Robert C. Huebert

3.4k total citations · 1 hit paper
46 papers, 2.3k citations indexed

About

Robert C. Huebert is a scholar working on Surgery, Hepatology and Molecular Biology. According to data from OpenAlex, Robert C. Huebert has authored 46 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Surgery, 24 papers in Hepatology and 15 papers in Molecular Biology. Recurrent topics in Robert C. Huebert's work include Liver physiology and pathology (18 papers), Pediatric Hepatobiliary Diseases and Treatments (10 papers) and Liver Diseases and Immunity (8 papers). Robert C. Huebert is often cited by papers focused on Liver physiology and pathology (18 papers), Pediatric Hepatobiliary Diseases and Treatments (10 papers) and Liver Diseases and Immunity (8 papers). Robert C. Huebert collaborates with scholars based in United States, Spain and France. Robert C. Huebert's co-authors include Nicholas F. LaRusso, Vijay H. Shah, Gregory J. Gores, Joseph A. Odin, Jesús M. Bañales, Sheng Cao, Livia Casciola‐Rosen, Antony Rosen, Mario Strazzabosco and Tom H. Karlsen and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Gastroenterology.

In The Last Decade

Robert C. Huebert

44 papers receiving 2.3k citations

Hit Papers

Cholangiocyte pathobiology 2019 2026 2021 2023 2019 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert C. Huebert United States 26 1.1k 841 808 715 248 46 2.3k
Atsushi Sugimura Japan 8 1.6k 1.4× 871 1.0× 387 0.5× 988 1.4× 265 1.1× 13 2.3k
H. P. Dienes Germany 21 712 0.7× 550 0.7× 700 0.9× 536 0.7× 466 1.9× 72 2.0k
Rebecca L. Aucott United Kingdom 14 803 0.7× 797 0.9× 670 0.8× 360 0.5× 324 1.3× 17 2.4k
Joachim C. Mertens Switzerland 24 724 0.7× 502 0.6× 653 0.8× 850 1.2× 733 3.0× 69 2.3k
Hisashi Takayama Japan 26 919 0.8× 1.0k 1.2× 454 0.6× 347 0.5× 575 2.3× 51 2.4k
Hiroko Ikeda Japan 27 476 0.4× 658 0.8× 368 0.5× 783 1.1× 436 1.8× 81 2.0k
Xinping Tan United States 17 800 0.7× 1.2k 1.4× 259 0.3× 621 0.9× 215 0.9× 20 1.9k
N Arakaki Japan 15 1.5k 1.4× 775 0.9× 471 0.6× 928 1.3× 275 1.1× 22 2.1k
Timothy T. Gordon‐Walker United Kingdom 7 718 0.7× 378 0.4× 680 0.8× 365 0.5× 301 1.2× 14 1.9k
Koichi Matsuzaki Japan 28 1.0k 0.9× 1.7k 2.0× 624 0.8× 284 0.4× 967 3.9× 53 2.8k

Countries citing papers authored by Robert C. Huebert

Since Specialization
Citations

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

Fields of papers citing papers by Robert C. Huebert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert C. Huebert

