Mary K. Doherty

4.6k total citations
78 papers, 3.5k citations indexed

About

Mary K. Doherty is a scholar working on Molecular Biology, Ecology and Spectroscopy. According to data from OpenAlex, Mary K. Doherty has authored 78 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 22 papers in Ecology and 16 papers in Spectroscopy. Recurrent topics in Mary K. Doherty's work include Advanced Proteomics Techniques and Applications (16 papers), Microbial Community Ecology and Physiology (14 papers) and Metabolomics and Mass Spectrometry Studies (10 papers). Mary K. Doherty is often cited by papers focused on Advanced Proteomics Techniques and Applications (16 papers), Microbial Community Ecology and Physiology (14 papers) and Metabolomics and Mass Spectrometry Studies (10 papers). Mary K. Doherty collaborates with scholars based in United Kingdom, United States and Sweden. Mary K. Doherty's co-authors include Robert J. Beynon, Simon J. Gaskell, Julie M. Pratt, Phillip D. Whitfield, Michael J. Clague, Dean E. Hammond, Deborah M. Simpson, Gillian Reid, Stephen K. Chapman and C. C. Whitehead and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Mary K. Doherty

74 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mary K. Doherty United Kingdom 36 2.1k 778 581 415 363 78 3.5k
Yishai Levin Israel 36 2.3k 1.1× 644 0.8× 193 0.3× 263 0.6× 238 0.7× 107 4.0k
Joëlle Vinh France 34 2.6k 1.2× 318 0.4× 207 0.4× 383 0.9× 221 0.6× 112 4.2k
Stéphane D. Lemaire France 47 4.9k 2.3× 258 0.3× 246 0.4× 597 1.4× 340 0.9× 131 6.6k
Leopold L. Ilag Sweden 36 2.0k 1.0× 686 0.9× 479 0.8× 184 0.4× 309 0.9× 85 3.5k
Cees J. A. van Echteld Netherlands 31 2.1k 1.0× 177 0.2× 464 0.8× 232 0.6× 401 1.1× 89 4.5k
Dongmin Kang South Korea 32 2.3k 1.1× 279 0.4× 214 0.4× 628 1.5× 291 0.8× 101 4.2k
Jean‐Michel Camadro France 40 2.9k 1.4× 198 0.3× 176 0.3× 514 1.2× 132 0.4× 125 4.3k
Mark W. Duncan United States 46 2.6k 1.2× 1.5k 1.9× 164 0.3× 273 0.7× 876 2.4× 126 6.2k
Minoru Suzuki Japan 43 2.1k 1.0× 480 0.6× 148 0.3× 331 0.8× 596 1.6× 315 6.9k
Steven C. Hand United States 16 1.9k 0.9× 151 0.2× 652 1.1× 524 1.3× 379 1.0× 25 3.9k

Countries citing papers authored by Mary K. Doherty

Since Specialization
Citations

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

Fields of papers citing papers by Mary K. Doherty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary K. Doherty. 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 Mary K. Doherty. The network helps show where Mary K. Doherty may publish in the future.

Co-authorship network of co-authors of Mary K. Doherty

This figure shows the co-authorship network connecting the top 25 collaborators of Mary K. Doherty. A scholar is included among the top collaborators of Mary K. Doherty 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 Mary K. Doherty. Mary K. Doherty 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
3.
Hammond, Dean E., Sergio Rodríguez‐Cuenca, Mary K. Doherty, et al.. (2023). CBL/CAP Is Essential for Mitochondria Respiration Complex I Assembly and Bioenergetics Efficiency in Muscle Cells. International Journal of Molecular Sciences. 24(4). 3399–3399. 3 indexed citations
4.
5.
Al-Otaibi, Noha, et al.. (2021). Disaccahrides-Based Cryo-Formulant Effect on Modulating Phospho/Mitochondrial Lipids and Biological Profiles of Human Leukaemia Cells. Cellular Physiology and Biochemistry. 55(2). 206–221. 1 indexed citations
6.
Shaw, Andrew, et al.. (2020). A proteomic signature for CNS adaptations to the valence of environmental stimulation. Behavioural Brain Research. 383. 112515–112515. 3 indexed citations
7.
Doherty, Mary K., Pablo Balseiro, Sigurd O. Handeland, et al.. (2020). Plasma proteome profiling of freshwater and seawater life stages of rainbow trout (Oncorhynchus mykiss). PLoS ONE. 15(1). e0227003–e0227003. 15 indexed citations
8.
Carboni, Stefano, Sofia C. Franco, Mary K. Doherty, et al.. (2020). Lipidomics analysis of juveniles’ blue mussels (Mytilus edulis L. 1758), a key economic and ecological species. PLoS ONE. 15(2). e0223031–e0223031. 23 indexed citations
9.
Kurzawa‐Akanbi, Marzena, Long Xie, Dean Hallam, et al.. (2020). Complement modulation reverses pathology in Y402H-retinal pigment epithelium cell model of AMD by restoring lysosomal function. Stem Cells Translational Medicine.
11.
Geary, Bethany, Phillip Cash, Holger Husi, et al.. (2018). Acute stress alters the rates of degradation of cardiac muscle proteins. Journal of Proteomics. 191. 124–130. 5 indexed citations
12.
Doherty, Mary K., Philip Brownridge, Matthew A.G. Owen, et al.. (2012). A proteomics strategy for determining the synthesis and degradation rates of individual proteins in fish. Journal of Proteomics. 75(14). 4471–4477. 15 indexed citations
13.
Doherty, Mary K. & Phillip D. Whitfield. (2011). Proteomics moves from expression to turnover: update and future perspective. Expert Review of Proteomics. 8(3). 325–334. 21 indexed citations
14.
Lanucara, Francesco, Philip Brownridge, Iain S. Young, Phillip D. Whitfield, & Mary K. Doherty. (2010). Degradative proteomics and disease mechanisms. PROTEOMICS - CLINICAL APPLICATIONS. 4(2). 133–142. 1 indexed citations
15.
Doherty, Mary K., Robert J. Beynon, & Phillip D. Whitfield. (2008). Proteomics and naturally occurring animal diseases: Opportunities for animal and human medicine. PROTEOMICS - CLINICAL APPLICATIONS. 2(2). 135–141. 20 indexed citations
16.
McLean, Lynn, Iain S. Young, Mary K. Doherty, et al.. (2007). Global cooling: Cold acclimation and the expression of soluble proteins in carp skeletal muscle. PROTEOMICS. 7(15). 2667–2681. 40 indexed citations
17.
McCullough, John, Paula E. Row, Óscar Lorenzo, et al.. (2006). Activation of the Endosome-Associated Ubiquitin Isopeptidase AMSH by STAM, a Component of the Multivesicular Body-Sorting Machinery. Current Biology. 16(2). 160–165. 163 indexed citations
18.
Beynon, Robert J., Mary K. Doherty, Julie M. Pratt, & Simon J. Gaskell. (2005). Multiplexed absolute quantification in proteomics using artificial QCAT proteins of concatenated signature peptides. Nature Methods. 2(8). 587–589. 349 indexed citations
19.
Doherty, Mary K., et al.. (2005). Proteome dynamics in complex organisms: Using stable isotopes to monitor individual protein turnover rates. PROTEOMICS. 5(2). 522–533. 128 indexed citations
20.
Doherty, Mary K., et al.. (2004). 2004 SPRING MEETING OF THE WPSA UK BRANCH PAPERS. British Poultry Science. 45(sup1). S27–S28. 10 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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