Jody V. Vykoukal

5.6k total citations · 2 hit papers
75 papers, 3.7k citations indexed

About

Jody V. Vykoukal is a scholar working on Molecular Biology, Surgery and Oncology. According to data from OpenAlex, Jody V. Vykoukal has authored 75 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 18 papers in Surgery and 16 papers in Oncology. Recurrent topics in Jody V. Vykoukal's work include Microfluidic and Bio-sensing Technologies (12 papers), Extracellular vesicles in disease (9 papers) and MicroRNA in disease regulation (8 papers). Jody V. Vykoukal is often cited by papers focused on Microfluidic and Bio-sensing Technologies (12 papers), Extracellular vesicles in disease (9 papers) and MicroRNA in disease regulation (8 papers). Jody V. Vykoukal collaborates with scholars based in United States, Germany and Netherlands. Jody V. Vykoukal's co-authors include Peter R. C. Gascoyne, Frederick F. Becker, Eckhard Alt, Ronald Pethig, Yanlan Huang, Matthias Ilmer, Mitja L. Heinemann, Johannes F. Fahrmann, Lukas Prantl and Samir Hanash and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Journal of Clinical Oncology.

In The Last Decade

Jody V. Vykoukal

73 papers receiving 3.6k citations

Hit Papers

Particle separation by dielectrophoresis 1995 2026 2005 2015 2002 1995 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
Jody V. Vykoukal United States 28 2.0k 1.1k 1.1k 559 371 75 3.7k
Han Wei Hou Singapore 31 3.1k 1.5× 674 0.6× 737 0.7× 217 0.4× 498 1.3× 72 4.1k
Bee Luan Khoo Hong Kong 25 2.4k 1.2× 623 0.5× 429 0.4× 574 1.0× 1.1k 2.9× 87 3.5k
Richard B. M. Schasfoort Netherlands 27 2.0k 1.0× 1.6k 1.4× 938 0.9× 107 0.2× 469 1.3× 84 3.8k
Yi‐Chung Tung Taiwan 32 4.0k 2.0× 887 0.8× 641 0.6× 296 0.5× 982 2.6× 109 5.2k
Yingxiao Wang United States 43 1.6k 0.8× 2.9k 2.5× 146 0.1× 315 0.6× 839 2.3× 159 6.2k
Farhad Kosari United States 31 592 0.3× 1.4k 1.2× 166 0.2× 614 1.1× 477 1.3× 68 2.7k
Edmond W. K. Young Canada 33 3.5k 1.7× 810 0.7× 523 0.5× 77 0.1× 418 1.1× 77 4.5k
Rosa S. Schneiderman Israel 24 1.4k 0.7× 762 0.7× 137 0.1× 232 0.4× 387 1.0× 77 3.8k
Irawati Kandela United States 21 1.1k 0.5× 636 0.6× 387 0.4× 154 0.3× 249 0.7× 44 2.4k
Jacoba van der Zee Netherlands 38 3.8k 1.9× 653 0.6× 134 0.1× 238 0.4× 397 1.1× 95 5.1k

Countries citing papers authored by Jody V. Vykoukal

Since Specialization
Citations

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

Fields of papers citing papers by Jody V. Vykoukal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jody V. Vykoukal. 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 Jody V. Vykoukal. The network helps show where Jody V. Vykoukal may publish in the future.

