Rolf Stucka

2.8k total citations
45 papers, 1.4k citations indexed

About

Rolf Stucka is a scholar working on Molecular Biology, Neurology and Cell Biology. According to data from OpenAlex, Rolf Stucka has authored 45 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 10 papers in Neurology and 8 papers in Cell Biology. Recurrent topics in Rolf Stucka's work include Fungal and yeast genetics research (13 papers), Myasthenia Gravis and Thymoma (10 papers) and RNA and protein synthesis mechanisms (10 papers). Rolf Stucka is often cited by papers focused on Fungal and yeast genetics research (13 papers), Myasthenia Gravis and Thymoma (10 papers) and RNA and protein synthesis mechanisms (10 papers). Rolf Stucka collaborates with scholars based in Germany, United Kingdom and Canada. Rolf Stucka's co-authors include Horst Feldmann, Hanns Lochmüller, Miguel Á. Blázquez, Angela Abicht, Joachim Hauber, Carlos Gancedo, Angela Huebner, M. Isabel González, Adolf Ellinger and Wolfgang Müller‐Felber and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Brain.

In The Last Decade

Rolf Stucka

45 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rolf Stucka Germany 24 1.1k 287 283 217 146 45 1.4k
Kenneth Robzyk Israel 11 1.4k 1.3× 199 0.7× 89 0.3× 124 0.6× 115 0.8× 12 1.7k
Mary Y. Hurwitz United States 17 1.1k 1.0× 194 0.7× 30 0.1× 116 0.5× 277 1.9× 36 1.6k
László Szilák Hungary 19 753 0.7× 361 1.3× 40 0.1× 125 0.6× 117 0.8× 41 1.3k
Lindsey N. Young United States 12 654 0.6× 349 1.2× 44 0.2× 143 0.7× 62 0.4× 16 1.3k
Dean Clift United Kingdom 17 1.1k 1.1× 481 1.7× 41 0.1× 165 0.8× 202 1.4× 21 1.7k
Katsumi Nogimori Japan 13 701 0.7× 198 0.7× 58 0.2× 60 0.3× 169 1.2× 22 1.3k
Heimo Riedel United States 22 1.2k 1.1× 182 0.6× 37 0.1× 68 0.3× 230 1.6× 55 1.8k
Qi Hao China 17 518 0.5× 124 0.4× 122 0.4× 774 3.6× 54 0.4× 37 1.4k
Rui Jia China 19 609 0.6× 471 1.6× 24 0.1× 71 0.3× 76 0.5× 35 1.5k
Jacob M. Wozniak United States 16 982 0.9× 203 0.7× 89 0.3× 27 0.1× 32 0.2× 33 1.3k

Countries citing papers authored by Rolf Stucka

Since Specialization
Citations

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

Fields of papers citing papers by Rolf Stucka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rolf Stucka

