Elisabeth Vogelsang

4.0k total citations · 1 hit paper
16 papers, 3.2k citations indexed

About

Elisabeth Vogelsang is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Elisabeth Vogelsang has authored 16 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Cell Biology and 3 papers in Genetics. Recurrent topics in Elisabeth Vogelsang's work include Developmental Biology and Gene Regulation (10 papers), Zebrafish Biomedical Research Applications (6 papers) and Hippo pathway signaling and YAP/TAZ (4 papers). Elisabeth Vogelsang is often cited by papers focused on Developmental Biology and Gene Regulation (10 papers), Zebrafish Biomedical Research Applications (6 papers) and Hippo pathway signaling and YAP/TAZ (4 papers). Elisabeth Vogelsang collaborates with scholars based in Germany, United States and Austria. Elisabeth Vogelsang's co-authors include Mary C. Mullins, Michael Granato, Pascal Haffter, Donald A. Kane, Yun‐Jin Jiang, Robert N. Kelsh, Michael Brand, Carl‐Philipp Heisenberg, Matthias Hammerschmidt and Christiane Nüsslein‐Volhard and has published in prestigious journals such as Cell, Molecular and Cellular Biology and Development.

In The Last Decade

Elisabeth Vogelsang

16 papers receiving 3.2k citations

Hit Papers

The identification of genes with unique and essential fun... 1996 2026 2006 2016 1996 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabeth Vogelsang Germany 13 2.3k 1.9k 465 342 324 16 3.2k
Dirk Beuchle Germany 20 3.8k 1.7× 2.1k 1.1× 834 1.8× 248 0.7× 534 1.6× 24 4.9k
Ursula Schach Germany 8 2.1k 0.9× 1.7k 0.9× 630 1.4× 153 0.4× 418 1.3× 8 3.1k
David J. Grunwald United States 31 4.2k 1.9× 1.6k 0.9× 1.0k 2.2× 391 1.1× 319 1.0× 58 5.5k
Andreas Fritz United States 25 3.0k 1.3× 937 0.5× 872 1.9× 281 0.8× 301 0.9× 41 4.1k
Frédéric Rosa France 38 3.1k 1.4× 1.2k 0.6× 545 1.2× 644 1.9× 348 1.1× 77 4.6k
Aidas Nasevicius United States 12 2.8k 1.2× 1.6k 0.8× 545 1.2× 541 1.6× 322 1.0× 12 4.0k
Charline Walker United States 26 3.5k 1.5× 2.1k 1.1× 1.1k 2.5× 193 0.6× 400 1.2× 34 4.8k
Brian A. Link United States 42 3.1k 1.4× 2.0k 1.1× 564 1.2× 137 0.4× 497 1.5× 114 4.7k
Hans‐Martin Maischein Germany 28 1.5k 0.7× 1.0k 0.6× 232 0.5× 220 0.6× 300 0.9× 37 2.3k
Kazuhide Asakawa Japan 26 1.9k 0.8× 1.4k 0.7× 437 0.9× 133 0.4× 557 1.7× 48 2.9k

Countries citing papers authored by Elisabeth Vogelsang

Since Specialization
Citations

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

Fields of papers citing papers by Elisabeth Vogelsang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Vogelsang

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth Vogelsang. A scholar is included among the top collaborators of Elisabeth Vogelsang 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 Elisabeth Vogelsang. Elisabeth Vogelsang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Mollá, Belén, et al.. (2025). Retromer promotes the lysosomal turnover of mtDNA. Science Advances. 11(14). eadr6415–eadr6415. 6 indexed citations
2.
Nolte, Hendrik, Elisabeth Vogelsang, Michiko Takeda, et al.. (2024). Differential regulation of the proteome and phosphoproteome along the dorso-ventral axis of the early Drosophila embryo. eLife. 13. 2 indexed citations
3.
Narasimha, Maithreyi, et al.. (2014). Cadherin switching during the formation and differentiation of theDrosophilamesoderm: implications for epithelial mesenchymal transitions. Journal of Cell Science. 127(Pt 7). 1511–22. 46 indexed citations
4.
Narasimha, Maithreyi, et al.. (2014). Cadherin switching during the formation and differentiation of the Drosophila mesoderm – implications for epithelial-to-mesenchymal transitions. Development. 141(9). e0907–e0907. 16 indexed citations
5.
Csiszár, Ágnes, Elisabeth Vogelsang, Hartmut Beug, & Maria Leptin. (2010). A Novel Conserved Phosphotyrosine Motif in the Drosophila Fibroblast Growth Factor Signaling Adaptor Dof with a Redundant Role in Signal Transmission. Molecular and Cellular Biology. 30(8). 2017–2027. 4 indexed citations
6.
Narasimha, Maithreyi, et al.. (2006). Analysis and reconstitution of the genetic cascade controlling early mesoderm morphogenesis in the Drosophila embryo. Mechanisms of Development. 124(3). 167–179. 57 indexed citations
7.
Wilson, Robert, Elisabeth Vogelsang, & Maria Leptin. (2005). FGF signalling and the mechanism of mesoderm spreading in Drosophila embryos. Development. 132(3). 491–501. 42 indexed citations
8.
Wilson, Robert, Alysia Battersby, Ágnes Csiszár, Elisabeth Vogelsang, & Maria Leptin. (2004). A Functional Domain of Dof That Is Required for Fibroblast Growth Factor Signaling. Molecular and Cellular Biology. 24(6). 2263–2276. 21 indexed citations
9.
Haffter, Pascal, Mary C. Mullins, Shuo Lin, et al.. (1996). Mutations affecting pigmentation and shape of the adult zebrafish. Development Genes and Evolution. 206(4). 260–276. 141 indexed citations
10.
Odenthal, Jörg, Pascal Haffter, Elisabeth Vogelsang, et al.. (1996). Mutations affecting the formation of the notochord in the zebrafish, Danio rerio. Development. 123(1). 103–115. 206 indexed citations
11.
Odenthal, Jörg, Pascal Haffter, Robert N. Kelsh, et al.. (1996). Mutations affecting xanthophore pigmentation in the zebrafish, Danio rerio. Development. 123(1). 391–398. 136 indexed citations
12.
Haffter, Pascal, Michael Granato, Michael Brand, et al.. (1996). The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio. Development. 123(1). 1–36. 1339 indexed citations breakdown →
13.
Kelsh, Robert N., Michael Brand, Yun‐Jin Jiang, et al.. (1996). Zebrafish pigmentation mutations and the processes of neural crest development. Development. 123(1). 369–389. 386 indexed citations
14.
Ransom, David G., Pascal Haffter, Jörg Odenthal, et al.. (1996). Characterization of zebrafish mutants with defects in embryonic hematopoiesis. Development. 123(1). 311–319. 220 indexed citations
15.
Chen, Jau‐Nian, Pascal Haffter, Jörg Odenthal, et al.. (1996). Mutations affecting the cardiovascular system and other internal organs in zebrafish. Development. 123(1). 293–302. 373 indexed citations
16.
Stein, David A., et al.. (1991). The polarity of the dorsoventral axis in the drosophila embryo is defined by an extracellular signal. Cell. 65(5). 725–735. 222 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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