Renae M. Ryan

3.2k total citations
56 papers, 2.4k citations indexed

About

Renae M. Ryan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Biochemistry. According to data from OpenAlex, Renae M. Ryan has authored 56 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 34 papers in Cellular and Molecular Neuroscience and 27 papers in Biochemistry. Recurrent topics in Renae M. Ryan's work include Neuroscience and Neuropharmacology Research (34 papers), Amino Acid Enzymes and Metabolism (27 papers) and Ion channel regulation and function (16 papers). Renae M. Ryan is often cited by papers focused on Neuroscience and Neuropharmacology Research (34 papers), Amino Acid Enzymes and Metabolism (27 papers) and Ion channel regulation and function (16 papers). Renae M. Ryan collaborates with scholars based in Australia, United States and Canada. Renae M. Ryan's co-authors include Robert J. Vandenberg, Olga Boudker, Dinesh Yernool, Keiko Shimamoto, Eric Gouaux, Joseph A. Mindell, Josep Font, Jane E. Carland, Ann D. Mitrovic and MacDonald J. Christie and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Renae M. Ryan

54 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Renae M. Ryan Australia 28 1.6k 1.2k 808 437 283 56 2.4k
Christof Grewer United States 33 1.7k 1.1× 1.5k 1.2× 912 1.1× 582 1.3× 221 0.8× 76 2.8k
Noa Zerangue United States 19 2.5k 1.6× 1.7k 1.4× 612 0.8× 398 0.9× 612 2.2× 21 4.4k
Christoph Fahlke Germany 42 3.4k 2.2× 2.5k 2.0× 347 0.4× 360 0.8× 142 0.5× 117 4.7k
Sela Mager United States 19 1.3k 0.8× 1.1k 0.9× 498 0.6× 146 0.3× 162 0.6× 25 2.0k
Sreekala Mandiyan United States 17 1.2k 0.8× 1.1k 0.9× 441 0.5× 153 0.4× 150 0.5× 23 2.1k
Naoko Utsunomiya‐Tate Japan 16 748 0.5× 334 0.3× 512 0.6× 130 0.3× 492 1.7× 43 1.7k
Shigeki Furuya Japan 30 2.0k 1.3× 837 0.7× 880 1.1× 67 0.2× 106 0.4× 95 3.1k
Tetsufumi Ueda United States 35 2.8k 1.8× 2.5k 2.0× 303 0.4× 276 0.6× 75 0.3× 79 4.1k
William F. Hood United States 28 1.4k 0.9× 1.1k 0.9× 265 0.3× 154 0.4× 148 0.5× 58 2.6k
Hiro Furukawa United States 32 2.4k 1.5× 2.4k 2.0× 187 0.2× 302 0.7× 159 0.6× 86 4.5k

Countries citing papers authored by Renae M. Ryan

Since Specialization
Citations

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

Fields of papers citing papers by Renae M. Ryan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Renae M. Ryan. 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 Renae M. Ryan. The network helps show where Renae M. Ryan may publish in the future.

