Elisabeth Gateff

2.9k total citations
40 papers, 2.4k citations indexed

About

Elisabeth Gateff is a scholar working on Molecular Biology, Immunology and Insect Science. According to data from OpenAlex, Elisabeth Gateff has authored 40 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Immunology and 9 papers in Insect Science. Recurrent topics in Elisabeth Gateff's work include Invertebrate Immune Response Mechanisms (14 papers), Insect symbiosis and bacterial influences (8 papers) and Neurobiology and Insect Physiology Research (7 papers). Elisabeth Gateff is often cited by papers focused on Invertebrate Immune Response Mechanisms (14 papers), Insect symbiosis and bacterial influences (8 papers) and Neurobiology and Insect Physiology Research (7 papers). Elisabeth Gateff collaborates with scholars based in Germany, United States and Sweden. Elisabeth Gateff's co-authors include Howard A. Schneiderman, Dan Hultmark, Péter Vilmos, István Andó, Jasmine Wismar, Éva Kurucz, Ursula Kurzik‐Dumke, Róbert Márkus, János Zsámboki and Thomas Löffler and has published in prestigious journals such as Science, Journal of Biological Chemistry and The EMBO Journal.

In The Last Decade

Elisabeth Gateff

40 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabeth Gateff Germany 26 1.3k 1.0k 603 586 529 40 2.4k
Carl Hashimoto United States 20 1.3k 1.0× 1.3k 1.3× 538 0.9× 529 0.9× 216 0.4× 25 2.6k
Bengt Åsling Sweden 10 949 0.7× 627 0.6× 307 0.5× 590 1.0× 379 0.7× 11 1.7k
Michèle Crozatier France 31 1.4k 1.1× 1.4k 1.4× 782 1.3× 993 1.7× 346 0.7× 55 2.8k
Christos Samakovlis Sweden 36 2.8k 2.1× 1.8k 1.8× 867 1.4× 957 1.6× 835 1.6× 63 4.5k
Cory J. Evans United States 17 919 0.7× 1.2k 1.2× 529 0.9× 715 1.2× 263 0.5× 19 2.0k
Péter Vilmos Hungary 15 782 0.6× 662 0.7× 500 0.8× 330 0.6× 273 0.5× 35 1.5k
Daniel Zachary France 19 650 0.5× 1.7k 1.7× 1.4k 2.3× 841 1.4× 135 0.3× 29 2.5k
Makoto Nakamura Japan 17 1.2k 0.9× 406 0.4× 180 0.3× 345 0.6× 236 0.4× 48 1.8k
Nadine T. Nehme France 10 393 0.3× 979 1.0× 622 1.0× 221 0.4× 195 0.4× 10 1.5k
Éva Kurucz Hungary 19 480 0.4× 1.5k 1.5× 1.1k 1.8× 694 1.2× 149 0.3× 38 1.9k

Countries citing papers authored by Elisabeth Gateff

Since Specialization
Citations

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

Fields of papers citing papers by Elisabeth Gateff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Gateff

