Thomas Macartney

6.3k total citations · 1 hit paper
76 papers, 4.3k citations indexed

About

Thomas Macartney is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Thomas Macartney has authored 76 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 23 papers in Cell Biology and 17 papers in Oncology. Recurrent topics in Thomas Macartney's work include Ubiquitin and proteasome pathways (26 papers), Protein Degradation and Inhibitors (15 papers) and DNA Repair Mechanisms (11 papers). Thomas Macartney is often cited by papers focused on Ubiquitin and proteasome pathways (26 papers), Protein Degradation and Inhibitors (15 papers) and DNA Repair Mechanisms (11 papers). Thomas Macartney collaborates with scholars based in United Kingdom, United States and Germany. Thomas Macartney's co-authors include Dario R. Alessi, Gopal P. Sapkota, David G. Campbell, John Rouse, Axel Knebel, Robert Gourlay, Mária Deák, Miratul M. K. Muqit, Helen I. Woodroof and Agne Kazlauskaite and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Thomas Macartney

74 papers receiving 4.3k citations

Hit Papers

align trajectories sort by overperformance

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.

PINK1 is activated by mitochondrial membrane potential depolarization and stimulates Parkin E3 ligase activity by phosphorylating Serine 65

2012 726 citations Chandana Kondapalli, Helen I. Woodroof et al. Open Biology profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Thomas Macartney	3.3k	847	843	825	609	76	4.3k
Gerald Marsischky	3.4k 1.0×	723 0.9×	429 0.5×	687 0.8×	857 1.4×	14	4.7k
Alban Ordureau	3.5k 1.1×	1.1k 1.3×	2.4k 2.8×	955 1.2×	460 0.8×	51	5.4k
Robert Gourlay	2.2k 0.7×	663 0.8×	1.1k 1.4×	571 0.7×	241 0.4×	40	3.3k
Charlotte Hubbert	3.5k 1.1×	274 0.3×	698 0.8×	791 1.0×	776 1.3×	8	4.2k
Lilian Phu	2.8k 0.9×	255 0.3×	930 1.1×	647 0.8×	625 1.0×	34	3.5k
Masayuki Komada	3.0k 0.9×	183 0.2×	498 0.6×	1.3k 1.6×	750 1.2×	80	4.8k
Yoshiharu Kawaguchi	3.2k 1.0×	243 0.3×	545 0.6×	713 0.9×	876 1.4×	17	4.2k
Shun-ichiro Iemura	3.4k 1.0×	198 0.2×	2.4k 2.8×	1.2k 1.4×	492 0.8×	28	5.3k
Christiane Susini	1.7k 0.5×	949 1.1×	2.1k 2.5×	257 0.3×	1.4k 2.3×	87	4.1k
Dominique Lallemand	2.0k 0.6×	456 0.5×	235 0.3×	775 0.9×	562 0.9×	28	3.1k

Countries citing papers authored by Thomas Macartney

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Macartney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Macartney

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Macartney. A scholar is included among the top collaborators of Thomas Macartney 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 Thomas Macartney. Thomas Macartney 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

Meijer, Hedda A., Sara Johnson, Richard P. Gallagher, et al.. (2025). NOTCH1 S2513 is critical for the regulation of NICD levels impacting the segmentation clock in hiPSC-derived PSM cells and somitoids. Genes & Development. 39(17-18). 1025–1044.

Singh, Pawan, Shalini Agarwal, Léa P. Wilhelm, et al.. (2025). Kinome screening identifies integrated stress response kinase EIF2AK1/HRI as a negative regulator of PINK1 mitophagy signaling. Science Advances. 11(19). eadn2528–eadn2528. 1 indexed citations

Dite, Toby A., Paweł Lis, Sandra Bell, et al.. (2025). NRBP1 pseudokinase binds to and activates the WNK pathway in response to osmotic stress. Science Advances. 11(29). eadv4636–eadv4636.

