Annette Draeger

4.8k total citations
87 papers, 4.0k citations indexed

About

Annette Draeger is a scholar working on Molecular Biology, Cell Biology and Physiology. According to data from OpenAlex, Annette Draeger has authored 87 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 22 papers in Cell Biology and 18 papers in Physiology. Recurrent topics in Annette Draeger's work include Lipid Membrane Structure and Behavior (21 papers), S100 Proteins and Annexins (17 papers) and Erythrocyte Function and Pathophysiology (12 papers). Annette Draeger is often cited by papers focused on Lipid Membrane Structure and Behavior (21 papers), S100 Proteins and Annexins (17 papers) and Erythrocyte Function and Pathophysiology (12 papers). Annette Draeger collaborates with scholars based in Switzerland, Germany and Austria. Annette Draeger's co-authors include Eduard B. Babiychuk, Katia Monastyrskaya, Fiona C. Burkhard, Susan Wray, Heidi Wolfmeier, J. Victor Small, Roman Schoenauer, Alan G. Weeds, Robin B. Fitzsimons and Hans Hoppeler and has published in prestigious journals such as Journal of Biological Chemistry, Circulation and The Journal of Cell Biology.

In The Last Decade

Annette Draeger

87 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Annette Draeger Switzerland 37 2.6k 737 494 442 435 87 4.0k
Uffe Birk Jensen Denmark 34 2.5k 1.0× 606 0.8× 382 0.8× 435 1.0× 356 0.8× 104 4.5k
Lorenza González‐Mariscal Mexico 41 3.6k 1.4× 1.0k 1.4× 619 1.3× 414 0.9× 342 0.8× 100 6.5k
George Posthuma Netherlands 32 2.0k 0.8× 509 0.7× 348 0.7× 446 1.0× 321 0.7× 64 3.7k
Fernando López‐Casillas Mexico 35 3.3k 1.3× 681 0.9× 483 1.0× 339 0.8× 354 0.8× 82 4.8k
Eduard B. Babiychuk Switzerland 29 1.9k 0.7× 501 0.7× 312 0.6× 313 0.7× 258 0.6× 64 2.8k
Kate J. Heesom United Kingdom 39 2.9k 1.1× 1.2k 1.7× 422 0.9× 681 1.5× 390 0.9× 156 5.4k
Tsutomu Tsuji Japan 37 2.4k 0.9× 691 0.9× 336 0.7× 536 1.2× 386 0.9× 168 4.9k
Otmar Huber Germany 47 5.4k 2.1× 1.4k 1.9× 520 1.1× 491 1.1× 511 1.2× 109 8.0k
Patrik Maurer Germany 42 2.0k 0.8× 524 0.7× 438 0.9× 343 0.8× 269 0.6× 60 4.7k
Simon Fredriksson Sweden 25 3.4k 1.3× 343 0.5× 489 1.0× 327 0.7× 294 0.7× 34 5.3k

Countries citing papers authored by Annette Draeger

Since Specialization
Citations

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

Fields of papers citing papers by Annette Draeger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annette Draeger

