Dorothea Godt

3.8k total citations
29 papers, 2.9k citations indexed

About

Dorothea Godt is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Dorothea Godt has authored 29 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 10 papers in Cell Biology. Recurrent topics in Dorothea Godt's work include Developmental Biology and Gene Regulation (15 papers), Neurobiology and Insect Physiology Research (9 papers) and Genomics and Chromatin Dynamics (7 papers). Dorothea Godt is often cited by papers focused on Developmental Biology and Gene Regulation (15 papers), Neurobiology and Insect Physiology Research (9 papers) and Genomics and Chromatin Dynamics (7 papers). Dorothea Godt collaborates with scholars based in Canada, United States and France. Dorothea Godt's co-authors include Ulrich Tepaß, Frank A. Laski, Susan Zollman, Jean‐Louis Couderc, Mark Peifer, Mitsuhiko Ikura, Gilbert G. Privé, Kevin Truong, J Couderc and Sarah E. Cramton and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Reviews Molecular Cell Biology.

In The Last Decade

Dorothea Godt

29 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dorothea Godt Canada 20 2.1k 958 651 498 386 29 2.9k
Enrique Martı́n-Blanco Spain 25 3.2k 1.5× 1.1k 1.2× 952 1.5× 653 1.3× 589 1.5× 54 4.1k
François Payre France 30 2.6k 1.2× 745 0.8× 572 0.9× 805 1.6× 317 0.8× 57 3.7k
Deborah J. Andrew United States 34 3.4k 1.6× 1.3k 1.4× 940 1.4× 697 1.4× 606 1.6× 81 4.5k
Hiroki Oda Japan 28 2.4k 1.1× 1.2k 1.3× 720 1.1× 427 0.9× 254 0.7× 77 3.4k
Jordi Casanova Spain 38 2.9k 1.4× 932 1.0× 839 1.3× 691 1.4× 571 1.5× 94 3.8k
Yi Sun Taiwan 28 2.0k 1.0× 686 0.7× 540 0.8× 471 0.9× 363 0.9× 74 2.8k
José F. de Celis Spain 35 3.8k 1.8× 1.1k 1.2× 1.3k 1.9× 688 1.4× 449 1.2× 73 4.4k
Acaimo González‐Reyes Spain 25 2.1k 1.0× 793 0.8× 387 0.6× 535 1.1× 247 0.6× 42 2.6k
Sonsoles Campuzano Spain 27 3.1k 1.5× 958 1.0× 1.3k 2.0× 557 1.1× 375 1.0× 43 3.7k
Wu‐Min Deng United States 29 2.3k 1.1× 1.1k 1.2× 510 0.8× 418 0.8× 463 1.2× 81 3.1k

Countries citing papers authored by Dorothea Godt

Since Specialization
Citations

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

Fields of papers citing papers by Dorothea Godt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorothea Godt

