William C. Hines

2.7k total citations · 1 hit paper
29 papers, 2.0k citations indexed

About

William C. Hines is a scholar working on Molecular Biology, Oncology and Physiology. According to data from OpenAlex, William C. Hines has authored 29 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Oncology and 9 papers in Physiology. Recurrent topics in William C. Hines's work include Cancer Cells and Metastasis (11 papers), Telomeres, Telomerase, and Senescence (8 papers) and Epigenetics and DNA Methylation (5 papers). William C. Hines is often cited by papers focused on Cancer Cells and Metastasis (11 papers), Telomeres, Telomerase, and Senescence (8 papers) and Epigenetics and DNA Methylation (5 papers). William C. Hines collaborates with scholars based in United States, Switzerland and Argentina. William C. Hines's co-authors include Mina J. Bissell, Paul Yaswen, Audrey Brenot, Zena Werb, Andrew J. Ewald, Kevin J. Cheung, Ryan S. Gray, Eliah R. Shamir, Jeffrey K. Griffith and Marco Bisoffi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

William C. Hines

29 papers receiving 2.0k citations

Hit Papers

Why don't we get more cancer? A proposed role of the micr... 2011 2026 2016 2021 2011 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William C. Hines United States 17 927 920 495 442 319 29 2.0k
Evanthia T. Roussos Torres United States 18 1.1k 1.2× 1.1k 1.1× 413 0.8× 513 1.2× 379 1.2× 62 2.4k
René Villadsen Denmark 23 1.6k 1.7× 1.3k 1.4× 605 1.2× 347 0.8× 267 0.8× 40 2.5k
Ana Cerezo Spain 13 841 0.9× 1.1k 1.2× 358 0.7× 677 1.5× 138 0.4× 16 2.0k
Fernando Calvo Spain 22 1.0k 1.1× 1.8k 1.9× 467 0.9× 1.1k 2.5× 217 0.7× 42 2.9k
Roya Navab Canada 25 694 0.7× 1.1k 1.2× 638 1.3× 237 0.5× 173 0.5× 46 2.0k
Sebastian Hoersch United States 16 672 0.7× 1.6k 1.7× 503 1.0× 350 0.8× 144 0.5× 23 2.6k
Daniela Tosoni Italy 16 1.2k 1.3× 1.8k 1.9× 531 1.1× 585 1.3× 99 0.3× 24 2.7k
Olav Engebraaten Norway 29 925 1.0× 1.3k 1.4× 700 1.4× 277 0.6× 230 0.7× 87 2.7k
Anthony R. Howlett United States 21 1.0k 1.1× 1.3k 1.4× 369 0.7× 521 1.2× 419 1.3× 34 2.5k
Maria‐Carla Parrini France 6 1.1k 1.2× 1.2k 1.3× 459 0.9× 442 1.0× 141 0.4× 7 2.2k

Countries citing papers authored by William C. Hines

Since Specialization
Citations

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

Fields of papers citing papers by William C. Hines

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William C. Hines. 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 William C. Hines. The network helps show where William C. Hines may publish in the future.

