Roswitha Krick

7.6k total citations
23 papers, 1.2k citations indexed

About

Roswitha Krick is a scholar working on Cell Biology, Molecular Biology and Epidemiology. According to data from OpenAlex, Roswitha Krick has authored 23 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cell Biology, 16 papers in Molecular Biology and 16 papers in Epidemiology. Recurrent topics in Roswitha Krick's work include Autophagy in Disease and Therapy (16 papers), Cellular transport and secretion (15 papers) and Endoplasmic Reticulum Stress and Disease (6 papers). Roswitha Krick is often cited by papers focused on Autophagy in Disease and Therapy (16 papers), Cellular transport and secretion (15 papers) and Endoplasmic Reticulum Stress and Disease (6 papers). Roswitha Krick collaborates with scholars based in Germany, United States and Russia. Roswitha Krick's co-authors include Michael Thumm, Petra Schlotterhose, Eeva‐Liisa Eskelinen, Evelyn Welter, Sebastian Bremer, Andreea Scacioc, Karin Kühnel, David S. Goldfarb, Jonathan I. Millen and Suresh Subramani and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Cell Biology.

In The Last Decade

Roswitha Krick

23 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roswitha Krick Germany 17 805 630 627 133 119 23 1.2k
Daniel Papinski Austria 11 781 1.0× 469 0.7× 523 0.8× 97 0.7× 157 1.3× 12 1.0k
Ester Rieter Netherlands 8 768 1.0× 458 0.7× 360 0.6× 136 1.0× 149 1.3× 8 988
Martina Schuschnig Austria 14 1.1k 1.4× 580 0.9× 649 1.0× 124 0.9× 200 1.7× 19 1.4k
Hiromi Kirisako Japan 15 1.2k 1.4× 746 1.2× 730 1.2× 129 1.0× 171 1.4× 20 1.5k
Chika Kondo‐Kakuta Japan 9 1.2k 1.5× 712 1.1× 640 1.0× 126 0.9× 226 1.9× 9 1.4k
Noriko Kondo‐Okamoto Japan 9 831 1.0× 283 0.4× 792 1.3× 114 0.9× 83 0.7× 9 1.2k
Shanta Nag United States 9 705 0.9× 380 0.6× 359 0.6× 114 0.9× 136 1.1× 10 913
Dorotea Fracchiolla Austria 11 782 1.0× 303 0.5× 537 0.9× 81 0.6× 116 1.0× 13 982
Hannah C. Dooley United Kingdom 9 1.2k 1.5× 592 0.9× 572 0.9× 200 1.5× 236 2.0× 13 1.5k
Christine Abert Austria 7 679 0.8× 347 0.6× 440 0.7× 68 0.5× 108 0.9× 9 837

Countries citing papers authored by Roswitha Krick

Since Specialization
Citations

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

Fields of papers citing papers by Roswitha Krick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roswitha Krick

