Marcus M. Nalaskowski

785 total citations
25 papers, 634 citations indexed

About

Marcus M. Nalaskowski is a scholar working on Molecular Biology, Cell Biology and Biophysics. According to data from OpenAlex, Marcus M. Nalaskowski has authored 25 papers receiving a total of 634 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 9 papers in Cell Biology and 3 papers in Biophysics. Recurrent topics in Marcus M. Nalaskowski's work include Nuclear Structure and Function (9 papers), RNA Research and Splicing (5 papers) and PI3K/AKT/mTOR signaling in cancer (4 papers). Marcus M. Nalaskowski is often cited by papers focused on Nuclear Structure and Function (9 papers), RNA Research and Splicing (5 papers) and PI3K/AKT/mTOR signaling in cancer (4 papers). Marcus M. Nalaskowski collaborates with scholars based in Germany and Norway. Marcus M. Nalaskowski's co-authors include Georg W. Mayr, Wolfgang Hampe, Werner Fanick, Christina Deschermeier, Sabine Windhorst, Maria A. Brehm, Manfred Jücker, Hongying Lin, Malte Stockebrand and Leticia Oliveira‐Ferrer and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Analytical Biochemistry.

In The Last Decade

Marcus M. Nalaskowski

24 papers receiving 628 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marcus M. Nalaskowski Germany 14 495 170 69 52 50 25 634
Chun So Hong Kong 12 473 1.0× 171 1.0× 40 0.6× 64 1.2× 95 1.9× 15 704
Thomas Küntziger Norway 18 710 1.4× 191 1.1× 35 0.5× 59 1.1× 72 1.4× 27 846
Nathalie Rocques France 9 489 1.0× 129 0.8× 135 2.0× 64 1.2× 73 1.5× 14 659
Bianca V. Gapp Austria 7 493 1.0× 52 0.3× 47 0.7× 56 1.1× 81 1.6× 9 619
Stefan Weitzer Austria 13 991 2.0× 126 0.7× 72 1.0× 52 1.0× 38 0.8× 15 1.1k
Meritxell Orpinell Switzerland 12 584 1.2× 230 1.4× 66 1.0× 21 0.4× 104 2.1× 12 746
Andrew C. Hedman United States 16 670 1.4× 438 2.6× 35 0.5× 87 1.7× 130 2.6× 24 948
Ingmar B. Schäfer Germany 15 697 1.4× 273 1.6× 53 0.8× 33 0.6× 23 0.5× 19 870
Jennifer A. Benanti United States 15 582 1.2× 182 1.1× 66 1.0× 72 1.4× 187 3.7× 24 777

Countries citing papers authored by Marcus M. Nalaskowski

Since Specialization
Citations

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

Fields of papers citing papers by Marcus M. Nalaskowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marcus M. Nalaskowski. 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 Marcus M. Nalaskowski. The network helps show where Marcus M. Nalaskowski may publish in the future.