This figure shows the co-authorship network connecting the top 25 collaborators of Annette Draeger. A scholar is included among the top collaborators of Annette Draeger 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 Annette Draeger. Annette Draeger 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.
2.
Gheinani, Ali Hashemi, Ulrich Baumgartner, Erik Vassella, et al.. (2018). Improved isolation strategies to increase the yield and purity of human urinary exosomes for biomarker discovery. Scientific Reports. 8(1). 3945–3945. 151 indexed citations
3.
Beckmann, Nadine, Stephanie Kadow, Fabian Schumacher, et al.. (2018). Pathological manifestations of Farber disease in a new mouse model. Biological Chemistry. 399(10). 1183–1202. 17 indexed citations
4.
Köffel, René, Heidi Wolfmeier, Roman Schoenauer, et al.. (2018). Host-Derived Microvesicles Carrying Bacterial Pore-Forming Toxins Deliver Signals to Macrophages: A Novel Mechanism of Shaping Immune Responses. Frontiers in Immunology. 9. 1688–1688. 19 indexed citations
5.
Drücker, Patrick, Andreas Rühling, David Grill, et al.. (2016). Imidazolium Salts Mimicking the Structure of Natural Lipids Exploit Remarkable Properties Forming Lamellar Phases and Giant Vesicles. Langmuir. 33(6). 1333–1342. 56 indexed citations
6.
Babiychuk, Eduard B. & Annette Draeger. (2015). Defying death: Cellular survival strategies following plasmalemmal injury by bacterial toxins. Seminars in Cell and Developmental Biology. 45. 39–47. 29 indexed citations
7.
Henry, Brian, Daniel R. Neill, Katrin Anne Becker, et al.. (2014). Engineered liposomes sequester bacterial exotoxins and protect from severe invasive infections in mice. Nature Biotechnology. 33(1). 81–88. 173 indexed citations
8.
Schoenauer, Roman, et al.. (2014). P2X7 receptors mediate resistance to toxin-induced cell lysis. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1843(5). 915–922. 20 indexed citations
9.
Monastyrskaya, Katia, Eduard B. Babiychuk, Annette Draeger, & Fiona C. Burkhard. (2013). Down-Regulation of Annexin A1 in the Urothelium Decreases Cell Survival After Bacterial Toxin Exposure. The Journal of Urology. 190(1). 325–333. 9 indexed citations
10.
Babiychuk, Eduard B., et al.. (2011). The Targeting of Plasmalemmal Ceramide to Mitochondria during Apoptosis. PLoS ONE. 6(8). e23706–e23706. 43 indexed citations
11.
Burkhard, Fiona C., et al.. (2009). MicroRNAs May Mediate the Down-Regulation of Neurokinin-1 Receptor in Chronic Bladder Pain Syndrome. American Journal Of Pathology. 176(1). 288–303. 92 indexed citations
12.
Monastyrskaya, Katia, et al.. (2006). Annexins as intracellular calcium sensors. Cell Calcium. 41(3). 207–219. 105 indexed citations
13.
Draeger, Annette, Katia Monastyrskaya, Fiona C. Burkhard, et al.. (2003). Membrane segregation and downregulation of raft markers during sarcolemmal differentiation in skeletal muscle cells. Developmental Biology. 262(2). 324–334. 24 indexed citations
14.
Rescher, Ursula, Volker Gerke, Hans Georg Mannherz, et al.. (2003). The expression levels of three raft-associated molecules in cultivated vascular cells are dependent on culture conditions. Cellular and Molecular Life Sciences. 60(12). 2702–2709. 8 indexed citations
15.
Babiychuk, Eduard B., Theodor Burdyga, Annette Draeger, & Susan Wray. (2002). Extraction of cholesterol abolishes phasic contraction of rat and guinea-pig ureter. Proceedings of The Physiological Society. 1 indexed citations
16.
Babiychuk, Eduard B., et al.. (2002). Stress fibres–a Ca2+-independent store for annexins?. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1600(1-2). 154–161. 8 indexed citations
17.
Rottner, Klemens, et al.. (1999). Intima-like smooth muscle cells: developmental link between endothelium and media?. Anatomy and Embryology. 200(3). 313–323. 25 indexed citations
18.
Draeger, Annette, et al.. (1991). Immunohistochemical localization of cytokeratins, smooth muscle actin and vimentin in human normal salivery glands and pleomorphic adenomas with particular reference to myoepithelial and basal cells. Apmis. 10 indexed citations
19.
Draeger, Annette, et al.. (1991). Developmental isoforms and a low molecular weight variant. FEBS Letters. 24–28. 9 indexed citations
20.
Draeger, Annette, et al.. (1991). Calponin Developmental isoforms and a low molecular weight variant. FEBS Letters. 291(1). 24–28. 47 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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