Rita-Eva Varga

417 total citations
6 papers, 277 citations indexed

About

Rita-Eva Varga is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology. According to data from OpenAlex, Rita-Eva Varga has authored 6 papers receiving a total of 277 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Cellular and Molecular Neuroscience, 2 papers in Cell Biology and 1 paper in Molecular Biology. Recurrent topics in Rita-Eva Varga's work include Hereditary Neurological Disorders (3 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genomics and Rare Diseases (1 paper). Rita-Eva Varga is often cited by papers focused on Hereditary Neurological Disorders (3 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genomics and Rare Diseases (1 paper). Rita-Eva Varga collaborates with scholars based in Germany, Austria and United Kingdom. Rita-Eva Varga's co-authors include Christian Beetz, Ingo Kurth, Nicole Hertel, Christian A. Hübner, Mukhran Khundadze, Michaela Auer‐Grumbach, Thomas Fothergill, Slave Trajanoski, Thomas Wieland and Vincent Timmerman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Analytical Biochemistry and The American Journal of Human Genetics.

In The Last Decade

Rita-Eva Varga

6 papers receiving 275 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rita-Eva Varga Germany	5	149	100	75	74	73	6	277
Maxime Boutry France	6	176 1.2×	101 1.0×	102 1.4×	94 1.3×	66 0.9×	7	334
Claudia Crimella Italy	8	234 1.6×	111 1.1×	137 1.8×	94 1.3×	56 0.8×	8	356
Laura Cox United Kingdom	6	120 0.8×	46 0.5×	97 1.3×	108 1.5×	100 1.4×	7	432
Tania Rizo Germany	5	98 0.7×	102 1.0×	122 1.6×	219 3.0×	33 0.5×	5	403
Giles Watts United States	7	54 0.4×	115 1.1×	47 0.6×	165 2.2×	87 1.2×	7	342
Katrina J. Llewellyn United States	10	50 0.3×	105 1.1×	53 0.7×	161 2.2×	113 1.5×	16	362
Elena I. Ilina Germany	9	123 0.8×	46 0.5×	26 0.3×	184 2.5×	27 0.4×	13	340
Christine M. Rostosky Germany	5	68 0.5×	81 0.8×	24 0.3×	153 2.1×	97 1.3×	5	312
Alleene V. Strickland United States	7	256 1.7×	105 1.1×	113 1.5×	185 2.5×	29 0.4×	7	417
Maria Schabhüttl Austria	9	202 1.4×	132 1.3×	101 1.3×	162 2.2×	13 0.2×	9	382

Countries citing papers authored by Rita-Eva Varga

Since Specialization

Citations

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

Fields of papers citing papers by Rita-Eva Varga

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rita-Eva Varga. 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 Rita-Eva Varga. The network helps show where Rita-Eva Varga may publish in the future.

Co-authorship network of co-authors of Rita-Eva Varga

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

All Works

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6 of 6 papers shown

1.

Khundadze, Mukhran, Nahal Brocke‐Ahmadinejad, Rita-Eva Varga, et al.. (2021). Mouse models for hereditary spastic paraplegia uncover a role of PI4K2A in autophagic lysosome reformation. Autophagy. 17(11). 3690–3706. 22 indexed citations

2.

Varga, Rita-Eva, Mukhran Khundadze, Markus Daμμe, et al.. (2015). In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11. PLoS Genetics. 11(8). e1005454–e1005454. 97 indexed citations

3.

Beetz, Christian, Adam Johnson, Amber L. Schuh, et al.. (2013). Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure. Proceedings of the National Academy of Sciences. 110(13). 5091–5096. 75 indexed citations

4.

Beetz, Christian, Thomas R. Pieber, Nicole Hertel, et al.. (2012). Exome Sequencing Identifies a REEP1 Mutation Involved in Distal Hereditary Motor Neuropathy Type V. The American Journal of Human Genetics. 91(1). 139–145. 69 indexed citations

5.

Kiehntopf, Michael, Rita-Eva Varga, Hans Georg Koch, & Christian Beetz. (2011). A homemade MLPA assay detects known CTNS mutations and identifies a novel deletion in a previously unresolved cystinosis family. Gene. 495(1). 89–92. 4 indexed citations

6.

Varga, Rita-Eva, Amir Jahić, Elena Sánchez-Ferrero, et al.. (2011). MLPA-based evidence for sequence gain: Pitfalls in confirmation and necessity for exclusion of false positives. Analytical Biochemistry. 421(2). 799–801. 10 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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