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth Gateff. A scholar is included among the top collaborators of Elisabeth Gateff 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 Gateff. Elisabeth Gateff 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.
Kurucz, Éva, Róbert Márkus, Barbara Laurinyecz, et al.. (2007). Definition ofDrosophilahemocyte subsets by cell-type specific antigens. Acta Biologica Hungarica. 58(Supplement 1). 95–111. 129 indexed citations
2.
Kurucz, Éva, Róbert Márkus, János Zsámboki, et al.. (2007). Nimrod, a Putative Phagocytosis Receptor with EGF Repeats in Drosophila Plasmatocytes. Current Biology. 17(7). 649–654. 262 indexed citations
3.
Vilmos, Péter, István Nagy, Éva Kurucz, et al.. (2003). A rapid rosetting method for separation of hemocyte sub-populations of Drosophila melanogaster. Developmental & Comparative Immunology. 28(6). 555–563. 30 indexed citations
4.
Wismar, Jasmine, Negusse Habtemichael, James T. Warren, et al.. (2000). The Mutation without childrenrgl Causes Ecdysteroid Deficiency in Third-Instar Larvae of Drosophila melanogaster. Developmental Biology. 226(1). 1–17. 47 indexed citations
5.
Gateff, Elisabeth, Ursula Kurzik‐Dumke, Jasmine Wismar, et al.. (1996). Drosophila differentiation genes instrumental in tumor suppression. The International Journal of Developmental Biology. 40(1). 149–156. 11 indexed citations
6.
Wismar, Jasmine, Thomas Löffler, Negusse Habtemichael, et al.. (1995). The Drosophila melanogaster tumor suppressor gene lethal(3)malignant brain tumor encodes a proline-rich protein with a novel zinc finger. Mechanisms of Development. 53(1). 141–154. 84 indexed citations
7.
Gateff, Elisabeth. (1994). Tumor suppressor and overgrowth suppressor genes of Drosophila melanogaster: developmental aspects. The International Journal of Developmental Biology. 38(4). 565–590. 61 indexed citations
8.
9.
Gateff, Elisabeth. (1994). Tumor‐Suppressor Genes, Hematopoietic Malignancies and Other Hematopoietic Disorders of Drosophila melanogastera. Annals of the New York Academy of Sciences. 712(1). 260–279. 20 indexed citations
10.
Roebroek, Anton, John W.M. Creemers, Ilse G.L. Pauli, et al.. (1992). Cloning and functional expression of Dfurin2, a subtilisin-like proprotein processing enzyme of Drosophila melanogaster with multiple repeats of a cysteine motif.. Journal of Biological Chemistry. 267(24). 17208–17215. 77 indexed citations
11.
Kurzik‐Dumke, Ursula, et al.. (1992). Genetic, cytogenetic and developmental analysis of the Drosophila melanogaster tumor suppressor gene lethal(2)tumorous imaginal discs (l(2)tid). Differentiation. 51(2). 91–104. 31 indexed citations
12.
Löffler, Thomas, Heinz Sass, Gerhard Becker, et al.. (1990). Genetic and molecular analysis of six tumor suppressor genes in Drosophila melanogaster. Environmental Health Perspectives. 88. 157–161. 4 indexed citations
13.
14.
Klose, W., et al.. (1980). Developmental studies on two ecdysone deficient mutants ofDrosophila melanogaster. Development Genes and Evolution. 189(1). 57–67. 51 indexed citations
15.
Gateff, Elisabeth, et al.. (1979). Pattern specification in imaginal discs ofDrosophila melanogaster. Development Genes and Evolution. 186(1). 1–25. 31 indexed citations
16.
Gateff, Elisabeth. (1978). Malignant Neoplasms of Genetic Origin in Drosophila melanogaster. Science. 200(4349). 1448–1459. 376 indexed citations
17.
Campos‐Ortega, José A. & Elisabeth Gateff. (1976). The development of ommatidial patterning in metamorphosed eye imaginal discs implants ofDrosophila melanogaster. Development Genes and Evolution. 179(4). 373–392. 27 indexed citations
18.
Gateff, Elisabeth & Howard A. Schneiderman. (1975). Developmental capacities of immature eye-antennal imaginal discs ofDrosophila melanogaster. Development Genes and Evolution. 176(3). 171–189. 26 indexed citations
19.
Gateff, Elisabeth, Hiroyuki Akai, & Howard A. Schneiderman. (1974). Correlations between developmental capacity and structure of tissue sublines derived from the eye-antennal imaginal disc ofDrosophila melanogaster. Development Genes and Evolution. 176(2). 89–123. 6 indexed citations
20.
Gateff, Elisabeth & Howard A. Schneiderman. (1974). Developmental capacities of benign and malignant neoplasms ofDrosophila. Development Genes and Evolution. 176(1). 23–65. 121 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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