Co-authorship network of co-authors of Marcus M. Nalaskowski

This figure shows the co-authorship network connecting the top 25 collaborators of Marcus M. Nalaskowski. A scholar is included among the top collaborators of Marcus M. Nalaskowski 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 Marcus M. Nalaskowski. Marcus M. Nalaskowski 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.
Horn, Stefan, Malte Kriegs, Michael P. Horn, et al.. (2024). Ikaros sets the threshold for negative B-cell selection by regulation of the signaling strength of the AKT pathway. Cell Communication and Signaling. 22(1). 360–360. 2 indexed citations
2.
Arnold, Julia T., Christoph Krisp, Hartmut Schlüter, et al.. (2020). Tubulin Tyrosine Ligase Like 4 (TTLL4) overexpression in breast cancer cells is associated with brain metastasis and alters exosome biogenesis. Journal of Experimental & Clinical Cancer Research. 39(1). 205–205. 37 indexed citations
3.
Kops, Christina de Bruyn, et al.. (2019). Analysis of the FLVR motif of SHIP1 and its importance for the protein stability of SH2 containing signaling proteins. Cellular Signalling. 63. 109380–109380. 9 indexed citations
4.
Nalaskowski, Marcus M., et al.. (2019). A toolkit for expression of Strep-tagged enhanced green fluorescent protein concatemers in mammalian cells. Analytical Biochemistry. 586. 113430–113430.
5.
Wellbrock, Jasmin, et al.. (2018). Effect of the actin- and calcium-regulating activities of ITPKB on the metastatic potential of lung cancer cells. Biochemical Journal. 475(12). 2057–2071. 7 indexed citations
6.
Nalaskowski, Marcus M., et al.. (2018). Nuclear accumulation of SHIP1 mutants derived from AML patients leads to increased proliferation of leukemic cells. Cellular Signalling. 49. 87–94. 8 indexed citations
7.
Horn, Stefan, Matthias Schaks, Marcus M. Nalaskowski, et al.. (2017). SHIP1, but not an AML-derived SHIP1 mutant, suppresses myeloid leukemia growth in a xenotransplantation mouse model. Gene Therapy. 24(11). 749–753. 16 indexed citations
8.
Böhm, Jennifer, et al.. (2017). A set of enhanced green fluorescent protein concatemers for quantitative determination of nuclear localization signal strength. Analytical Biochemistry. 533. 48–55. 5 indexed citations
9.
Brehm, Maria A., et al.. (2014). Efficacious inhibition of Importin α/β-mediated nuclear import of human inositol phosphate multikinase. Biochimie. 102. 117–123. 7 indexed citations
10.
Schneider, Katrin, Christiane Fuchs, Akos Dobay, et al.. (2013). Dissection of cell cycle–dependent dynamics of Dnmt1 by FRAP and diffusion-coupled modeling. Nucleic Acids Research. 41(9). 4860–4876. 43 indexed citations
11.
Nalaskowski, Marcus M., et al.. (2012). A toolkit for graded expression of green fluorescent protein fusion proteins in mammalian cells. Analytical Biochemistry. 428(1). 24–27. 13 indexed citations
12.
Nalaskowski, Marcus M., et al.. (2012). A Plasmodium multi-domain protein possesses multiple inositol phosphate kinase activities. Molecular and Biochemical Parasitology. 186(2). 134–138. 3 indexed citations
13.
Nalaskowski, Marcus M., et al.. (2011). The inositol 5-phosphatase SHIP1 is a nucleo-cytoplasmic shuttling protein and enzymatically active in cell nuclei. Cellular Signalling. 24(3). 621–628. 19 indexed citations
14.
Nalaskowski, Marcus M., et al.. (2011). A novel Entamoeba histolytica inositol phosphate kinase catalyzes the formation of 5PP-Ins(1,2,3,4,6)P5. Molecular and Biochemical Parasitology. 181(1). 49–52. 4 indexed citations
15.
Nalaskowski, Marcus M., Ralf Fliegert, Maria A. Brehm, et al.. (2010). Human Inositol 1,4,5-Trisphosphate 3-Kinase Isoform B (IP3KB) Is a Nucleocytoplasmic Shuttling Protein Specifically Enriched at Cortical Actin Filaments and at Invaginations of the Nuclear Envelope. Journal of Biological Chemistry. 286(6). 4500–4510. 28 indexed citations
16.
Windhorst, Sabine, Hongying Lin, Christian Elling, et al.. (2008). Ins(1,4,5)P3 3-kinase-A overexpression induces cytoskeletal reorganization via a kinase-independent mechanism. Biochemical Journal. 414(3). 407–417. 28 indexed citations
17.
Nalaskowski, Marcus M., et al.. (2007). Nuclear localization of enhanced green fluorescent protein homomultimers. Analytical Biochemistry. 368(1). 95–99. 159 indexed citations
18.
Nalaskowski, Marcus M., Sabine Windhorst, Malte Stockebrand, & Georg W. Mayr. (2006). Subcellular localisation of human inositol 1,4,5-trisphosphate 3-kinase C: species-specific use of alternative export sites for nucleo-cytoplasmic shuttling indicates divergent roles of the catalytic and N-terminal domains. Biological Chemistry. 387(5). 583–593. 11 indexed citations
19.
Nalaskowski, Marcus M. & Georg W. Mayr. (2004). The Families of Kinases Removing the Ca2+ Releasing Second Messenger Ins(1,4,5)P3. Current Molecular Medicine. 4(3). 277–290. 23 indexed citations
20.
Nalaskowski, Marcus M., Uwe Bertsch, Werner Fanick, et al.. (2003). Rat Inositol 1,4,5-Trisphosphate 3-Kinase C Is Enzymatically Specialized for Basal Cellular Inositol Trisphosphate Phosphorylation and Shuttles Actively between Nucleus and Cytoplasm. Journal of Biological Chemistry. 278(22). 19765–19776. 31 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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