Roger E. Karess

6.6k total citations · 1 hit paper
56 papers, 5.4k citations indexed

About

Roger E. Karess is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Roger E. Karess has authored 56 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 35 papers in Cell Biology and 20 papers in Plant Science. Recurrent topics in Roger E. Karess's work include Microtubule and mitosis dynamics (33 papers), Genomics and Chromatin Dynamics (12 papers) and Chromosomal and Genetic Variations (11 papers). Roger E. Karess is often cited by papers focused on Microtubule and mitosis dynamics (33 papers), Genomics and Chromatin Dynamics (12 papers) and Chromosomal and Genetic Variations (11 papers). Roger E. Karess collaborates with scholars based in France, United States and United Kingdom. Roger E. Karess's co-authors include Gerald M. Rubin, Anne Royou, William Sullivan, Hidesaburô Hanafusa, David M. Glover, Sanjay Kulkarni, Renata Basto, David G. Russell, Enrique Medina‐Acosta and Eulalie Buffin and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Roger E. Karess

54 papers receiving 5.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Analysis of P transposable element functions in drosophila

1984 669 citations Roger E. Karess, Gerald M. Rubin Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roger E. Karess France	34	4.1k	2.8k	986	671	431	56	5.4k
Christopher G. Burd United States	48	7.4k 1.8×	3.5k 1.3×	585 0.6×	596 0.9×	372 0.9×	81	9.5k
Bruce Bowerman United States	50	7.0k 1.7×	2.8k 1.0×	810 0.8×	907 1.4×	446 1.0×	99	9.7k
Cayetano González Spain	38	4.2k 1.0×	3.1k 1.1×	940 1.0×	704 1.0×	512 1.2×	94	5.2k
John W. Tamkun United States	39	7.9k 1.9×	1.1k 0.4×	1.1k 1.2×	1.3k 1.9×	416 1.0×	54	9.6k
Thomas E. Kreis Switzerland	37	3.7k 0.9×	4.1k 1.5×	212 0.2×	343 0.5×	294 0.7×	46	5.6k
Carolyn A. Worby United States	31	3.7k 0.9×	931 0.3×	287 0.3×	853 1.3×	828 1.9×	56	5.7k
Susan M. Abmayr United States	40	5.0k 1.2×	936 0.3×	548 0.6×	918 1.4×	700 1.6×	72	6.0k
Masanori Taira Japan	42	5.0k 1.2×	728 0.3×	279 0.3×	957 1.4×	368 0.9×	133	6.0k
Scott B. Selleck United States	36	4.5k 1.1×	3.4k 1.2×	274 0.3×	969 1.4×	814 1.9×	69	6.2k

Countries citing papers authored by Roger E. Karess

Since Specialization

Citations

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

Fields of papers citing papers by Roger E. Karess

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roger E. Karess. 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 Roger E. Karess. The network helps show where Roger E. Karess may publish in the future.

Co-authorship network of co-authors of Roger E. Karess

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

All Works

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20 of 20 papers shown

Raich, Natacha, et al.. (2022). Microbiological and molecular screening of Candida spp. isolated from genital tract of asymptomatic pregnant women. Journal of Medical Microbiology. 71(9). 3 indexed citations

Raich, Natacha, Vincent Contremoulins, & Roger E. Karess. (2020). Immunostaining of Whole-Mount <em>Drosophila</em> Testes for 3D Confocal Analysis of Large Spermatocytes. Journal of Visualized Experiments.