Co-authorship network of co-authors of William C. Hines

This figure shows the co-authorship network connecting the top 25 collaborators of William C. Hines. A scholar is included among the top collaborators of William C. Hines 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 William C. Hines. William C. Hines 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.
Sayaman, Rosalyn W., et al.. (2024). Transcriptomic analysis of the 12 major human breast cell types reveals mechanisms of cell and tissue function. PLoS Biology. 22(11). e3002820–e3002820. 2 indexed citations
2.
Crabtree, William, et al.. (2024). Breast pericytes: a newly identified driver of tumor cell proliferation. Frontiers in Oncology. 14. 1455484–1455484. 1 indexed citations
3.
Hines, William C.. (2023). Lost in transduction: Critical considerations when using viral vectors. Frontiers in Cell and Developmental Biology. 10. 1080265–1080265. 1 indexed citations
4.
Wang, Chunqing, Xing Zhang, Liping Luo, et al.. (2022). COX-2 Deficiency Promotes White Adipogenesis via PGE2-Mediated Paracrine Mechanism and Exacerbates Diet-Induced Obesity. Cells. 11(11). 1819–1819. 16 indexed citations
5.
Foulke‐Abel, Jennifer, et al.. (2022). Ulcerative Colitis: Novel Epithelial Insights Provided by Single Cell RNA Sequencing. Frontiers in Medicine. 9. 868508–868508. 13 indexed citations
6.
Hines, William C., Irene Kuhn, James C. Garbe, et al.. (2015). 184AA3: a xenograft model of ER+ breast adenocarcinoma. Breast Cancer Research and Treatment. 155(1). 37–52. 7 indexed citations
7.
Hines, William C., Paul Yaswen, & Mina J. Bissell. (2015). Modelling breast cancer requires identification and correction of a critical cell lineage-dependent transduction bias. Nature Communications. 6(1). 6927–6927. 24 indexed citations
8.
Hines, William C., et al.. (2014). Sorting Out the FACS: A Devil in the Details. Cell Reports. 6(5). 779–781. 62 indexed citations
9.
Pirone, Jason R., Monica D’Arcy, Delisha A. Stewart, et al.. (2012). Age-Associated Gene Expression in Normal Breast Tissue Mirrors Qualitative Age-at-Incidence Patterns for Breast Cancer. Cancer Epidemiology Biomarkers & Prevention. 21(10). 1735–1744. 35 indexed citations
10.
Bazarov, Alexey V., Won Jae Lee, William C. Hines, et al.. (2012). The specific role of pRb in p16INK4A-mediated arrest of normal and malignant human breast cells. Cell Cycle. 11(5). 1008–1013. 20 indexed citations
11.
Cheung, Kevin J., Audrey Brenot, Eliah R. Shamir, et al.. (2012). ECM microenvironment regulates collective migration and local dissemination in normal and malignant mammary epithelium. Proceedings of the National Academy of Sciences. 109(39). E2595–604. 350 indexed citations
12.
Trujillo, Kristina A., et al.. (2011). Breast Field Cancerization: Isolation and Comparison of Telomerase-Expressing Cells in Tumor and Tumor Adjacent, Histologically Normal Breast Tissue. Molecular Cancer Research. 9(9). 1209–1221. 21 indexed citations
13.
Bissell, Mina J. & William C. Hines. (2011). Why don't we get more cancer? A proposed role of the microenvironment in restraining cancer progression. Nature Medicine. 17(3). 320–329. 1134 indexed citations breakdown →
14.
Mukhopadhyay, Rituparna, Sylvain V. Costes, Alexey V. Bazarov, et al.. (2010). Promotion of variant human mammary epithelial cell outgrowth by ionizing radiation: an agent-based model supported by in vitro studies. Breast Cancer Research. 12(1). R11–R11. 19 indexed citations
15.
Hines, William C., Alexey V. Bazarov, Rituparna Mukhopadhyay, & Paul Yaswen. (2010). BORIS (CTCFL) Is Not Expressed in Most Human Breast Cell Lines and High Grade Breast Carcinomas. PLoS ONE. 5(3). e9738–e9738. 19 indexed citations
16.
Bazarov, Alexey V., Marjolein van Sluis, William C. Hines, et al.. (2010). p16INK4a‐mediated suppression of telomerase in normal and malignant human breast cells. Aging Cell. 9(5). 736–746. 19 indexed citations
17.
Bazarov, Alexey V., et al.. (2009). Telomerase activation by c-Myc in human mammary epithelial cells requires additional genomic changes. Cell Cycle. 8(20). 3373–3378. 16 indexed citations
18.
Heaphy, Christopher M., William C. Hines, Kimberly S. Butler, et al.. (2007). Assessment of the Frequency of Allelic Imbalance in Human Tissue Using a Multiplex Polymerase Chain Reaction System. Journal of Molecular Diagnostics. 9(2). 266–271. 5 indexed citations
19.
Heaphy, Christopher M., Marco Bisoffi, Colleen Fordyce, et al.. (2006). Telomere DNA content and allelic imbalance demonstrate field cancerization in histologically normal tissue adjacent to breast tumors. International Journal of Cancer. 119(1). 108–116. 67 indexed citations
20.
Hines, William C., et al.. (2006). Protease nexin-1 expression is altered in human breast cancer. Cancer Cell International. 6(1). 16–16. 22 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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