This figure shows the co-authorship network connecting the top 25 collaborators of Rolf Stucka. A scholar is included among the top collaborators of Rolf Stucka 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 Rolf Stucka. Rolf Stucka 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.
Roos, Andreas, Martin Häusler, Laxmikanth Kollipara, et al.. (2024). HNRNPA1 de novo Variant Associated with Early Childhood Onset, Rapidly Progressive Generalized Myopathy. Journal of Neuromuscular Diseases. 11(5). 1131–1137. 2 indexed citations
2.
Schäfer, Carola, et al.. (2016). Targeted HIV-1 Latency Reversal Using CRISPR/Cas9-Derived Transcriptional Activator Systems. PLoS ONE. 11(6). e0158294–e0158294. 65 indexed citations
3.
Hauber, Ilona, Jan Chemnitz, Janet Chusainow, et al.. (2013). Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice. PLoS Pathogens. 9(9). e1003587–e1003587. 47 indexed citations
4.
Gallenmüller, Constanze, Wolfgang Müller‐Felber, Marina Dusl, et al.. (2013). Salbutamol-responsive limb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK. Neuromuscular Disorders. 24(1). 31–35. 47 indexed citations
5.
Larochelle, Nancy, Rolf Stucka, Norman Rieger, et al.. (2010). Genomic integration of adenoviral gene transfer vectors following transduction of fertilized mouse oocytes. Transgenic Research. 20(1). 123–135. 3 indexed citations
6.
Seeger, Jürgen, Bertold Schrank, Angela Pyle, et al.. (2010). Clinical and neuropathological findings in patients with TACO1 mutations. Neuromuscular Disorders. 20(11). 720–724. 26 indexed citations
7.
Müller, Juliane, Angela Abicht, H.‐J. Christen, et al.. (2004). A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome. Neuromuscular Disorders. 14(11). 744–749. 19 indexed citations
8.
Kiefer, Reinhard, Rolf Stucka, Christoph König, et al.. (2004). Synaptic Congenital Myasthenic Syndrome in Three Patients due to a Novel Missense Mutation (T441A) of theCOLQGene. Neuropediatrics. 35(3). 183–189. 20 indexed citations
9.
Larochelle, Nancy, Christian Thirion, Rolf Stucka, et al.. (2003). Expression of dystrophin driven by the 1.35-kb MCK promoter ameliorates muscular dystrophy in fast, but not in slow muscles of transgenic mdx mice. Molecular Therapy. 8(1). 80–89. 38 indexed citations
10.
Schmidt, Carolin, Angela Abicht, K Krampfl, et al.. (2003). Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferase. Neuromuscular Disorders. 13(3). 245–251. 41 indexed citations
11.
Horváth, Rita, Hanns Lochmüller, Rolf Stucka, et al.. (2000). Characterization of Human SCO1 and COX17 Genes in Mitochondrial Cytochrome-c-Oxidase Deficiency. Biochemical and Biophysical Research Communications. 276(2). 530–533. 26 indexed citations
12.
Abicht, Angela, Rolf Stucka, Veronika Karcagi, et al.. (1999). A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin. Neurology. 53(7). 1564–1564. 77 indexed citations
13.
Briza, Peter, Adolf Ellinger, Tillman Schuster, et al.. (1992). DIT101 (CSD2, CAL1), a cell cycle‐regulated yeast gene required for synthesis of chitin in cell walls and chitosan in spore walls. Yeast. 8(12). 1089–1099. 115 indexed citations
14.
González, M. Isabel, et al.. (1992). Molecular cloning of CIF1, a yeast gene necessary for growth on glucose. Yeast. 8(3). 183–192. 91 indexed citations
15.
Stucka, Rolf, et al.. (1991). New genes for tRNAPhe, tRNALeu, and tRNAThrfromSaccharomyces cerevisiae. Nucleic Acids Research. 19(1). 179–179. 8 indexed citations
16.
Stucka, Rolf & Horst Feldmann. (1990). An element of symmetry in yeast TATA‐box binding protein transcription factor IID. FEBS Letters. 261(2). 223–225. 12 indexed citations
17.
Hauber, Joachim, et al.. (1988). Analysis of yeast chromosomal regions carrying members of the glutamate tRNA gene family: various transposable elements are associated with them. Nucleic Acids Research. 16(22). 10623–10634. 32 indexed citations
18.
Stucka, Rolf & Horst Feldmann. (1988). Structure of aSaccharomyces cerevisiaegene encoding minor (AGY)tRNASer. Nucleic Acids Research. 16(8). 3583–3583. 19 indexed citations
19.
Stucka, Rolf, Joachim Hauber, & Horst Feldmann. (1987). One member of the tRNA(Glu) gene family in yeast codes for a minor GAGtRNA(Glu) species and is associated with several short transposable elements. Current Genetics. 12(5). 323–328. 8 indexed citations
20.
Stucka, Rolf, Joachim Hauber, & Horst Feldmann. (1986). Conserved and non-conserved features among the yeast T-y elements. Current Genetics. 11(3). 193–200. 14 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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