Andrew S. Liss

4.2k total citations
56 papers, 1.8k citations indexed

About

Andrew S. Liss is a scholar working on Oncology, Molecular Biology and Cancer Research. According to data from OpenAlex, Andrew S. Liss has authored 56 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Oncology, 25 papers in Molecular Biology and 24 papers in Cancer Research. Recurrent topics in Andrew S. Liss's work include Pancreatic and Hepatic Oncology Research (29 papers), Cancer Cells and Metastasis (11 papers) and Cancer Genomics and Diagnostics (11 papers). Andrew S. Liss is often cited by papers focused on Pancreatic and Hepatic Oncology Research (29 papers), Cancer Cells and Metastasis (11 papers) and Cancer Genomics and Diagnostics (11 papers). Andrew S. Liss collaborates with scholars based in United States, Japan and Germany. Andrew S. Liss's co-authors include Sarah P. Thayer, Maximilian Weniger, Kim C. Honselmann, Mari Mino–Kenudson, Andrew L. Warshaw, Carlos Fernández‐del Castillo, Keith D. Lillemoe, Meritxell Rovira, Jan Jensen and Steven D. Leach and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Journal of Clinical Oncology.

In The Last Decade

Andrew S. Liss

55 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew S. Liss United States 23 1.1k 735 572 541 183 56 1.8k
Henning Wege Germany 20 526 0.5× 660 0.9× 431 0.8× 345 0.6× 219 1.2× 64 1.8k
Renê Gerhard Brazil 21 985 0.9× 615 0.8× 385 0.7× 365 0.7× 119 0.7× 41 1.8k
Trine Tramm Denmark 21 540 0.5× 626 0.9× 440 0.8× 687 1.3× 173 0.9× 78 1.9k
Hee Jung An South Korea 27 818 0.8× 1.3k 1.7× 313 0.5× 766 1.4× 286 1.6× 76 2.5k
Abha Khanna United States 12 761 0.7× 764 1.0× 504 0.9× 402 0.7× 101 0.6× 28 1.8k
Dahmane Oukrif United Kingdom 18 780 0.7× 671 0.9× 455 0.8× 434 0.8× 128 0.7× 36 1.8k
Meghna Waghray United States 15 623 0.6× 663 0.9× 229 0.4× 261 0.5× 192 1.0× 15 1.4k
Ai Sato Japan 16 592 0.6× 630 0.9× 162 0.3× 352 0.7× 275 1.5× 45 1.4k
Luca Emanuele Pollina Italy 22 1.1k 1.0× 750 1.0× 418 0.7× 566 1.0× 86 0.5× 63 2.1k
Jishu Wei China 27 1.1k 1.0× 904 1.2× 445 0.8× 654 1.2× 418 2.3× 99 2.0k

Countries citing papers authored by Andrew S. Liss

Since Specialization
Citations

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

Fields of papers citing papers by Andrew S. Liss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew S. Liss. 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 Andrew S. Liss. The network helps show where Andrew S. Liss may publish in the future.

