Alexander Gasch

2.8k total citations
39 papers, 2.3k citations indexed

About

Alexander Gasch is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Alexander Gasch has authored 39 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 10 papers in Cardiology and Cardiovascular Medicine and 7 papers in Cell Biology. Recurrent topics in Alexander Gasch's work include Muscle Physiology and Disorders (13 papers), Cardiomyopathy and Myosin Studies (7 papers) and RNA modifications and cancer (5 papers). Alexander Gasch is often cited by papers focused on Muscle Physiology and Disorders (13 papers), Cardiomyopathy and Myosin Studies (7 papers) and RNA modifications and cancer (5 papers). Alexander Gasch collaborates with scholars based in Germany, United States and Spain. Alexander Gasch's co-authors include Nam‐Hai Chua, Renate Renkawitz‐Pohl, Robert G. Roeder, Alexander Hoffmann, Masami Horikoshi, Siegfried Labeit, Taku Takahashi, N. K. Nishizawa, Uwe Hinz and Michael Sattler and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Alexander Gasch

39 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexander Gasch Germany 25 1.9k 424 264 233 229 39 2.3k
Hiroshi Kanazawa Japan 26 1.3k 0.7× 198 0.5× 267 1.0× 180 0.8× 94 0.4× 100 2.2k
Elisabetta Mattei Italy 22 1.4k 0.7× 263 0.6× 106 0.4× 263 1.1× 60 0.3× 51 1.8k
Mônica Beltrame Italy 25 2.1k 1.1× 175 0.4× 188 0.7× 367 1.6× 137 0.6× 48 2.8k
Alex H. Hutagalung United States 12 1.4k 0.8× 121 0.3× 1.1k 4.0× 107 0.5× 205 0.9× 13 2.0k
Lori L. Wallrath United States 36 3.6k 1.9× 1.0k 2.5× 316 1.2× 515 2.2× 61 0.3× 70 4.0k
Masaya Yamamoto Japan 15 1.1k 0.6× 216 0.5× 676 2.6× 86 0.4× 71 0.3× 24 1.6k
Joh‐E Ikeda Japan 28 1.1k 0.6× 261 0.6× 260 1.0× 264 1.1× 41 0.2× 53 2.0k
Antje Gohla Germany 22 1.4k 0.8× 92 0.2× 515 2.0× 102 0.4× 101 0.4× 37 2.2k
Kazuko Iida Japan 20 994 0.5× 799 1.9× 558 2.1× 40 0.2× 110 0.5× 36 1.8k
Rika Suzuki Japan 18 1.6k 0.8× 141 0.3× 201 0.8× 696 3.0× 35 0.2× 57 2.3k

Countries citing papers authored by Alexander Gasch

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Gasch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Gasch

