Peter T. Northcote

5.3k total citations · 1 hit paper
67 papers, 4.1k citations indexed

About

Peter T. Northcote is a scholar working on Molecular Biology, Organic Chemistry and Oncology. According to data from OpenAlex, Peter T. Northcote has authored 67 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 26 papers in Organic Chemistry and 25 papers in Oncology. Recurrent topics in Peter T. Northcote's work include Marine Sponges and Natural Products (23 papers), Cancer Treatment and Pharmacology (22 papers) and Microtubule and mitosis dynamics (20 papers). Peter T. Northcote is often cited by papers focused on Marine Sponges and Natural Products (23 papers), Cancer Treatment and Pharmacology (22 papers) and Microtubule and mitosis dynamics (20 papers). Peter T. Northcote collaborates with scholars based in New Zealand, United States and Spain. Peter T. Northcote's co-authors include John W. Blunt, Murray H. G. Munro, John H. Miller, Brent R. Copp, Michèle R. Prinsep, Lyndon M. West, Chris Battershill, J. Fernando Dı́az, Jerry Pelletier and Wan‐Ping Hu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Peter T. Northcote

66 papers receiving 4.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Marine natural products

2010 386 citations John W. Blunt, Brent R. Copp et al. Natural Product Reports profile →

Peers

Peter T. Northcote

BIOTE

PHARM

Carmen Cuevas Spain

Susumu Ikegami Japan

Bradley S. Davidson United States

Zhengchao Tu China

Mary Kay Harper United States

James J. La Clair United States

Pascal Verdier‐Pinard United States

Michael H.G. Kubbutat Germany

Andrew J. Phillips United States

Isabel Barasoaı́n Spain

Carmen Cuevas Spain

Peter T. Northcote

1.8k ×1.0

1.4k ×0.9

BIOTE

2.3k ×1.9

1.4k ×1.3

PHARM

162 ×0.2

Citations per year, relative to Peter T. Northcote Peter T. Northcote (= 1×) peers Carmen Cuevas

Countries citing papers authored by Peter T. Northcote

Since Specialization

Citations

This map shows the geographic impact of Peter T. Northcote'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 Peter T. Northcote with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter T. Northcote more than expected).

Fields of papers citing papers by Peter T. Northcote

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter T. Northcote. 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 Peter T. Northcote. The network helps show where Peter T. Northcote may publish in the future.

Co-authorship network of co-authors of Peter T. Northcote

This figure shows the co-authorship network connecting the top 25 collaborators of Peter T. Northcote. A scholar is included among the top collaborators of Peter T. Northcote 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 Peter T. Northcote. Peter T. Northcote is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Watson, P. R., Paul Teesdale‐Spittle, Peter T. Northcote, et al.. (2025). Potent inhibition of human monoamine oxidase A and B by phenolic compounds and polyunsaturated fatty acids in tobacco smoke. Chemico-Biological Interactions. 413. 111477–111477.

Hull, Kenneth G., Regina Cencic, Mingzhao Zhu, et al.. (2021). Functional mimicry revealed by the crystal structure of an eIF4A:RNA complex bound to the interfacial inhibitor, desmethyl pateamine A. Cell chemical biology. 28(6). 825–834.e6. 26 indexed citations

Paterson, Ian, et al.. (2017). Induction of accelerated senescence by the microtubule-stabilizing agent peloruside A. Investigational New Drugs. 35(6). 706–717. 10 indexed citations

Singh, A. Jonathan, et al.. (2016). Peloruside A, a microtubule-stabilizing agent, induces aneuploidy in ovarian cancer cells. Investigational New Drugs. 34(4). 424–438. 2 indexed citations

González-Almela, Esther, Miguel Ángel Sanz, Manuel García-Moreno, et al.. (2015). Differential action of pateamine A on translation of genomic and subgenomic mRNAs from Sindbis virus. Virology. 484. 41–50. 18 indexed citations

Hanna, Reem, David R. Maass, Paul H. Atkinson, et al.. (2013). Characterizing the laulimalide–peloruside binding site using site-directed mutagenesis of TUB2 in S. cerevisiae. Molecular BioSystems. 10(1). 110–116. 2 indexed citations

