Emmanuel Käs

3.1k total citations
32 papers, 2.7k citations indexed

About

Emmanuel Käs is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Emmanuel Käs has authored 32 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 9 papers in Plant Science and 4 papers in Genetics. Recurrent topics in Emmanuel Käs's work include Genomics and Chromatin Dynamics (13 papers), RNA Research and Splicing (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). Emmanuel Käs is often cited by papers focused on Genomics and Chromatin Dynamics (13 papers), RNA Research and Splicing (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). Emmanuel Käs collaborates with scholars based in France, Switzerland and United States. Emmanuel Käs's co-authors include Ulrich K. Laemmli, Yasuhisa Adachi, Leonora Poljak, Lawrence A. Chasin, Elisa Izaurralde, Gail Urlaub, Adelaide M. Carothers, Keji Zhao, Elma González and Pamela J. Mitchell and has published in prestigious journals such as Cell, The EMBO Journal and PLoS ONE.

In The Last Decade

Emmanuel Käs

32 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emmanuel Käs France 24 2.4k 471 450 182 152 32 2.7k
J L Corden United States 21 3.0k 1.3× 788 1.7× 268 0.6× 275 1.5× 243 1.6× 24 3.5k
Nahum Sonenberg Canada 19 2.6k 1.1× 225 0.5× 181 0.4× 150 0.8× 239 1.6× 24 3.0k
M P Calos United States 18 1.7k 0.7× 777 1.6× 192 0.4× 366 2.0× 210 1.4× 24 2.4k
J H Miller United States 11 1.2k 0.5× 475 1.0× 186 0.4× 239 1.3× 182 1.2× 11 1.8k
Sadaaki Kawai Japan 17 1.2k 0.5× 704 1.5× 287 0.6× 260 1.4× 219 1.4× 29 1.9k
Stephen F. Anderson United States 20 1.9k 0.8× 645 1.4× 154 0.3× 394 2.2× 265 1.7× 26 2.4k
Serafı́n Piñol-Roma United States 20 2.9k 1.2× 228 0.5× 182 0.4× 126 0.7× 238 1.6× 21 3.4k
G E Mark United States 21 1.3k 0.5× 358 0.8× 144 0.3× 339 1.9× 294 1.9× 32 2.0k
Donal S. Luse United States 36 4.6k 1.9× 969 2.1× 327 0.7× 221 1.2× 202 1.3× 70 5.1k
Robert C. Kingsbury United States 5 2.1k 0.9× 963 2.0× 303 0.7× 237 1.3× 386 2.5× 12 2.9k

Countries citing papers authored by Emmanuel Käs

Since Specialization
Citations

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

Fields of papers citing papers by Emmanuel Käs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuel Käs

