Mathieu Rappas

2.6k total citations
29 papers, 1.7k citations indexed

About

Mathieu Rappas is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Mathieu Rappas has authored 29 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 15 papers in Genetics and 6 papers in Ecology. Recurrent topics in Mathieu Rappas's work include Bacterial Genetics and Biotechnology (15 papers), RNA and protein synthesis mechanisms (12 papers) and Bacteriophages and microbial interactions (6 papers). Mathieu Rappas is often cited by papers focused on Bacterial Genetics and Biotechnology (15 papers), RNA and protein synthesis mechanisms (12 papers) and Bacteriophages and microbial interactions (6 papers). Mathieu Rappas collaborates with scholars based in United Kingdom, United States and Germany. Mathieu Rappas's co-authors include Xiaodong Zhang, Martin Buck, Jörg Schumacher, Daniel Bose, A.S. Dore, Sivaramesh Wigneshweraraj, Nicolas Joly, Laurence H. Pearl, Antony W. Oliver and Hajime Niwa and has published in prestigious journals such as Nature, Science and Nucleic Acids Research.

In The Last Decade

Mathieu Rappas

29 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mathieu Rappas United Kingdom 22 1.4k 520 244 226 193 29 1.7k
Emily Tate United States 15 1.6k 1.2× 365 0.7× 166 0.7× 128 0.6× 227 1.2× 21 2.4k
Johannes H. Bauer United States 24 1.1k 0.8× 271 0.5× 515 2.1× 130 0.6× 231 1.2× 35 2.2k
Didier Busso France 18 1.2k 0.9× 238 0.5× 103 0.4× 78 0.3× 155 0.8× 47 1.5k
Shigeki Takeda Japan 24 1.1k 0.8× 195 0.4× 327 1.3× 332 1.5× 77 0.4× 71 1.6k
Maria Pellegrini United States 27 1.7k 1.2× 209 0.4× 528 2.2× 76 0.3× 318 1.6× 98 2.4k
Erik Ahrné Switzerland 16 1.3k 1.0× 352 0.7× 117 0.5× 119 0.5× 75 0.4× 23 1.7k
Sanduo Zheng China 20 1.4k 1.0× 179 0.3× 297 1.2× 95 0.4× 97 0.5× 35 1.8k
Mamoru Mizuno Japan 25 2.1k 1.5× 205 0.4× 181 0.7× 86 0.4× 67 0.3× 86 2.4k
Vera Pingoud Germany 16 1.3k 0.9× 306 0.6× 95 0.4× 116 0.5× 152 0.8× 32 1.5k
Asser S. Andersen Denmark 25 1.4k 1.0× 192 0.4× 170 0.7× 40 0.2× 118 0.6× 43 2.1k

Countries citing papers authored by Mathieu Rappas

Since Specialization
Citations

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

Fields of papers citing papers by Mathieu Rappas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathieu Rappas

