James Hulit

3.1k total citations
31 papers, 2.4k citations indexed

About

James Hulit is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, James Hulit has authored 31 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 12 papers in Oncology and 8 papers in Cancer Research. Recurrent topics in James Hulit's work include Cancer-related Molecular Pathways (9 papers), Cancer, Hypoxia, and Metabolism (6 papers) and Wnt/β-catenin signaling in development and cancer (6 papers). James Hulit is often cited by papers focused on Cancer-related Molecular Pathways (9 papers), Cancer, Hypoxia, and Metabolism (6 papers) and Wnt/β-catenin signaling in development and cancer (6 papers). James Hulit collaborates with scholars based in United States, United Kingdom and Canada. James Hulit's co-authors include Michael P. Lisanti, Richard G. Pestell, Federica Sotgia, Chris Albanese, Rebecca Lamb, Rachel B. Hazan, Anthony Howell, Ubaldo Martinez‐Outschoorn, Georgia Agiostratidou and Maofu Fu 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

James Hulit

31 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James Hulit United States 26 1.7k 772 596 466 210 31 2.4k
Nicolas Dumaz France 26 2.2k 1.3× 1.3k 1.7× 459 0.8× 376 0.8× 147 0.7× 59 2.8k
Gianluca Bossi Italy 30 1.4k 0.8× 988 1.3× 547 0.9× 167 0.4× 209 1.0× 53 2.2k
Takaki Hiwasa Japan 25 1.3k 0.8× 474 0.6× 386 0.6× 297 0.6× 135 0.6× 132 2.1k
Cécile Demur France 29 2.0k 1.2× 1.0k 1.3× 352 0.6× 698 1.5× 111 0.5× 79 3.4k
Matthew G. Annis Canada 27 2.0k 1.2× 835 1.1× 827 1.4× 246 0.5× 213 1.0× 44 3.0k
Stefania D’Atri Italy 33 2.2k 1.3× 1.2k 1.5× 746 1.3× 244 0.5× 129 0.6× 117 3.2k
Elda Grabocka United States 13 2.6k 1.5× 1.1k 1.4× 1.2k 2.0× 621 1.3× 265 1.3× 20 3.8k
Jessie Villanueva United States 18 1.6k 1.0× 799 1.0× 361 0.6× 314 0.7× 88 0.4× 30 2.1k
Gerhard Siemeister Germany 32 2.2k 1.3× 959 1.2× 594 1.0× 488 1.0× 101 0.5× 68 3.3k
José M.A. Moreira Denmark 31 1.8k 1.1× 656 0.8× 670 1.1× 193 0.4× 147 0.7× 79 2.8k

Countries citing papers authored by James Hulit

Since Specialization
Citations

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

Fields of papers citing papers by James Hulit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Hulit