Hainline, Sarah G., et al.. (2015). A maternal effectrough dealmutation suggesting multiple pathways regulating Drosophila RZZ kinetochore recruitment. Journal of Cell Science. 128(6). 1204–16. 5 indexed citations

Raich, Natacha, Régine Terracol, Xavier Baudin, et al.. (2015). RZZ and Mad1 dynamics in Drosophila mitosis. Chromosome Research. 23(2). 333–342. 17 indexed citations

Pascal, Aude, et al.. (2015). Spindle assembly checkpoint inactivation fails to suppress neuroblast tumour formation in aurA mutant Drosophila. Nature Communications. 6(1). 8879–8879. 16 indexed citations

Karess, Roger E., Katja Wassmann, & Zohra Rahmani. (2013). New Insights into the Role of BubR1 in Mitosis and Beyond. International review of cell and molecular biology. 306. 223–273. 29 indexed citations

Karess, Roger E., et al.. (2012). Inducing “cytokinesis” without mitosis in unfertilized Drosophila eggs. Cell Cycle. 11(15). 2856–2863. 5 indexed citations

Katsani, Katerina R., Roger E. Karess, Nathalie Dostatni, & Valérie Doye. (2008). In Vivo Dynamics of Drosophila Nuclear Envelope Components. Molecular Biology of the Cell. 19(9). 3652–3666. 101 indexed citations

Buffin, Eulalie, et al.. (2007). Flies without a spindle checkpoint. Nature Cell Biology. 9(5). 565–572. 99 indexed citations

10.

Lee, Jun Hee, Hyongjong Koh, Myung-Jin Kim, et al.. (2007). Energy-dependent regulation of cell structure by AMP-activated protein kinase. Nature. 447(7147). 1017–1020. 334 indexed citations

11.

Karess, Roger E.. (2005). Rod–Zw10–Zwilch: a key player in the spindle checkpoint. Trends in Cell Biology. 15(7). 386–392. 171 indexed citations

12.

Buffin, Eulalie, Christophe Lefebvre, Jun-Yong Huang, Mary E. Gagou, & Roger E. Karess. (2005). Recruitment of Mad2 to the Kinetochore Requires the Rod/Zw10 Complex. Current Biology. 15(9). 856–861. 159 indexed citations

13.

Basto, Renata, Frédéric Scaërou, Sarah Mische, et al.. (2004). In Vivo Dynamics of the Rough Deal Checkpoint Protein during Drosophila Mitosis. Current Biology. 14(1). 56–61. 86 indexed citations

14.

Royou, Anne, Christine M. Field, John C. Sisson, William Sullivan, & Roger E. Karess. (2003). Reassessing the Role and Dynamics of Nonmuscle Myosin II during Furrow Formation in Early Drosophila Embryos. Molecular Biology of the Cell. 15(2). 838–850. 233 indexed citations

15.

Royou, Anne, William Sullivan, & Roger E. Karess. (2002). Cortical recruitment of nonmuscle myosin II in early syncytial Drosophila embryos. The Journal of Cell Biology. 158(1). 127–137. 189 indexed citations

16.

Wojcik, Edward, Renata Basto, Madeline Serr, et al.. (2001). Kinetochore dynein: its dynamics and role in the transport of the Rough deal checkpoint protein. Nature Cell Biology. 3(11). 1001–1007. 173 indexed citations

17.

Medina‐Acosta, Enrique, Roger E. Karess, & David G. Russell. (1993). Structually distinct genes for the surface protease of Leishmania mexicana are developmentally regulated. Molecular and Biochemical Parasitology. 57(1). 31–45. 71 indexed citations

18.

Karess, Roger E., et al.. (1991). The regulatory light chain of nonmuscle myosin is encoded by spaghetti-squash, a gene required for cytokinesis in Drosophila. Cell. 65(7). 1177–1189. 243 indexed citations

19.

Button, Linda L., David G. Russell, Hannah L. Klein, et al.. (1989). Genes encoding the major surface glycoprotein in Leishmania are tandemly linked at a single chromosomal locus and are constitutively transcribed. Molecular and Biochemical Parasitology. 32(2-3). 271–283. 113 indexed citations

20.

Karess, Roger E. & Gerald M. Rubin. (1984). A genetic approach to the dissection of P transposable element functions in Drosophila. Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 307(1132). 231–238. 1 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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