Lachlan D. Rash

4.6k total citations
58 papers, 3.0k citations indexed

About

Lachlan D. Rash is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Lachlan D. Rash has authored 58 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 19 papers in Cellular and Molecular Neuroscience and 19 papers in Genetics. Recurrent topics in Lachlan D. Rash's work include Ion channel regulation and function (40 papers), Ion Transport and Channel Regulation (21 papers) and Nicotinic Acetylcholine Receptors Study (20 papers). Lachlan D. Rash is often cited by papers focused on Ion channel regulation and function (40 papers), Ion Transport and Channel Regulation (21 papers) and Nicotinic Acetylcholine Receptors Study (20 papers). Lachlan D. Rash collaborates with scholars based in Australia, Switzerland and France. Lachlan D. Rash's co-authors include Wayne C. Hodgson, Glenn F. King, Pierre Escoubas, Mehdi Mobli, Ben Cristofori‐Armstrong, Natalie J. Saez, Eivind A. B. Undheim, Michel Lazdunski, Sylvie Diochot and Paul F. Alewood and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Angewandte Chemie International Edition and Physiological Reviews.

In The Last Decade

Lachlan D. Rash

55 papers receiving 2.9k citations

Peers

Countries citing papers authored by Lachlan D. Rash

Since Specialization

Citations

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

Fields of papers citing papers by Lachlan D. Rash

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lachlan D. Rash. 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 Lachlan D. Rash. The network helps show where Lachlan D. Rash may publish in the future.

Co-authorship network of co-authors of Lachlan D. Rash

This figure shows the co-authorship network connecting the top 25 collaborators of Lachlan D. Rash. A scholar is included among the top collaborators of Lachlan D. Rash 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 Lachlan D. Rash. Lachlan D. Rash 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

