Rudolf A. Kley

9.4k total citations
58 papers, 2.0k citations indexed

About

Rudolf A. Kley is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Rudolf A. Kley has authored 58 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 25 papers in Cellular and Molecular Neuroscience and 25 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Rudolf A. Kley's work include Muscle Physiology and Disorders (27 papers), Genetic Neurodegenerative Diseases (25 papers) and Cardiomyopathy and Myosin Studies (25 papers). Rudolf A. Kley is often cited by papers focused on Muscle Physiology and Disorders (27 papers), Genetic Neurodegenerative Diseases (25 papers) and Cardiomyopathy and Myosin Studies (25 papers). Rudolf A. Kley collaborates with scholars based in Germany, United States and United Kingdom. Rudolf A. Kley's co-authors include Matthias Vorgerd, Dirk Fischer, Mike P. Wattjes, Dieter O. Fürst, Peter F. M. van der Ven, Rolf Schröder, Montse Olivé, Hanns Lochmüller, Lev G. Goldfarb and Mark A. Tarnopolsky and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Rudolf A. Kley

56 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rudolf A. Kley Germany 26 1.2k 700 529 455 322 58 2.0k
B. Eymard France 29 1.5k 1.2× 771 1.1× 439 0.8× 245 0.5× 336 1.0× 82 2.6k
Andreas Roos Germany 25 1.3k 1.0× 195 0.3× 501 0.9× 492 1.1× 218 0.7× 134 2.1k
Juan J. Vílchez Spain 32 1.5k 1.2× 258 0.4× 1.5k 2.9× 351 0.8× 209 0.6× 130 3.0k
Sharon Keers United Kingdom 18 1.8k 1.5× 376 0.5× 553 1.0× 326 0.7× 136 0.4× 28 2.1k
Duygu Selcen United States 35 2.3k 1.9× 979 1.4× 765 1.4× 1.1k 2.4× 481 1.5× 87 3.8k
C. Jimenez‐Mallebrera Spain 25 1.5k 1.2× 273 0.4× 256 0.5× 303 0.7× 108 0.3× 78 1.9k
Jens Reimann Germany 22 845 0.7× 221 0.3× 265 0.5× 296 0.7× 130 0.4× 55 1.3k
Gerald Pfeffer Canada 22 1.2k 1.0× 159 0.2× 307 0.6× 143 0.3× 140 0.4× 75 1.9k
Göknur Haliloğlu Türkiye 23 922 0.8× 161 0.2× 224 0.4× 183 0.4× 110 0.3× 116 1.7k
Leslie Bridges United Kingdom 27 887 0.7× 217 0.3× 222 0.4× 132 0.3× 492 1.5× 78 2.4k

Countries citing papers authored by Rudolf A. Kley

Since Specialization
Citations

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

Fields of papers citing papers by Rudolf A. Kley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rudolf A. Kley. 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 Rudolf A. Kley. The network helps show where Rudolf A. Kley may publish in the future.