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanuel Käs. A scholar is included among the top collaborators of Emmanuel Käs 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 Emmanuel Käs. Emmanuel Käs 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.
Afanasyeva, Arina, Anne Schreiber, Dina Grohmann, et al.. (2014). Lytic Water Dynamics Reveal Evolutionarily Conserved Mechanisms of ATP Hydrolysis by TIP49 AAA+ ATPases. Structure. 22(4). 549–559. 14 indexed citations
2.
Petukhov, Michael, Martin Bommer, Tracey Barrett, et al.. (2012). Large-Scale Conformational Flexibility Determines the Properties of AAA+ TIP49 ATPases. Structure. 20(8). 1321–1331. 25 indexed citations
3.
4.
Papin, Christophe, Odile Humbert, Anna A. Kalashnikova, et al.. (2010). 3′‐ to 5′ DNA unwinding by TIP49b proteins. FEBS Journal. 277(12). 2705–2714. 12 indexed citations
5.
Emberly, Eldon, Roxane Blattes, Bernd Schuettengruber, et al.. (2008). BEAF Regulates Cell-Cycle Genes through the Controlled Deposition of H3K9 Methylation Marks into Its Conserved Dual-Core Binding Sites. PLoS Biology. 6(12). e327–e327. 54 indexed citations
6.
Blattes, Roxane, Caroline Monod, Olivier Cuvier, et al.. (2006). Displacement of D1, HP1 and topoisomerase II from satellite heterochromatin by a specific polyamide. The EMBO Journal. 25(11). 2397–2408. 49 indexed citations
7.
Blattes, Roxane, et al.. (2005). Target Practice: Aiming at Satellite Repeats with DNA Minor Groove Binders. PubMed. 5(4). 409–420. 13 indexed citations
8.
Dennis, Cynthia, et al.. (2004). RuvAB‐directed branch migration of individual Holliday junctions is impeded by sequence heterology. The EMBO Journal. 23(12). 2413–2422. 24 indexed citations
9.
Poljak, Leonora, et al.. (2003). Analysis of NCp7-dependent Activation of HIV-1 cDNA Integration and its Conservation Among Retroviral Nucleocapsid Proteins. Journal of Molecular Biology. 329(3). 411–421. 35 indexed citations
10.
Monod, Caroline, Nathalie Aulner, Olivier Cuvier, & Emmanuel Käs. (2002). Modification of position‐effect variegation by competition for binding to Drosophila satellites. EMBO Reports. 3(8). 747–752. 11 indexed citations
11.
Cuvier, Olivier, Craig M. Hart, Emmanuel Käs, & Ulrich K. Laemmli. (2002). Identification of a multicopy chromatin boundary element at the borders of silenced chromosomal domains. Chromosoma. 110(8). 519–531. 40 indexed citations
12.
Vernis, Laurence, Leonora Poljak, Marion Chasles, et al.. (2001). Only Centromeres Can Supply the Partition System Required for ARS Function in the Yeast Yarrowia lipolytica. Journal of Molecular Biology. 305(2). 203–217. 33 indexed citations
13.
Beaujean, Nathalie, Christine Baly, Caroline Monod, et al.. (2000). Induction of Early Transcription in One-Cell Mouse Embryos by Microinjection of the Nonhistone Chromosomal Protein HMG-I. Developmental Biology. 221(2). 337–354. 39 indexed citations
14.
Slama‐Schwok, Anny, K. Zakrzewska, Gabriel C. Léger, et al.. (2000). Structural Changes Induced by Binding of the High-Mobility Group I Protein to a Mouse Satellite DNA Sequence. Biophysical Journal. 78(5). 2543–2559. 24 indexed citations
15.
Jullien, Denis, Michèle Crozatier, & Emmanuel Käs. (1997). cDNA sequence and expression pattern of the Drosophila melanogaster PAPS synthetase gene: a new salivary gland marker. Mechanisms of Development. 68(1-2). 179–186. 23 indexed citations
16.
Käs, Emmanuel & Ulrich K. Laemmli. (1992). In vivo topoisomerase II cleavage of the Drosophila histone and satellite III repeats: DNA sequence and structural characteristics.. The EMBO Journal. 11(2). 705–716. 163 indexed citations
17.
Käs, Emmanuel, Elisa Izaurralde, & Ulrich K. Laemmli. (1989). Specific inhibition of DNA Binding to nuclear scaffolds and histone H1 by distamycin. Journal of Molecular Biology. 210(3). 587–599. 123 indexed citations
18.
Izaurralde, Elisa, Emmanuel Käs, & Ulrich K. Laemmli. (1989). Highly preferential nucleation of histone H1 assembly on scaffold-associated regions. Journal of Molecular Biology. 210(3). 573–585. 148 indexed citations
19.
Käs, Emmanuel & Lawrence A. Chasin. (1987). Anchorage of the Chinese hamster dihydrofolate reductase gene to the nuclear scaffold occurs in an intragenic region. Journal of Molecular Biology. 198(4). 677–692. 83 indexed citations
20.
Mitchell, Pamela J., Adelaide M. Carothers, Jang H. Han, et al.. (1986). Multiple transcription start sites, DNase I-hypersensitive sites, and an opposite-strand exon in the 5' region of the CHO dhfr gene.. Molecular and Cellular Biology. 6(2). 425–440. 150 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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