Herbert Levine

37.0k total citations · 3 hit papers
461 papers, 24.0k citations indexed

About

Herbert Levine is a scholar working on Molecular Biology, Cell Biology and Condensed Matter Physics. According to data from OpenAlex, Herbert Levine has authored 461 papers receiving a total of 24.0k indexed citations (citations by other indexed papers that have themselves been cited), including 158 papers in Molecular Biology, 87 papers in Cell Biology and 81 papers in Condensed Matter Physics. Recurrent topics in Herbert Levine's work include Cellular Mechanics and Interactions (66 papers), Cancer Cells and Metastasis (54 papers) and Theoretical and Computational Physics (49 papers). Herbert Levine is often cited by papers focused on Cellular Mechanics and Interactions (66 papers), Cancer Cells and Metastasis (54 papers) and Theoretical and Computational Physics (49 papers). Herbert Levine collaborates with scholars based in United States, Israel and India. Herbert Levine's co-authors include David A. Kessler, Wouter‐Jan Rappel, Mohit Kumar Jolly, Joel Koplik, Eshel Ben‐Jacob, José N. Onuchic, Dongya Jia, Inon Cohen, Stuart F. Schlossman and Lev S. Tsimring and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Herbert Levine

456 papers receiving 23.3k citations

Hit Papers

Pattern selection in fingered growth phenomena 1982 2026 1996 2011 1988 2001 1982 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Herbert Levine United States 84 7.5k 4.2k 3.6k 3.5k 3.2k 461 24.0k
Benjamin D. Simons United Kingdom 74 8.7k 1.1× 3.9k 0.9× 2.8k 0.8× 1.9k 0.5× 1.5k 0.5× 241 20.4k
Hiroshi Okamoto Japan 85 5.1k 0.7× 2.0k 0.5× 791 0.2× 3.2k 0.9× 1.1k 0.3× 1.4k 33.5k
Eshel Ben‐Jacob Israel 72 4.6k 0.6× 1.4k 0.3× 1.4k 0.4× 4.8k 1.3× 307 0.1× 325 22.3k
Eytan Domany Israel 68 8.2k 1.1× 1.9k 0.4× 773 0.2× 3.8k 1.1× 716 0.2× 275 17.0k
Akira Hasegawa Japan 98 9.6k 1.3× 708 0.2× 1.4k 0.4× 2.0k 0.6× 2.0k 0.6× 1.2k 45.0k
Stephen R. Quake United States 115 18.7k 2.5× 2.8k 0.7× 1.0k 0.3× 564 0.2× 4.6k 1.4× 354 50.5k
Alfred Zippelius Switzerland 58 2.8k 0.4× 5.2k 1.2× 285 0.1× 1.6k 0.5× 5.0k 1.6× 281 13.3k
Ronald D. Vale United States 97 23.0k 3.0× 2.5k 0.6× 18.6k 5.2× 1.2k 0.3× 3.0k 0.9× 216 35.3k
Akira Suzuki Japan 76 13.8k 1.8× 3.0k 0.7× 2.0k 0.5× 240 0.1× 2.7k 0.9× 998 32.6k
Philip K. Maini United Kingdom 66 6.3k 0.8× 2.0k 0.5× 4.0k 1.1× 525 0.1× 679 0.2× 396 16.2k

Countries citing papers authored by Herbert Levine

Since Specialization
Citations

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

Fields of papers citing papers by Herbert Levine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Herbert Levine

