations

3.

Laššuthová, Petra, Katharina Vill, Sevim Erdem‐Özdamar, et al.. (2018). Novel SBF2 mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2. Clinical Genetics. 94(5). 467–472. 7 indexed citations

4.

Boczonadi, Veronika, Martin King, Anthony C. Smith, et al.. (2018). Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease. Genetics in Medicine. 20(10). 1224–1235. 40 indexed citations

5.

Boczonadi, Veronika, Kathrin Meyer, Helen Griffin, et al.. (2018). Mutations in glycyl-tRNA synthetase impair mitochondrial metabolism in neurons. Human Molecular Genetics. 27(12). 2187–2204. 26 indexed citations

6.

Bánsági, Boglárka, Helen Griffin, Roger G. Whittaker, et al.. (2017). Genetic heterogeneity of motor neuropathies. Neurology. 88(13). 1226–1234. 69 indexed citations

7.

Bánsági, Boglárka, David Lewis‐Smith, Endre Pál, et al.. (2016). Phenotypic convergence of Menkes and Wilson disease. Neurology Genetics. 2(6). e119–e119. 13 indexed citations

8.

Bánsági, Boglárka, Thalia Antoniadi, Sinéad M. Murphy, et al.. (2015). Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland. Journal of Neurology. 262(8). 1899–1908. 32 indexed citations

9.

Evangelista, Teresinha, Boglárka Bánsági, Angela Pyle, et al.. (2015). Phenotypic variability of TRPV4 related neuropathies. Neuromuscular Disorders. 25(6). 516–521. 25 indexed citations

10.

Whittaker, Roger G., David N. Herrmann, Boglárka Bánsági, et al.. (2015). Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome. Neurology. 85(22). 1964–1971. 40 indexed citations

11.

Herrmann, D., Rita Horváth, Janet E. Sowden, et al.. (2014). Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy. The American Journal of Human Genetics. 95(4). 472–472. 2 indexed citations

12.

Kovács, Tamás, Boglárka Bánsági, Ogúz Kelemen, & Szabolcs Kéri. (2014). Neuregulin 1-Induced AKT and ERK Phosphorylation in Patients with Fragile X Syndrome (FXS) and Intellectual Disability Associated with Obstetric Complications. Journal of Molecular Neuroscience. 54(1). 119–124. 3 indexed citations

13.

Herrmann, D., Rita Horváth, Janet E. Sowden, et al.. (2014). Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy. The American Journal of Human Genetics. 95(3). 332–339. 81 indexed citations

14.

Boczonadi, Veronika, Emanuele Barca, Angela Pyle, et al.. (2014). ANO10 mutations cause ataxia and coenzyme Q10 deficiency. Journal of Neurology. 261(11). 2192–2198. 61 indexed citations

15.

Boczonadi, Veronika, Boglárka Bánsági, & Rita Horváth. (2014). Reversible infantile mitochondrial diseases. Journal of Inherited Metabolic Disease. 38(3). 427–435. 26 indexed citations

16.

Szabó, Léna, et al.. (2012). A detailed semiologic analysis of childhood psychogenic nonepileptic seizures. Epilepsia. 53(3). 565–570. 80 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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