Roland Dosch

3.2k total citations · 1 hit paper
33 papers, 2.5k citations indexed

About

Roland Dosch is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Roland Dosch has authored 33 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 10 papers in Cell Biology and 9 papers in Genetics. Recurrent topics in Roland Dosch's work include Zebrafish Biomedical Research Applications (10 papers), Developmental Biology and Gene Regulation (10 papers) and Animal Genetics and Reproduction (6 papers). Roland Dosch is often cited by papers focused on Zebrafish Biomedical Research Applications (10 papers), Developmental Biology and Gene Regulation (10 papers) and Animal Genetics and Reproduction (6 papers). Roland Dosch collaborates with scholars based in Germany, United States and Switzerland. Roland Dosch's co-authors include Christof Niehrs, Hajo Delius, Volker Gawantka, Mary C. Mullins, Daria Onichtchouk, Daniel S. Wagner, Claudia Blumenstock, Joan Massagué, Ye-Guang Chen and Keith A. Mintzer and has published in prestigious journals such as Nature, Science and The EMBO Journal.

In The Last Decade

Roland Dosch

31 papers receiving 2.5k citations

Hit Papers

Silencing of TGF-β signalling by the pseudoreceptor BAMBI 1999 2026 2008 2017 1999 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roland Dosch Germany 19 2.0k 461 440 164 151 33 2.5k
Daria Onichtchouk Germany 20 2.3k 1.2× 302 0.7× 388 0.9× 105 0.6× 124 0.8× 32 2.7k
Danica Živković Netherlands 19 1.3k 0.7× 336 0.7× 472 1.1× 64 0.4× 125 0.8× 36 1.8k
Enrico Moro Italy 33 2.2k 1.1× 565 1.2× 1.4k 3.3× 188 1.1× 135 0.9× 71 3.3k
Andreas Jenny United States 31 2.9k 1.5× 1.1k 2.3× 771 1.8× 101 0.6× 259 1.7× 56 3.5k
Leslie Dale United Kingdom 19 1.3k 0.7× 205 0.4× 219 0.5× 250 1.5× 128 0.8× 32 1.7k
Chang‐Yeol Yeo South Korea 26 2.2k 1.1× 302 0.7× 322 0.7× 72 0.4× 72 0.5× 48 2.7k
Esmond J. Sanders Canada 26 936 0.5× 229 0.5× 346 0.8× 66 0.4× 136 0.9× 59 1.8k
Aleyde Van Eynde Belgium 27 3.3k 1.7× 511 1.1× 397 0.9× 107 0.7× 79 0.5× 52 3.9k
André W. Brändli Switzerland 30 1.8k 0.9× 408 0.9× 422 1.0× 87 0.5× 362 2.4× 44 2.4k
Naohiro Hashimoto Japan 23 1.5k 0.8× 377 0.8× 278 0.6× 637 3.9× 145 1.0× 55 2.3k

Countries citing papers authored by Roland Dosch

Since Specialization
Citations

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

Fields of papers citing papers by Roland Dosch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roland Dosch

