Diego F. Calvisi

21.6k total citations · 3 hit papers
215 papers, 11.5k citations indexed

About

Diego F. Calvisi is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Diego F. Calvisi has authored 215 papers receiving a total of 11.5k indexed citations (citations by other indexed papers that have themselves been cited), including 139 papers in Molecular Biology, 59 papers in Oncology and 56 papers in Cancer Research. Recurrent topics in Diego F. Calvisi's work include Cancer, Hypoxia, and Metabolism (30 papers), Cancer-related Molecular Pathways (29 papers) and Cancer Mechanisms and Therapy (29 papers). Diego F. Calvisi is often cited by papers focused on Cancer, Hypoxia, and Metabolism (30 papers), Cancer-related Molecular Pathways (29 papers) and Cancer Mechanisms and Therapy (29 papers). Diego F. Calvisi collaborates with scholars based in Germany, United States and Italy. Diego F. Calvisi's co-authors include Xin Chen, Snorri S. Thorgeirsson, Sara Ladu, Ju‐Seog Lee, Matthias Evert, Valentina M. Factor, Frank Dombrowski, Rosa M. Pascale, Francesco Feo and In‐Sun Chu and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Diego F. Calvisi

211 papers receiving 11.4k citations

Hit Papers

A novel prognostic subtype of human hepatocellular carcin... 2004 2026 2011 2018 2006 2004 2006 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Diego F. Calvisi Germany 55 7.0k 3.4k 2.4k 2.2k 1.7k 215 11.5k
Ju‐Seog Lee United States 61 7.9k 1.1× 3.9k 1.2× 3.7k 1.5× 1.9k 0.9× 1.4k 0.8× 218 13.3k
Terence K. Lee Hong Kong 59 6.3k 0.9× 3.5k 1.0× 4.3k 1.8× 1.9k 0.8× 876 0.5× 170 10.8k
Valentina M. Factor United States 55 5.1k 0.7× 2.2k 0.7× 2.1k 0.9× 2.7k 1.2× 1.2k 0.7× 109 8.7k
Satdarshan P. Monga United States 58 6.9k 1.0× 1.4k 0.4× 1.6k 0.7× 4.2k 1.9× 2.1k 1.2× 229 11.7k
Hui‐Chuan Sun China 58 5.0k 0.7× 4.2k 1.2× 3.1k 1.3× 3.7k 1.7× 2.0k 1.1× 308 11.8k
Shoji Nakamori Japan 55 3.6k 0.5× 2.0k 0.6× 4.4k 1.9× 1.6k 0.7× 1.5k 0.9× 276 10.1k
Stephanie Ma Hong Kong 47 5.0k 0.7× 3.0k 0.9× 3.9k 1.6× 1.4k 0.6× 598 0.3× 125 8.8k
Koji Umeshita Japan 51 2.6k 0.4× 1.8k 0.5× 2.2k 0.9× 3.4k 1.5× 1.6k 0.9× 290 8.5k
Nathan W. Werneburg United States 42 2.9k 0.4× 1.2k 0.3× 1.2k 0.5× 930 0.4× 2.6k 1.5× 56 6.3k
Wolfgang Mikulits Austria 44 4.1k 0.6× 1.6k 0.5× 2.4k 1.0× 955 0.4× 531 0.3× 116 6.9k

Countries citing papers authored by Diego F. Calvisi

Since Specialization
Citations

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

Fields of papers citing papers by Diego F. Calvisi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Diego F. Calvisi. 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 Diego F. Calvisi. The network helps show where Diego F. Calvisi may publish in the future.