This figure shows the co-authorship network connecting the top 25 collaborators of Herbert Levine. A scholar is included among the top collaborators of Herbert Levine 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 Herbert Levine. Herbert Levine 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.
Chakraborty, Priyanka, Jason T. George, Wendy A. Woodward, Herbert Levine, & Mohit Kumar Jolly. (2021). Gene expression profiles of inflammatory breast cancer reveal high heterogeneity across the epithelial-hybrid-mesenchymal spectrum. Translational Oncology. 14(4). 101026–101026. 15 indexed citations
2.
Eliaz, Yossi, François Nédélec, Greg Morrison, Herbert Levine, & Margaret S. Cheung. (2020). Insights from graph theory on the morphologies of actomyosin networks with multilinkers. Physical review. E. 102(6). 62420–62420. 5 indexed citations
3.
He, Ting-Fang, Ruo‐Qian Wang, Daniel Schmolze, et al.. (2020). Occupancy and Fractal Dimension Analyses of the Spatial Distribution of Cytotoxic (CD8+) T Cells Infiltrating the Tumor Microenvironment in Triple Negative Breast Cancer. Biophysical Reviews and Letters. 15(2). 83–98. 2 indexed citations
4.
Eliaz, Yossi, Nicholas P. Schafer, M. Neal Waxham, et al.. (2020). The role of the Arp2/3 complex in shaping the dynamics and structures of branched actomyosin networks. Proceedings of the National Academy of Sciences. 117(20). 10825–10831. 24 indexed citations
5.
George, Jason T. & Herbert Levine. (2019). Sustained Coevolution in a Stochastic Model of Cancer–Immune Interaction. Cancer Research. 80(4). 811–819. 12 indexed citations
6.
Jia, Dongya, Mingyang Lu, Kwang Hwa Jung, et al.. (2019). Elucidating cancer metabolic plasticity by coupling gene regulation with metabolic pathways. Proceedings of the National Academy of Sciences. 116(9). 3909–3918. 236 indexed citations
7.
Li, Xuefei, Tina Gruosso, Dongmei Zuo, et al.. (2019). Infiltration of CD8 + T cells into tumor cell clusters in triple-negative breast cancer. Proceedings of the National Academy of Sciences. 116(9). 3678–3687. 91 indexed citations
8.
Sinha, Sudipta Kumar, et al.. (2019). Anticipating critical transitions in epithelial–hybrid-mesenchymal cell-fate determination. Proceedings of the National Academy of Sciences. 116(52). 26343–26352. 35 indexed citations
9.
Bocci, Federico, S. C. Tripathi, Jason T. George, et al.. (2019). NRF2 activates a partial epithelial-mesenchymal transition and is maximally present in a hybrid epithelial/mesenchymal phenotype. Integrative Biology. 11(6). 251–263. 104 indexed citations
10.
Shinde, Aparna, Shana D. Hardy, Dong Wook Kim, et al.. (2019). Spleen Tyrosine Kinase–Mediated Autophagy Is Required for Epithelial–Mesenchymal Plasticity and Metastasis in Breast Cancer. Cancer Research. 79(8). 1831–1843. 97 indexed citations
11.
Kang, Tae-Yun, Federico Bocci, Mohit Kumar Jolly, et al.. (2019). Pericytes enable effective angiogenesis in the presence of proinflammatory signals. Proceedings of the National Academy of Sciences. 116(47). 23551–23561. 52 indexed citations
12.
Bocci, Federico, Larisa Gearhart-Serna, Marcelo Boareto, et al.. (2018). Toward understanding cancer stem cell heterogeneity in the tumor microenvironment. Proceedings of the National Academy of Sciences. 116(1). 148–157. 225 indexed citations
13.
Evans, Myron K., Michael C. Brown, Joseph Geradts, et al.. (2018). XIAP Regulation by MNK Links MAPK and NFκB Signaling to Determine an Aggressive Breast Cancer Phenotype. Cancer Research. 78(7). 1726–1738. 44 indexed citations
14.
Tripathi, S. C., Johannes F. Fahrmann, Müge Çeliktaş, et al.. (2017). MCAM Mediates Chemoresistance in Small-Cell Lung Cancer via the PI3K/AKT/SOX2 Signaling Pathway. Cancer Research. 77(16). 4414–4425. 85 indexed citations
15.
George, Jason T., Mohit Kumar Jolly, Shengnan Xu, Jason A. Somarelli, & Herbert Levine. (2017). Survival Outcomes in Cancer Patients Predicted by a Partial EMT Gene Expression Scoring Metric. Cancer Research. 77(22). 6415–6428. 170 indexed citations
16.
Li, Xuefei, et al.. (2017). On the mechanism of long-range orientational order of fibroblasts. Proceedings of the National Academy of Sciences. 114(34). 8974–8979. 49 indexed citations
17.
Yu, Linglin, Mingyang Lu, Dongya Jia, et al.. (2017). Modeling the Genetic Regulation of Cancer Metabolism: Interplay between Glycolysis and Oxidative Phosphorylation. Cancer Research. 77(7). 1564–1574. 203 indexed citations
18.
Skoge, Monica, Michael Erickstad, Albert Bae, et al.. (2014). Cellular memory in eukaryotic chemotaxis. Proceedings of the National Academy of Sciences. 111(40). 14448–14453. 96 indexed citations
19.
Levine, Herbert, et al.. (2012). Coupling actin flow, adhesion, and morphology in a computational cell motility model. Proceedings of the National Academy of Sciences. 109(18). 6851–6856. 190 indexed citations
20.
Nadkarni, Suhita, Thomas M. Bartol, Terrence J. Sejnowski, & Herbert Levine. (2010). Modelling Vesicular Release at Hippocampal Synapses. PLoS Computational Biology. 6(11). e1000983–e1000983. 50 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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