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, Helen I. Woodroof, Miratul M. K. Muqit 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

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 →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	NOTCH1 S2513 is critical for the regulation of NICD levels impacting the segmentation clock in hiPSC-derived PSM cells and somitoids 2025 ·Genes & Development ·Hedda A. Meijer, (unknown), Sara Johnson, Richard P. Gallagher, (unknown), (unknown), (unknown), (unknown), (unknown), Thomas Macartney, L. S. P. Davidson, David I. K. Martin, Marek Gierliński, Paul Davies, Katharina F. Sonnen, Philip J. Murray, J. Kim Dale	0
2	Kinome screening identifies integrated stress response kinase EIF2AK1/HRI as a negative regulator of PINK1 mitophagy signaling 2025 ·Science Advances ·Pawan Singh, Shalini Agarwal, (unknown), Léa P. Wilhelm, (unknown), (unknown), Thomas Macartney, Rachel Toth, Adrien Rousseau, Glenn R. Masson, Ian G. Ganley, Miratul M. K. Muqit	1
3	NRBP1 pseudokinase binds to and activates the WNK pathway in response to osmotic stress 2025 ·Science Advances ·(unknown), Toby A. Dite, Paweł Lis, Sandra Bell, Fiona Brown, Clare Johnson, (unknown), Samantha Raggett, Mark Dorward, (unknown), Thomas Macartney, Renata F. Soares, Frédéric Lamoliatte, Dario R. Alessi	0
4	Chemo-Phosphoproteomic Profiling with ATR Inhibitors Berzosertib and Gartisertib Uncovers New Biomarkers and DNA Damage Response Regulators 2024 ·Molecular & Cellular Proteomics ·(unknown), Florian Weiland, Sylvie M. Noordermeer, Thomas Carroll, Yuandi Gao, Jianming Wang, Houjiang Zhou, Frédéric Lamoliatte, Rachel Toth, Thomas Macartney, Fiona Brown, C. James Hastie, Constance Alabert, Haico van Attikum, Frank T. Zenke, (unknown), John Rouse	2
5	The UFM1 E3 ligase recognizes and releases 60S ribosomes from ER translocons 2024 ·Nature ·(unknown), Joshua Peter, (unknown), (unknown), David Millrine, (unknown), (unknown), Joby Varghese, Frédéric Lamoliatte, (unknown), Thomas Macartney, Antonio N. Calabrese, Elton Zeqiraj, Yogesh Kulathu	23
6	A novel FAM83G variant from palmoplantar keratoderma patient disrupts WNT signalling via loss of FAM83G-CK1α interaction 2024 ·Open Biology ·(unknown), Marta Codina‐Solà, Mar Xunclà, (unknown), Elena García‐Arumí, Eduardo F. Tizzano, Nicola T. Wood, Thomas Macartney, (unknown), Gopal P. Sapkota	2
7	Mapping of a N-terminal α-helix domain required for human PINK1 stabilization, Serine228 autophosphorylation and activation in cells 2022 ·Open Biology ·(unknown), (unknown), Olawale G. Raimi, Andrew M. Shaw, (unknown), James R. Ault, Sophie Burel, Kathrin Brockmann, Atul Kumar, (unknown), E. Krysztofinska, Thomas Macartney, Richard Bayliss, Julia C. Fitzgerald, Miratul M. K. Muqit	20
8	An RNF12-USP26 amplification loop drives germ cell specification and is disrupted by disease-associated mutations 2022 ·Science Signaling ·(unknown), (unknown), Francisco Bustos, Houjiang Zhou, Feng Wang, Rachel Toth, Thomas Macartney, Ingolf Bach, Gino Nardocci, Greg M. Findlay	6
9	Development of BromoTag: A “Bump-and-Hole”–PROTAC System to Induce Potent, Rapid, and Selective Degradation of Tagged Target Proteins 2021 ·Journal of Medicinal Chemistry ·Adam G. Bond, Conner Craigon, Kwok-Ho Chan, Andrea Testa, Athanasios Karapetsas, (unknown), Thomas Macartney, J. Julian Blow, Dario R. Alessi, Alessio Ciulli	63
10	Reconstitution of human CMG helicase ubiquitylation by CUL2LRR1 and multiple E2 enzymes 2021 ·Biochemical Journal ·(unknown), (unknown), (unknown), Thomas Macartney, Karim Labib	7
