Daniel Bopp

7.3k total citations · 2 hit papers
42 papers, 4.4k citations indexed

About

Daniel Bopp is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Daniel Bopp has authored 42 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 24 papers in Molecular Biology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Daniel Bopp's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Developmental Biology and Gene Regulation (14 papers) and Neurobiology and Insect Physiology Research (11 papers). Daniel Bopp is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Developmental Biology and Gene Regulation (14 papers) and Neurobiology and Insect Physiology Research (11 papers). Daniel Bopp collaborates with scholars based in Switzerland, United States and Germany. Daniel Bopp's co-authors include Markus Noll, Maya Burri, Gabriella Frigerio, Stefan Baumgartner, Paul Schedl, Jamila I. Horabin, Monika Hediger, Giuseppe Saccone, Christiane Nüsslein‐Volhard and Thomas W. Cline and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Daniel Bopp

41 papers receiving 4.4k citations

Hit Papers

The role of localization of bicoid RNA in organizing the ... 1986 2026 1999 2012 1988 1986 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Bopp Switzerland 29 3.4k 1.7k 761 598 546 42 4.4k
John M. Belote United States 34 2.2k 0.6× 2.2k 1.3× 554 0.7× 765 1.3× 414 0.8× 62 4.2k
Harald Vaessin United States 20 3.3k 0.9× 902 0.5× 266 0.3× 1.1k 1.9× 518 0.9× 26 4.1k
Kent G. Golic United States 27 4.6k 1.3× 1.1k 0.7× 397 0.5× 782 1.3× 1.2k 2.2× 49 5.4k
Helen White‐Cooper United Kingdom 29 2.2k 0.6× 742 0.4× 507 0.7× 526 0.9× 436 0.8× 44 3.4k
Robin E. Denell United States 34 2.9k 0.8× 1.3k 0.8× 541 0.7× 786 1.3× 644 1.2× 69 3.5k
John Roote United Kingdom 24 1.9k 0.5× 841 0.5× 263 0.3× 385 0.6× 628 1.2× 39 2.6k
Monika Hediger Switzerland 13 1.5k 0.4× 646 0.4× 488 0.6× 558 0.9× 306 0.6× 14 2.2k
Kenneth C. Burtis United States 22 1.7k 0.5× 1.3k 0.8× 477 0.6× 854 1.4× 245 0.4× 29 2.8k
Harald Biessmann United States 37 2.7k 0.8× 602 0.4× 529 0.7× 649 1.1× 1.6k 3.0× 80 3.8k
Uwe Walldorf Germany 28 2.9k 0.8× 854 0.5× 166 0.2× 1.0k 1.7× 370 0.7× 53 3.5k

Countries citing papers authored by Daniel Bopp

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Bopp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Bopp

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Bopp. A scholar is included among the top collaborators of Daniel Bopp 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 Daniel Bopp. Daniel Bopp 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.
Li, Xuan, S.L. Visser, Jae Hak Son, et al.. (2024). Divergent evolution of male-determining loci on proto-Y chromosomes of the housefly. Nature Communications. 15(1). 5984–5984.
3.
Wu, Yanli, Ian Morilla, Ernst A. Wimmer, et al.. (2017). Male sex in houseflies is determined by Mdmd , a paralog of the generic splice factor gene CWC22. Science. 356(6338). 642–645. 99 indexed citations
4.
Meccariello, Angela, et al.. (2017). CRISPR-Cas9 targeted disruption of the yellow ortholog in the housefly identifies the brown body locus. Scientific Reports. 7(1). 4582–4582. 25 indexed citations
5.
Meccariello, Angela, Simona Maria Monti, Alessandra Romanelli, et al.. (2017). Highly efficient DNA-free gene disruption in the agricultural pest Ceratitis capitata by CRISPR-Cas9 ribonucleoprotein complexes. Scientific Reports. 7(1). 10061–10061. 53 indexed citations
6.
Verhulst, Eveline C., Jeremy Lynch, Daniel Bopp, Leo W. Beukeboom, & Louis van de Zande. (2013). A New Component of the Nasonia Sex Determining Cascade Is Maternally Silenced and Regulates Transformer Expression. PLoS ONE. 8(5). e63618–e63618. 28 indexed citations
7.
Meier, Nicole, et al.. (2013). Genetic Control of Courtship Behavior in the Housefly: Evidence for a Conserved Bifurcation of the Sex-Determining Pathway. PLoS ONE. 8(4). e62476–e62476. 28 indexed citations
8.
Bopp, Daniel, Giuseppe Saccone, & Martin Beye. (2013). Sex Determination in Insects: Variations on a Common Theme. Sexual Development. 8(1-3). 20–28. 114 indexed citations
9.
Bopp, Daniel. (2010). About females and males: continuity and discontinuity in flies. Journal of Genetics. 89(3). 315–323. 17 indexed citations
10.
Maróy, Péter, et al.. (2009). Hormones and Sex-Specific Transcription Factors Jointly Control Yolk Protein Synthesis inMusca domestica. PubMed. 2009. 1–9. 5 indexed citations
11.
Hediger, Monika, et al.. (2005). The transformer2 gene in Musca domestica is required for selecting and maintaining the female pathway of development. Development Genes and Evolution. 215(4). 165–176. 71 indexed citations
12.
Hediger, Monika, et al.. (2003). Sex determination in Drosophila melanogaster and Musca domestica converges at the level of the terminal regulator doublesex. Development Genes and Evolution. 214(1). 29–42. 111 indexed citations
13.
Bellotto, Manolo, Daniel Bopp, Kirsten-André Senti, et al.. (2002). Maternal-effect loci involved in Drosophila oogenesis and embryogenesis: P element-induced mutations on the third chromosome. The International Journal of Developmental Biology. 46(1). 149–157. 20 indexed citations
14.
Dübendorfer, Andreas, et al.. (2002). Musca domestica, a window on the evolution of sex-determining mechanisms in insects. The International Journal of Developmental Biology. 46(1). 75–79. 111 indexed citations
15.
McGregor, Alistair P., Philip J. Shaw, John M. Hancock, et al.. (2001). Rapid restructuring of bicoid‐dependent hunchback promoters within and between Dipteran species: implications for molecular coevolution. Evolution & Development. 3(6). 397–407. 54 indexed citations
16.
Hediger, Monika, Markus Nießen, Ernst A. Wimmer, Andreas Dübendorfer, & Daniel Bopp. (2001). Genetic transformation of the housefly Musca domestica with the lepidopteran derived transposon piggyBac. Insect Molecular Biology. 10(2). 113–119. 73 indexed citations
17.
Horabin, Jamila I., et al.. (2000). Sex Determination in the Drosophila Germline Is Dictated by the Sexual Identity of the Surrounding Soma. Genetics. 155(4). 1741–1756. 26 indexed citations
18.
Horabin, Jamila I., et al.. (1995). Selection and maintenance of sexual identity in the Drosophila germline.. Genetics. 141(4). 1521–1535. 35 indexed citations
19.
Dambly‐Chaudière, Christine, Élisabeth Jamet, Maya Burri, et al.. (1992). The paired box gene pox neuro: A determiant of poly-innervated sense organs in Drosophila. Cell. 69(1). 159–172. 117 indexed citations
20.
Parkhurst, Susan M., Daniel Bopp, & David Ish‐Horowicz. (1990). X:A ratio, the primary sex-determining signal in Drosophila, is transduced by helix-loop-helix proteins. Cell. 63(6). 1179–1191. 144 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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