Field, Jessica J., Benet Pera, Enrique Calvo, et al.. (2012). Zampanolide, a Potent New Microtubule-Stabilizing Agent, Covalently Reacts with the Taxane Luminal Site in Tubulin α,β-Heterodimers and Microtubules. Chemistry & Biology. 19(6). 686–698. 75 indexed citations

Kanakkanthara, Arun, Pisana Rawson, Peter T. Northcote, & John H. Miller. (2012). Acquired Resistance to Peloruside A and Laulimalide is Associated with Downregulation of Vimentin in Human Ovarian Carcinoma Cells. Pharmaceutical Research. 29(11). 3022–3032. 15 indexed citations

Kanakkanthara, Arun, Anja Wilmes, Aurora O’Brate, et al.. (2011). Peloruside- and Laulimalide-Resistant Human Ovarian Carcinoma Cells Have βI-Tubulin Mutations and Altered Expression of βII- and βIII-Tubulin Isotypes. Molecular Cancer Therapeutics. 10(8). 1419–1429. 33 indexed citations

10.

Blunt, John W., Brent R. Copp, Murray H. G. Munro, Peter T. Northcote, & Michèle R. Prinsep. (2010). Marine natural products. Natural Product Reports. 28(2). 196–268. 386 indexed citations breakdown →

11.

Pera, Benet, Mina Razzak, Chiara Trigili, et al.. (2010). Molecular Recognition of Peloruside A by Microtubules. The C24 Primary Alcohol is Essential for Biological Activity. ChemBioChem. 11(12). 1669–1678. 22 indexed citations

12.

Blunt, John W., Brent R. Copp, Murray H. G. Munro, Peter T. Northcote, & Michèle R. Prinsep. (2010). Marine natural products. Natural Product Reports. 27(2). 165–165. 319 indexed citations

13.

Wilmes, Anja, David O’Sullivan, Ian Paterson, et al.. (2010). Synergistic interactions between peloruside A and other microtubule-stabilizing and destabilizing agents in cultured human ovarian carcinoma cells and murine T cells. Cancer Chemotherapy and Pharmacology. 68(1). 117–126. 27 indexed citations

14.

Wilmes, Anja, Pisana Rawson, Lifeng Peng, et al.. (2010). Effects of the microtubule stabilizing agent peloruside A on the proteome of HL-60 cells. Investigational New Drugs. 29(4). 544–553. 8 indexed citations

15.

Andreae, Peter, et al.. (2010). Peloruside A inhibits microtubule dynamics in a breast cancer cell line MCF7. Investigational New Drugs. 29(4). 615–626. 19 indexed citations

16.

Blunt, John W., et al.. (2007). Marine natural products. Natural Product Reports. 24(1). 31–31. 334 indexed citations

17.

Mazrouï, Rachid, Rami Sukarieh, Randal J. Kaufman, et al.. (2006). Inhibition of Ribosome Recruitment Induces Stress Granule Formation Independently of Eukaryotic Initiation Factor 2α Phosphorylation. Molecular Biology of the Cell. 17(10). 4212–4219. 269 indexed citations

18.

Matthews, James, Lisa Lindqvist, Olivia Novac, et al.. (2005). Stimulation of mammalian translation initiation factor eIF4A activity by a small molecule inhibitor of eukaryotic translation. Proceedings of the National Academy of Sciences. 102(30). 10460–10465. 180 indexed citations

19.

Page, Michael J., Lyndon M. West, Peter T. Northcote, Christopher N. Battershill, & Michelle Kelly. (2005). Spatial and Temporal Variability of Cytotoxic Metabolites in Populations of the New Zealand Sponge Mycale hentscheli. Journal of Chemical Ecology. 31(5). 1161–1174. 79 indexed citations

20.

Miller, John H., Thomas N. Gaitanos, Kylie Hood, et al.. (2004). Peloruside A enhances apoptosis in H-ras-transformed cells and is cytotoxic to proliferating T cells. APOPTOSIS. 9(6). 785–796. 33 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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