Co-authorship network of co-authors of Jody V. Vykoukal

This figure shows the co-authorship network connecting the top 25 collaborators of Jody V. Vykoukal. A scholar is included among the top collaborators of Jody V. Vykoukal 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 Jody V. Vykoukal. Jody V. Vykoukal 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.
Chen, Yihui, So‐Young Park, Jody V. Vykoukal, et al.. (2025). Citrullinated ENO1 Vaccine Enhances PD-1 Blockade in Mice Implanted with Murine Triple-Negative Breast Cancer Cells. Vaccines. 13(6). 629–629.
2.
Chen, Yihui, Rongzhang Dou, Ehsan Irajizad, et al.. (2025). Integrated Metabolomics and Spatial Transcriptomics of Cystic Pancreatic Cancer Precursors Reveals Dysregulated Polyamine Metabolism as a Biomarker of Progression. Clinical Cancer Research. 31(12). 2454–2465.
3.
Chen, Yihui, et al.. (2023). c-MYC-Driven Polyamine Metabolism in Ovarian Cancer: From Pathogenesis to Early Detection and Therapy. Cancers. 15(3). 623–623. 8 indexed citations
4.
Fahrmann, Johannes F., Ehsan Irajizad, Edwin J. Ostrin, et al.. (2023). Mortality benefit of a blood-based biomarker panel for lung cancer and the PLCO cohort.. Journal of Clinical Oncology. 41(16_suppl). 8560–8560. 1 indexed citations
5.
Chen, Yihui, Ranran Wu, Ehsan Irajizad, et al.. (2023). Kynureninase Upregulation Is a Prominent Feature of NFR2-Activated Cancers and Is Associated with Tumor Immunosuppression and Poor Prognosis. Cancers. 15(3). 834–834. 18 indexed citations
6.
Manyam, Ganiraju C., Jody V. Vykoukal, Johannes F. Fahrmann, et al.. (2023). SPOP Mutations Target STING1 Signaling in Prostate Cancer and Create Therapeutic Vulnerabilities to PARP Inhibitor–Induced Growth Suppression. Clinical Cancer Research. 29(21). 4464–4478. 11 indexed citations
7.
Irajizad, Ehsan, Johannes F. Fahrmann, Tracey L. Marsh, et al.. (2023). Mortality Benefit of a Blood-Based Biomarker Panel for Lung Cancer on the Basis of the Prostate, Lung, Colorectal, and Ovarian Cohort. Journal of Clinical Oncology. 41(27). 4360–4368. 10 indexed citations
8.
Fahrmann, Johannes F., Tracey L. Marsh, Ehsan Irajizad, et al.. (2022). Blood-Based Biomarker Panel for Personalized Lung Cancer Risk Assessment. Journal of Clinical Oncology. 40(8). 876–883. 57 indexed citations
9.
Vykoukal, Jody V., Johannes F. Fahrmann, Nikul Patel, et al.. (2022). Contributions of Circulating microRNAs for Early Detection of Lung Cancer. Cancers. 14(17). 4221–4221. 21 indexed citations
10.
Irajizad, Ehsan, Chae Young Han, Joseph Celestino, et al.. (2022). A Blood-Based Metabolite Panel for Distinguishing Ovarian Cancer from Benign Pelvic Masses. Clinical Cancer Research. 28(21). 4669–4676. 10 indexed citations
11.
Vykoukal, Jody V., et al.. (2021). Extracellular Vesicles in Lung Cancer: Prospects for Diagnostic and Therapeutic Applications. Cancers. 13(18). 4604–4604. 17 indexed citations
12.
Kobayashi, Makoto, Hiroyuki Katayama, Ehsan Irajizad, et al.. (2020). Proteome Profiling Uncovers an Autoimmune Response Signature That Reflects Ovarian Cancer Pathogenesis. Cancers. 12(2). 485–485. 7 indexed citations
13.
Vykoukal, Jody V., Johannes F. Fahrmann, Justin R. Gregg, et al.. (2020). Caveolin-1-mediated sphingolipid oncometabolism underlies a metabolic vulnerability of prostate cancer. Nature Communications. 11(1). 4279–4279. 50 indexed citations
14.
Anker, Alexandra, Lukas Prantl, Catharina Strauss, et al.. (2020). Clinical Impact of DIEP Flap Perforator Characteristics – A Prospective Indocyanine Green Fluorescence Imaging Study. Journal of Plastic Reconstructive & Aesthetic Surgery. 73(8). 1526–1533. 16 indexed citations
15.
Fahrmann, Johannes F., et al.. (2020). Extracellular Vesicles Mediate B Cell Immune Response and Are a Potential Target for Cancer Therapy. Cells. 9(6). 1518–1518. 38 indexed citations
16.
Fahrmann, Johannes F., Xiangying Mao, Ehsan Irajizad, et al.. (2020). Plasma-Derived Extracellular Vesicles Convey Protein Signatures That Reflect Pathophysiology in Lung and Pancreatic Adenocarcinomas. Cancers. 12(5). 1147–1147. 20 indexed citations
17.
Ilmer, Matthias, et al.. (2015). Improved Method for Isolation of Neonatal Rat Cardiomyocytes with Increased Yield of C-Kit+ Cardiac Progenitor Cells. Journal of Stem Cell Research & Therapy. 5(9). 1–8. 20 indexed citations
18.
Ilmer, Matthias, Ivonne Regel, Kenji Yokoi, et al.. (2015). RSPO2 Enhances Canonical Wnt Signaling to Confer Stemness-Associated Traits to Susceptible Pancreatic Cancer Cells. Cancer Research. 75(9). 1883–1896. 59 indexed citations
19.
Ghosn, Mohamad G., Daryl G. Schulz, Jody V. Vykoukal, et al.. (2015). FRESH ADIPOSE TISSUE DERIVED STEM CELLS SIGNIFICANTLY ENHANCE VENTRICULAR FUNCTION IN A CHRONIC PORCINE MYOCARDIAL INFARCTION MODEL. Journal of the American College of Cardiology. 65(10). A1911–A1911. 1 indexed citations
20.
Gehmert, Sebastian, Sanga Gehmert, Lukas Prantl, et al.. (2010). Breast cancer cells attract the migration of adipose tissue-derived stem cells via the PDGF-BB/PDGFR-β signaling pathway. Biochemical and Biophysical Research Communications. 398(3). 601–605. 53 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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