This figure shows the co-authorship network connecting the top 25 collaborators of Robert C. Huebert. A scholar is included among the top collaborators of Robert C. Huebert 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 Robert C. Huebert. Robert C. Huebert 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.
Aseem, Sayed Obaidullah, Jing Wang, Derrick Zhao, et al.. (2025). Aramchol attenuates fibrosis in mouse models of biliary fibrosis and blocks the TGFβ-induced fibroinflammatory mediators in cholangiocytes. Hepatology Communications. 9(8). 1 indexed citations
2.
Amiot, Bruce, Nidhi Jalan‐Sakrikar, Michele Smart, et al.. (2023). Biodegradable biliary stents coated with mesenchymal stromal cells in a porcine choledochojejunostomy model. Cytotherapy. 25(5). 483–489. 2 indexed citations
3.
Jalan‐Sakrikar, Nidhi, Thiago M. de Assuncao, Feda H. Hamdan, et al.. (2021). Induced Pluripotent Stem Cells From Subjects With Primary Sclerosing Cholangitis Develop a Senescence Phenotype Following Biliary Differentiation. Hepatology Communications. 6(2). 345–360. 18 indexed citations
4.
Sehrawat, Tejasav S., Nidhi Jalan‐Sakrikar, Nicholas Pirius, et al.. (2021). Long non-coding RNA ACTA2-AS1 promotes ductular reaction by interacting with the p300/ELK1 complex. Journal of Hepatology. 76(4). 921–933. 30 indexed citations
5.
Haak, Andrew J., et al.. (2021). Traf2 and NCK Interacting Kinase Is a Critical Regulator of Procollagen I Trafficking and Hepatic Fibrogenesis in Mice. Hepatology Communications. 6(3). 593–609. 11 indexed citations
6.
Kamboj, Amrit K., et al.. (2020). A Curious Case of Confusion in a Patient With Cirrhosis. Gastroenterology. 159(6). 2036–2038. 2 indexed citations
7.
Aseem, Sayed Obaidullah, Nidhi Jalan‐Sakrikar, Cheng Chi, et al.. (2020). Epigenomic Evaluation of Cholangiocyte Transforming Growth Factor-β Signaling Identifies a Selective Role for Histone 3 Lysine 9 Acetylation in Biliary Fibrosis. Gastroenterology. 160(3). 889–905.e10. 39 indexed citations
8.
Jalan‐Sakrikar, Nidhi, Thiago M. de Assuncao, Sayed Obaidullah Aseem, et al.. (2019). Proteasomal Degradation of Enhancer of Zeste Homologue 2 in Cholangiocytes Promotes Biliary Fibrosis. Hepatology. 70(5). 1674–1689. 24 indexed citations
9.
Aseem, Sayed Obaidullah & Robert C. Huebert. (2019). Epigenetic Mechanisms of Pancreatobiliary Fibrosis. Current Treatment Options in Gastroenterology. 17(3). 342–356. 4 indexed citations
10.
Martín‐Mateos, Rosa, Thiago M. de Assuncao, Juan Pablo Arab, et al.. (2018). Enhancer of Zeste Homologue 2 Inhibition Attenuates TGF-β Dependent Hepatic Stellate Cell Activation and Liver Fibrosis. Cellular and Molecular Gastroenterology and Hepatology. 7(1). 197–209. 54 indexed citations
11.
Mathison, Angela, Monique Williams, Asha Nair, et al.. (2017). Combined AURKA and H3K9 Methyltransferase Targeting Inhibits Cell Growth By Inducing Mitotic Catastrophe. Molecular Cancer Research. 15(8). 984–997. 12 indexed citations
12.
Assuncao, Thiago M. de, Nidhi Jalan‐Sakrikar, Steve F. Bronk, et al.. (2017). Development and characterization of cholangioids from normal and diseased human cholangiocytes as an in vitro model to study primary sclerosing cholangitis. Laboratory Investigation. 97(11). 1385–1396. 37 indexed citations
13.
Wang, Ruisi, Qian Ding, Thiago M. de Assuncao, et al.. (2016). Hepatic Stellate Cell Selective Disruption of Dynamin-2 GTPase Increases Murine Fibrogenesis through Up-Regulation of Sphingosine-1 Phosphate–Induced Cell Migration. American Journal Of Pathology. 187(1). 134–145. 5 indexed citations
14.
Wang, Ruisi, Qian Ding, Usman Yaqoob, et al.. (2015). Exosome Adherence and Internalization by Hepatic Stellate Cells Triggers Sphingosine 1-Phosphate-dependent Migration. Journal of Biological Chemistry. 290(52). 30684–30696. 179 indexed citations
15.
Huebert, Robert C. & Jorge Rakela. (2014). Cellular Therapy for Liver Disease. Mayo Clinic Proceedings. 89(3). 414–424. 56 indexed citations
16.
Thabut, Dominique, Chittaranjan Routray, Gwen Lomberk, et al.. (2011). Complementary vascular and matrix regulatory pathways underlie the beneficial mechanism of action of sorafenib in liver fibrosis. Hepatology. 54(2). 573–585. 88 indexed citations
17.
Huebert, Robert C., Kumaravelu Jagavelu, Bing Huang, et al.. (2010). Immortalized liver endothelial cells: a cell culture model for studies of motility and angiogenesis. Laboratory Investigation. 90(12). 1770–1781. 50 indexed citations
18.
Cao, Sheng, Usman Yaqoob, Amitava Das, et al.. (2010). Neuropilin-1 promotes cirrhosis of the rodent and human liver by enhancing PDGF/TGF-β signaling in hepatic stellate cells. Journal of Clinical Investigation. 120(7). 2379–2394. 125 indexed citations
19.
Huebert, Robert C., Uday Shergill, Amitava Das, et al.. (2010). Aquaporin-1 Facilitates Angiogenic Invasion in the Pathological Neovasculature that Accompanies Cirrhosis. Hepatology. 52(1). 238–248. 54 indexed citations
20.
Allina, Jorge, Bin Hu, Daniel M. Sullivan, et al.. (2006). T cell targeting and phagocytosis of apoptotic biliary epithelial cells in primary biliary cirrhosis. Journal of Autoimmunity. 27(4). 232–241. 74 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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