Co-authorship network of co-authors of Andrew S. Liss

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew S. Liss. A scholar is included among the top collaborators of Andrew S. Liss 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 Andrew S. Liss. Andrew S. Liss 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.
Ma, Hua, Shadi A. Esfahani, Bahar Ataeinia, et al.. (2024). Allysine-Targeted Molecular MRI Enables Early Prediction of Chemotherapy Response in Pancreatic Cancer. Cancer Research. 84(15). 2549–2560. 4 indexed citations
2.
3.
Ono, Yusuke, Akihiro Hayashi, Kenji Takahashi, et al.. (2023). Multiplex Digital PCR Assay to Detect Multiple KRAS and GNAS Mutations Associated with Pancreatic Carcinogenesis from Minimal Specimen Amounts. Journal of Molecular Diagnostics. 25(6). 367–377. 6 indexed citations
4.
Ferguson, Scott, Katherine S. Yang, Piotr Zelga, et al.. (2022). Single-EV analysis (sEVA) of mutated proteins allows detection of stage 1 pancreatic cancer. Science Advances. 8(16). eabm3453–eabm3453. 75 indexed citations
5.
Birnbaum, David Jérémie, Pascal Finetti, Charles Vanderburg, et al.. (2021). Transcriptomic Analysis of Laser Capture Microdissected Tumors Reveals Cancer- and Stromal-Specific Molecular Subtypes of Pancreatic Ductal Adenocarcinoma. Clinical Cancer Research. 27(8). 2314–2325. 11 indexed citations
6.
Liu, Zhenyang, Tomohiro Kurokawa, Amy Ly, et al.. (2020). A fast, simple, and cost-effective method of expanding patient-derived xenograft mouse models of pancreatic ductal adenocarcinoma. Journal of Translational Medicine. 18(1). 10 indexed citations
7.
Yang, Katherine S., Debora Ciprani, Aileen O’Shea, et al.. (2020). Extracellular Vesicle Analysis Allows for Identification of Invasive IPMN. Gastroenterology. 160(4). 1345–1358.e11. 65 indexed citations
8.
Bausch, Dirk, Stefan Fritz, Louisa Bolm, et al.. (2020). Hedgehog signaling promotes angiogenesis directly and indirectly in pancreatic cancer. Angiogenesis. 23(3). 479–492. 42 indexed citations
9.
Park, Joo Kyung, Thomas Hank, Keith D. Lillemoe, et al.. (2019). Primary and Metastatic Pancreatic Cancer Cells Exhibit Differential Migratory Potentials. Pancreas. 49(1). 128–134.
10.
Weniger, Maximilian, Kim C. Honselmann, & Andrew S. Liss. (2018). The Extracellular Matrix and Pancreatic Cancer: A Complex Relationship. Cancers. 10(9). 316–316. 203 indexed citations
11.
Konnikova, Liza, Gilles Boschetti, Adeeb Rahman, et al.. (2018). High-dimensional immune phenotyping and transcriptional analyses reveal robust recovery of viable human immune and epithelial cells from frozen gastrointestinal tissue. Mucosal Immunology. 11(6). 1684–1693. 25 indexed citations
12.
Saung, May Tun, Armon Sharei, Viktor A. Adalsteinsson, et al.. (2016). A Size‐Selective Intracellular Delivery Platform. Small. 12(42). 5873–5881. 31 indexed citations
13.
Yamaguchi, Junpei, Mari Mino–Kenudson, Andrew S. Liss, et al.. (2016). Loss of Trefoil Factor 2 From Pancreatic Duct Glands Promotes Formation of Intraductal Papillary Mucinous Neoplasms in Mice. Gastroenterology. 151(6). 1232–1244.e10. 38 indexed citations
14.
Valsangkar, Nakul P., Thun Ingkakul, Camilo Correa‐Gallego, et al.. (2015). Survival in ampullary cancer: Potential role of different KRAS mutations. Surgery. 157(2). 260–268. 32 indexed citations
15.
Cauley, Christy E., Martha B. Pitman, Jiahua Zhou, et al.. (2015). Circulating Epithelial Cells in Patients with Pancreatic Lesions: Clinical and Pathologic Findings. Journal of the American College of Surgeons. 221(3). 699–707. 62 indexed citations
16.
Kulemann, Birte, Martha B. Pitman, Andrew S. Liss, et al.. (2015). Circulating Tumor Cells Found in Patients With Localized and Advanced Pancreatic Cancer. Pancreas. 44(4). 547–550. 82 indexed citations
17.
Yamaguchi, Junpei, Andrew S. Liss, Alexandra Sontheimer-Phelps, et al.. (2015). Pancreatic duct glands (PDGs) are a progenitor compartment responsible for pancreatic ductal epithelial repair. Stem Cell Research. 15(1). 190–202. 45 indexed citations
18.
Rovira, Meritxell, et al.. (2009). Isolation and characterization of centroacinar/terminal ductal progenitor cells in adult mouse pancreas. Proceedings of the National Academy of Sciences. 107(1). 75–80. 225 indexed citations
19.
Tong, Songyang, Andrew S. Liss, M. James You, & Henry R. Bose. (2006). The activation of TC10, a Rho small GTPase, contributes to v-Rel-mediated transformation. Oncogene. 26(16). 2318–2329. 4 indexed citations
20.
Králová, Jarmila, et al.. (1998). AP-1 Factors Play an Important Role in Transformation Induced by the v- rel Oncogene. Molecular and Cellular Biology. 18(5). 2997–3009. 34 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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