Weiland, Florian, Sylvie M. Noordermeer, Thomas Carroll, et al.. (2024). Chemo-Phosphoproteomic Profiling with ATR Inhibitors Berzosertib and Gartisertib Uncovers New Biomarkers and DNA Damage Response Regulators. Molecular & Cellular Proteomics. 23(8). 100802–100802. 2 indexed citations

Peter, Joshua, David Millrine, Joby Varghese, et al.. (2024). The UFM1 E3 ligase recognizes and releases 60S ribosomes from ER translocons. Nature. 627(8003). 437–444. 23 indexed citations

Raimi, Olawale G., Andrew M. Shaw, James R. Ault, et al.. (2022). Mapping of a N-terminal α-helix domain required for human PINK1 stabilization, Serine228 autophosphorylation and activation in cells. Open Biology. 12(1). 210264–210264. 20 indexed citations

Bustos, Francisco, Houjiang Zhou, Feng Wang, et al.. (2022). An RNF12-USP26 amplification loop drives germ cell specification and is disrupted by disease-associated mutations. Science Signaling. 15(742). eabm5995–eabm5995. 6 indexed citations

Macartney, Thomas, et al.. (2021). Reconstitution of human CMG helicase ubiquitylation by CUL2LRR1 and multiple E2 enzymes. Biochemical Journal. 478(14). 2825–2842. 7 indexed citations

Bond, Adam G., Conner Craigon, Kwok-Ho Chan, et al.. (2021). Development of BromoTag: A “Bump-and-Hole”–PROTAC System to Induce Potent, Rapid, and Selective Degradation of Tagged Target Proteins. Journal of Medicinal Chemistry. 64(20). 15477–15502. 63 indexed citations

10.

Dunbar, Karen J., Thomas Macartney, & Gopal P. Sapkota. (2020). IMiDs induce FAM83F degradation via an interaction with CK1α to attenuate Wnt signalling. Life Science Alliance. 4(2). e202000804–e202000804. 6 indexed citations

11.

Dunbar, Karen J., Rebecca A. Jones, Kevin S. Dingwell, et al.. (2020). FAM83F regulates canonical Wnt signalling through an interaction with CK1α. Life Science Alliance. 4(2). e202000805–e202000805. 10 indexed citations

12.

Fulcher, Luke J., Lin Mei, Thomas Macartney, et al.. (2019). FAM 83D directs protein kinase CK 1α to the mitotic spindle for proper spindle positioning. EMBO Reports. 20(9). e47495–e47495. 38 indexed citations

13.

Malik, Nazma, Raja Sekhar Nirujogi, Julien Peltier, et al.. (2019). Phosphoproteomics reveals that the hVPS34 regulated SGK3 kinase specifically phosphorylates endosomal proteins including Syntaxin-7, Syntaxin-12, RFIP4 and WDR44. Biochemical Journal. 476(20). 3081–3107. 13 indexed citations

14.

Lis, Paweł, Wondwossen M Yeshaw, Paulina S. Wawro, et al.. (2019). PPM1H phosphatase counteracts LRRK2 signaling by selectively dephosphorylating Rab proteins. eLife. 8. 80 indexed citations

15.

Cummins, Timothy D., Kevin Z. L. Wu, Polyxeni Bozatzi, et al.. (2018). PAWS1 controls cytoskeletal dynamics and cell migration through association with the SH3 adaptor CD2AP. Journal of Cell Science. 131(1). 49 indexed citations

16.

Fulcher, Luke J., Polyxeni Bozatzi, Kevin Z. L. Wu, et al.. (2018). The DUF1669 domain of FAM83 family proteins anchor casein kinase 1 isoforms. Science Signaling. 11(531). 87 indexed citations

17.

Muñoz, Iván, Michael Morgan, Julien Peltier, et al.. (2018). Phosphoproteomic screening identifies physiological substrates of the CDKL 5 kinase. The EMBO Journal. 37(24). 53 indexed citations

18.

Strickson, Sam, Christoph H. Emmerich, Eddy T. H. Goh, et al.. (2017). Roles of the TRAF6 and Pellino E3 ligases in MyD88 and RANKL signaling. Proceedings of the National Academy of Sciences. 114(17). E3481–E3489. 88 indexed citations

19.

Lai, Yu‐Chiang, Chandana Kondapalli, James B Procter, et al.. (2015). Phosphoproteomic screening identifies Rab GTP ases as novel downstream targets of PINK 1. The EMBO Journal. 34(22). 2840–2861. 135 indexed citations

20.

Zhang, Ning, Maximilian Fritsch, David G. Campbell, et al.. (2015). Phosphorylation of Synaptic Vesicle Protein 2A at Thr84 by Casein Kinase 1 Family Kinases Controls the Specific Retrieval of Synaptotagmin-1. Journal of Neuroscience. 35(6). 2492–2507. 61 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