Co-authorship network of co-authors of Diego F. Calvisi

This figure shows the co-authorship network connecting the top 25 collaborators of Diego F. Calvisi. A scholar is included among the top collaborators of Diego F. Calvisi 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 Diego F. Calvisi. Diego F. Calvisi 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.
Liao, Wei‐Ting, Yi Zhang, Jingxiao Wang, et al.. (2025). β-Catenin regulates distinct pathways from YAP and suppresses ONECUT1 to drive hepatoblastoma development in mice and humans. Hepatology. 83(2). 215–230. 1 indexed citations
2.
Zushin, Peter‐James H., Hyo Min Park, Sharon M. Louie, et al.. (2024). FATP5 Is Indispensable for the Growth of Intrahepatic Cholangiocarcinoma. Molecular Cancer Research. 22(6). 585–595. 3 indexed citations
3.
Deng, Shanshan, Xinjun Lu, Xue Wang, et al.. (2024). Overexpression of TBX3 suppresses tumorigenesis in experimental and human cholangiocarcinoma. Cell Death and Disease. 15(6). 441–441. 1 indexed citations
4.
Scheiter, Alexander, Felix Keil, Cédric Coulouarn, et al.. (2022). Wnt/β-Catenin-Pathway Alterations and Homologous Recombination Deficiency in Cholangiocarcinoma Cell Lines and Clinical Samples: Towards Specific Vulnerabilities. Journal of Personalized Medicine. 12(8). 1270–1270. 3 indexed citations
5.
Mancarella, Serena, Grazia Serino, Isabella Gigante, et al.. (2022). CD90 is regulated by notch1 and hallmarks a more aggressive intrahepatic cholangiocarcinoma phenotype. Journal of Experimental & Clinical Cancer Research. 41(1). 16 indexed citations
6.
Pellegrino, Rossella, Abhishek Thavamani, Diego F. Calvisi, et al.. (2021). Serum Response Factor (SRF) Drives the Transcriptional Upregulation of the MDM4 Oncogene in HCC. Cancers. 13(2). 199–199. 8 indexed citations
7.
Scheiter, Alexander, Florian Lüke, Felix Keil, et al.. (2021). STRN-ALKFusion in a Case of Malignant Peritoneal Mesothelioma: Mixed Response to Crizotinib, Mode of Resistance, and Brigatinib Sequential Therapy. JCO Precision Oncology. 5(5). 1507–1513. 4 indexed citations
8.
Evert, Katja, Thomas Dienemann, Christoph Brochhausen, et al.. (2021). Autopsy findings after long-term treatment of COVID-19 patients with microbiological correlation. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 479(1). 97–108. 34 indexed citations
9.
Chen, Xinyan, Xinyan Chen, András Kiss, et al.. (2020). CDK9 is dispensable for YAP‐driven hepatoblastoma development. Pediatric Blood & Cancer. 67(5). e28221–e28221. 3 indexed citations
10.
Xu, Meng, Haichuan Wang, Jingxiao Wang, et al.. (2020). mTORC2 Signaling Is Necessary for Timely Liver Regeneration after Partial Hepatectomy. American Journal Of Pathology. 190(4). 817–829. 14 indexed citations
11.
Chen, Bin, Lana X. Garmire, Diego F. Calvisi, et al.. (2020). Publisher Correction: Harnessing big ‘omics’ data and AI for drug discovery in hepatocellular carcinoma. Nature Reviews Gastroenterology & Hepatology. 2 indexed citations
12.
Wang, Jingxiao, Haichuan Wang, Ning Ding, et al.. (2019). Loss of Fbxw7 synergizes with activated Akt signaling to promote c-Myc dependent cholangiocarcinogenesis. Journal of Hepatology. 71(4). 742–752. 47 indexed citations
13.
Méndez‐Lucas, Andrés, Xiaolei Li, Junjie Hu, et al.. (2017). Glucose Catabolism in Liver Tumors Induced by c-MYC Can Be Sustained by Various PKM1/PKM2 Ratios and Pyruvate Kinase Activities. Cancer Research. 77(16). 4355–4364. 67 indexed citations
14.
Brooks, Jennifer D., Bettina Fleischmann-Mundt, Norman Woller, et al.. (2017). Perioperative, Spatiotemporally Coordinated Activation of T and NK Cells Prevents Recurrence of Pancreatic Cancer. Cancer Research. 78(2). 475–488. 55 indexed citations
15.
Calvisi, Diego F., Hyuk Moon, Silvia Ribback, et al.. (2015). Transgenic mouse model expressing P53R172H, luciferase, EGFP and KRASG12D in a single open reading frame for live imaging of tumor. Scientific Reports. 5(1). 8053–8053. 10 indexed citations
16.
Song, Su Jung, Min Sup Song, Soonjoung Kim, et al.. (2009). Aurora A Regulates Prometaphase Progression by Inhibiting the Ability of RASSF1A to Suppress APC-Cdc20 Activity. Cancer Research. 69(6). 2314–2323. 40 indexed citations
17.
Calvisi, Diego F., Howard Donninger, Michele D. Vos, et al.. (2009). NORE1A Tumor Suppressor Candidate Modulates p21CIP1 via p53. Cancer Research. 69(11). 4629–4637. 50 indexed citations
18.
Calvisi, Diego F., Federico Pinna, Sara Ladu, et al.. (2008). Dual-Specificity Phosphatase 1 Ubiquitination in Extracellular Signal-Regulated Kinase–Mediated Control of Growth in Human Hepatocellular Carcinoma. Cancer Research. 68(11). 4192–4200. 107 indexed citations
19.
Miglio, Maria R. De, Patrizia Virdis, Diego F. Calvisi, et al.. (2006). Mapping a Sex Hormone–Sensitive Gene Determining Female Resistance to Liver Carcinogenesis in a Congenic F344.BN- Hcs4 Rat. Cancer Research. 66(21). 10384–10390. 6 indexed citations
20.
Novoselov, Sergey V., Diego F. Calvisi, Vyacheslav M. Labunskyy, et al.. (2005). Selenoprotein deficiency and high levels of selenium compounds can effectively inhibit hepatocarcinogenesis in transgenic mice. Oncogene. 24(54). 8003–8011. 98 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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