This figure shows the co-authorship network connecting the top 25 collaborators of Roland Dosch. A scholar is included among the top collaborators of Roland Dosch 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 Roland Dosch. Roland Dosch 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.
Möbius, Wiebke, Ralf Heinrich, Torben Ruhwedel, et al.. (2025). Patient-specific mutation of contact site protein Tomm70 causes neurodegeneration. Disease Models & Mechanisms. 18(4).
2.
Ruhwedel, Torben, Patricia Scholz, Till Ischebeck, et al.. (2024). Axon demyelination and degeneration in a zebrafish spastizin model of hereditary spastic paraplegia. Open Biology. 14(11). 240100–240100. 1 indexed citations
3.
Klein, Sabine, Roland Dosch, Sven Reiche, & Wilfried A. Kues. (2024). Dynamic maternal synthesis and segregation of the germ plasm organizer, Bucky ball, in chicken oocytes and follicles. Scientific Reports. 14(1). 27753–27753. 1 indexed citations
5.
Göpfert, Martin C., et al.. (2022). A Markerless Pose Estimator Applicable to Limbless Animals. Frontiers in Behavioral Neuroscience. 16. 819146–819146. 5 indexed citations
6.
Klein, Sabine, et al.. (2022). Identification of chicken LOC420478 as Bucky ball equivalent and potential germ plasm organizer in birds. Scientific Reports. 12(1). 16858–16858. 1 indexed citations
7.
Schnabel, Viktor, Frauke Alves, Damian J. Ralser, et al.. (2022). Evolutionary distinct roles of γ-secretase subunit nicastrin in zebrafish and humans. Journal of Dermatological Science. 105(2). 80–87. 2 indexed citations
8.
Gautier‐Stein, Amandine, et al.. (2014). Souffle/Spastizin Controls Secretory Vesicle Maturation during Zebrafish Oogenesis. PLoS Genetics. 10(6). e1004449–e1004449. 21 indexed citations
9.
Bontems, Franck, et al.. (2011). Efficient mutation identification in zebrafish by microarray capturing and next generation sequencing. Biochemical and Biophysical Research Communications. 405(3). 373–376. 5 indexed citations
10.
Brennan, Caroline H., Roland Dosch, Anna-Pavlina G. Haramis, et al.. (2010). Report of the European Zebrafish Principal Investigator Meeting in Padua, Italy, March 18–22, 2010. Zebrafish. 7(3). 305–310. 2 indexed citations
11.
Holloway, Beth, Sol Gómez de la Torre Canny, Ying Ye, et al.. (2009). A Novel Role for MAPKAPK2 in Morphogenesis during Zebrafish Development. PLoS Genetics. 5(3). e1000413–e1000413. 44 indexed citations
12.
Bontems, Franck, Amandine Gautier‐Stein, Florence L. Marlow, et al.. (2009). Bucky Ball Organizes Germ Plasm Assembly in Zebrafish. Current Biology. 19(5). 414–422. 178 indexed citations
13.
Hogg, Ron C., et al.. (2007). An automated system for intracellular and intranuclear injection. Journal of Neuroscience Methods. 169(1). 65–75. 51 indexed citations
14.
Panzer, Jessica A., Sarah Gibbs, Roland Dosch, et al.. (2005). Neuromuscular synaptogenesis in wild-type and mutant zebrafish. Developmental Biology. 285(2). 340–357. 82 indexed citations
15.
Schneider, Valérie, Evelyn Santana, Roland Dosch, et al.. (2005). Genetic screens for genes controlling motor nerve–muscle development and interactions. Developmental Biology. 280(1). 162–176. 40 indexed citations
16.
Wagner, Daniel S., Roland Dosch, Keith A. Mintzer, Anthony P. Wiemelt, & Mary C. Mullins. (2004). Maternal Control of Development at the Midblastula Transition and beyond. Developmental Cell. 6(6). 781–790. 115 indexed citations
17.
Dosch, Roland, Daniel S. Wagner, Keith A. Mintzer, et al.. (2004). Maternal Control of Vertebrate Development before the Midblastula Transition. Developmental Cell. 6(6). 771–780. 192 indexed citations
18.
Dosch, Roland & Christof Niehrs. (2000). Requirement for anti-dorsalizing morphogenetic protein in organizer patterning. Mechanisms of Development. 90(2). 195–203. 55 indexed citations
19.
Niehrs, Christof, Roland Dosch, & Daria Onichtchouk. (2000). Embryonic Patterning of Xenopus Mesoderm by Bmp-4. PubMed. 165–190. 5 indexed citations
20.
Onichtchouk, Daria, Ye-Guang Chen, Roland Dosch, et al.. (1999). Silencing of TGF-β signalling by the pseudoreceptor BAMBI. Nature. 401(6752). 480–485. 584 indexed citations breakdown →

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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