This figure shows the co-authorship network connecting the top 25 collaborators of Dorothea Godt. A scholar is included among the top collaborators of Dorothea Godt 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 Dorothea Godt. Dorothea Godt 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.
Park, Karen Sophia, Dorothea Godt, & Daniel Kalderon. (2018). Dissection and Staining of <em>Drosophila </em>Pupal Ovaries. Journal of Visualized Experiments. 3 indexed citations
2.
3.
Li, Tongchao, Νικόλαος Γιαγτζόγλου, Daniel F. Eberl, et al.. (2016). The E3 ligase Ubr3 regulates Usher syndrome and MYH9 disorder proteins in the auditory organs of Drosophila and mammals. eLife. 5. 22 indexed citations
4.
Chen, Xi, et al.. (2014). Myosin VIIA regulates microvillus morphogenesis and interacts with cadherin Cad99C in Drosophila oogenesis. Journal of Cell Science. 127(Pt 22). 4821–32. 18 indexed citations
5.
Sarpal, Ritu, et al.. (2012). Mutational analysis supports a core role for Drosophila α-Catenin in adherens junction function. Journal of Cell Science. 125(1). 233–245. 67 indexed citations
6.
Atallah, Joel, et al.. (2009). Cell dynamics and developmental bias in the ontogeny of a complex sexually dimorphic trait inDrosophila melanogaster. Evolution & Development. 11(2). 191–204. 15 indexed citations
7.
Wang, Fay, et al.. (2007). Expression profile of the cadherin family in the developing Drosophila brain. The Journal of Comparative Neurology. 506(3). 469–488. 31 indexed citations
8.
Tanentzapf, Guy, Danelle Devenport, Dorothea Godt, & Nicholas H. Brown. (2007). Integrin-dependent anchoring of a stem-cell niche. Nature Cell Biology. 9(12). 1413–1418. 168 indexed citations
9.
D’Alterio, Cecilia, et al.. (2005). Drosophila melanogaster Cad99C, the orthologue of human Usher cadherin PCDH15, regulates the length of microvilli. The Journal of Cell Biology. 171(3). 549–558. 59 indexed citations
10.
Godt, Dorothea & Ulrich Tepaß. (2003). Organogenesis: keeping in touch with the germ cells. Current Biology. 13(17). R683–R685. 7 indexed citations
11.
Koo, Karen, et al.. (2003). The large Maf factor Traffic Jam controls gonad morphogenesis in Drosophila. Nature Cell Biology. 5(11). 994–1000. 219 indexed citations
12.
Godt, Dorothea, et al.. (2002). Expression pattern of Gal4 enhancer trap insertions into the bric à brac locus generated by P element replacement. genesis. 34(1-2). 62–65. 31 indexed citations
13.
Bardot, Olivier, Dorothea Godt, Frank A. Laski, & Jean‐Louis Couderc. (2002). Expressing UAS‐bab1 and UAS‐bab2: A comparative study of gain‐of‐function effects and the potential to rescue the bric à brac mutant phenotype. genesis. 34(1-2). 66–70. 4 indexed citations
14.
Chen, Jiong, Dorothea Godt, Kristin C. Gunsalus, et al.. (2001). Cofilin/ADF is required for cell motility during Drosophila ovary development and oogenesis. Nature Cell Biology. 3(2). 204–209. 114 indexed citations
15.
Tepaß, Ulrich, Kevin Truong, Dorothea Godt, Mitsuhiko Ikura, & Mark Peifer. (2000). Cadherins in embryonic and neural morphogenesis. Nature Reviews Molecular Cell Biology. 1(2). 91–100. 387 indexed citations
16.
Godt, Dorothea & Ulrich Tepaß. (1998). Drosophila oocyte localization is mediated by differential cadherin-based adhesion. Nature. 395(6700). 387–391. 274 indexed citations
17.
Sahut‐Barnola, Isabelle, Dorothea Godt, Frank A. Laski, & Jean‐Louis Couderc. (1995). Drosophila Ovary Morphogenesis: Analysis of Terminal Filament Formation and Identification of a Gene Required for This Process. Developmental Biology. 170(1). 127–135. 78 indexed citations
18.
Zollman, Susan, Dorothea Godt, Gilbert G. Privé, J Couderc, & Frank A. Laski. (1994). The BTB domain, found primarily in zinc finger proteins, defines an evolutionarily conserved family that includes several developmentally regulated genes in Drosophila.. Proceedings of the National Academy of Sciences. 91(22). 10717–10721. 385 indexed citations
19.
Godt, Dorothea, Jean‐Louis Couderc, Sarah E. Cramton, & Frank A. Laski. (1993). Pattern formation in the limbs of Drosophila: bric à brac is expressed in both a gradient and a wave-like pattern and is required for specification and proper segmentation of the tarsus. Development. 119(3). 799–812. 173 indexed citations
20.
Godt, Dorothea, et al.. (1991). The Distribution of Transcripts of Neurogenic Genes in Neurogenic Mutants of Drosophila Melanogaster. Journal of Neurogenetics. 7(4). 241–252. 8 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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