This figure shows the co-authorship network connecting the top 25 collaborators of Roswitha Krick. A scholar is included among the top collaborators of Roswitha Krick 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 Roswitha Krick. Roswitha Krick 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.
Neumann, Piotr, Roswitha Krick, Narain Karedla, et al.. (2020). Atg21 organizes Atg8 lipidation at the contact of the vacuole with the phagophore. Autophagy. 17(6). 1458–1478. 26 indexed citations
2.
Schlotterhose, Petra, et al.. (2015). PI 3P binding by Atg21 organises Atg8 lipidation. The EMBO Journal. 34(7). 955–973. 76 indexed citations
3.
Scacioc, Andreea, et al.. (2015). Characterization of PROPPIN-Phosphoinositide Binding and Role of Loop 6CD in PROPPIN-Membrane Binding. Biophysical Journal. 108(9). 2223–2234. 34 indexed citations
4.
Scacioc, Andreea, Javier M. Hernández, Roswitha Krick, et al.. (2013). Qualitative and quantitative characterization of protein-phosphoinositide interactions with liposome-based methods. Autophagy. 9(5). 770–777. 23 indexed citations
5.
Welter, Evelyn, Robert Reinhold, Petra Schlotterhose, et al.. (2013). Uth1 is a mitochondrial inner membrane protein dispensable for post‐log‐phase and rapamycin‐induced mitophagy. FEBS Journal. 280(20). 4970–4982. 36 indexed citations
6.
Thumm, Michael, Andreea Scacioc, Milena Stephan, et al.. (2012). It takes two to tango. Autophagy. 9(1). 106–107. 11 indexed citations
7.
Krick, Roswitha, Andreea Scacioc, Milena Stephan, et al.. (2012). Structural and functional characterization of the two phosphoinositide binding sites of PROPPINs, a β-propeller protein family. Proceedings of the National Academy of Sciences. 109(30). E2042–9. 125 indexed citations
8.
Nair, Usha, Michael Thumm, Daniel J. Klionsky, & Roswitha Krick. (2011). GFP-Atg8 protease protection as a tool to monitor autophagosome biogenesis. Autophagy. 7(12). 1546–1550. 74 indexed citations
9.
Krick, Roswitha, Sebastian Bremer, Evelyn Welter, Eeva‐Liisa Eskelinen, & Michael Thumm. (2011). Cheating on ubiquitin with Atg8. Autophagy. 7(2). 250–251. 2 indexed citations
10.
Welter, Evelyn, Michael Thumm, & Roswitha Krick. (2010). Quantification of nonselective bulk autophagy inS. cerevisiaeusing Pgk1-GFP. Autophagy. 6(6). 794–797. 58 indexed citations
11.
Krick, Roswitha, Sebastian Bremer, Evelyn Welter, et al.. (2010). Cdc48/p97 and Shp1/p47 regulate autophagosome biogenesis in concert with ubiquitin-like Atg8. The Journal of Cell Biology. 190(6). 965–973. 105 indexed citations
12.
Millen, Jonathan I., et al.. (2009). Measuring piecemeal microautophagy of the nucleus inSaccharomyces cerevisiae. Autophagy. 5(1). 75–81. 37 indexed citations
13.
Krick, Roswitha, et al.. (2009). Turnover of organelles by autophagy in yeast. Current Opinion in Cell Biology. 21(4). 522–530. 92 indexed citations
14.
Krick, Roswitha, et al.. (2009). Piecemeal microautophagy of the nucleus: Genetic and morphological traits. Autophagy. 5(2). 270–272. 38 indexed citations
15.
Krick, Roswitha, et al.. (2008). Dissecting the localization and function of Atg18, Atg21 and Ygr223c. Autophagy. 4(7). 896–910. 78 indexed citations
16.
Krick, Roswitha, Sebastian Bremer, Petra Schlotterhose, et al.. (2008). Piecemeal Microautophagy of the Nucleus Requires the Core Macroautophagy Genes. Molecular Biology of the Cell. 19(10). 4492–4505. 147 indexed citations
17.
Krick, Roswitha, et al.. (2006). The relevance of the phosphatidylinositolphosphat‐binding motif FRRGT of Atg18 and Atg21 for the Cvt pathway and autophagy. FEBS Letters. 580(19). 4632–4638. 81 indexed citations
18.
Krick, Roswitha, et al.. (2006). CK2-dependent C-terminal phosphorylation at T300 directs the nuclear transport of TSPY protein. Biochemical and Biophysical Research Communications. 341(2). 343–350. 8 indexed citations
19.
Meiling-Wesse, Khuyen, Ulrike D. Epple, Roswitha Krick, et al.. (2005). Trs85 (Gsg1), a Component of the TRAPP Complexes, Is Required for the Organization of the Preautophagosomal Structure during Selective Autophagy via the Cvt Pathway. Journal of Biological Chemistry. 280(39). 33669–33678. 81 indexed citations
20.
Krick, Roswitha, Sibylle Jakubiczka, & Joachim Arnemann. (2003). Expression, alternative splicing and haplotype analysis of transcribed testis specific protein (TSPY) genes. Gene. 302(1-2). 11–19. 17 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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