Co-authorship network of co-authors of Rudolf A. Kley

This figure shows the co-authorship network connecting the top 25 collaborators of Rudolf A. Kley. A scholar is included among the top collaborators of Rudolf A. Kley 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 Rudolf A. Kley. Rudolf A. Kley 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.
Eggers, Britta, Julian Uszkoreit, Robert Rehmann, et al.. (2022). Target formation in muscle fibres indicates reinnervation – A proteomic study in muscle samples from peripheral neuropathies. Neuropathology and Applied Neurobiology. 49(1). e12853–e12853. 5 indexed citations
2.
Güttsches, Anne‐Katrin, Frank Jacobsen, Martin Tegenthoff, et al.. (2019). Chaperones in sporadic inclusion body myositis—Validation of proteomic data. Muscle & Nerve. 61(1). 116–121. 7 indexed citations
3.
Ciryam, Prajwal, Matthew Antalek, Fernando Maureira Cid, et al.. (2019). A metastable subproteome underlies inclusion formation in muscle proteinopathies. Acta Neuropathologica Communications. 7(1). 197–197. 19 indexed citations
4.
Maerkens, A., Montse Olivé, Joachim Schessl, et al.. (2016). New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analyses. Acta Neuropathologica Communications. 4(1). 8–8. 47 indexed citations
5.
Winter, Lilli, Ilka Wittig, Viktoriya Peeva, et al.. (2016). Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue. Acta Neuropathologica. 132(3). 453–473. 51 indexed citations
6.
Claeys, Kristl G., et al.. (2016). Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNC. Neuromuscular Disorders. 27(1). 73–77. 13 indexed citations
7.
Chevessier, Frédéric, Zacharias Orfanos, A. Maerkens, et al.. (2015). Myofibrillar instability exacerbated by acute exercise in filaminopathy. Human Molecular Genetics. 24(25). 7207–7220. 45 indexed citations
8.
Dekomien, Gabriele, Kristl G. Claeys, Maja von der Hagen, et al.. (2015). Two novel nebulin variants in an adult patient with congenital nemaline myopathy. Neuromuscular Disorders. 25(5). 392–396. 3 indexed citations
9.
Tasca, Giorgio, Mauro Monforte, Chiara De Fino, et al.. (2015). Magnetic resonance imaging pattern recognition in sporadic inclusion‐body myositis. Muscle & Nerve. 52(6). 956–962. 87 indexed citations
10.
Kley, Rudolf A., et al.. (2014). ATOH8: a novel marker in human muscle fiber regeneration. Histochemistry and Cell Biology. 143(5). 443–452. 20 indexed citations
11.
Sauer, Florian, Prisca Boisguérin, Zacharias Orfanos, et al.. (2013). Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling. Molecular Biology of the Cell. 24(20). 3215–3226. 32 indexed citations
12.
Nilsson, Mats I., Dhuha Al‐Sajee, Mark A. Tarnopolsky, et al.. (2013). Xin Is a Marker of Skeletal Muscle Damage Severity in Myopathies. American Journal Of Pathology. 183(6). 1703–1709. 29 indexed citations
13.
Kley, Rudolf A., Piraye Oflazer, Zagaa Odgerel, et al.. (2012). Pathophysiology of protein aggregation and extended phenotyping in filaminopathy. Brain. 135(9). 2642–2660. 61 indexed citations
14.
Fürst, Dieter O., Lev G. Goldfarb, Rudolf A. Kley, et al.. (2012). Filamin C-related myopathies: pathology and mechanisms. Acta Neuropathologica. 125(1). 33–46. 89 indexed citations
15.
Kley, Rudolf A., A. Maerkens, Verena Theis, et al.. (2012). A Combined Laser Microdissection and Mass Spectrometry Approach Reveals New Disease Relevant Proteins Accumulating in Aggregates of Filaminopathy Patients. Molecular & Cellular Proteomics. 12(1). 215–227. 66 indexed citations
16.
Kley, Rudolf A., Peter F. M. van der Ven, Montse Olivé, et al.. (2012). Impairment of protein degradation in myofibrillar myopathy caused by FLNC/filamin C mutations. Autophagy. 9(3). 422–423. 27 indexed citations
17.
Schwenkreis, Peter, Michael Voigt, Monika Hasenbring, et al.. (2011). Central mechanisms during fatiguing muscle exercise in muscular dystrophy and fibromyalgia syndrome: A study with transcranial magnetic stimulation. Muscle & Nerve. 43(4). 479–484. 23 indexed citations
18.
Kley, Rudolf A., et al.. (2008). Creatine treatment in muscle disorders: a meta-analysis of randomised controlled trials. Journal of Neurology Neurosurgery & Psychiatry. 79(4). 366–367. 18 indexed citations
19.
Löwe, Thomas, Rudolf A. Kley, Peter F. M. van der Ven, et al.. (2007). The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathy. Human Molecular Genetics. 16(11). 1351–1358. 35 indexed citations
20.
Rommel, O., Rudolf A. Kley, Gabriele Dekomien, et al.. (2006). Muscle pain in myophosphorylase deficiency (McArdle’s disease): The role of gender, genotype, and pain-related coping. Pain. 124(3). 295–304. 23 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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