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Gasch. A scholar is included among the top collaborators of Alexander Gasch 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 Alexander Gasch. Alexander Gasch 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.
Bogomolovas, Julius, Jennifer R. Fleming, Barbara Franke, et al.. (2021). Titin kinase ubiquitination aligns autophagy receptors with mechanical signals in the sarcomere. EMBO Reports. 22(10). e48018–e48018. 31 indexed citations
2.
Gasch, Alexander, et al.. (2020). Skeletal Muscle Anti-Atrophic Effects of Leucine Involve Myostatin Inhibition. DNA and Cell Biology. 39(12). 2289–2299. 13 indexed citations
3.
Nguyen, Thanh Hung, T. Scott Bowen, Antje Augstein, et al.. (2020). Expression of MuRF1 or MuRF2 is essential for the induction of skeletal muscle atrophy and dysfunction in a murine pulmonary hypertension model. Skeletal Muscle. 10(1). 12–12. 26 indexed citations
4.
Gasch, Alexander, et al.. (2017). Actualización en la estratificación de riesgo del tromboembolismo pulmonar agudo sintomático. Revista Clínica Española. 217(6). 342–350. 3 indexed citations
5.
Bowen, T. Scott, Volker Adams, Sarah Werner, et al.. (2017). Small‐molecule inhibition of MuRF1 attenuates skeletal muscle atrophy and dysfunction in cardiac cachexia. Journal of Cachexia Sarcopenia and Muscle. 8(6). 939–953. 79 indexed citations
6.
Bogomolovas, Julius, et al.. (2016). Cardiac specific titin N2B exon is a novel sensitive serological marker for cardiac injury. International Journal of Cardiology. 212. 232–234. 11 indexed citations
7.
Rudolf, Rüdiger, Julius Bogomolovas, S. Strack, et al.. (2012). Regulation of nicotinic acetylcholine receptor turnover by MuRF1 connects muscle activity to endo/lysosomal and atrophy pathways. AGE. 35(5). 1663–1674. 55 indexed citations
8.
Chung, Charles S., Julius Bogomolovas, Alexander Gasch, et al.. (2011). Titin‐Actin Interaction: PEVK‐Actin‐Based Viscosity in a Large Animal. BioMed Research International. 2011(1). 310791–310791. 24 indexed citations
9.
Mackereth, Cameron D., Tobias Madl, Sophie Bonnal, et al.. (2011). Multi-domain conformational selection underlies pre-mRNA splicing regulation by U2AF. Nature. 475(7356). 408–411. 167 indexed citations
10.
Hata, Shoji, Christian Witt, Yasuko Ono, et al.. (2007). Muscle RING-Finger Protein-1 (MuRF1) as a Connector of Muscle Energy Metabolism and Protein Synthesis. Journal of Molecular Biology. 376(5). 1224–1236. 130 indexed citations
11.
Oddone, Anna, Esben Lorentzen, J. Basquin, et al.. (2006). Structural and biochemical characterization of the yeast exosome component Rrp40. EMBO Reports. 8(1). 63–69. 46 indexed citations
12.
Gasch, Alexander, et al.. (2001). Tumor de células de Leydig, ginecomastia y trombosis de vena cava inferior. Anales de Medicina Interna. 18(8). 432–4. 1 indexed citations
13.
Gasch, Alexander, et al.. (1999). Rapid detection of Listeria monocytogenes by PCR-ELISA. Letters in Applied Microbiology. 29(6). 416–420. 20 indexed citations
14.
Takahashi, Taku, et al.. (1998). Identification by PCR of receptor-like protein kinases from Arabidopsis flowers. Plant Molecular Biology. 37(4). 587–596. 35 indexed citations
15.
Hong, Yan, Makoto Takano, Chunming Liu, et al.. (1996). Expression of three members of the calcium-dependent protein kinase gene family in Arabidopsis thaliana. Plant Molecular Biology. 30(6). 1259–1275. 70 indexed citations
16.
Gasch, Alexander, et al.. (1995). Mapping of a human rRNA gene in the YAC contig surrounding the SMA candidate gene. Human Genetics. 96(3). 335–8. 2 indexed citations
17.
Kern, Rainer, Alexander Gasch, Mária Deák, S. A. Kay, & Nam‐Hai Chua. (1993). phyB of Tobacco, a New Member of the Phytochrome Family. PLANT PHYSIOLOGY. 102(4). 1363–1364. 17 indexed citations
18.
Nikolov, Dimitar B., Shuhong Hu, Judith C. Lin, et al.. (1992). Crystal structure of TFIID TATA-box binding protein. Nature. 360(6399). 40–46. 352 indexed citations
19.
Gasch, Alexander, et al.. (1988). The expression of β1 and β3 tubulin genes of Drosophila melanogaster is spatially regulated during embryogenesis. Molecular and General Genetics MGG. 211(1). 8–16. 44 indexed citations
20.
Faust, Daniela M., Renate Renkawitz‐Pohl, Alexander Gasch, et al.. (1986). Cloning and identification of the gene coding for the 140-kd subunit of Drosophila RNA polymerase II. The EMBO Journal. 5(4). 741–746. 13 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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