This figure shows the co-authorship network connecting the top 25 collaborators of James Hulit. A scholar is included among the top collaborators of James Hulit 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 James Hulit. James Hulit 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.
Shabo, Ivan, Joar Svanvik, Annelie Lindström, et al.. (2020). Roles of cell fusion, hybridization and polyploid cell formation in cancer metastasis. World Journal of Clinical Oncology. 11(3). 121–135. 58 indexed citations
2.
Barrow‐McGee, Rachel, Carine Joffre, Ludovic Ménard, et al.. (2016). Beta 1-integrin–c-Met cooperation reveals an inside-in survival signalling on autophagy-related endomembranes. Nature Communications. 7(1). 11942–11942. 89 indexed citations
3.
Mercier, Isabelle Le, Donna Gonzales, Kevin Quann, et al.. (2014). CAPER, a novel regulator of human breast cancer progression. Cell Cycle. 13(8). 1256–1264. 26 indexed citations
4.
Salem, Ahmed F., Mazhar Salim Al Zoubi, Diana Whitaker‐Menezes, et al.. (2013). Cigarette smoke metabolically promotes cancer, via autophagy and premature aging in the host stromal microenvironment. Cell Cycle. 12(5). 818–825. 41 indexed citations
5.
Sánchez‐Alvarez, Rosa, Ubaldo Martinez‐Outschoorn, Lin Zhao, et al.. (2013). Ethanol exposure induces the cancer-associated fibroblast phenotype and lethal tumor metabolism. Cell Cycle. 12(2). 289–301. 45 indexed citations
6.
Qian, Xia, James Hulit, K Suyama, et al.. (2012). p21CIP1 mediates reciprocal switching between proliferation and invasion during metastasis. Oncogene. 32(18). 2292–2303. 39 indexed citations
7.
Hulit, James, Dmitriy Kedrin, Bojana Gligorijevic, et al.. (2012). The Use of Fluorescent Proteins for Intravital Imaging of Cancer Cell Invasion. Methods in molecular biology. 872. 15–30. 8 indexed citations
8.
Sotgia, Federica, Diana Whitaker‐Menezes, Ubaldo Martinez‐Outschoorn, et al.. (2012). Mitochondria “fuel” breast cancer metabolism: Fifteen markers of mitochondrial biogenesis label epithelial cancer cells, but are excluded from adjacent stromal cells. Cell Cycle. 11(23). 4390–4401. 139 indexed citations
9.
Agiostratidou, Georgia, Maomi Li, Kimita Suyama, et al.. (2009). Loss of Retinal Cadherin Facilitates Mammary Tumor Progression and Metastasis. Cancer Research. 69(12). 5030–5038. 38 indexed citations
10.
Bouzahzah, Boumediene, Vyacheslav Yurchenko, Fnu Nagajyothi, et al.. (2008). Regulation of host cell cyclin D1 byTrypanosoma cruziin myoblasts. Cell Cycle. 7(4). 500–503. 9 indexed citations
11.
Hulit, James, Kimita Suyama, Su Wol Chung, et al.. (2007). N-Cadherin Signaling Potentiates Mammary Tumor Metastasis via Enhanced Extracellular Signal-Regulated Kinase Activation. Cancer Research. 67(7). 3106–3116. 173 indexed citations
12.
Agiostratidou, Georgia, James Hulit, Greg R. Phillips, & Rachel B. Hazan. (2007). Differential Cadherin Expression: Potential Markers for Epithelial to Mesenchymal Transformation During Tumor Progression. Journal of Mammary Gland Biology and Neoplasia. 12(2-3). 127–133. 77 indexed citations
13.
Albanese, Chris, Kongming Wu, Mark D’Amico, et al.. (2003). IKKα Regulates Mitogenic Signaling through Transcriptional Induction of Cyclin D1 via Tcf. Molecular Biology of the Cell. 14(2). 585–599. 131 indexed citations
14.
Wang, Chenguang, Nagarajan Pattabiraman, Jian Zhou, et al.. (2003). Cyclin D1 Repression of Peroxisome Proliferator-Activated Receptor γ Expression and Transactivation. Molecular and Cellular Biology. 23(17). 6159–6173. 165 indexed citations
15.
Albanese, Chris, James Hulit, Toshiyuki Sakamaki, & Richard G. Pestell. (2002). Recent advances in inducible expression in transgenic mice. Seminars in Cell and Developmental Biology. 13(2). 129–141. 39 indexed citations
16.
Park, David, Hyangkyu Lee, Philippe G. Frank, et al.. (2002). Caveolin-1-deficient Mice Show Accelerated Mammary Gland Development During Pregnancy, Premature Lactation, and Hyperactivation of the Jak-2/STAT5a Signaling Cascade. Molecular Biology of the Cell. 13(10). 3416–3430. 90 indexed citations
17.
Hulit, James, Richard J. Lee, Robert G. Russell, & Richard G. Pestell. (2002). ErbB-2-induced mammary tumor growth: the role of cyclin D1 and p27Kip1. Biochemical Pharmacology. 64(5-6). 827–836. 30 indexed citations
18.
Hulit, James, Dolores Di Vizio, & Richard G. Pestell. (2001). Inducible transgenics. New lessons on events governing the induction and commitment in mammary tumorigenesis.. Breast Cancer Research. 3(4). 209–209. 10 indexed citations
19.
Hulit, James, Maofu Fu, Ferruccio Galbiati, et al.. (2000). The Cyclin D1 Gene Is Transcriptionally Repressed by Caveolin-1. Journal of Biological Chemistry. 275(28). 21203–21209. 123 indexed citations
20.
Augenlicht, Leonard H., Roger J. Davis, Michael P. Lisanti, et al.. (2000). The Integrin-linked Kinase Regulates the Cyclin D1 Gene through Glycogen Synthase Kinase 3β and cAMP-responsive Element-binding Protein-dependent Pathways. Journal of Biological Chemistry. 275(42). 32649–32657. 215 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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