Douglas Strathdee

4.2k total citations
40 papers, 1.6k citations indexed

About

Douglas Strathdee is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Douglas Strathdee has authored 40 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 9 papers in Cell Biology and 6 papers in Oncology. Recurrent topics in Douglas Strathdee's work include Mitochondrial Function and Pathology (9 papers), Cellular Mechanics and Interactions (5 papers) and CRISPR and Genetic Engineering (5 papers). Douglas Strathdee is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Cellular Mechanics and Interactions (5 papers) and CRISPR and Genetic Engineering (5 papers). Douglas Strathdee collaborates with scholars based in United Kingdom, United States and Canada. Douglas Strathdee's co-authors include Karen Blyth, David Stevenson, Colin Nixon, Owen J. Sansom, Sheila Bryson, Karen H. Vousden, Ken Brown, Noboru H. Komiyama, Seth G. N. Grant and Dimitris Athineos and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Douglas Strathdee

37 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Douglas Strathdee United Kingdom 18 1.0k 342 297 275 221 40 1.6k
Yufang Zheng China 24 989 1.0× 180 0.5× 289 1.0× 156 0.6× 239 1.1× 64 1.7k
Pengcheng Zhou China 19 1.0k 1.0× 198 0.6× 316 1.1× 343 1.2× 139 0.6× 34 1.6k
Maria V. Barbolina United States 23 847 0.8× 323 0.9× 495 1.7× 253 0.9× 189 0.9× 38 1.6k
Daniel J. Knauer United States 22 847 0.8× 441 1.3× 259 0.9× 224 0.8× 292 1.3× 51 1.8k
Julia Billiard United States 17 1.1k 1.1× 332 1.0× 304 1.0× 134 0.5× 120 0.5× 26 1.6k
Chris Shelley United States 22 953 0.9× 403 1.2× 266 0.9× 148 0.5× 281 1.3× 39 1.7k
Ralf Schwanbeck Germany 21 1.1k 1.1× 188 0.5× 231 0.8× 130 0.5× 106 0.5× 34 1.5k
John E. Landers United States 33 1.5k 1.5× 131 0.4× 409 1.4× 313 1.1× 285 1.3× 53 2.6k
Giuseppe Lamorte Italy 22 1.5k 1.5× 441 1.3× 804 2.7× 226 0.8× 262 1.2× 44 2.5k
Yoshihisa Sakai United States 16 1.2k 1.2× 216 0.6× 287 1.0× 149 0.5× 297 1.3× 37 1.8k

Countries citing papers authored by Douglas Strathdee

Since Specialization
Citations

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

Fields of papers citing papers by Douglas Strathdee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Douglas Strathdee