#	Work	Indexed citations
1	Exaptation of an evolutionary constraint enables behavioural control over the composition of secreted venom in a giant centipede 2024 ·Nature Ecology & Evolution ·(unknown), Brett R. Hamilton, Samuel D. Robinson, Kathryn Green, (unknown), Darren L. Brown, Jennifer L. Stow, (unknown), Kjetil Lysne Voje, S. Sean Millard, Irina Vetter, Lachlan D. Rash, Eivind A. B. Undheim	1
2	The funnel-web spider venom derived single knot peptide Hc3a modulates acid-sensing ion channel 1a desensitisation 2024 ·Biochemical Pharmacology ·(unknown), (unknown), (unknown), Alison Obergrussberger, Nadine Becker, Richard J. Clark, K. Johan Rosengren, Lachlan D. Rash, Ben Cristofori‐Armstrong	1
3	Acid-sensing (proton-gated) ion channels (ASICs) in GtoPdb v.2023.1 2023 ·IUPHAR/BPS Guide to Pharmacology CITE ·Stephan Kellenberger, Lachlan D. Rash	0
4	The modulation of acid-sensing ion channel 1 by PcTx1 is pH-, subtype- and species-dependent: Importance of interactions at the channel subunit interface and potential for engineering selective analogues 2019 ·Biochemical Pharmacology ·Ben Cristofori‐Armstrong, Natalie J. Saez, Irène R. Chassagnon, Glenn F. King, Lachlan D. Rash	28
5	The tarantula toxin β/δ-TRTX-Pre1a highlights the importance of the S1-S2 voltage-sensor region for sodium channel subtype selectivity 2017 ·Scientific Reports ·Joshua S. Wingerd, (unknown), (unknown), (unknown), Yanni K.‐Y. Chin, Ben Cristofori‐Armstrong, Thomas Durek, John M. Gilchrist, Christopher W. Vaughan, Frank Bosmans, David J. Adams, Richard J. Lewis, Paul F. Alewood, Mehdi Mobli, MacDonald J. Christie, Lachlan D. Rash	15
6	Potent neuroprotection after stroke afforded by a double-knot spider-venom peptide that inhibits acid-sensing ion channel 1a 2017 ·Proceedings of the National Academy of Sciences ·Irène R. Chassagnon, Claudia A. McCarthy, Yanni K.‐Y. Chin, Sandy S. Pineda, Angelo Keramidas, Mehdi Mobli, Vi Pham, T. Michael De Silva, Joseph W. Lynch, Robert E. Widdop, Lachlan D. Rash, Glenn F. King	166
7	The Aromatic Head Group of Spider Toxin Polyamines Influences Toxicity to Cancer Cells 2017 ·Toxins ·David T. Wilson, Glen M. Boyle, (unknown), Matthew J. Nolan, Peter G. Parsons, Jennifer J. Smith, Leon Tribolet, Alex Loukas, Michael J. Liddell, Lachlan D. Rash, Norelle L. Daly	18
8	Discovery and molecular interaction studies of a highly stable, tarantula peptide modulator of acid-sensing ion channel 1 2017 ·Neuropharmacology ·(unknown), Ben Cristofori‐Armstrong, Pierre Escoubas, Lachlan D. Rash	27
9	Modulation of Ion Channels by Cysteine-Rich Peptides 2017 ·Advances in pharmacology ·Mehdi Mobli, Eivind A. B. Undheim, Lachlan D. Rash	18
10	The structure, dynamics and selectivity profile of a NaV1.7 potency-optimised huwentoxin-IV variant 2017 ·PLoS ONE ·(unknown), Jennifer R. Deuis, Fernanda C. Cardoso, (unknown), Richard J. Lewis, Lachlan D. Rash, Glenn F. King, Irina Vetter, Mehdi Mobli	36
11	Acid-Sensing Ion Channel Pharmacology, Past, Present, and Future … 2017 ·Advances in pharmacology ·Lachlan D. Rash	45
12	A Dynamic Pharmacophore Drives the Interaction between Psalmotoxin-1 and the Putative Drug Target Acid-Sensing Ion Channel 1a 2011 ·Molecular Pharmacology ·Natalie J. Saez, Mehdi Mobli, Michael Bieri, Irène R. Chassagnon, Alpeshkumar K. Malde, Roland Gamsjaeger, Alan E. Mark, Paul R. Gooley, Lachlan D. Rash, Glenn F. King	67
13	Inhibition of voltage‐gated Na⁺ currents in sensory neurones by the sea anemone toxin APETx2 2011 ·British Journal of Pharmacology ·Maxime G. Blanchard, Lachlan D. Rash, Stephan Kellenberger	66
14	Venomics: a new paradigm for natural products-based drug discovery 2010 ·Amino Acids ·Irina Vetter, (unknown), Lachlan D. Rash, Raveendra Anangi, Mehdi Mobli, Paul F. Alewood, Richard J. Lewis, Glenn F. King	160
15	De novo sequencing of peptides from the parotid secretion of the cane toad, Bufo marinus (Rhinella marina) 2010 ·Toxicon ·Lachlan D. Rash, Rodrigo A. V. Morales, (unknown), Paul F. Alewood	30
16	A new sea anemone peptide, APETx2, inhibits ASIC3, a major acid‐sensitive channel in sensory neurons 2004 ·The EMBO Journal ·Sylvie Diochot, Anne Baron, Lachlan D. Rash, Emmanuel Deval, Pierre Escoubas, Sabine Scarzello, Miguel Salinas, Michel Lazdunski	306
17	Pharmacology and biochemistry of spider venoms 2002 ·Toxicon ·Lachlan D. Rash, Wayne C. Hodgson	253
18	Neurotoxic activity of venom from the Australian Eastern mouse spider (Missulena bradleyi) involves modulation of sodium channel gating 2000 ·British Journal of Pharmacology ·Lachlan D. Rash, Liesl C. Birinyi-Strachan, Graham M. Nicholson, Wayne C. Hodgson	30
19	Sex differences in the pharmacological activity of venom from the white-tailed spider (Lampona cylindrata) 2000 ·Toxicon ·Lachlan D. Rash, Roger G. King, Wayne C. Hodgson	31
20	Evidence that histamine is the principal pharmacological component of venom from an Australian wolf spider (Lycosa godeffroyi) 1998 ·Toxicon ·Lachlan D. Rash, Roger G. King, Wayne C. Hodgson	28

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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