Gerhard Meng

1.4k total citations
17 papers, 300 citations indexed

About

Gerhard Meng is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Gerhard Meng has authored 17 papers receiving a total of 300 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 6 papers in Genetics. Recurrent topics in Gerhard Meng's work include Muscle Physiology and Disorders (15 papers), Cardiomyopathy and Myosin Studies (8 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Gerhard Meng is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Cardiomyopathy and Myosin Studies (8 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Gerhard Meng collaborates with scholars based in Germany, United States and Austria. Gerhard Meng's co-authors include T. Grimm, Wolfram Kreß, B. Müller, T. Bettecken, Sabina Liechti‐Gallati, C R Müller, Clemens R. Müller, C. R. Müller, Michael Kottlors and Franz X. Glocker and has published in prestigious journals such as Genomics, Journal of Medical Genetics and Muscle & Nerve.

In The Last Decade

Gerhard Meng

15 papers receiving 287 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gerhard Meng Germany 10 245 98 76 70 63 17 300
Royston Ong Australia 6 229 0.9× 127 1.3× 82 1.1× 103 1.5× 55 0.9× 10 330
R. Skinner United Kingdom 11 245 1.0× 68 0.7× 55 0.7× 94 1.3× 77 1.2× 18 335
John F. Harper United States 7 255 1.0× 72 0.7× 94 1.2× 64 0.9× 50 0.8× 11 332
T O'Brien United Kingdom 8 382 1.6× 48 0.5× 147 1.9× 73 1.0× 115 1.8× 11 483
Morena Cadaldini Italy 8 221 0.9× 87 0.9× 75 1.0× 29 0.4× 77 1.2× 11 306
Meharji Arumilli Finland 12 214 0.9× 50 0.5× 127 1.7× 40 0.6× 37 0.6× 24 332
Xavière Lornage France 10 186 0.8× 105 1.1× 43 0.6× 40 0.6× 54 0.9× 19 243
Hülya Gündeşli Türkiye 7 343 1.4× 76 0.8× 38 0.5× 55 0.8× 75 1.2× 12 417
Tomoko Chiyo Japan 10 263 1.1× 38 0.4× 72 0.9× 47 0.7× 42 0.7× 15 347
Milena Cau Italy 10 313 1.3× 256 2.6× 52 0.7× 122 1.7× 45 0.7× 19 533

Countries citing papers authored by Gerhard Meng

Since Specialization
Citations

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

Fields of papers citing papers by Gerhard Meng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gerhard Meng

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

All Works

17 of 17 papers shown
1.
Rudnik‐Schöneborn, Sabine, et al.. (2019). Early onset facioscapulohumeral muscular dystrophy – Long-term follow-up of a patient with total facial diplegia. Neuromuscular Disorders. 29(12). 973–976. 2 indexed citations
2.
Ceccon, Garry, Helmar C. Lehmann, Eva Neuen-Jacob, et al.. (2017). „Therapierefraktäre Polymyositis“ – stimmt die Diagnose?. Zeitschrift für Rheumatologie. 76(7). 640–643. 3 indexed citations
3.
Rost, Simone, et al.. (2017). The Genetic Approach: Next-Generation Sequencing-Based Diagnosis of Congenital and Infantile Myopathies/Muscle Dystrophies. Neuropediatrics. 48(4). 242–246. 11 indexed citations
4.
Raskopf, E, Kija Shah‐Hosseini, Gerhard Meng, et al.. (2017). Die Versorgungsforschung-Datenbank PhytoVIS – eine retrospektive Befragung zur Anwendungserfahrung mit Phytopharmaka. Zeitschrift für Phytotherapie. 38. 1 indexed citations
5.
Grimm, T., Wolfram Kreß, Gerhard Meng, & Clemens R. Müller. (2012). Risk assessment and genetic counseling in families with Duchenne muscular dystrophy.. PubMed. 31(3). 179–83. 32 indexed citations
6.
Kottlors, Michael, Wolfram Kreß, Gerhard Meng, & Franz X. Glocker. (2010). Facioscapulohumeral muscular dystrophy presenting with isolated axial myopathy and bent spine syndrome. Muscle & Nerve. 42(2). 273–275. 26 indexed citations
7.
Grimm, T., et al.. (2009). Muskeldystrophien Duchenne und Becker. Medizinische Genetik. 21(3). 327–331. 1 indexed citations
8.
Jenne, Dieter E., Matthias Vorgerd, J. M. Schröder, et al.. (2005). Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3. Biological Chemistry. 386(1). 61–7. 10 indexed citations
9.
Finsterer, Josef, Claudia Stöllberger, & Gerhard Meng. (2004). Cardiac Involvement in Facioscapulohumeral Muscular Dystrophy. Cardiology. 103(2). 81–83. 11 indexed citations
10.
11.
Grimm, T., Gerhard Meng, Sabina Liechti‐Gallati, et al.. (1994). On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.. Journal of Medical Genetics. 31(3). 183–186. 84 indexed citations
12.
Müller, B., Gerhard Meng, Sabina Liechti‐Gallati, et al.. (1992). Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD). Human Genetics. 89(2). 204–206. 9 indexed citations
13.
14.
Dominguez-Steglich, M., Gerhard Meng, Thomas Bettecken, Clemens R. Müller, & Michael Schmid. (1990). The dystrophin gene is autosomally located on a microchromosome in chicken. Genomics. 8(3). 536–540. 14 indexed citations
15.
Hejtmancik, J. Fielding, G. Romeo, Mikael Lindlöf, et al.. (1989). A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus. Genomics. 4(1). 105–109. 17 indexed citations
16.
Grimm, T., et al.. (1989). Hot spot of recombination within DXS164 in the Duchenne muscular dystrophy gene.. PubMed. 45(3). 368–72. 31 indexed citations
17.
Meng, Gerhard. (1955). Zur Diagnose der Residuen von tuberkulösen Bronchial-Lymphknotenperforationen im Bronchialbaum. Respiration. 12(6). 446–467. 1 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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