This figure shows the co-authorship network connecting the top 25 collaborators of Douglas Strathdee. A scholar is included among the top collaborators of Douglas Strathdee 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 Douglas Strathdee. Douglas Strathdee 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
1.
Najumudeen, Arafath K., Sigrid K. Fey, Catriona A. Ford, et al.. (2024). KRAS allelic imbalance drives tumour initiation yet suppresses metastasis in colorectal cancer in vivo. Nature Communications. 15(1). 100–100. 8 indexed citations
2.
Wang, Suya, Haiyan Wu, Xu Yang, et al.. (2023). Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome. Human Molecular Genetics. 32(12). 2055–2067. 10 indexed citations
3.
Screen, Michael, Louise S. Matheson, Andrew J.M. Howden, et al.. (2023). RNA helicase EIF4A1-mediated translation is essential for the GC response. Life Science Alliance. 7(2). e202302301–e202302301. 3 indexed citations
4.
Liu, Ming, et al.. (2023). Phenotypic Characterization of Female Carrier Mice Heterozygous for Tafazzin Deletion. Biology. 12(9). 1238–1238. 1 indexed citations
5.
Hennequart, Marc, Steven E. Pilley, Christiaan F. Labuschagne, et al.. (2023). ALDH1L2 regulation of formate, formyl-methionine, and ROS controls cancer cell migration and metastasis. Cell Reports. 42(6). 112562–112562. 22 indexed citations
6.
Baudot, Alice D., Victoria M.-Y. Wang, Jim O’Prey, et al.. (2022). Glycan degradation promotes macroautophagy. Proceedings of the National Academy of Sciences. 119(26). e2111506119–e2111506119. 7 indexed citations
7.
Humpton, Timothy J., Andreas Hock, Christos Kiourtis, et al.. (2022). A noninvasive iRFP713 p53 reporter reveals dynamic p53 activity in response to irradiation and liver regeneration in vivo. Science Signaling. 15(720). eabd9099–eabd9099. 3 indexed citations
8.
Swaminathan, Karthic, Andrew D. Campbell, Vassilis Papalazarou, et al.. (2020). The RAC1 Target NCKAP1 Plays a Crucial Role in the Progression of Braf;Pten-Driven Melanoma in Mice. Journal of Investigative Dermatology. 141(3). 628–637.e15. 12 indexed citations
9.
Ren, Mindong, Yang Xu, Hediye Erdjument‐Bromage, et al.. (2019). Extramitochondrial cardiolipin suggests a novel function of mitochondria in spermatogenesis. The Journal of Cell Biology. 218(5). 1491–1502. 37 indexed citations
10.
Mitchell, Louise, Kirsteen J. Campbell, Rachel A. Ridgway, et al.. (2019). Brf1 loss and not overexpression disrupts tissues homeostasis in the intestine, liver and pancreas. Cell Death and Differentiation. 26(12). 2535–2550. 6 indexed citations
11.
Christodoulou, Neophytos, Antonia Weberling, Douglas Strathdee, et al.. (2019). Morphogenesis of extra-embryonic tissues directs the remodelling of the mouse embryo at implantation. Nature Communications. 10(1). 3557–3557. 65 indexed citations
12.
Porter, Andrew P., Gavin White, Zoi Diamantopoulou, et al.. (2018). STEF/TIAM2-mediated Rac1 activity at the nuclear envelope regulates the perinuclear actin cap. Nature Communications. 9(1). 2124–2124. 44 indexed citations
13.
Warren, Sean, Max Nobis, Astrid Magenau, et al.. (2018). Removing physiological motion from intravital and clinical functional imaging data. eLife. 7. 31 indexed citations
14.
Konjar, Špela, Cristina Ferreira, Reinhard Hinterleitner, et al.. (2018). Mitochondria maintain controlled activation state of epithelial-resident T lymphocytes. Science Immunology. 3(24). 47 indexed citations
15.
Lagemaat, Louie N. van de, Lianne Stanford, Douglas Strathdee, et al.. (2016). Standardized experiments in mutant mice reveal behavioural similarity on 129S5 and C57BL / 6J backgrounds. Genes Brain & Behavior. 16(4). 409–418. 5 indexed citations
16.
Walton, Josephine, Julianna Blagih, Darren Ennis, et al.. (2016). CRISPR/Cas9-Mediated Trp53 and Brca2 Knockout to Generate Improved Murine Models of Ovarian High-Grade Serous Carcinoma. Cancer Research. 76(20). 6118–6129. 150 indexed citations
17.
Woodham, Emma F., et al.. (2016). Loss of strumpellin in the melanocytic lineage impairs theWASHComplex but does not affect coat colour. Pigment Cell & Melanoma Research. 29(5). 559–571. 15 indexed citations
18.
Mitchell, Louise, Cynthia Lavoie, Virginie Sanguin‐Gendreau, et al.. (2016). Rab11-FIP1C Is a Critical Negative Regulator in ErbB2-Mediated Mammary Tumor Progression. Cancer Research. 76(9). 2662–2674. 26 indexed citations
19.
Cadalbert, Laurence, David Stevenson, Sheila Bryson, et al.. (2015). Mouse Tafazzin Is Required for Male Germ Cell Meiosis and Spermatogenesis. PLoS ONE. 10(6). e0131066–e0131066. 14 indexed citations
20.
Strathdee, Douglas, Bruce Whitelaw, & Anthony Clark. (2008). Distal Transgene Insertion Affects CpG Island Maintenance during Differentiation. Journal of Biological Chemistry. 283(17). 11509–11515. 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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