Co-authorship network of co-authors of Renae M. Ryan

This figure shows the co-authorship network connecting the top 25 collaborators of Renae M. Ryan. A scholar is included among the top collaborators of Renae M. Ryan 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 Renae M. Ryan. Renae M. Ryan 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.
Font, Josep, et al.. (2024). An elastic siderophore synthetase and rubbery substrates assemble multimeric linear and macrocyclic hydroxamic acid metal chelators. Chemical Science. 16(5). 2180–2190. 2 indexed citations
2.
Zeng, Yi C., Meghna Sobti, Nicola J. Smith, et al.. (2023). Structural basis of promiscuous substrate transport by Organic Cation Transporter 1. Nature Communications. 14(1). 6374–6374. 36 indexed citations
3.
Ryan, Renae M., et al.. (2022). Characterizing unexpected interactions of a glutamine transporter inhibitor with members of the SLC1A transporter family. Journal of Biological Chemistry. 298(8). 102178–102178. 8 indexed citations
4.
5.
Aguilar, Jenny I., Mary Hongying Cheng, Josep Font, et al.. (2021). Psychomotor impairments and therapeutic implications revealed by a mutation associated with infantile Parkinsonism-Dystonia. eLife. 10. 15 indexed citations
6.
Pant, Shashank, Rosemary J. Cater, Meghna Sobti, et al.. (2021). Glutamate transporters have a chloride channel with two hydrophobic gates. Nature. 591(7849). 327–331. 48 indexed citations
7.
Holst, Jeff, et al.. (2020). Amino Acid Transporters and Exchangers from the SLC1A Family: Structure, Mechanism and Roles in Physiology and Cancer. Neurochemical Research. 45(6). 1268–1286. 45 indexed citations
8.
Geldermalsen, Michelle van, Lake‐Ee Quek, Nigel Turner, et al.. (2018). Benzylserine inhibits breast cancer cell growth by disrupting intracellular amino acid homeostasis and triggering amino acid response pathways. BMC Cancer. 18(1). 689–689. 56 indexed citations
9.
Font, Josep, et al.. (2017). Structural characterisation reveals insights into substrate recognition by the glutamine transporter ASCT2/SLC1A5. Nature Communications. 9(1). 38–38. 62 indexed citations
10.
Vandenberg, Robert J., et al.. (2015). Glycine transporter2 inhibitors: Getting the balance right. Neurochemistry International. 98. 89–93. 17 indexed citations
11.
Vandenberg, Robert J., et al.. (2015). Transport Rates of a Glutamate Transporter Homologue Are Influenced by the Lipid Bilayer. Journal of Biological Chemistry. 290(15). 9780–9788. 26 indexed citations
12.
Heinzelmann, Germano, et al.. (2014). Na+ Interactions with the Neutral Amino Acid Transporter ASCT1. Journal of Biological Chemistry. 289(25). 17468–17479. 22 indexed citations
13.
Cater, Rosemary J., Robert J. Vandenberg, & Renae M. Ryan. (2014). The Domain Interface of the Human Glutamate Transporter EAAT1 Mediates Chloride Permeation. Biophysical Journal. 107(3). 621–629. 32 indexed citations
14.
Bailey, Charles G., Renae M. Ryan, Annora Thoeng, et al.. (2010). Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria. Journal of Clinical Investigation. 121(1). 446–453. 105 indexed citations
15.
Vandenberg, Robert J., Shiwei Huang, & Renae M. Ryan. (2008). Slips, leaks and channels in glutamate transporters. Channels. 2(1). 51–58. 28 indexed citations
16.
Huang, Shiwei, Renae M. Ryan, & Robert J. Vandenberg. (2008). The Role of Cation Binding in Determining Substrate Selectivity of Glutamate Transporters. Journal of Biological Chemistry. 284(7). 4510–4515. 17 indexed citations
17.
Ryan, Renae M. & Joseph A. Mindell. (2007). The uncoupled chloride conductance of a bacterial glutamate transporter homolog. Nature Structural & Molecular Biology. 14(5). 365–371. 88 indexed citations
18.
Boudker, Olga, Renae M. Ryan, Dinesh Yernool, Keiko Shimamoto, & Eric Gouaux. (2007). Coupling substrate and ion binding to extracellular gate of a sodium-dependent aspartate transporter. Nature. 445(7126). 387–393. 392 indexed citations
19.
Ryan, Renae M., Ann D. Mitrovic, & Robert J. Vandenberg. (2004). The Chloride Permeation Pathway of a Glutamate Transporter and Its Proximity to the Glutamate Translocation Pathway. Journal of Biological Chemistry. 279(20). 20742–20751. 100 indexed citations
20.
Ryan, Renae M. & Robert J. Vandenberg. (2002). Distinct Conformational States Mediate the Transport and Anion Channel Properties of the Glutamate Transporter EAAT-1. Journal of Biological Chemistry. 277(16). 13494–13500. 63 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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