This figure shows the co-authorship network connecting the top 25 collaborators of Mathieu Rappas. A scholar is included among the top collaborators of Mathieu Rappas 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 Mathieu Rappas. Mathieu Rappas 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.
Vakili, Mohammad, Huijong Han, Christina Schmidt, et al.. (2023). Mix-and-extrude: high-viscosity sample injection towards time-resolved protein crystallography. Journal of Applied Crystallography. 56(4). 1038–1045. 10 indexed citations
2.
Robertson, N.J., Mathieu Rappas, A.S. Dore, et al.. (2018). Structure of the complement C5a receptor bound to the extra-helical antagonist NDT9513727. Nature. 553(7686). 111–114. 108 indexed citations
3.
4.
Ehrenmann, Janosch, Jendrik Schöppe, Christoph Klenk, et al.. (2018). High-resolution crystal structure of parathyroid hormone 1 receptor in complex with a peptide agonist. Nature Structural & Molecular Biology. 25(12). 1086–1092. 86 indexed citations
5.
Jazayeri, Ali, Mathieu Rappas, Alastair Brown, et al.. (2017). Crystal structure of the GLP-1 receptor bound to a peptide agonist. Nature. 546(7657). 254–258. 136 indexed citations
6.
Oswald, Christine, Mathieu Rappas, James Kean, et al.. (2016). Intracellular allosteric antagonism of the CCR9 receptor. Nature. 540(7633). 462–465. 196 indexed citations
7.
Qu, Meng, Mathieu Rappas, Valérie Garcia, et al.. (2013). Phosphorylation-Dependent Assembly and Coordination of the DNA Damage Checkpoint Apparatus by Rad4TopBP1. Molecular Cell. 51(6). 723–736. 22 indexed citations
8.
Boos, Dominik, Luis Sánchez‐Pulido, Mathieu Rappas, et al.. (2011). Regulation of DNA Replication through Sld3-Dpb11 Interaction Is Conserved from Yeast to Humans. Current Biology. 21(13). 1152–1157. 115 indexed citations
9.
Rappas, Mathieu, Antony W. Oliver, & Laurence H. Pearl. (2010). Structure and function of the Rad9-binding region of the DNA-damage checkpoint adaptor TopBP1. Nucleic Acids Research. 39(1). 313–324. 65 indexed citations
10.
Burrows, Patricia C., Nicolas Joly, Wendy Cannon, et al.. (2009). Coupling σ Factor Conformation to RNA Polymerase Reorganisation for DNA Melting. Journal of Molecular Biology. 387(2). 306–319. 13 indexed citations
11.
Bose, Daniel, Tillmann Pape, Patricia C. Burrows, et al.. (2008). Organization of an Activator-Bound RNA Polymerase Holoenzyme. Molecular Cell. 32(3). 337–346. 62 indexed citations
12.
Wigneshweraraj, Sivaramesh, Daniel Bose, Patricia C. Burrows, et al.. (2008). Modus operandi of the bacterial RNA polymerase containing the σ54 promoter‐specificity factor. Molecular Microbiology. 68(3). 538–546. 97 indexed citations
13.
Muzzolini, Laura, Fabienne Beuron, Ardan Patwardhan, et al.. (2007). Different Quaternary Structures of Human RECQ1 Are Associated with Its Dual Enzymatic Activity. PLoS Biology. 5(2). e20–e20. 58 indexed citations
14.
Joly, Nicolas, Mathieu Rappas, Martin Buck, & Xiaodong Zhang. (2007). Trapping of a Transcription Complex Using a New Nucleotide Analogue: AMP Aluminium Fluoride. Journal of Molecular Biology. 375(5). 1206–1211. 13 indexed citations
15.
Rappas, Mathieu, Jörg Schumacher, Hajime Niwa, Martin Buck, & Xiaodong Zhang. (2006). Structural Basis of the Nucleotide Driven Conformational Changes in the AAA+ Domain of Transcription Activator PspF. Journal of Molecular Biology. 357(2). 481–492. 75 indexed citations
16.
Schumacher, Jörg, Nicolas Joly, Mathieu Rappas, Xiaodong Zhang, & Martin Buck. (2006). Structures and organisation of AAA+ enhancer binding proteins in transcriptional activation. Journal of Structural Biology. 156(1). 190–199. 88 indexed citations
17.
Rappas, Mathieu, Daniel Bose, & Xiaodong Zhang. (2006). Bacterial enhancer-binding proteins: unlocking σ54-dependent gene transcription. Current Opinion in Structural Biology. 17(1). 110–116. 84 indexed citations
18.
Buck, Martin, Daniel Bose, Patricia C. Burrows, et al.. (2006). A second paradigm for gene activation in bacteria. Biochemical Society Transactions. 34(6). 1067–1071. 26 indexed citations
19.
Rappas, Mathieu, Jörg Schumacher, Fabienne Beuron, et al.. (2005). Structural Insights into the Activity of Enhancer-Binding Proteins. Science. 307(5717). 1972–1975. 138 indexed citations
20.
Huo, Yi‐Xin, Zhe‐Xian Tian, Mathieu Rappas, et al.. (2005). Protein‐induced DNA bending clarifies the architectural organization of the σ 54 ‐dependent glnA p2 promoter. Molecular Microbiology. 59(1). 168–180. 34 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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