Sandeep Dhayade

1.9k total citations
17 papers, 893 citations indexed

About

Sandeep Dhayade is a scholar working on Molecular Biology, Oncology and Immunology. According to data from OpenAlex, Sandeep Dhayade has authored 17 papers receiving a total of 893 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Oncology and 5 papers in Immunology. Recurrent topics in Sandeep Dhayade's work include Cancer, Hypoxia, and Metabolism (5 papers), Cancer-related Molecular Pathways (3 papers) and Cancer Research and Treatments (2 papers). Sandeep Dhayade is often cited by papers focused on Cancer, Hypoxia, and Metabolism (5 papers), Cancer-related Molecular Pathways (3 papers) and Cancer Research and Treatments (2 papers). Sandeep Dhayade collaborates with scholars based in United Kingdom, Germany and United States. Sandeep Dhayade's co-authors include Karen Blyth, Gillian Mackay, Alexei Vázquez, Colin Nixon, Johan Vande Voorde, Robert Feil, Zachary T. Schug, Eyal Gottlieb, Andrew H. Sims and Evdokia Michalopoulou and has published in prestigious journals such as Nature Communications, Genes & Development and PLoS ONE.

In The Last Decade

Sandeep Dhayade

17 papers receiving 889 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandeep Dhayade United Kingdom 13 576 251 165 139 136 17 893
Martina Sboarina Belgium 11 775 1.3× 513 2.0× 220 1.3× 65 0.5× 217 1.6× 12 1.2k
Yanling Jing China 10 669 1.2× 468 1.9× 140 0.8× 43 0.3× 85 0.6× 17 929
Max Hamaker United States 6 795 1.4× 721 2.9× 111 0.7× 99 0.7× 70 0.5× 9 1.1k
Annalisa Zecchin Belgium 10 449 0.8× 187 0.7× 118 0.7× 38 0.3× 106 0.8× 12 701
Ahmad A. Cluntun United States 12 964 1.7× 690 2.7× 165 1.0× 104 0.7× 163 1.2× 20 1.5k
Tomoyuki Nakano Japan 18 591 1.0× 107 0.4× 88 0.5× 133 1.0× 107 0.8× 54 843
Jun‐Kyu Byun South Korea 13 568 1.0× 443 1.8× 143 0.9× 67 0.5× 65 0.5× 25 965
Vivian Rodriguez‐Cruz United States 8 474 0.8× 265 1.1× 169 1.0× 37 0.3× 79 0.6× 11 819
Byung‐Gyu Kim South Korea 21 732 1.3× 201 0.8× 121 0.7× 44 0.3× 81 0.6× 44 1.0k

Countries citing papers authored by Sandeep Dhayade

Since Specialization
Citations

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

Fields of papers citing papers by Sandeep Dhayade

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandeep Dhayade

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

All Works

17 of 17 papers shown
1.
Campbell, Kirsteen J., Susan Mason, Catherine Cloix, et al.. (2021). Breast cancer dependence on MCL-1 is due to its canonical anti-apoptotic function. Cell Death and Differentiation. 28(9). 2589–2600. 31 indexed citations
2.
Kilbey, Anna, Tesa Severson, Sandeep Dhayade, et al.. (2020). The MSP‐RON axis stimulates cancer cell growth in models of triple negative breast cancer. Molecular Oncology. 14(8). 1868–1880. 12 indexed citations
3.
Dhayade, Sandeep, Matthias Pietzke, Jacqueline Tait-Mulder, et al.. (2020). Impact of Formate Supplementation on Body Weight and Plasma Amino Acids. Nutrients. 12(8). 2181–2181. 4 indexed citations
4.
Humpton, Timothy J., Koji Nomura, Julia Weber, et al.. (2020). Differential requirements for MDM2 E3 activity during embryogenesis and in adult mice. Genes & Development. 35(1-2). 117–132. 8 indexed citations
5.
Oizel, Kristell, Jacqueline Tait-Mulder, Jorge Fernández-de-Cossio-Díaz, et al.. (2020). Formate induces a metabolic switch in nucleotide and energy metabolism. Cell Death and Disease. 11(5). 310–310. 41 indexed citations
6.
Kay, Emily, Lisa J. Neilson, Juan R. Hernández‐Fernaud, et al.. (2020). Abstract B76: Pyruvate dehydrogenase: A key to epigenetic regulation in CAFs. Clinical Cancer Research. 26(13_Supplement). B76–B76. 1 indexed citations
7.
Purdie, Karin J., Jun Wang, Catherine Harwood, et al.. (2019). A Unique Panel of Patient-Derived Cutaneous Squamous Cell Carcinoma Cell Lines Provides a Preclinical Pathway for Therapeutic Testing. International Journal of Molecular Sciences. 20(14). 3428–3428. 19 indexed citations
8.
Meiser, Johannes, Anne Schuster, Matthias Pietzke, et al.. (2018). Increased formate overflow is a hallmark of oxidative cancer. Nature Communications. 9(1). 1368–1368. 83 indexed citations
9.
Campbell, Kirsteen J., Sandeep Dhayade, Nicola Ferrari, et al.. (2018). MCL-1 is a prognostic indicator and drug target in breast cancer. Cell Death and Disease. 9(2). 19–19. 144 indexed citations
10.
Dornier, Emmanuel, Nicolas Rabas, Louise Mitchell, et al.. (2017). Glutaminolysis drives membrane trafficking to promote invasiveness of breast cancer cells. Nature Communications. 8(1). 2255–2255. 84 indexed citations
11.
Rumney, Robin M. H., et al.. (2017). PyMT-Maclow: A novel, inducible, murine model for determining the role of CD68 positive cells in breast tumor development. PLoS ONE. 12(12). e0188591–e0188591. 15 indexed citations
12.
Bulusu, Vinay, Sergey Tumanov, Evdokia Michalopoulou, et al.. (2017). Acetate Recapturing by Nuclear Acetyl-CoA Synthetase 2 Prevents Loss of Histone Acetylation during Oxygen and Serum Limitation. Cell Reports. 18(3). 647–658. 191 indexed citations
13.
Dhayade, Sandeep, Susanne Kaesler, Tobias Sinnberg, et al.. (2016). Sildenafil Potentiates a cGMP-Dependent Pathway to Promote Melanoma Growth. Cell Reports. 14(11). 2599–2610. 62 indexed citations
14.
Müller, Paul Markus, Sandeep Dhayade, Martin Thunemann, et al.. (2012). H2O2 lowers the cytosolic Ca2+ concentration via activation of cGMP-dependent protein kinase Iα. Free Radical Biology and Medicine. 53(8). 1574–1583. 24 indexed citations
15.
Bucci, Mariarosaria, Andreas Papapetropoulos, Valentina Vellecco, et al.. (2012). cGMP-Dependent Protein Kinase Contributes to Hydrogen Sulfide-Stimulated Vasorelaxation. PLoS ONE. 7(12). e53319–e53319. 116 indexed citations
16.
Kase, Satoru, Yan Qiu, Alexander H. R. Varey, et al.. (2010). Recombinant Human VEGF(165)b Inhibits Experimental Choroidal Neovascularization. UCL Discovery (University College London). 4 indexed citations
17.
Hua, Jing, Christine Spee, Satoru Kase, et al.. (2010). Recombinant Human VEGF165b Inhibits Experimental Choroidal Neovascularization. Investigative Ophthalmology & Visual Science. 51(8). 4282–4282. 54 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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