Helen R. Mott

5.2k total citations · 3 hit papers
77 papers, 4.1k citations indexed

About

Helen R. Mott is a scholar working on Molecular Biology, Cell Biology and Materials Chemistry. According to data from OpenAlex, Helen R. Mott has authored 77 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 26 papers in Cell Biology and 15 papers in Materials Chemistry. Recurrent topics in Helen R. Mott's work include Protein Kinase Regulation and GTPase Signaling (43 papers), Protein Structure and Dynamics (15 papers) and Enzyme Structure and Function (15 papers). Helen R. Mott is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (43 papers), Protein Structure and Dynamics (15 papers) and Enzyme Structure and Function (15 papers). Helen R. Mott collaborates with scholars based in United Kingdom, South Sudan and United States. Helen R. Mott's co-authors include Darerca Owen, Daniel Nietlispach, Ernest D. Laue, Christopher M. Dobson, Anthony W. P. Fitzpatrick, Michele Vendruscolo, Tuomas P. J. Knowles, Mark E. Welland, Sarah Meehan and Peter R. Nielsen and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Helen R. Mott

76 papers receiving 4.0k citations

Hit Papers

Role of Intermolecular Fo... 2002 2026 2010 2018 2007 2002 2013 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
Helen R. Mott United Kingdom 30 3.1k 614 606 504 389 77 4.1k
Meytal Landau Israel 31 3.2k 1.0× 338 0.6× 1.4k 2.3× 592 1.2× 509 1.3× 76 4.7k
Richard A. Kammerer Switzerland 43 3.5k 1.1× 1.5k 2.5× 314 0.5× 538 1.1× 419 1.1× 101 5.2k
R.L. Brady United Kingdom 39 3.3k 1.1× 334 0.5× 366 0.6× 475 0.9× 591 1.5× 87 4.7k
Yuting Yang China 36 3.0k 1.0× 278 0.5× 964 1.6× 669 1.3× 283 0.7× 143 5.0k
John R. Silvius Canada 50 6.8k 2.2× 1.5k 2.4× 615 1.0× 362 0.7× 218 0.6× 114 7.9k
Dimitri Y. Chirgadze United Kingdom 35 2.5k 0.8× 398 0.6× 243 0.4× 389 0.8× 382 1.0× 78 3.4k
Michel Seigneuret France 28 2.2k 0.7× 385 0.6× 385 0.6× 227 0.5× 148 0.4× 53 3.2k
Jörg Gsponer Canada 30 3.0k 1.0× 413 0.7× 442 0.7× 208 0.4× 707 1.8× 68 3.7k
Akiko Koide United States 46 4.4k 1.4× 279 0.5× 348 0.6× 229 0.5× 379 1.0× 110 5.8k
Jody M. Mason United Kingdom 26 2.2k 0.7× 223 0.4× 639 1.1× 285 0.6× 209 0.5× 81 3.1k

Countries citing papers authored by Helen R. Mott

Since Specialization
Citations

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

Fields of papers citing papers by Helen R. Mott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helen R. Mott. 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 Helen R. Mott. The network helps show where Helen R. Mott may publish in the future.