11	IMiDs induce FAM83F degradation via an interaction with CK1α to attenuate Wnt signalling 2020 ·Life Science Alliance ·Karen J. Dunbar, Thomas Macartney, Gopal P. Sapkota	6
12	FAM83F regulates canonical Wnt signalling through an interaction with CK1α 2020 ·Life Science Alliance ·Karen J. Dunbar, Rebecca A. Jones, Kevin S. Dingwell, Thomas Macartney, James C. Smith, Gopal P. Sapkota	10
13	FAM 83D directs protein kinase CK 1α to the mitotic spindle for proper spindle positioning 2019 ·EMBO Reports ·Luke J. Fulcher, (unknown), Lin Mei, Thomas Macartney, Nicola T. Wood, Alan R. Prescott, (unknown), Joby Varghese, Robert Gourlay, Graeme Ball, Rosemary G. Clarke, David G. Campbell, Christopher A. Maxwell, Gopal P. Sapkota	38
14	Phosphoproteomics reveals that the hVPS34 regulated SGK3 kinase specifically phosphorylates endosomal proteins including Syntaxin-7, Syntaxin-12, RFIP4 and WDR44 2019 ·Biochemical Journal ·Nazma Malik, Raja Sekhar Nirujogi, Julien Peltier, Thomas Macartney, Melanie Wightman, Alan R. Prescott, Robert Gourlay, Matthias Trost, Dario R. Alessi, Athanasios Karapetsas	13
15	PPM1H phosphatase counteracts LRRK2 signaling by selectively dephosphorylating Rab proteins 2019 ·eLife ·(unknown), Paweł Lis, Wondwossen M Yeshaw, Paulina S. Wawro, Raja Sekhar Nirujogi, Melanie Wightman, Thomas Macartney, Mark Dorward, Axel Knebel, Francesca Tonelli, Suzanne R. Pfeffer, Dario R. Alessi	80
16	PAWS1 controls cytoskeletal dynamics and cell migration through association with the SH3 adaptor CD2AP 2018 ·Journal of Cell Science ·Timothy D. Cummins, Kevin Z. L. Wu, Polyxeni Bozatzi, Kevin S. Dingwell, Thomas Macartney, Nicola T. Wood, Joby Varghese, Robert Gourlay, David G. Campbell, Alan R. Prescott, Eric R. Griffis, James C. Smith, Gopal P. Sapkota	49
17	The DUF1669 domain of FAM83 family proteins anchor casein kinase 1 isoforms 2018 ·Science Signaling ·Luke J. Fulcher, Polyxeni Bozatzi, (unknown), Kevin Z. L. Wu, Timothy D. Cummins, Joshua C. Bufton, Daniel M. Pinkas, Karen J. Dunbar, (unknown), Nicola T. Wood, Simone Weidlich, Thomas Macartney, Joby Varghese, Robert Gourlay, David G. Campbell, Kevin S. Dingwell, James C. Smith, Alex N. Bullock, Gopal P. Sapkota	87
18	Roles of the TRAF6 and Pellino E3 ligases in MyD88 and RANKL signaling 2017 ·Proceedings of the National Academy of Sciences ·Sam Strickson, Christoph H. Emmerich, Eddy T. H. Goh, Jiazhen Zhang, Ian R. Kelsall, Thomas Macartney, C. James Hastie, Axel Knebel, Mark Peggie, Francesco Marchesi, J. Simon C. Arthur, Philip Cohen	88
19	Phosphoproteomic screening identifies Rab GTP ases as novel downstream targets of PINK 1 2015 ·The EMBO Journal ·Yu‐Chiang Lai, Chandana Kondapalli, (unknown), James B Procter, Brian D. Dill, Helen I. Woodroof, Robert Gourlay, Mark Peggie, Thomas Macartney, Olga Corti, Jean‐Christophe Corvol, David G. Campbell, Aymelt Itzen, Matthias Trost, Miratul M. K. Muqit	135
20	Phosphorylation of Synaptic Vesicle Protein 2A at Thr84 by Casein Kinase 1 Family Kinases Controls the Specific Retrieval of Synaptotagmin-1 2015 ·Journal of Neuroscience ·Ning Zhang, (unknown), Maximilian Fritsch, (unknown), David G. Campbell, Robert Gourlay, Srikannathasan Velupillai, Thomas Macartney, Mark Peggie, Daan M. F. van Aalten, Michael A. Cousin, Dario R. Alessi	61

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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