Co-authorship network of co-authors of Helen R. Mott

This figure shows the co-authorship network connecting the top 25 collaborators of Helen R. Mott. A scholar is included among the top collaborators of Helen R. Mott 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 Helen R. Mott. Helen R. Mott 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.
Mott, Helen R., et al.. (2023). ACKnowledging the role of the Activated-Cdc42 associated kinase (ACK) in regulating protein stability in cancer. Small GTPases. 14(1). 14–25. 1 indexed citations
3.
Owen, Darerca, et al.. (2022). Membrane extraction by calmodulin underpins the disparate signalling of RalA and RalB. BioEssays. 44(6). e2200011–e2200011. 1 indexed citations
4.
Wood, George, et al.. (2020). 1H, 15N and 13C resonance assignments of the HR1c domain of PRK1, a protein kinase C-related kinase. Biomolecular NMR Assignments. 14(2). 245–250. 1 indexed citations
5.
Mott, Helen R., et al.. (2020). Class IA PI3K regulatory subunits: p110-independent roles and structures. Biochemical Society Transactions. 48(4). 1397–1417. 56 indexed citations
6.
Campbell, Louise J., et al.. (2020). NMR resonance assignments for the active and inactive conformations of the small G protein RalA. Biomolecular NMR Assignments. 14(1). 87–91. 2 indexed citations
7.
Revell, Jefferson D., et al.. (2020). The discovery and maturation of peptide biologics targeting the small G-protein Cdc42: A bioblockade for Ras-driven signaling. Journal of Biological Chemistry. 295(9). 2866–2884. 12 indexed citations
8.
Owen, Darerca & Helen R. Mott. (2018). CRIB effector disorder: exquisite function from chaos. Biochemical Society Transactions. 46(5). 1289–1302. 6 indexed citations
9.
Nietlispach, Daniel, et al.. (2016). 1H, 13C and 15N resonance assignments of the Cdc42-binding domain of TOCA1. Biomolecular NMR Assignments. 10(2). 407–411. 1 indexed citations
10.
Campbell, Louise J., et al.. (2011). 1H, 13C and 15N resonance assignments of the GTPase-activating (GAP) and Ral binding domains (GBD) of RLIP76 (RalBP1). Biomolecular NMR Assignments. 6(2). 119–122. 3 indexed citations
11.
Gautier, Antoine, Helen R. Mott, Mark J. Bostock, John Kirkpatrick, & Daniel Nietlispach. (2010). Structure determination of the seven-helix transmembrane receptor sensory rhodopsin II by solution NMR spectroscopy. Nature Structural & Molecular Biology. 17(6). 768–774. 164 indexed citations
12.
Thomson, Russell, et al.. (2009). Hydrodynamic gene delivery of baboon trypanosome lytic factor eliminates both animal and human-infective African trypanosomes. Proceedings of the National Academy of Sciences. 106(46). 19509–19514. 47 indexed citations
13.
Campbell, Louise J., et al.. (2008). The Structure of Binder of Arl2 (BART) Reveals a Novel G Protein Binding Domain. Journal of Biological Chemistry. 284(2). 992–999. 9 indexed citations
14.
Fenwick, R. Bryn, Sunil Prasannan, Louise J. Campbell, et al.. (2008). 1H, 13C and 15N resonance assignments for the active conformation of the small G protein RalB in complex with its effector RLIP76. Biomolecular NMR Assignments. 2(2). 179–182. 3 indexed citations
15.
Fenwick, R. Bryn, Sunil Prasannan, Louise J. Campbell, et al.. (2008). Resonance assignments for the RLIP76 Ral binding domain in its free form and in complex with the small G protein RalB. Biomolecular NMR Assignments. 2(2). 191–194. 2 indexed citations
16.
Bligh, S. W. Annie, et al.. (2004). Fluorescence Properties of Green Fluorescent Protein FRET Pairs Concatenated with the Small G Protein, Rac, and Its Interacting Domain of the Kinase, p21-Activated Kinase. Assay and Drug Development Technologies. 2(6). 659–673. 3 indexed citations
17.
Nietlispach, Daniel, et al.. (2004). Structure Determination of Protein Complexes by NMR. Humana Press eBooks. 278. 255–288. 11 indexed citations
19.
Laue, Ernest D., Meenakshi Venkatesan, Helen R. Mott, et al.. (2000). Structure of Cdc42 bound to the GTPase binding domain of PAK.. Nature Structural Biology. 7(5). 384–388. 152 indexed citations
20.
Mott, Helen R., Paul C. Driscoll, Jonathan Boyd, et al.. (1992). Secondary structure of human interleukin 2 from 3D heteronuclear NMR experiments. Biochemistry. 31(33). 7741–7744. 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026